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-- Host:                         127.0.0.1
-- Server version:               5.7.22-0ubuntu18.04.1 - (Ubuntu)
-- Server OS:                    Linux
-- HeidiSQL Version:             9.5.0.5280
-- --------------------------------------------------------

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/*!40101 SET NAMES utf8 */;
/*!50503 SET NAMES utf8mb4 */;
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-- Dumping database structure for gslbase
CREATE DATABASE IF NOT EXISTS `gslbase` /*!40100 DEFAULT CHARACTER SET utf8 */;
USE `gslbase`;

-- Dumping structure for table gslbase.coexpressions
CREATE TABLE IF NOT EXISTS `coexpressions` (
  `agi_id` varchar(255) COLLATE utf8_unicode_ci NOT NULL DEFAULT '',
  `gene_name` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  `protein_name` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  `synonym` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  `entrez_gene` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  `refseq_mrna` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  `refseq_protein` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  `uniprot` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  `ec_number` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  `length` int(11) DEFAULT NULL,
  `gsl_type` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  PRIMARY KEY (`agi_id`),
  KEY `agi_id` (`agi_id`),
  KEY `uniprot` (`uniprot`)
) ENGINE=InnoDB DEFAULT CHARSET=utf8 COLLATE=utf8_unicode_ci;

-- Dumping data for table gslbase.coexpressions: ~778 rows (approximately)
/*!40000 ALTER TABLE `coexpressions` DISABLE KEYS */;
INSERT INTO `coexpressions` (`agi_id`, `gene_name`, `protein_name`, `synonym`, `entrez_gene`, `refseq_mrna`, `refseq_protein`, `uniprot`, `ec_number`, `length`, `gsl_type`) VALUES
	('AT1G01120', 'KCS1', '3-ketoacyl-CoA synthase 1 ', 'EL1', '839395', 'NM_099994.4', 'NP_171620.2', 'Q9MAM3', '2.3.1.199', 528, 'Potential GSL genes'),
	('AT1G01390', 'UGT72B2', 'UDP-glycosyltransferase 72B2 ', 'F6F3.19', '837790', 'NM_100021.3', 'NP_171646.1', 'Q8W4C2', '2.4.1.-', 480, 'Potential GSL genes'),
	('AT1G01470', 'LEA14', 'Probable desiccation-related protein LEA14', 'F22L4.3', '837071', 'NM_100029.6', 'NP_171654.1', 'O03983', '', 151, 'Potential GSL genes'),
	('AT1G01480', 'ACS2', '1-aminocyclopropane-1-carboxylate synthase 2 ', 'ACC1', '837082', '?NM_100030.4?', 'NP_171655.1?', 'Q06402', '', 496, 'Potential camalexin genes'),
	('AT1G01560', 'MPK11', 'Mitogen-activated protein kinase 11 ', 'F22L4.10', '839523', '?NM_001123738.2?', 'NP_001117210.1?', 'Q9LMM5', '2.7.11.24', 369, 'Potential camalexin genes'),
	('AT1G02500', 'SAM1', 'S-adenosylmethionine synthase 1 ', 'T14P4.17 ', '839501', '?NM_100131.3', 'NP_171751.1?', 'P23686', '2.5.1.6', 393, 'Potential camalexin genes'),
	('AT1G02920', 'GSTF7', 'Glutathione S-transferase F7  ', 'GST11', '839295', 'NM_100173.4', 'NP_171791.1', 'Q9SRY5', '2.5.1.18', 209, 'Potential GSL genes'),
	('AT1G02930', 'GSTF6', 'Glutathione S-transferase F6', 'ERD11', '839515', 'NM_100174.3', 'NP_171792.1', 'P42760', '2.5.1.18', 208, 'Potential GSL genes'),
	('AT1G02940', 'GSTF5', 'Glutathione S-transferase F5 ', 'F22D16.5', '839479', 'NM_100175.2', 'NP_171793.1', 'Q9SRY6', '2.5.1.18', 256, 'Potential GSL genes'),
	('AT1G02950', 'GSTF4', 'Glutathione S-transferase F4 ', 'GST31', '838240', 'NM_179250.1', 'NP_849581.1', 'Q84TK0', '2.5.1.18', 245, 'Potential GSL genes'),
	('AT1G03400', 'F21B7.39', '1-aminocyclopropane-1-carboxylate oxidase homolog 4', 'F21B7.39', '838751', 'NM_100222.3', 'NP_171839.1', 'Q94A78', '1.14.-.-', 351, 'Potential GSL genes'),
	('AT1G03410', '2A6 ', '1-aminocyclopropane-1-carboxylate oxidase homolog 5', 'F21B7.3', '838763', 'NM_100223.3', 'NP_171840.2', 'Q43383', '1.14.-.-', 398, 'Potential GSL genes'),
	('AT1G03820', 'F11M21.25', 'Putative uncharacterized protein At1g03820', '', '839400', 'NM_100261', 'NP_171878', 'Q9ZWA4', '', 222, 'Potential GSL genes'),
	('AT1G03980', 'ATPCS2', 'Glutathione gamma-glutamylcysteinyltransferase 2 ', 'PCS2', '839354', 'NM_100279', 'NP_171894', 'Q9ZWB7', '2.3.2.15', 452, 'Potential GSL genes'),
	('AT1G04350', 'F19P19.22', '1-aminocyclopropane-1-carboxylate oxidase homolog 6', 'F19P19.22', '839542', 'NM_100315.4', 'NP_171930.1', 'P93824', '1.14.-.-', 360, 'Potential GSL genes'),
	('AT1G04380', 'F19P19.18', '1-aminocyclopropane-1-carboxylate oxidase homolog 7', 'F19P19.18   ', '839535', 'NM_100318.5', 'NP_171933.1', 'P93821', '1.14.-.-', 345, 'Potential GSL genes'),
	('AT1G04710', 'KAT1', '3-ketoacyl-CoA thiolase 1, peroxisomal ', 'T1G11.4', '839434', 'NM_100351.5', 'NP_171965.1', 'Q8LF48', '2.3.1.16 ', 443, 'Potential GSL genes'),
	('AT1G05010', 'ACO4', '1-aminocyclopropane-1-carboxylate oxidase 4 ', 'ACO1', '839345', '?NM_100380.4', 'NP_171994.1?', 'Q06588', '', 323, 'Potential camalexin genes'),
	('AT1G05560', 'UGT1', 'UDP-glycosyltransferase 75B1 ', 'T25N20.20', '837058', '?NM_100435.3', 'NP_563742.1?', 'Q9LR44', '', 469, 'Potential camalexin genes'),
	('AT1G05680', 'UGT74E2', 'UDP-glycosyltransferase 74E2 ', 'F3F20.13', '837075', '?NM_100448.4', 'NP_172059.1?', 'Q9SYK9', '', 453, 'Potential camalexin genes'),
	('AT1G06000', 'UGT89C1', 'UDP-glycosyltransferase 89C1 ', 'T21E18.5', '837109', 'NM_100480.3', 'NP_563756.1', 'Q9LNE6', '2.4.1.- ', 435, 'Potential GSL genes'),
	('AT1G06160', 'ERF094', 'Ethylene-responsive transcription factor ERF094 ', 'ORA59', '837125', 'NM_100497', 'NP_172106', 'Q9LND1', '', 244, 'Potential GSL genes TF'),
	('AT1G06570', 'HPD', '4-hydroxyphenylpyruvate dioxygenase ', 'PDS1', '837168', '?NM_100536.4?', 'NP_172144.3?', 'P93836', '', 445, 'Potential camalexin genes'),
	('AT1G06620', 'F12K11.24 ', '1-aminocyclopropane-1-carboxylate oxidase homolog 1', '  ', '837171', 'NM_100539.3', 'NP_172147.2', 'Q84MB3', '1.14.-.-', 365, 'Potential GSL genes'),
	('AT1G06640', 'AT1G06640', '1-aminocyclopropane-1-carboxylate oxidase homolog 2', 'F12K11.27', '837173', 'NM_202045', 'NP_973774', 'Q9C5K7', '', 369, 'Potential GSL genes'),
	('AT1G06645', 'F12K11.6', '2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein', ' ', '3766668', 'NM_001160843.2', 'NP_001154315.2', 'F4IDQ2', '', 379, 'Potential GSL genes'),
	('AT1G06830', 'GRXS11', 'Monothiol glutaredoxin-S11 ', 'ROXY6', '837195', 'NM_100560', 'NP_172168', 'Q9M9Y9', '', 99, 'Potential GSL genes'),
	('AT1G07260', 'UGT71C3', 'UDP-glycosyltransferase 71C3 ', 'F10K1.3', '837237', 'NM_100600', 'NP_172206', 'Q9LML7', '2.4.1.-', 476, 'Potential GSL genes'),
	('AT1G07610', 'MT1C', 'Metallothionein-like protein 1C ', 'F22G5_34', '837274', 'NM_100634.2', 'NP_172240.1', 'Q38804', '', 45, 'Potential GSL genes'),
	('AT1G07780', 'PAI1', 'N-5\'-phosphoribosylanthranilate isomerase 1, chloroplastic ', 'TRP6', '837292', 'NM_202055', 'NP_973784', 'Q42440', '5.3.1.24', 275, 'Potential GSL genes'),
	('AT1G07890', 'APX1', 'L-ascorbate peroxidase 1, cytosolic ', 'F24B9.2', '837304', 'NM_202057.2', 'NP_973786.1', 'Q05431', '1.11.1.11', 250, 'Potential GSL genes'),
	('AT1G07920', 'A3', 'Elongation factor 1-alpha 3 ', 'T6D22.2', '836161', 'NM_100668.3', 'NP_563801.1', 'Q0WL56', '', 449, 'Potential GSL genes'),
	('AT1G07930', 'A2', 'Elongation factor 1-alpha 2 ', 'T6D22.31', '836161', 'NM_100668.3', 'NP_563801.1', 'Q8W4H7', '', 449, 'Potential GSL genes'),
	('AT1G07940', 'A1', 'Elongation factor 1-alpha 1 ', 'T6D22.3', '836161', 'NM_100668.3', 'NP_563801.1', 'P0DH99', '', 449, 'Potential GSL genes'),
	('AT1G08920', 'SUGTL2', 'Sugar transporter ERD6-like 3 ', 'F7G19.20', '837413', 'NM_179287', 'NP_849618', 'Q94KE0', '', 470, 'Potential GSL genes'),
	('AT1G08930', 'ERD6', 'Sugar transporter ERD6 ', 'SUGTL1', '837414', 'NM_100765', 'NP_563830', 'O04036', '', 496, 'Potential GSL genes'),
	('AT1G09240', 'NAS3', 'Nicotianamine synthase 3 ', 'T12M4.5', '837444', '?NM_100794.4', 'NP_172395.1?', 'O80483', '', 320, 'Potential camalexin genes'),
	('AT1G09430', 'ACLA-3', 'ATP-citrate synthase alpha chain protein 3 ', 'F19J9.9', '837466', '?NM_100814.4', 'NP_172414.1?', 'O80526', '2.3.3.8, 6.2.1.5', 424, 'Potential camalexin genes'),
	('AT1G09500', 'At1g09500', 'At1g09500/F14J9_16 ', 'F14J9.16 ', '837475', '?NM_100821.3', 'NP_172421.1?', 'O80533', '', 325, 'Potential camalexin genes'),
	('AT1G10060', 'BCAT-1', 'Branched-chain-amino-acid aminotransferase 1, mitochondrial ', 'ATBCAT-1', '837542', 'NM_179298', 'NP_849629', 'Q93Y32', '2.6.1.42', 384, 'Potential GSL genes'),
	('AT1G10070', 'BCAT-2', 'Branched-chain-amino-acid aminotransferase 2, chloroplastic ', 'ATBCAT-2', '837543', 'NM_100881', 'NP_172478', 'Q9M439', '2.6.1.42', 388, 'Potential GSL genes'),
	('AT1G10630', 'ATARFA1F', 'ADP-ribosylation factor A1F ', 'F20B24.7', '837606', '?NM_001331919.1', 'NP_001321560.1?', 'Q6ID97', '', 181, 'Potential camalexin genes'),
	('AT1G10900', 'PIP5K7', 'Phosphatidylinositol 4-phosphate 5-kinase 7 ', 'P5K2', '837633', 'NM_100965.5', 'NP_172559.2', 'Q9SUI2', '2.7.1.68', 754, 'Potential GSL genes'),
	('AT1G11580', 'ATPMEPCRA', 'Pectinesterase/pectinesterase inhibitor 18 ', 'PMEPCRA', '837701', 'NM_101031', 'NP_172624', 'Q1JPL7', '3.1.1.11\n3.2.2.22', 557, 'Potential GSL genes'),
	('AT1G11790', 'ADT1', 'Arogenate dehydratase/prephenate dehydratase 1, chloroplastic ', 'PDT1', '837725', '?NM_001035947.1?', 'NP_001031024.1?', 'Q9SA96', '4.2.1.51', 392, 'Potential camalexin genes'),
	('AT1G11840', 'GLX1', 'Lactoylglutathione lyase GLX1 ', 'F12F1.32', '837731', 'NM_179313.2', 'NP_849644.2', 'O65398', '4.4.1.5', 283, 'Potential GSL genes'),
	('AT1G11860', 'GDCST', 'Aminomethyltransferase, mitochondrial ', 'GDT1', '837733', 'NM_179315.1', 'NP_849646.1', 'O65396', '2.1.2.10', 408, 'Potential GSL genes'),
	('AT1G12110', 'NPF6.3', 'Protein NRT1/ PTR FAMILY 6.3 ', 'CHL1', '837763', 'NM_101083.4', 'NP_563899.1', 'Q05085', '', 590, 'Potential GSL genes'),
	('AT1G12130', 'FMO GS-OX-like 6', 'Flavin-containing monooxygenase FMO GS-OX-like 6', 'T28K15.13', '837765', 'NM_101085.2', 'NP_172677.1', 'Q9FWW3', '1.8.-.-', 470, 'Potential GSL genes'),
	('AT1G12160', 'FMO GS-OX-like 1', 'Flavin-containing monooxygenase FMO GS-OX-like 1', 'T28K15.10', '837768', 'NM_101088.4', 'NP_172680.1', 'Q9FWW6', '1.8.-.-', 468, 'Potential GSL genes'),
	('AT1G12200', 'AT1G12200', 'Flavin-containing monooxygenase FMO GS-OX-like 2 ', 'T28K15.7', '837773', 'NM_101092', 'NP_172684', 'Q9FWW9', '1.8.-.-', 465, 'Potential GSL genes'),
	('AT1G13430', 'STO9', 'Cytosolic sulfotransferase 9 ', 'ST4C', '837903', 'NM_101213.3', 'NP_172800.2', 'Q9FX55', '2.8.2.- ', 351, 'Potential GSL genes'),
	('AT1G14120', 'At1g14120', '2-oxoglutarate 2OG and FeII-dependent oxygenase superfamily protein', 'F7A19.20', '837971', 'NM_101277.3', 'NP_172864.1', 'Q9XI76', '', 312, 'Potential GSL genes'),
	('AT1G14130', 'F7A19.21', '2-oxoglutarate 2OG and FeII-dependent oxygenase-like protein', 'At1g14130', '837972', 'NM_101278', 'NP_172865', 'Q9XI75', '', 308, 'Potential GSL genes'),
	('AT1G14370', 'PBL2', 'Probable serine/threonine-protein kinase PBL2 ', 'APK2A', '837999', '?NM_101304.4', 'NP_172889.1?', 'O49839', '', 426, 'Potential camalexin genes'),
	('AT1G14870', 'PCR2', 'Protein PLANT CADMIUM RESISTANCE 2 ', 'F10B6.27', '838052', '?NM_101356.5', 'NP_172940.1?', 'Q9LQU4', '', 152, 'Potential camalexin genes'),
	('AT1G15520', 'ABCG40', 'ABC transporter G family member 40 ', 'PDR12', '838122', '?NM_101421.3', 'NP_173005.1?', 'Q9M9E1', '', 1423, 'Potential camalexin genes'),
	('AT1G15750', 'TPL', 'Protein TOPLESS (WUS-interacting protein 1)', 'WSIP1', '838144', '?NM_001035973.3', 'NP_001031050.1?', 'Q94AI7', '', 1131, 'Potential camalexin genes'),
	('AT1G15950', 'CCR1', 'Cinnamoyl-CoA reductase 1', 'IRX4', '838165', 'NM_101463.4', 'NP_173047.1', 'Q9S9N9', '1.2.1.44 ', 344, 'Potential GSL genes'),
	('AT1G16030', 'HSP70-5', 'Heat shock 70 kDa protein 5 ', 'HSP70B', '838174', 'NM_101471.3', 'NP_173055.1', 'Q9S9N1', '', 646, 'Potential GSL genes'),
	('AT1G16060', 'ADAP', 'AP2-like ethylene-responsive transcription factor At1g16060', 'T24D18.16', '838176', 'NM_202110', 'NP_973839', 'Q94AN4', '', 345, 'Potential GSL genes TF'),
	('AT1G17380', 'TIFY11A', 'Protein TIFY 11A ', 'JAZ5', '838310', 'NM_101599.3', 'NP_564019.1', 'Q9LDU5', '', 274, 'Potential GSL genes'),
	('AT1G17420', 'LOX3', 'Lipoxygenase 3, chloroplastic ', 'At1g17420', '838314', 'NM_101603.3', 'NP_564021.1', 'Q9LNR3', '1.13.11.12', 919, 'Potential GSL genes'),
	('AT1G17745', 'PGDH2', 'D-3-phosphoglycerate dehydrogenase 2, chloroplastic ', '3-PGDH', '838352', 'NM_101636.3', 'NP_564034.1', 'O04130', '1.1.1.95', 624, 'Potential GSL genes'),
	('AT1G18500', 'MAML-4', '2-isopropylmalate synthase 1, chloroplastic ', 'IPMS1', '838431', 'NM_101708', 'NP_173285', 'Q9LPR4', '2.3.3.13', 631, 'Potential GSL genes'),
	('AT1G18570', 'MYB51', 'Transcription factor MYB51 ', 'HIG1', '838438', '?NM_101715.4', 'NP_173292.1?', 'O49782', '', 352, 'Potential camalexin genes TF'),
	('AT1G18870', 'ICS2', 'Isochorismate synthase 2, chloroplastic ', 'F6A14.3', '838468', '?NM_001160879.1', 'NP_001154351.1?', 'Q9M9V6', '5.4.4.2', 562, 'Potential camalexin genes'),
	('AT1G18880', 'NPF2.9', 'Protein NRT1/ PTR FAMILY 2.9 AtNPF2.9 ', 'NRT1.9', '838469', 'NM_101745.5', 'NP_173322.1', 'Q9M9V7', '', 587, 'Potential GSL genes'),
	('AT1G19180', 'TIFY10A', 'Protein TIFY 10A Jasmonate ZIM domain-containing protein 1', 'JAZ1', '838501', 'NM_101776.3', 'NP_564075.1', 'Q9LMA8', '', 253, 'Potential GSL genes'),
	('AT1G19300', 'GATL1', 'Probable galacturonosyltransferase-like 1  ', 'GLZ1', '838512', 'NM_101787.3', 'NP_564077.1', 'Q9LN68', '2.4.1.-', 351, 'Potential GSL genes'),
	('AT1G19640', 'JMT', 'Jasmonate O-methyltransferase ', 'F14P1.3', '838551', '?NM_101820.4', 'NP_173394.1?', 'Q9AR07', '', 389, 'Potential camalexin genes'),
	('AT1G19670', 'ATCLH1', 'Chlorophyllase-1 ', 'CORI1', '838554', 'NM_101823', 'NP_564094', 'O22527', '3.1.1.14', 324, 'Potential GSL genes'),
	('AT1G19920', 'APS2', 'ATP sulfurylase 2 ', 'ASA1', '838580', 'NM_101847', 'NP_564099', 'Q43870', '2.7.7.4', 476, 'Potential GSL genes'),
	('AT1G20160', 'CRSP', 'CO2-response secreted protease ', 'SBT5.2', '838606', 'NM_101870.3', 'NP_564107.1', 'Q9LNU1', '3.4.14.10', 769, 'Potential GSL genes'),
	('AT1G20510', 'OPCL1', '4-coumarate--CoA ligase-like 5 ', '', '838639', 'NM_202143', 'NP_973872', 'Q84P21', '6.2.1.-', 546, 'Potential GSL genes'),
	('AT1G20560', 'AAE1', 'Probable acyl-activating enzyme 1, peroxisomal ', 'AMPBP1', '838644', 'NM_101906.4', 'NP_564116.1', 'F4HUK6', '6.2.1.-', 556, 'Potential GSL genes'),
	('AT1G20620', 'CAT3', 'Catalase-3 ', 'F2D10.40', '838651', 'NM_202144', 'NP_973873', 'Q42547', '1.11.1.6', 492, 'Potential GSL genes'),
	('AT1G20823', 'ATL80', 'RING-H2 finger protein ATL80 ', 'At1g20823', '838674', 'NM_101935.3', 'NP_173506.1', 'Q9LM69', '2.3.2.27', 197, 'Potential GSL genes'),
	('AT1G21110', 'IGMT3 ', 'Indole glucosinolate O-methyltransferase 3', 'At1g21110', '838707', 'NM_101965.3', 'NP_173535.1', 'Q9LPU6', '2.1.1.-', 373, 'Potential GSL genes'),
	('AT1G21130', 'IGMT4', 'Indole glucosinolate O-methyltransferase 4 ', 'T22I11.4', '838709', 'NM_179362', 'NP_849693', 'Q9LPU8', '2.1.1.-', 373, 'Potential GSL genes'),
	('AT1G21250', 'WAK1', 'Wall-associated receptor kinase 1', 'PRO25', '838721', 'NM_101978.5', 'NP_564137.1', 'Q39191', '2.7.11.-', 735, 'Potential GSL genes'),
	('AT1G21440', 'F24J8.7', 'Phosphoenolpyruvate carboxylase family protein', '', '838742', 'NM_101995', 'NP_173565', 'Q501F7', '', 336, 'Potential GSL genes'),
	('AT1G21590', 'F24J8.18', 'Kinase with adenine nucleotide alpha hydrolases-like domain-containing protein', 'F24J8_18', '838760', 'NM_102008.5', 'NP_173578.2', 'Q8VZG4', '', 756, 'Potential GSL genes'),
	('AT1G22360', 'AtUGT85A2', 'UDP-glycosyltransferase 85A2 ', 'UGT85A2', '838843', 'NM_102086', 'NP_173653', 'Q9ZWJ3', '2.4.1.-', 481, 'Potential GSL genes'),
	('AT1G22380', 'UGT85A3', 'UDP-glycosyltransferase 85A3 ', 'F12K8.28 ', '838845', '?NM_102088.3', 'NP_173655.2?', 'Q9LMF1', '', 488, 'Potential camalexin genes'),
	('AT1G22410', 'F12K8.24', 'Phospho-2-dehydro-3-deoxyheptonate aldolase ', '', '838847', 'NM_102090', 'NP_173657', 'Q9SK84', '2.5.1.54', 527, 'Potential GSL genes'),
	('AT1G22710', 'SUC2', 'Sucrose transport protein SUC2', 'SUT1', '838877', 'NM_102118.4', 'NP_173685.1', 'Q39231', '', 512, 'Potential GSL genes'),
	('AT1G23020', 'FRO3', 'Ferric reduction oxidase 3, mitochondrial ', 'FROHC', '838910', '?NM_001198138.1?', 'NP_001185067.1?', 'F4I4K7', '', 717, 'Potential camalexin genes'),
	('AT1G23310', 'GGAT1', 'Glutamate--glyoxylate aminotransferase 1 ', 'AOAT1', '838940', '?NM_001036006.1?', 'NP_001031083.1?', 'Q9LR30', '', 481, 'Potential camalexin genes'),
	('AT1G23800', 'ALDH2B7', 'Aldehyde dehydrogenase family 2 member B7, mitochondrial ALDH2b ', 'ALDH3', '838991', 'NM_102228.4', 'NP_564204.1', 'Q8S528', '1.2.1.3', 534, 'Potential GSL genes'),
	('AT1G23850', 'AT1G23850', 'Putative uncharacterized protein At1g23850 ', 'T23E23.1', '838996', 'NM_102233', 'NP_564207', 'Q9LRA9', '', 354, 'Potential GSL genes'),
	('AT1G24575', 'At1g24575', 'DEAD-box ATP-dependent RNA helicase-like protein', '', '839072', 'NM_102300.3', 'NP_564220.1', 'Q8LAL6', '', 88, 'Potential GSL genes'),
	('AT1G25220', 'ASB1', 'Anthranilate synthase beta subunit 1, chloroplastic ', 'TRP4', '839103', 'NM_102331.3', 'NP_173893.1', 'Q42565', '', 276, 'Potential GSL genes'),
	('AT1G26380', 'FOX1', 'Berberine bridge enzyme-like 3 ', 'FOX', '839180', '?NM_102402.4', 'NP_564244.1?', 'Q9FZC4', '', 535, 'Potential camalexin genes'),
	('AT1G26410', 'FOX4', 'Berberine bridge enzyme-like 6 ', 'T1K7.21', '839183', '?NM_102405.3', 'NP_173965.1?', 'Q9FZC7', '', 552, 'Potential camalexin genes'),
	('AT1G26420', 'FOX5', 'Berberine bridge enzyme-like 7 ', 'T1K7.20', '839184', '?NM_102406.3', 'NP_173966.1?', 'Q9FZC8', '', 529, 'Potential camalexin genes'),
	('AT1G27030', 'AT1G27030', 'At1g27030/T7N9_9 ', '', '839592', 'NM_102465', 'NP_564270', 'Q9LFY3', '', 310, 'Potential GSL genes'),
	('AT1G27130', 'GSTU13', 'Glutathione S-transferase U13 ', 'GST12', '839602', 'NM_102475', 'NP_174033', 'Q9FUS6', '2.5.1.18', 227, 'Potential GSL genes '),
	('AT1G27450', 'APT1', 'Adenine phosphoribosyltransferase 1, chloroplastic ', 'APT', '839636', '?NM_001332762.1?', 'NP_001323015.1?', 'P31166', '2.4.2.7', 243, 'Potential camalexin genes'),
	('AT1G28600', 'At1g28600', 'GDSL esterase/lipase At1g28600 ', 'F1K23.6', '839760', 'NM_102628.4', 'NP_174182.1', 'Q94F40', '3.1.1.- ', 393, 'Potential GSL genes'),
	('AT1G28610', 'AT1G28610', 'GDSL esterase/lipase At1g28610 ', 'F1K23.16', '839761', 'NM_202203', 'NP_973932', 'Q9SHP6', '3.1.1.-', 383, 'Potential GSL genes'),
	('AT1G28680', 'At1g28680', 'Uncharacterized protein', 'AXX17_At1g29150', '839768', 'NM_102635.3', 'NP_174189.1', 'A0A178WKU1', '', 451, 'Potential GSL genes'),
	('AT1G29410', 'PAI3', 'PHOSPHORIBOSYLANTHRANILATE ISOMERASE 3', 'F15D2.31', '839817', 'NM_180623', 'NP_850954', 'Q8LPI9', '5.3.1.24', 244, 'Potential GSL genes'),
	('AT1G29900', 'CARB', 'Carbamoyl-phosphate synthase large chain, chloroplastic ', 'VEN3', '839868', '?NM_102730.2', 'NP_564338.1?', 'Q42601', '6.3.5.5', 1187, 'Potential camalexin genes'),
	('AT1G30120', 'PDH-E1 BETA', 'Pyruvate dehydrogenase E1 component subunit beta-2, chloroplastic ', 'E1-BETA-1', '839891', '?NM_102751.5', 'NP_174304.1?', 'Q9C6Z3', '', 406, 'Potential camalexin genes'),
	('AT1G30530', 'UGT78D1', 'UDP-glycosyltransferase 78D1 ', 'F26G16.15', '839933', '?NM_102790.4', 'NP_564357.1?', 'Q9S9P6', '', 453, 'Potential camalexin genes'),
	('AT1G30700', 'At1g30700', 'Berberine bridge enzyme-like 8 ', 'T5I8.15', '839950', '?NM_102806.3', 'NP_174357.1?', 'Q9SA85', '', 527, 'Potential camalexin genes'),
	('AT1G31180', 'IMDH1', '3-isopropylmalate dehydrogenase 1, chloroplastic ', 'F28K20.14', '840006', 'NM_102856.3', 'NP_174403.1', 'Q9SA14', '1.1.1.85', 404, 'Potential GSL genes'),
	('AT1G31230', 'AT1G31230', 'Bifunctional aspartokinase/homoserine dehydrogenase 1, chloroplastic', 'F28K20.19', '840011', 'NM_102861', 'NP_174408', 'Q9SA18', '2.7.2.4\n1.1.1.3', 911, 'Potential GSL genes'),
	('AT1G31550', 'At1g31550', 'GDSL esterase/lipase At1g31550 ', 'F27M3.22', '840045', 'NM_102894.4', 'NP_174440.2', 'Q9C857', '3.1.1.-', 394, 'Potential GSL genes'),
	('AT1G31710', 'AT1G31710', 'Amine oxidase ', 'F27M3_9', '840058', 'NM_102906', 'NP_174452', 'Q8GZ62', '1.4.3.-', 557, 'Potential GSL genes'),
	('AT1G31770', 'ABCG14', 'ABC transporter G family member 14 ', '', '840064', 'NM_102911', 'NP_564383', 'Q9C6W5', '', 649, 'Potential GSL genes'),
	('AT1G32480', 'IDH-IV', 'Putative isocitrate dehydrogenase [NAD] subunit-like 4 ', 'F5D14.26', '840142', 'NM_102983', 'NP_174526', 'Q9LQK9', '', 294, 'Potential GSL genes'),
	('AT1G32870', 'ANAC13', 'NAC domain-containing protein 13 ', 'NTL1', '840181', '?NM_001123929.1', 'NP_001117401.1?', 'F4IED2', '', 528, 'Potential camalexin genes'),
	('AT1G33260', 'At1g33260', 'Probable receptor-like protein kinase', 'T16O9.6', '840220', 'NM_202227.1', 'NP_973956.1', 'P0DKI6', '2.7.11.1', 349, 'Potential GSL genes'),
	('AT1G34430', 'EMB3003', 'Dihydrolipoyllysine-residue acetyltransferase component 5 of pyruvate dehydrogenase complex, chloroplastic ', 'F12K21.24', '840346', '?NM_103166.4', 'NP_174703.1?', 'Q9C8P0', '', 465, 'Potential camalexin genes'),
	('AT1G35260', 'MLP165', 'MLP-like protein 165', 'T9I1.17', '840415', 'NM_103224', 'NP_564456', 'Q9C7I7', '', 152, 'Potential GSL genes'),
	('AT1G35720', 'ANN1', 'Annexin D1 AnnAt1 Annexin A1', 'ANNAT1', '840476', 'NM_103274.4', 'NP_174810.1', 'Q9SYT0', '', 317, 'Potential GSL genes'),
	('AT1G36160', 'ACC1', 'Acetyl-CoA carboxylase 1 AtACC1  ', 'EMB22', '840521', 'NM_103313.4', 'NP_174849.2', 'Q38970', '6.4.1.2\n6.3.4.14', 2254, 'Potential GSL genes'),
	('AT1G37130', 'NIA2', 'Nitrate reductase [NADH] 2 ', 'NR2', '840630', 'NM_103364', 'NP_174901', 'P11035', '1.7.1.1', 917, 'Potential GSL genes'),
	('AT1G43160', 'RAP2.6', 'Ethylene-responsive transcription factor RAP2-6 ', 'ERF108', '840915', 'NM_103468', 'NP_175008', 'Q7G1L2', '', 192, 'Potential GSL genes TF'),
	('AT1G44100', 'AAP5', 'Amino acid permease 5 ', 'At1g44100', '841013', 'NM_103536.4', 'NP_175076.2', 'Q8GUM3', '', 480, 'Potential GSL genes'),
	('AT1G44170', 'ALDH3H1', 'Aldehyde dehydrogenase family 3 member H1 ', 'ALDH4', '841020', 'NM_103541.3', 'NP_849770.1', 'Q70DU8', '1.2.1.3', 484, 'Potential GSL genes'),
	('AT1G44350', 'ILL6', 'IAA-amino acid hydrolase ILR1-like 6 ', 'GR1', '841026', 'NM_103546', 'NP_175086', 'Q8VYX0', '3.5.1.-', 464, 'Potential GSL genes'),
	('AT1G44800', 'AT1G44800', 'WAT1-related protein At1g44800', 'T12C22.7', '841044', 'NM_103561', 'NP_175101', 'Q9LPF1', '', 370, 'Potential GSL genes'),
	('AT1G48850', 'EMB1144', 'Chorismate synthase, chloroplastic ', 'F27K7.1', '841307', 'NM_103779', 'NP_564534', 'P57720', '4.2.3.5', 436, 'Potential GSL genes'),
	('AT1G49230', 'ATL78', 'RING-H2 finger protein', 'F27J15.2', '841346', 'NM_103813', 'NP_175349', 'Q6NQG7', '', 219, 'Potential GSL genes'),
	('AT1G49470', 'F13F21.10', 'F13F21.10 protein Uncharacterized protein', '', '841370', 'NM_103835', 'NP_564546', 'Q9XIB3', '', 302, 'Potential GSL genes'),
	('AT1G49860', 'GSTF14', 'Glutathione S-transferase F14 ', 'F10F5.9', '841409', 'NM_103873.5', 'NP_175408.1', 'Q9C6C8', '2.5.1.18 ', 254, 'Potential GSL genes'),
	('AT1G50090', 'BCAT7', 'Putative branched-chain-amino-acid aminotransferase 7 ', 'F2J10.5', '841432', 'NM_103896', 'NP_175430', 'Q9LPM8', '', 367, 'Potential GSL genes'),
	('AT1G51490', 'TGG6 ', 'Putative myrosinase 6', 'At1g51490', '841574', 'NM_001333491.1', 'NP_001319196.1', 'Q9C8K1', '3.2.1.147', 484, 'Potential GSL genes'),
	('AT1G51680', '4CL1', '4-coumarate--CoA ligase 1', 'F19C24.11', '841593', 'NM_104046.3', 'NP_849793.1', 'Q42524', '6.2.1.12 ', 561, 'Potential GSL genes'),
	('AT1G52000', 'JAL5', 'Jacalin-related lectin 5', 'F5F19.6', '841629', 'NM_104081.4', 'NP_175612.1', 'Q9ZU23', '', 730, 'Potential GSL genes'),
	('AT1G52400', 'BGL1', 'Beta-D-glucopyranosyl abscisate beta-glucosidase ', 'BGLU18', '841670', 'NM_104118', 'NP_175649', 'Q9SE50', '3.2.1.175', 528, 'Potential GSL genes'),
	('AT1G52410', 'TSA1', 'TSK-associating protein 1', 'F19K6.14', '841671', 'NM_179466', 'NP_849797', 'F4ICX9', '', 759, 'Potential GSL genes'),
	('AT1G53440', 'T3F20.24', 'Probable LRR receptor-like serine/threonine-protein kinase At1g53440 ', 'AT1G53440', '841779', 'NM_104222', 'NP_175749', 'C0LGG9', '2.7.11.1', 1035, 'Potential GSL genes'),
	('AT1G54030', 'MVP1', 'Inactive GDSL esterase/lipase-like protein 25 ', 'ERMO3', '841841', 'NM_104280', 'NP_175805', 'Q7XA74', '', 417, 'Potential GSL genes'),
	('AT1G54100', 'ALDH7B4', 'Aldehyde dehydrogenase family 7 member B4 ', 'F15I1.19', '841849', '?NM_104287.5', 'NP_175812.1?', 'Q9SYG7', '', 508, 'Potential camalexin genes'),
	('AT1G54340', 'ICDH', 'Peroxisomal isocitrate dehydrogenase [NADP] ', 'F20D21.16', '841875', 'NM_104312', 'NP_175836', 'Q9SLK0', '1.1.1.42', 416, 'Potential GSL genes'),
	('AT1G54350', 'ABCC2', 'ABC transporter D family member 2, chloroplastic ', 'PMP1', '841876', 'NM_104313.4', 'NP_175837.2', 'Q6NLC1', '3.6.3.-', 706, 'Potential GSL genes'),
	('AT1G55020', 'LOX1', 'Linoleate 9S-lipoxygenase 1 ', 'F14C21.3', '841944', 'NM_104376.3', 'NP_175900.1', 'Q06327', '1.13.11.58', 859, 'Potential GSL genes'),
	('AT1G55090', 'T7N22.4', 'Glutamine-dependent NAD', '', '841952', 'NM_104383', 'NP_175906', 'Q9C723', '6.3.5.1', 725, 'Potential GSL genes'),
	('AT1G55210', 'DIR20', 'Dirigent protein 20', 'F7A10.7', '841964', 'NM_104394.4', 'NP_175917.1', 'Q9C891', '', 187, 'Potential GSL genes'),
	('AT1G55450', 'T5A14.14', 'S-adenosyl-L-methionine-dependent methyltransferases superfamily protein', '', '841992', 'NM_104421', 'NP_564689', 'Q9ZVU4', '', 311, 'Potential GSL genes'),
	('AT1G55810', 'UKL3', 'Uridine kinase-like protein 3 [Includes: Uridine kinase ', 'F20N2.21', '842031', '?NM_001333736.1?', 'NP_001323277.1?', 'Q8VYB2', '2.7.1.48', 466, 'Potential camalexin genes'),
	('AT1G55920', 'ATSERAT2;1', 'Serine acetyltransferase 1, chloroplastic ', 'SAT1', '842043', 'NM_104470', 'NP_175988', 'Q42588', '2.3.1.30', 314, 'Potential GSL genes'),
	('AT1G56160', 'MYB72', 'Myb domain protein 72 ', 'T6H22.4', '842069', 'NM_104495', 'NP_176012', 'Q9SGU3', '', 296, 'Potential GSL genes TF'),
	('AT1G56430', 'ATNAS4', 'Probable nicotianamine synthase 4 ', 'NAS4', '842096', 'NM_104521', 'NP_176038', 'Q9C7X5', '2.5.1.43', 324, 'Potential GSL genes'),
	('AT1G56650', 'MYB75', 'Transcription factor MYB75 ', 'PAP1', '842120', '?NM_104541.4', 'NP_176057.1?', 'Q9FE25', '', 248, 'Potential camalexin genes TF'),
	('AT1G57630', 'At1g57630', 'Disease resistance protein RPP1-WsB, putative ', 'T8L23.10', '842139', '?NM_104560.2', 'NP_176076.1?', 'Q9FVT9', '', 172, 'Potential camalexin genes'),
	('AT1G58260', 'CYP79C2 ', 'Cytochrome P450, putative', 'At1g58260', '842194', 'NM_104606.2', 'NP_176122.2', 'Q9LQB7', '', 530, 'Potential GSL genes'),
	('AT1G58265', 'At1g58265', 'Cytochrome P450 superfamily protein', 'At1g58265', '842195', 'NM_179494.1', 'NP_849825.1', 'Q3E7Q8', '', 159, 'Potential GSL genes'),
	('AT1G59700', 'GSTU16', 'Glutathione S-transferase U16 ', 'F23H11.1', '842261', '?NM_104662.4', 'NP_176178.1?', 'Q9XIF8', '', 234, 'Potential camalexin genes'),
	('AT1G59740', 'NPF4.3', 'Protein NRT1/ PTR FAMILY 4.3 ', 'NRT1.14', '842267', 'NM_104667.3', 'NP_176183.1', 'Q93VV5', '', 591, 'Potential GSL genes'),
	('AT1G59870', 'ABCG36', 'ABC transporter G family member 36 ', 'PDR8 PEN3', '842281', '?NM_104680.3', 'NP_176196.1?', 'Q9XIE2', '', 1469, 'Potential camalexin genes'),
	('AT1G60680', 'AGD2', 'Probable aldo-keto reductase 2 ', 'F8A5.20', '842362', '?NM_104751.5', 'NP_176267.3?', 'Q84M96', '', 346, 'Potential camalexin genes'),
	('AT1G60810', 'ACLA-2', 'ATP-citrate synthase alpha chain protein 2 ', 'F23C21.5', '842375', '?NM_001333917.1', 'NP_001320572.1?', 'O22718', '2.3.3.8, 6.2.1.5', 423, 'Potential camalexin genes'),
	('AT1G61120', 'GES', '(E,E)-geranyllinalool synthase ', 'TPS04', '842405', '?NM_104793.3', 'NP_564772.1?', 'Q93YV0', '', 877, 'Potential camalexin genes'),
	('AT1G61610', 'AK2', 'Putative G-type lectin S-receptor-like serine/threonine-protein kinase At1g61610 ', 'AK-LYS2', '842457', 'NM_104843', 'NP_176355', 'Q9FKF5', '2.7.11.1', 134, 'Potential GSL genes'),
	('AT1G61660', 'BHLH112', 'Transcription factor bHLH112 ', 'EN64', '842462', 'NM_179505.1', 'NP_849836.1', 'Q94JL3', '', 393, 'Potential GSL genes'),
	('AT1G61820', 'BGLU46', 'Beta-glucosidase 46 ', 'F8K4.3', '842479', 'NM_202338', 'NP_974067', 'O80690', '3.2.1.21', 516, 'Potential GSL genes'),
	('AT1G62580', 'T3P18.14', 'Flavin-containing monooxygenase FMO GS-OX-like 7', 'At1g62580 ', '842555', 'NM_104936.2', 'NP_176446.1', 'Q9SXD9', '1.8.-.-', 464, 'Potential GSL genes'),
	('AT1G62600', 'T3P18.16', 'Flavin-containing monooxygenase FMO GS-OX-like 4', 'At1g62600 ', '842557', 'NM_104938.5', ' NP_176448.1', 'Q94BV5', '1.8.-.-', 452, 'Potential GSL genes'),
	('AT1G62620', 'T3P18.18', 'Flavin-containing monooxygenase FMO GS-OX-like 3', 'At1g62620 ', '842559', ' NM_104940.4', ' NP_176450.2', 'Q9SXD5', '1.8.-.-', 450, 'Potential GSL genes'),
	('AT1G62660', 'BFRUCT3', 'Acid beta-fructofuranosidase 3, vacuolar ', 'BETAFRUCT3', '842563', 'NM_104943', 'NP_564798', 'Q43348', '3.2.1.26', 648, 'Potential GSL genes'),
	('AT1G62800', 'ASP4', 'Aspartate aminotransferase, cytoplasmic isozyme 2', 'F23N19.17', '842579', 'NM_179507', 'NP_849838', 'P46646', '2.6.1.1', 403, 'Potential GSL genes'),
	('AT1G62810', 'AT1G62810', 'Primary amine oxidase ', 'F23N19.18', '842580', 'NM_104959', 'NP_176469', 'Q8H1H9', '1.4.3.21', 712, 'Potential GSL genes'),
	('AT1G63010', 'F16M19.18', 'SPX domain-containing membrane protein', 'F16P17.18', '842604', 'NM_202344.2', 'NP_974073.2', 'Q2V4F9', ' ', 697, 'Potential GSL genes'),
	('AT1G63340', 'F9N12.4', 'Putative flavin-containing monooxygenase FMO GS-OX-like 10', 'At1g63340 ', '842640', 'NM_105013.4', 'NP_176523.4', 'Q9C8T8', '1.8.-.-', 448, 'Potential GSL genes'),
	('AT1G63370', 'F2K11.25 ', 'Flavin-containing monooxygenase FMO GS-OX-like 5', 'At1g63370 ', '842643', 'NM_105016.2', ' NP_176526.1', 'Q9C8U0', '1.8.-.-', 450, 'Potential GSL genes'),
	('AT1G63390', 'F2K11.23', 'Putative flavin-containing monooxygenase FMO GS-OX-like 11', 'At1g63390 ', '842645', 'NM_001334089.1', ' NP_001319303.1', 'Q9SH25', '1.8.-.-', 168, 'Potential GSL genes'),
	('AT1G63660', 'At1g63660', 'At1g63660 ', 'F24D7.15', '842670', '?NM_105043.4', 'NP_176553.1?', 'Q9CAD1', '6.3.5.2', 534, 'Potential camalexin genes'),
	('AT1G63730', 'At1g63730', 'Disease resistance protein (TIR-NBS-LRR class) family ', 'F24D7.8', '842677', '?NM_105050.1', 'NP_176560.1?', 'Q9CAD8', '', 966, 'Potential camalexin genes'),
	('AT1G64370', 'F15H21.1', 'Filaggrin-like protein', 'F15H21_1', '842744', 'NM_105112.4', 'NP_564833.1', 'Q9C7W1', '', 178, 'Potential GSL genes'),
	('AT1G64400', 'LACS3', 'Long chain acyl-CoA synthetase 3', 'F15H21.7', '842748', 'NM_105115.4', 'NP_176622.1', 'Q9C7W4', '6.2.1.3', 665, 'Potential GSL genes'),
	('AT1G64660', 'MGL', 'Methionine gamma-lyase ', 'F1N19.23', '842774', '?NM_105141.3', 'NP_176647.1?', 'Q9SGU9', '', 441, 'Potential camalexin genes'),
	('AT1G66200', 'GLN1-2', 'Glutamine synthetase cytosolic isozyme 1-2 ', 'GSR2', '842935', 'NM_105291', 'NP_176794', 'Q8LCE1', '6.3.1.2', 356, 'Potential GSL genes'),
	('AT1G66540', 'F28G11_4', 'Cytochrome P450 superfamily protein', 'At1g66540 ', '842972', 'NM_001124086.1', 'NP_001117558.1', 'Q0WVW6', '', 327, 'Potential GSL genes'),
	('AT1G67550', 'URE', 'Urease ', 'F12B7.10', '843076', '?NM_105422.4', 'NP_176922.1?', 'Q9SR52', '3.5.1.5', 838, 'Potential camalexin genes'),
	('AT1G67810', 'SUFE2', 'SufE-like protein 2, chloroplastic ', 'F12A21.6', '843107', '?NM_105449.4', 'NP_176947.1?', 'Q9FXE3', '', 258, 'Potential camalexin genes'),
	('AT1G67870', 'T23K23.28', 'At1g67870/T23K23_28 ', '', '843115', 'NM_105457', 'NP_564912', 'Q93VS6', '', 279, 'Potential GSL genes'),
	('AT1G68320', 'MYB62', 'Transcription factor MYB62 ', 'T22E19.5', '843161', '?NM_105503.3', 'NP_176999.1?', 'Q9C9G7', '', 286, 'Potential camalexin genes TF'),
	('AT1G69920', 'GSTU12', 'Glutathione S-transferase U12 ', 'T17F3.5', '843328', '?NM_105660.6', 'NP_177150.2?', 'Q6NMS0', '', 254, 'Potential camalexin genes'),
	('AT1G70580', 'GGAT2', 'Glutamate--glyoxylate aminotransferase 2 ', 'AOAT2 GGT2', '843395', '?NM_001036185.1', 'NP_001031262.1?', 'Q9S7E9', '', 481, 'Potential camalexin genes'),
	('AT1G70700', 'TIFY7', 'Jasmonate ZIM domain-containing protein 9', 'JAZ9', '843407', 'NM_105738.8', 'NP_177227.5', 'Q8W4J8', '', 267, 'Potential GSL genes'),
	('AT1G70810', 'CAR7', 'Protein C2-DOMAIN ABA-RELATED 7', 'F15H11.6', '843418', 'NM_105749.3', 'NP_565002.1', 'Q9SSL1', '', 165, 'Potential GSL genes'),
	('AT1G70890', 'MLP43', 'MLP-like protein 43', 'F15H11.12', '843427', 'NM_105756.4', 'NP_177245.1', 'Q9SSK5', '', 158, 'Potential GSL genes'),
	('AT1G72450', 'TIFY11B', 'Jasmonate ZIM domain-containing protein 6', 'JAZ6', '843577', 'NM_105904.4', 'NP_565043.1', 'Q9C9E3', '', 269, 'Potential GSL genes'),
	('AT1G72810', 'TS2', 'Threonine synthase 2, chloroplastic ', 'F3N23.1', '843612', 'NM_105939', 'NP_565047', 'Q9SSP5', '4.2.3.1', 516, 'Potential GSL genes'),
	('AT1G72900', 'F3N23.10', 'Similar to part of disease resistance protein ', '', '843621', 'NM_105948', 'NP_177433', 'Q9SSN6', '', 363, 'Potential GSL genes'),
	('AT1G72920', 'At1g72920', 'Toll-Interleukin-Resistance TIR domain family protein', 'F3N23.12', '843623', 'NM_105950.4', 'NP_177435.1', 'Q9SSN4', '', 275, 'Potential GSL genes'),
	('AT1G73120', 'At1g73120', 'At1g73120 ', 'T18K17.22', '843643', '?NM_105970.3', 'NP_177455.1?', 'Q9CAS9', '', 109, 'Potential camalexin genes'),
	('AT1G73260', 'KTI1', 'Kunitz trypsin inhibitor 1 ', 'TPI', '843660', '?NM_105985.3?', 'NP_565061.1?', 'Q8RXD5', '', 215, 'Potential camalexin genes'),
	('AT1G73330', 'DR4', 'Dr4 protein ', 'T9L24.45', '843668', 'NM_105993', 'NP_177476', 'Q39091', '', 209, 'Potential GSL genes'),
	('AT1G74040', 'IMS1', '2-isopropylmalate synthase 2, chloroplastic ', 'MAML-3', '843742', 'NM_106063', 'NP_177544', 'Q9C550', '2.3.3.13', 631, 'Potential GSL genes'),
	('AT1G74590', 'GSTU10', 'Glutathione S-transferase U10 ', 'F1M20.27', '843799', '?NM_106118.3', 'NP_177598.1?', 'Q9CA57', '', 232, 'Potential camalexin genes'),
	('AT1G74640', 'At1g74640', 'Alpha/beta-Hydrolases superfamily protein', 'F1M20.32', '843803', 'NM_106122.3', 'NP_565087.1', 'Q8L475', '', 370, 'Potential GSL genes'),
	('AT1G74710', 'EDS16', 'Isochorismate synthase 1, chloroplastic ', 'F1M20.39', '843810', '?NM_106129.4?', 'NP_565090.1?', 'Q9S7H8', '5.4.4.2', 569, 'Potential camalexin genes'),
	('AT1G74950', 'TIFY10B', 'Jasmonate ZIM domain-containing protein 2', 'JAZ2', '843834', 'NM_106153.4', 'NP_565096.1', 'Q9S7M2', '', 249, 'Potential GSL genes'),
	('AT1G75280', 'At1g75280', 'Isoflavone reductase homolog P3 ', 'F22H5.17', '843865', 'NM_106183.4', 'NP_565107.1', 'P52577', '1.3.1.-', 310, 'Potential GSL genes'),
	('AT1G76360', 'At1g76360', 'Protein kinase superfamily protein', 'F15M4.14', '843968', 'NM_106285.6', 'NP_177762.3', 'A4FVS9', '', 484, 'Potential GSL genes'),
	('AT1G76790', 'IGMT5 ', 'Indole glucosinolate O-methyltransferase 5', 'At1g76790 ', '844013', 'NM_106329.3', ' NP_177805.1', 'Q9SRD4', '2.1.1.-', 367, 'Potential GSL genes'),
	('AT1G76800', 'AT1G76800', 'Vacuolar iron transporter homolog 2 ', 'F28O16.17', '844014', 'NM_106330', 'NP_177806', 'Q9SRD3', '', 196, 'Potential GSL genes'),
	('AT1G77420', 'F2P24.13', 'Alpha/beta-Hydrolases superfamily protein ', 'At1g77420', '844079', 'NM_106392.4', 'NP_177867.1', 'Q9FVW6', '', 382, 'Potential GSL genes'),
	('AT1G77530', 'T5M16.12', 'O-methyltransferase family protein ', 'At1g77530  ', '844089', 'NM_106402.2', 'NP_177877.1', 'Q9CAQ3', '', 381, 'Potential GSL genes'),
	('AT1G77760', 'NIA1', 'Nitrate reductase [NADH] 1 ', 'T32E8.9', '844112', 'NM_106425.3', 'NP_177899.1', 'P11832', '1.7.1.1', 917, 'Potential GSL genes'),
	('AT1G77920', 'TGA7', 'Transcription factor TGA7 ', 'BZIP50', '844127', 'NM_106441.4', 'NP_565162.1', 'Q93ZE2', '', 368, 'Potential GSL genes'),
	('AT1G77990', 'SULTR2;2', 'Sulfate transporter 2.2', 'F28K19.21', '844134', 'NM_106448.4', 'NP_565165.2', 'P92946', '', 677, 'Potential GSL genes'),
	('AT1G78050', 'PGM', 'Phosphoglycerate/bisphosphoglycerate mutase', 'F28K19.30', '844140', '?NM_106454.4', 'NP_177928.2?', 'F4I8M8', '5.4.2.11', 332, 'Potential camalexin genes'),
	('AT1G78320', 'ATGSTU23', 'Glutathione S-transferase U23 ', 'GSTU23', '844167', 'NM_106481', 'NP_177955', 'Q9M9F1', '2.5.1.18', 220, 'Potential GSL genes'),
	('AT1G78370', 'GSTU20', 'Glutathione S-transferase U20 ', 'FIP1', '844173', '?NM_106484.4', 'NP_177958.1?', 'Q8L7C9', '', 217, 'Potential camalexin genes'),
	('AT1G78380', 'GSTU19', 'Glutathione S-transferase U19 ', 'ATGSTU19', '844174', 'NM_106485', 'NP_565178', 'Q9ZRW8', '2.5.1.18', 219, 'Potential GSL genes'),
	('AT1G78490', 'CYP708A3', 'CYTOCHROME P450, FAMILY 708, SUBFAMILY A, POLYPEPTIDE 3 ', 'T30F21.17', '844185', 'NM_106496', 'NP_177970', 'Q8VZC2', '', 479, 'Potential GSL genes'),
	('AT1G78660', 'GGH1', 'Gamma-glutamyl hydrolase 1 ', 'T30F21.1', '844202', '?NM_106513.5?', 'NP_177987.1?', 'Q9SYL6', '3.4.19.9', 348, 'Potential camalexin genes'),
	('AT1G78670', 'GGH3', 'Probable gamma-glutamyl hydrolase 3 ', 'F9K20.29', '844203', 'NM_106514.4', 'NP_177988.1', 'Q9ZV85', '3.4.19.9', 352, 'Potential GSL genes'),
	('AT1G78680', 'GGH2', 'Gamma-glutamyl hydrolase 2 ', 'GGH1', '844204', 'NM_106515.4', 'NP_565186.2', 'O65355', '3.4.19.9', 347, 'Potential GSL genes'),
	('AT1G79010', 'YUP8H12R.37', 'NADH dehydrogenase [ubiquinone] iron-sulfur protein 8-A, mitochondrial ', 'YUP8H12R_21', '844242', 'NM_106551.4', 'NP_178022.1', 'Q42599', '1.6.5.3\n1.6.99.3', 222, 'Potential GSL genes'),
	('AT1G79370', 'CYP79C1 ', 'Cytochrome P450, family 79, subfamily C, polypeptide 1', 'At1g79370', '844275', 'NM_106585.2', 'NP_178055.2', 'F4IF38', '', 546, 'Potential GSL genes'),
	('AT1G79680', 'WAKL10', 'Wall-associated receptor kinase-like 10 ', 'F20B17.10', '844307', '?NM_106617.4', 'NP_178086.1?', 'Q8VYA3', '', 769, 'Potential camalexin genes'),
	('AT1G79750', 'NADP-ME4', 'NADP-dependent malic enzyme 4, chloroplastic ', 'F19K16.27', '844314', '?NM_106624.5', 'NP_178093.1?', 'Q9CA83', '', 646, 'Potential camalexin genes'),
	('AT1G80050', 'APT2', 'Adenine phosphoribosyltransferase 2 ', 'F18B13.14', '844345', '?NM_106654.3', 'NP_178122.1?', 'Q42563', '2.4.2.7', 192, 'Potential camalexin genes'),
	('AT1G80555', 'AT1G80555', 'Isocitrate/isopropylmalate dehydrogenase family protein', '', '5007861', 'NM_001084388', 'NP_001077857', 'Q1G324', '', 130, 'Potential GSL genes'),
	('AT1G80560', 'IMDH2', '3-isopropylmalate dehydrogenase 2, chloroplastic ', 'IMDH', '844395', 'NM_106704.4', 'NP_178171.1', 'P93832', '1.1.1.85', 405, 'Potential GSL genes'),
	('AT1G80760', 'NIP6;1', 'Aquaporin NIP6-1 ', 'NLM7', '844415', 'NM_106724', 'NP_178191', 'Q9SAI4', '', 305, 'Potential GSL genes'),
	('AT1G80820', 'CCR2', 'Cinnamoyl-CoA reductase 2 ', 'F23A5.17', '844421', '?NM_106730.4', 'NP_178197.1?', 'Q9SAH9', '', 332, 'Potential camalexin genes'),
	('AT2G02010', 'GAD4', 'Glutamate decarboxylase 4 ', 'F14H20.8', '814732', '?NM_126262.2', 'NP_178310.1?', 'Q9ZPS3', '4.1.1.15', 493, 'Potential camalexin genes'),
	('AT2G02390', 'ATGSTZ1', 'Glutathione S-transferase Z1 ', 'GST18 GSTZ', '814770', '?NM_126296.5?', 'NP_178344.1?', 'Q9ZVQ3', '', 221, 'Potential camalexin genes'),
	('AT2G02930', 'GSTF3', 'Glutathione S-transferase F3 ', 'GST16', '814822', 'NM_126346.3', 'NP_178394.1', 'Q9SLM6', '2.5.1.18', 212, 'Potential GSL genes'),
	('AT2G03760', 'SOT12', 'Cytosolic sulfotransferase 12 ', 'RAR047', '814903', 'NM_126423', 'NP_178471', 'P52839', '2.8.2.-', 326, 'Potential GSL genes'),
	('AT2G03770', 'SOT13', 'Cytosolic sulfotransferase 13 ', 'F19B11', '814904', 'NM_126424.2', 'NP_178472.1', 'Q9ZPQ5', '2.8.2.-', 324, 'Potential GSL genes'),
	('AT2G04350', 'LACS8', 'Long chain acyl-CoA synthetase 8 ', 'T1O3', '814974', 'NM_179603.2', 'NP_849934.1', 'Q9SJD4', '6.2.1.3', 720, 'Potential GSL genes'),
	('AT2G04400', 'AT2G04400/T1O3.19', 'Indole-3-glycerol phosphate synthase, chloroplastic', 'T1O3.19', '814980', 'NM_126473', 'NP_178521', 'P49572', '4.1.1.48', 402, 'Potential GSL genes'),
	('AT2G05710', 'ACO2', 'Aconitate hydratase 2, mitochondrial ', 'T3P4.5', '815120', 'NM_126589', 'NP_178634', 'Q9SIB9', '4.2.1.3', 990, 'Potential GSL genes'),
	('AT2G05940', 'RIPK', 'Serine/threonine-protein kinase RIPK ', 'PBL14', '815147', 'NM_126607.3', 'NP_178651.1', 'Q9ZUF4', '2.7.11.1 ', 462, 'Potential GSL genes'),
	('AT2G06050', 'OPR3', '12-oxophytodienoate reductase 3 ', 'DDE1', '815160', 'NM_201702', 'NP_973431', 'Q9FUP0', '1.3.1.42', 391, 'Potential GSL genes'),
	('AT2G13560', 'NAD-ME1', 'NAD-dependent malic enzyme 1, mitochondrial ', 'T10F5.10', '815842', '?NM_126936.4', 'NP_178980.1?', 'Q9SIU0', '', 623, 'Potential camalexin genes'),
	('AT2G14750', 'APK1', 'Adenylyl-sulfate kinase 1, chloroplastic ', 'AKN1', '815963', '?NM_127039.4', 'NP_179082.1?', 'Q43295', '2.7.1.25', 276, 'Potential camalexin genes'),
	('AT2G14920', 'SOT10', 'Cytosolic sulfotransferase 10 ', 'ST4A', '815981', 'NM_127056.1', 'NP_179098.1', 'O82330', '2.8.2.-', 333, 'Potential GSL genes'),
	('AT2G15080', 'AtRLP19', 'Receptor-like protein 19 ', 'T15J14.12', '815997', '?NM_127070.3', 'NP_179112.1?', 'Q9ZUK3', '', 983, 'Potential camalexin genes'),
	('AT2G15620', 'NIR1', 'Ferredoxin--nitrite reductase, chloroplastic ', 'NIR', '816055', 'NM_127123', 'NP_179164', 'Q39161', '1.7.7.1', 586, 'Potential GSL genes'),
	('AT2G16570', 'ASE1', 'Amidophosphoribosyltransferase 1, chloroplastic ', 'GPRAT1', '816156', '?NM_127208.2', 'NP_179247.1?', 'Q9SI61', '2.4.2.14', 566, 'Potential camalexin genes'),
	('AT2G16660', 'AT2G16660', 'Major facilitator superfamily protein ', 'T24I21.7', '816167', 'NM_127218', 'NP_179257', 'Q9SLF1', '', 546, 'Potential GSL genes'),
	('AT2G16740', 'UBC29', 'Ubiquitin-conjugating enzyme E2 29 ', 'T24I21.15', '816175', 'NM_127226', 'NP_565391', 'Q9SLE4', '2.3.2.23', 148, 'Potential GSL genes'),
	('AT2G16890', 'UGT90A1', 'UDP-glycosyltransferase 90A1 ', 'F12A24.7', '816190', 'NM_180661', 'NP_850992', 'Q9ZVX4', '2.4.1.-', 478, 'Potential GSL genes'),
	('AT2G17130', 'IDH2', 'Isocitrate dehydrogenase [NAD] regulatory subunit 2, mitochondrial ', 'F6P23.14', '816218', '?NM_127267.3?', 'NP_179304.1?', 'P93032', '', 367, 'Potential camalexin genes'),
	('AT2G17265', 'HSK', 'Homoserine kinase ', 'DMR1', '816232', '?NM_127281.2', 'NP_179318.1?', 'Q8L7R2', '2.7.1.39', 370, 'Potential camalexin genes'),
	('AT2G18450', 'SDH1-2', 'Succinate dehydrogenase [ubiquinone] flavoprotein subunit 2, mitochondrial ', 'T30D6.4', '816359', '?NM_127401.3', 'NP_179435.1?', 'Q9ZPX5', '1.3.5.1', 632, 'Potential camalexin genes'),
	('AT2G19900', 'NADP-ME1', 'NADP-dependent malic enzyme 1 ', 'F6F22.7', '816509', '?NM_127548.4', 'NP_179580.1?', 'O82191', '', 581, 'Potential camalexin genes'),
	('AT2G20340', 'ELI5', 'Tyrosine decarboxylase 1 ', 'F11A3.11', '816553', 'NM_179668', 'NP_849999', 'Q8RY79', '4.1.1.25', 490, 'Potential GSL genes'),
	('AT2G20630', 'PIA1', 'Probable protein phosphatase 2C 20 ', '', '816590', 'NM_201761', 'NP_973490', 'Q9SIU8', '3.1.3.16', 290, 'Potential GSL genes'),
	('AT2G22430', 'ATHB-6', 'Homeobox-leucine zipper protein ATHB-6 ', 'F14M13.17', '816775', 'NM_127808.3', 'NP_565536.1', 'P46668', '', 311, 'Potential GSL genes'),
	('AT2G22930', 'UGT79B8', 'UDP-glycosyltransferase 79B8 ', 'T20K9.14', '816824', 'NM_127858', 'NP_179877', 'O81010', '2.4.1.-', 442, 'Potential GSL genes'),
	('AT2G23190', 'CYP81D7  ', 'Cytochrome P450, family 81, subfamily D, polypeptide 7', 'At2g23190 ', '816851', 'NM_127883.1', 'NP_179900.1', 'O22188', '', 543, 'Potential GSL genes'),
	('AT2G23220', 'CYP81D6', 'Cytochrome P450, family 81, subfamily D, polypeptide 6 ', 'At2g23220', '816854', 'NM_127886.1. ', 'NP_179903.1', 'O22185', '', 515, 'Potential GSL genes'),
	('AT2G23610', 'ATMES3', 'Methylesterase 3 ', 'MES3', '816893', 'NM_127925', 'NP_179942', 'O80477', '3.1.1.-', 263, 'Potential GSL genes'),
	('AT2G23960', 'GGP4', 'Gamma-glutamyl peptidase 4 ', 'At2g23960', '816929', 'NM_001335877.1', 'NP_001323529.1', 'F4INN2', '3.4.19.-', 251, 'Potential GSL genes'),
	('AT2G23970', 'GGP5', 'Gamma-glutamyl peptidase 5', 'At2g23970', '816930', 'NM_127959.2', 'NP_179975.1', 'O82225', '3.4.19.-', 251, 'Potential GSL genes'),
	('AT2G24180', 'CYP71B6', 'Cytochrome P450 71B6 ', 'F27D4.9', '816952', '?NM_127979.3', 'NP_179995.1?', 'O65787', '', 503, 'Potential camalexin genes'),
	('AT2G24200', 'LAP1', 'Leucine aminopeptidase 1 ', 'PM25', '816954', 'NM_127981', 'NP_179997', 'P30184', '3.4.11.1\n3.4.11.5', 520, 'Potential GSL genes'),
	('AT2G24850', 'TAT3', 'Probable aminotransferase TAT3  ', 'F27C12.23', '817022', 'NM_128044.3', 'NP_180058.1', 'Q9SK47', '2.6.1.-', 445, 'Potential GSL genes'),
	('AT2G25160', 'CYP82F1', 'At2g25160 ', 'F13D4.120', '817054', '?NM_128073.3', 'NP_180088.1?', 'Q7Y222', '', 527, 'Potential camalexin genes'),
	('AT2G25735', 'AT2G25735', 'Expressed protein Uncharacterized protein ', '', '817115', 'NM_128133', 'NP_565608', 'Q8RUI1', '', 119, 'Potential GSL genes'),
	('AT2G26170', 'CYP711A1', 'Cytochrome P450 711A1  ', 'MAX1', '817157', 'NM_179743.2', 'NP_850074.1', 'B9DFU2', '1.14.-.-', 522, 'Potential GSL genes'),
	('AT2G26400', 'ARD', '1,2-dihydroxy-3-keto-5-methylthiopentene dioxygenase 1 ', 'T9J22.7', '817180', '?NM_128197.4', 'NP_180208.1?', 'O48707', '1.13.11.54', 199, 'Potential camalexin genes'),
	('AT2G26560', 'PLP2', 'Patatin-like protein 2 ', 'PLA2A', '817197', 'NM_128213', 'NP_180224', 'O48723', '3.1.1.-', 407, 'Potential GSL genes'),
	('AT2G26640', 'KCS11', '3-ketoacyl-CoA synthase 11 ', 'F18A8.1', '817205', '?NM_128221.6', 'NP_180232.1?', 'O48780', '2.3.1.199, 2.3.1.180', 509, 'Potential camalexin genes'),
	('AT2G27360', 'At2g27360', 'GDSL esterase/lipase At2g27360 ', 'F12K2.6', '817279', 'NM_128295.5', 'NP_180304.1', 'Q9ZQI3', ' 3.1.1.-', 394, 'Potential GSL genes'),
	('AT2G27450', 'AT2G27450', 'N-carbamoylputrescine amidase ', 'CPA', '817290', 'NM_179770', 'NP_850101', 'Q8VYF5', '3.5.1.53', 326, 'Potential GSL genes'),
	('AT2G27690', 'CYP94C1', 'Cytochrome P450 94C1 ', 'F15K20.21', '817315', 'NM_128328', 'NP_180337', 'Q9ZUX1', '1.14.-.-', 495, 'Potential GSL genes'),
	('AT2G28760', 'UXS6', 'UDP-glucuronic acid decarboxylase 6 ', 'F8N16.5', '817426', 'NM_201826.3', 'NP_973555.1', 'Q9ZV36', ' 4.1.1.35', 343, 'Potential GSL genes'),
	('AT2G28850', 'CYP710A3', 'Cytochrome P450 710A3 ', 'F8N16.14', '817434', '?NM_128444.2', 'NP_180451.1?', 'Q9ZV29', '', 493, 'Potential camalexin genes'),
	('AT2G28880', 'ADCS', 'Aminodeoxychorismate synthase, chloroplastic ', 'EMB1997', '817437', '?NM_179796.2', 'NP_850127.1?', 'Q8LPN3', '4.1.3.27, 2.6.1.85', 919, 'Potential camalexin genes'),
	('AT2G29330', 'TRI', 'Tropinone reductase homolog At2g29330 ', 'F16P2.29', '817482', '?NM_128487.3', 'NP_180494.1?', 'Q9ZW16', '', 260, 'Potential camalexin genes'),
	('AT2G29440', 'ATGSTU6', 'Glutathione S-transferase U6 ', 'GSTU6', '817493', 'NM_128498', 'NP_180505', 'Q9ZW26', '2.5.1.18', 223, 'Potential GSL genes'),
	('AT2G29460', 'GSTU4', 'Glutathione S-transferase U4 ', 'GST22', '817495', '?NM_128500.4', 'NP_180507.1?', 'Q9ZW27', '', 224, 'Potential camalexin genes'),
	('AT2G29470', 'GSTU3', 'Glutathione S-transferase U3 ', 'GST21', '817496', '?NM_128501.4', 'NP_180508.1?', 'Q9ZW28', '', 225, 'Potential camalexin genes'),
	('AT2G29690', 'ASA2', 'Anthranilate synthase alpha subunit 2, chloroplastic ', 'T27A16.21', '817519', '?NM_128523.5', 'NP_180530.1?', 'P32069', '4.1.3.27', 621, 'Potential camalexin genes'),
	('AT2G29720', 'CTF2B', 'FAD/NAD', 'T27A16.18 ', '817522', '?NM_128526.2', 'NP_565688.1?', 'O82384', '', 427, 'Potential camalexin genes'),
	('AT2G30830', 'F7F1.4', '2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein', 'At2g30830', '817634', 'NM_128636.2', 'NP_180641.1', 'O80850', '', 358, 'Potential GSL genes'),
	('AT2G30840', 'F7F1.5', '2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein ', 'At2g30840', '817635', 'NM_128637.4', 'NP_180642.1', 'O80851', '', 362, 'Potential GSL genes'),
	('AT2G30860', 'GSTF9', 'Glutathione S-transferase F9 ', 'GSTF7', '817636', '?NM_001084514.1?', 'NP_001077983.1?', 'O80852', '2.5.1.18', 215, 'Potential camalexin genes'),
	('AT2G30870', 'GSTF10', 'Glutathione S-transferase F10 ', 'ERD13 GSTF4', '817637', '?NM_128639.4', 'NP_180644.1?', 'P42761', '2.5.1.18', 215, 'Potential camalexin genes'),
	('AT2G30950', 'VAR2', 'ATP-dependent zinc metalloprotease FTSH 2, chloroplastic ', 'VAR2', '817646', '?NM_001336310.1', 'NP_001323510.1?', 'O80860', '', 695, 'Potential camalexin genes'),
	('AT2G30970', 'ASP1', 'Aspartate aminotransferase, mitochondrial ', 'F7F1.18', '817648', '?NM_001124949.1', 'NP_001118421.1?', 'P46643', '2.6.1.1', 430, 'Potential camalexin genes'),
	('AT2G30990', 'AT2G30990', 'Protein of unknown function DUF688', '', '817650', 'NM_128653', 'NP_180656', 'F4IPV3', '', 593, 'Potential GSL genes'),
	('AT2G31180', 'MYB14', 'Transcription factor MYB14 ', 'F16D14.2', '817674', '?NM_128674.4', 'NP_180676.1?', 'Q9SJX8', '', 249, 'Potential camalexin genes TF'),
	('AT2G31230', 'ERF15', 'Ethylene-responsive transcription factor 15 ', 'ERF-15', '817680', 'NM_179831.2', 'NP_850162.1', 'Q8VYM0', '', 243, 'Potential GSL genes'),
	('AT2G31880', 'SOBIR1', 'Leucine-rich repeat receptor-like serine/threonine/tyrosine-protein kinase SOBIR1 ', 'EVR', '817746', '?NM_128746.3', 'NP_180747.1?', 'Q9SKB2', '', 641, 'Potential camalexin genes'),
	('AT2G32720', 'CYTB5-B', 'Cytochrome b5 isoform B ', 'CB5-B', '817832', 'NM_128831.4', 'NP_180831.1', 'O48845', '', 134, 'Potential GSL genes'),
	('AT2G32860', 'BGLU33', 'Beta-glucosidase 33 ', 'T21L14.20', '817847', 'NM_201858', 'NP_973587', 'O48779', '3.2.1.21', 614, 'Potential GSL genes'),
	('AT2G33230', 'YUC7', 'Probable indole-3-pyruvate monooxygenase YUCCA7 ', 'YUCCA7', '817885', '?NM_128882.2', 'NP_180881.1?', 'O49312', '', 431, 'Potential camalexin genes'),
	('AT2G34490', 'CYP710A2', 'Cytochrome P450 710A2 ', 'F13P17.22', '818012', 'NM_129001', 'NP_180996', 'O64698', '1.14.19.41', 499, 'Potential GSL genes'),
	('AT2G36880', 'METK3', 'S-adenosylmethionine synthase 3 ', 'T1J8.6', '818260', 'NM_129243.4', 'NP_181225.1', 'Q9SJL8', '2.5.1.6', 390, 'Potential GSL genes'),
	('AT2G36900', 'MEMB11', 'Membrin-11', 'T1J8.8', '818264', 'NM_129246.3', 'NP_181227.1', 'Q9SJL6', '', 225, 'Potential GSL genes'),
	('AT2G37040', 'PAL1', 'Phenylalanine ammonia-lyase 1', 'T1J8.22', '818280', 'NM_129260.3', 'NP_181241.1', 'P35510', ' 4.3.1.24', 725, 'Potential GSL genes'),
	('AT2G37460', 'AT2G37460', 'WAT1-related protein At2g37460', 'F3G5.25', '818323', 'NM_129301', 'NP_181282', 'Q9ZUS1', '', 380, 'Potential GSL genes'),
	('AT2G37690', 'F13M22.19', 'Phosphoribosylaminoimidazole carboxylase like protein ', 'F13M22_19', '818346', 'NM_129325.6', 'NP_181305.2', 'Q84TI2', '', 642, 'Potential GSL genes'),
	('AT2G37710', 'LECRK41', 'L-type lectin-domain containing receptor kinase IV.1 ', 'LECRKE', '818348', 'NM_129327.4', 'NP_181307.1', 'O80939', '2.7.11.1', 675, 'Potential GSL genes'),
	('AT2G37760', 'AKR4C8', 'Aldo-keto reductase family 4 member C8 ', 'F13M22', '818353', 'NM_201898', 'NP_973627', 'O80944', '1.1.1.-', 311, 'Potential GSL genes'),
	('AT2G38470', 'WRKY33', 'Probable WRKY transcription factor 33 ', 'T19C21.4', '818429', '?NM_129404.4', 'NP_181381.2?', 'Q8S8P5', '', 519, 'Potential camalexin genes TF'),
	('AT2G38640', 'At2g38640', 'Protein LURP-one-related 8', 'T6A23.16', '818446', 'NM_129421.4', 'NP_181398.1', 'Q9ZVI6', '', 196, 'Potential GSL genes'),
	('AT2G38750', 'ANN4', 'Annexin D4 ', 'ANNAT4', '818457', 'NM_129432', 'NP_181409', 'Q9ZVJ6', '', 319, 'Potential GSL genes'),
	('AT2G38860', 'YLS5', 'DJ-1 protein homolog E', 'YLS5', '818470', 'NM_179972', 'NP_850303', 'Q9ZV19', '', 398, 'Potential GSL genes'),
	('AT2G38910', 'CPK20', 'Calcium-dependent protein kinase 20 ', 'T7F6.8', '818476', '?NM_129449.2', 'NP_181425.1?', 'Q9ZV15', '', 583, 'Potential camalexin genes'),
	('AT2G39030', 'AT2G39030', 'L-ornithine N5-acetyltransferase NATA1 ', 'T7F6.20', '818489', 'NM_129460', 'NP_565898', 'Q9ZV05', '2.3.1.-', 228, 'Potential GSL genes'),
	('AT2G39310', 'JAL22', 'Jacalin-related lectin 22 ', 'T16B24.5', '818516', 'NM_129488.4', 'NP_181463.1', 'O80950', '', 458, 'Potential GSL genes'),
	('AT2G39330', 'JAL23', 'Jacalin-related lectin 23 ', 'T16B24.3', '818518', 'NM_129490', 'NP_181465', 'O80948', '', 459, 'Potential GSL genes'),
	('AT2G39800', 'P5CSA', 'Delta-1-pyrroline-5-carboxylate synthase A ', 'P5CS1', '818566', '?NM_001202785.1?', 'NP_001189714.1?', 'P54887', '1.2.1.41, 2.7.2.11', 717, 'Potential camalexin genes'),
	('AT2G39850', 'SBT4.1', 'Subtilisin-like protease SBT4.1 ', 'T5I7.15', '818572', 'NM_129544', 'NP_565915', 'F4IG09', '3.4.21.-', 775, 'Potential GSL genes'),
	('AT2G40460', 'NPF5.1', 'Protein NRT1/ PTR FAMILY 5.1 ', 'T2P4.19', '818640', 'NM_129607.4', 'NP_181578.1', 'Q8VZR7', '', 583, 'Potential GSL genes'),
	('AT2G41100', 'CML12', 'Calmodulin-like protein 12 ', 'ATCAL4', '818709', 'NM_180012', 'NP_850343', 'P25071', '', 324, 'Potential GSL genes'),
	('AT2G41180', 'SIB2', 'Sigma factor binding protein 2, chloroplastic ', 'VQ16', '818717', 'NM_129683', 'NP_030663', 'O80669', '', 141, 'Potential GSL genes'),
	('AT2G41220', 'GLU2', 'Ferredoxin-dependent glutamate synthase 2, chloroplastic ', 'F13H10.23', '818721', '?NM_129687.5', 'NP_181655.1?', 'Q9T0P4', '', 1629, 'Potential camalexin genes'),
	('AT2G41880', 'GK-1', 'Guanylate kinase 1 ', 'AGK1', '818788', '?NM_001336943.1', 'NP_001323632.1?', 'P93757', '2.7.4.8', 387, 'Potential camalexin genes'),
	('AT2G42610', 'LSH10', 'Protein LIGHT-DEPENDENT SHORT HYPOCOTYLS 10 ', 'OBO10', '818861', 'NM_180043', 'NP_850374', 'Q9S7R3', '', 177, 'Potential GSL genes'),
	('AT2G42760', 'At2g42760', 'DUF1685 family protein', 'F7D19.24', '818876', 'NM_129837.4', 'NP_181804.1', 'Q9SJI0', '', 267, 'Potential GSL genes'),
	('AT2G42790', 'CSY3', 'Citrate synthase 3, peroxisomal ', 'F7D19.21', '818879', '?NM_129840.5', 'NP_181807.1?', 'Q9SJH7', '', 509, 'Potential camalexin genes'),
	('AT2G43090', 'AT2G43090', '3-isopropylmalate dehydratase small subunit 3 ', 'MFL8.15', '818911', 'NM_129870', 'NP_181837', 'Q9ZW85', '4.2.1.33', 251, 'Potential GSL genes'),
	('AT2G43100', 'IPMI2', '3-isopropylmalate dehydratase small subunit 1 ', 'MFL8.14', '818912', '?NM_129871.3', 'NP_181838.1?', 'Q9ZW84', '4.2.1.33', 256, 'Potential camalexin genes'),
	('AT2G43530', 'ATTI3', 'Defensin-like protein 194 ', 'T01O24.27', '818954', 'NM_129914.4', 'NP_181881.2', 'O22867', '', 83, 'Potential GSL genes'),
	('AT2G43550', 'ATTI6', 'Defensin-like protein 197 ', 'T01O24.29', '818957', 'NM_129917', 'NP_566002', 'O22869', '', 89, 'Potential GSL genes'),
	('AT2G43820', 'UGT74F2', 'UDP-glycosyltransferase 74F2 ', 'SAGT1', '818986', '?NM_129944.3', 'NP_181910.1?', 'O22822', '', 449, 'Potential camalexin genes'),
	('AT2G43840', 'UGT74F1 ', 'UDP-glycosyltransferase 74F1', 'At2g43840', '818988', ' NM_129946.3', 'NP_181912.1', 'O22820', '2.4.1.-', 449, 'Potential GSL genes'),
	('AT2G44350', 'CSY4', 'Citrate synthase 4, mitochondrial ', 'F4I1.16', '819042', '?NM_001337082.1?', 'NP_001324514.1?', 'P20115', '', 474, 'Potential camalexin genes'),
	('AT2G45200', 'GOS12', 'Golgi SNAP receptor complex member 1-2', 'F4L23.29', '819128', 'NM_130083.5', 'NP_182045.1', 'O22151', '', 257, 'Potential GSL genes'),
	('AT2G45440', 'DHDPS2', '4-hydroxy-tetrahydrodipicolinate synthase 2, chloroplastic ', 'F4L23.5', '819152', '?NM_130106.3', 'NP_182068.1?', 'Q9FVC8', '4.3.3.7', 365, 'Potential camalexin genes'),
	('AT2G45580', 'CYP76C3', 'Cytochrome P450 76C3 ', 'F17K2.11', '819166', '?NM_130120.4', 'NP_182082.2?', 'O64638', '', 515, 'Potential camalexin genes'),
	('AT2G46370', 'JAR1', 'Jasmonic acid-amido synthetase JAR1  ', 'FIN219', '819244', 'NM_180122.4', 'NP_850453.1', 'Q9SKE2', '6.3.2.-', 575, 'Potential GSL genes'),
	('AT2G46510', 'AIB', 'Transcription factor ABA-INDUCIBLE bHLH-TYPE AtAIB', 'BHLH17', '819262', 'NM_130216.3', 'NP_566078.1', 'Q9ZPY8', '', 566, 'Potential GSL genes'),
	('AT2G46630', 'AT2G46630', 'Putative extensin Uncharacterized protein', '', '3768746', 'NM_130228', 'NP_182186', 'Q9ZNU3', '', 394, 'Potential GSL genes'),
	('AT2G46690', 'SAUR32', 'Auxin-responsive protein SAUR32 ', 'AAM1', '819281', 'NM_130234', 'NP_182192', 'Q9ZUZ3', '', 121, 'Potential GSL genes'),
	('AT2G47160', 'BOR1', 'Boron transporter 1', 'T3D7.3', '819329', 'NM_180138', 'NP_850469', 'Q8VYR7', '', 704, 'Potential GSL genes'),
	('AT2G47730', 'GSTF8', 'Glutathione S-transferase F8, chloroplastic ', 'GST6', '819386', 'NM_180148.5', 'NP_850479.1', 'Q96266', '2.5.1.18', 263, 'Potential GSL genes'),
	('AT3G01120', 'MTO1', 'Cystathionine gamma-synthase 1, chloroplastic ', 'CGS1', '821292', 'NM_110977', 'NP_186761', 'P55217', '2.5.1.48', 563, 'Potential GSL genes'),
	('AT3G01420', 'DOX1', 'Alpha-dioxygenase 1 ', 'DIOX1', '821135', '?NM_111008.3', 'NP_186791.1?', 'Q9SGH6', '', 639, 'Potential camalexin genes'),
	('AT3G01530', 'MYB57', 'Transcription factor MYB57 ', 'F4P13.8', '821113', '?NM_111019.2', 'NP_186802.1?', 'Q9SSA1', '', 206, 'Potential camalexin genes TF'),
	('AT3G01670', 'SEOA', 'Protein SIEVE ELEMENT OCCLUSION A ', 'SEOR2', '821096', 'NM_111033.3', 'NP_566145.1', 'Q93XX2', '', 822, 'Potential GSL genes'),
	('AT3G02020', 'AK3', 'Aspartokinase 3, chloroplastic ', 'AK-LYS3', '821287', '?NM_111068.4', 'NP_186851.1?', 'Q9S702', '2.7.2.4', 559, 'Potential camalexin genes'),
	('AT3G02090', 'At3g02090', 'Probable mitochondrial-processing peptidase subunit beta, mitochondrial Beta-MPP', 'F1C9.12', '821084', 'NM_180169.1', 'NP_850500.1', 'Q42290', '3.4.24.64 ', 531, 'Potential GSL genes'),
	('AT3G02840', 'At3g02840', 'ARM repeat superfamily protein ', 'F13E7.22', '821225', '?NM_111152.2', 'NP_566184.1?', 'Q9M8S5', '', 379, 'Potential camalexin genes'),
	('AT3G03190', 'GSTF11', 'Glutathione S-transferase F11 ', 'GSTF6', '821227', '?NM_111189.3', 'NP_186969.1?', 'Q96324', '2.5.1.18', 214, 'Potential camalexin genes'),
	('AT3G03630', 'At3g03630', 'Probable S-sulfocysteine synthase, chloroplastic  Beta-substituted Ala synthase 5;1 ARAth-Bsas5;1 CS26 O-acetylserine sulfhydrylase', 'T12J13.9', '821203', 'NM_111234.5', 'NP_187013.1', 'O22682', '2.5.1.47', 404, 'Potential GSL genes'),
	('AT3G03780', 'MS2', '5-methyltetrahydropteroyltriglutamate--homocysteine methyltransferase 2 ', 'F20H23.19', '821147', '?NM_001125092.1', 'NP_001118564.1?', 'Q9SRV5', '2.1.1.14', 765, 'Potential camalexin genes'),
	('AT3G03900', 'APK3', 'Adenylyl-sulfate kinase 3 ', 'F20H23.5', '821077', 'NM_111261', 'NP_187040', 'Q9SRW7', '2.7.1.25', 208, 'Potential GSL genes'),
	('AT3G03910', 'GSH3', 'Probable glutamate dehydrogenase 3 ', 'F20H23.4', '821072', '?NM_111262.2', 'NP_187041.1?', 'Q9S7A0', '', 411, 'Potential camalexin genes'),
	('AT3G04000', 'ChlADR2', 'NADPH-dependent aldehyde reductase 2, chloroplastic ', 'T11I18.11', '819555', '?NM_111271.3', 'NP_566221.2?', 'Q9SQR2', '', 272, 'Potential camalexin genes'),
	('AT3G04110', 'GLR1.1', 'Glutamate receptor 1.1 AtGLR1 Ligand-gated ion channel 1.1', 'GLR1', '819566', 'NM_111282.3', 'NP_187061.1', 'Q9M8W7', '', 808, 'Potential GSL genes'),
	('AT3G04390', 'At3g04390', 'Aldehyde oxidase/xanthine dehydrogenase, molybdopterin binding protein ', 'T27C4.3', '819594', '?NM_111310.1', 'NP_187089.1?', 'Q9M847', '', 79, 'Potential camalexin genes'),
	('AT3G04520', 'THA2', 'Probable low-specificity L-threonine aldolase 2 ', 'T27C4.17', '819608', 'NM_111323', 'NP_566228', 'Q9FPH3', '4.1.2.48', 355, 'Potential GSL genes'),
	('AT3G04720', 'HEL', 'Hevein-like preproprotein [Cleaved into: CB-HEL; CD-HEL  RNase]', 'F7O18.21', '819632', 'NM_111344.6', 'NP_187123.1', 'P43082', '3.1.-.-', 212, 'Potential GSL genes'),
	('AT3G04940', 'CYSD1', 'Bifunctional L-3-cyanoalanine synthase/cysteine synthase D1  ', 'OAS3', '819654', 'NM_111366.4', 'NP_566243.1', 'Q9S6Z7', '2.5.1.47\n4.4.1.9', 324, 'Potential GSL genes'),
	('AT3G05650', 'RLP32', 'Putative disease resistance protein ', 'F18C1.8', '819732', 'NM_111438', 'NP_187216', 'Q9M9X0', '', 868, 'Potential GSL genes'),
	('AT3G06350', 'EMB3004', 'Bifunctional 3-dehydroquinate dehydratase/shikimate dehydrogenase, chloroplastic ', 'F24P17.18', '819809', '?NM_111510.4', 'NP_187286.1?', 'Q9SQT8', '1.1.1.25, 4.2.1.10', 603, 'Potential camalexin genes'),
	('AT3G06650', 'ACLB-1', 'ATP-citrate synthase beta chain protein 1 ', 'F5E6.2', '819845', '?NM_001337675.1', 'NP_001326324.1?', 'Q9C522', '6.2.1.5', 608, 'Potential camalexin genes'),
	('AT3G07300', 'T1B9.3', 'NagB/RpiA/CoA transferase-like superfamily protein', 'At3g07300', '819918', 'NM_111610.5', 'NP_187386.2', 'Q9SFW0', '', 407, 'Potential GSL genes'),
	('AT3G07630', 'ADT2', 'Arogenate dehydratase/prephenate dehydratase 2, chloroplastic ', 'PDT2', '819954', '?NM_001337726.1', 'NP_001325505.1?', 'Q9SSE7', '4.2.1.51', 381, 'Potential camalexin genes'),
	('AT3G08640', 'RER3', 'Protein RETICULATA-RELATED 3, chloroplastic', 'F17O14.11', '820011', 'NM_111698', 'NP_187476', 'Q9C9Z2', '', 337, 'Potential GSL genes'),
	('AT3G09260', 'PYK10', 'Beta-glucosidase 23 ', 'PSR3.1', '820082', 'NM_111760', 'NP_187537', 'Q9SR37', '3.2.1.21', 524, 'Potential GSL genes'),
	('AT3G09270', 'GSTU8', 'Glutathione S-transferase U8 ', 'F3L24.14', '820083', '?NM_111761.3', 'NP_187538.1?', 'Q9SR36', '', 224, 'Potential camalexin genes'),
	('AT3G09440', 'HSP70-3', 'Heat shock 70 kDa protein 3 ', 'HSC70-3', '820102', 'NM_111778.4', 'NP_187555.1', 'O65719', '', 649, 'Potential GSL genes'),
	('AT3G09940', 'MDAR3', 'Monodehydroascorbate reductase 3 ', 'MDAR2', '820155', '?NM_111829.4?', 'NP_566361.1?', 'Q9SR59', '', 441, 'Potential camalexin genes'),
	('AT3G10050', 'OMR1', 'Threonine dehydratase biosynthetic, chloroplastic ', 'T22K18.12', '820166', 'NM_111840', 'NP_187616', 'Q9ZSS6', '4.3.1.19', 592, 'Potential GSL genes'),
	('AT3G10260', 'RTNLB8', 'Reticulon-like protein B8 ', 'F14P13.14', '820188', 'NM_180221.3', 'NP_850552.1', 'Q9SS37', '', 247, 'Potential GSL genes'),
	('AT3G11660', 'NHL1', 'NDR1/HIN1-like protein 1', 'T19F11.6', '820338', 'NM_111998.3', 'NP_566396.1', 'Q9SRN0', '', 209, 'Potential GSL genes'),
	('AT3G12520', 'SULTR4;2', 'Probable sulfate transporter 4.2', 'MQC3.34', '820431', 'NM_112087.3', 'NP_187858.1', 'Q8GYH8', '', 677, 'Potential GSL genes'),
	('AT3G12580', 'MED37C', 'Probable mediator of RNA polymerase II transcription subunit 37c ', 'HSC70-4', '820438', 'NM_112093.3', 'NP_187864.1', 'Q9LHA8', '', 650, 'Potential GSL genes'),
	('AT3G12670', 'emb2742', 'CTP synthase ', 'T2E22.2', '820447', '?NM_112102.3', 'NP_187873.1?', 'Q9LTW8', '6.3.4.2', 591, 'Potential camalexin genes'),
	('AT3G12750', 'ZIP1', 'Zinc transporter 1 ', 'MBK21.13', '820457', 'NM_112111.3', 'NP_187881.1', 'O81123', '', 355, 'Potential GSL genes'),
	('AT3G13110', 'ATSERAT2;2', 'Serine acetyltransferase 3, mitochondrial', 'SATA', '820499', 'NM_112150', 'NP_187918', 'Q39218', '2.3.1.30', 391, 'Potential GSL genes'),
	('AT3G13650', 'DIR7', 'Dirigent protein 7 ', 'MMM17.4', '820569', 'NM_112211.3', 'NP_187974.1', 'Q9LID5', '', 186, 'Potential GSL genes'),
	('AT3G14210', 'ESM1', 'GDSL esterase/lipase ESM1 ', 'MAG2.6', '820639', '?NM_112278.3', 'NP_188037.1?', 'Q9LJG3', '', 392, 'Potential camalexin genes'),
	('AT3G14225', 'GLIP4', 'GDSL esterase/lipase 4 ', 'MLE3.2', '820641', '?NM_001338115.1', 'NP_001325624.1?', 'Q9LJP1', '', 377, 'Potential camalexin genes'),
	('AT3G14350', 'SRF7', 'Protein STRUBBELIG-RECEPTOR FAMILY 7 ', 'MLN21.15', '820655', 'NM_202583', 'NP_974312', 'Q9LUL4', '', 717, 'Potential GSL genes'),
	('AT3G14620', 'CYP72A8', 'Cytochrome P450, family 72, subfamily A, polypeptide 8', '', '820690', 'NM_112323.5', 'NP_188080.1', 'Q9LUD2', '', 515, 'Potential GSL genes'),
	('AT3G14640', 'CYP72A10', 'Cytochrome P450, family 72, subfamily A, polypeptide 10', '', '820692', '?NM_001338128.1', 'NP_001319552.1?', 'F4IW83', '', 514, 'Potential camalexin genes'),
	('AT3G14680', 'CYP72A14', 'Cytochrome P450 72A14 ', 'MIE1.18', '820696', '?NM_112329.4', 'NP_188086.1?', 'Q9LUC6', '', 512, 'Potential camalexin genes'),
	('AT3G14690', 'CYP72A15', 'Cytochrome P450 72A15 ', 'MIE1.20', '820697', '?NM_112330.4', 'NP_188087.1?', 'Q9LUC5', '', 512, 'Potential camalexin genes'),
	('AT3G14990', 'DJ1A', 'Protein DJ-1 homolog A ', 'K15M2.13', '820728', 'NM_180257', 'NP_850588', 'Q9FPF0', '', 392, 'Potential GSL genes'),
	('AT3G15290', 'At3g15290', '3-hydroxyacyl-CoA dehydrogenase family protein ', '', '820760', 'NM_112392.4', 'NP_188147.1', 'Q9LDF5', '', 294, 'Potential GSL genes'),
	('AT3G15650', 'At3g15650', 'Alpha/beta-Hydrolases superfamily protein', '', '820808', 'NM_112435.3', 'NP_188186.1', 'Q9LW14', '', 255, 'Potential GSL genes'),
	('AT3G15810', 'MSJ11.21', 'Protein LURP-one-related 12', '', '820824', 'NM_112451.4', 'NP_566526.1', 'Q9LVZ8', '', 220, 'Potential GSL genes'),
	('AT3G15840', 'PIFI', 'Post-illumination chlorophyll fluorescence increase', '', '820827', '?NM_112454.3', 'NP_566528.1?', 'Q9LVZ5', '', 268, 'Potential camalexin genes'),
	('AT3G15950', 'NAI2', 'TSA1-like protein ', 'MVC8.9', '820839', 'NM_112465', 'NP_188216', 'Q9LSB4', '', 772, 'Potential GSL genes'),
	('AT3G15990', 'SULTR3;4', 'Probable sulfate transporter 3.4', 'MSL1.3', '820844', 'NM_112469', 'NP_188220', 'Q9LW86', '', 653, 'Potential GSL genes'),
	('AT3G16460', 'JAL34 ', 'Jacalin-related lectin 34', 'T02O04.4', '820894', 'NM_202595', 'NP_974324', 'O04310', '', 705, 'Potential GSL genes'),
	('AT3G16470', 'JAL35 ', 'Jacalin-related lectin 35 ', 'JR1', '820895', 'NM_112518', 'NP_566547', 'O04309', '', 451, 'Potential GSL genes'),
	('AT3G16530', 'MDC8.16', 'Lectin-like protein At3g16530', '', '820901', 'NM_112525.3', 'NP_188274.1', 'Q9LK72', '', 276, 'Potential GSL genes'),
	('AT3G16890', 'PPR40', 'Putative pentatricopeptide repeat-containing protein At3g16890, mitochondrial ', 'K14A17.14', '820944', '?NM_112565.2', 'NP_188314.1?', 'Q9LSQ2', '', 659, 'Potential camalexin genes'),
	('AT3G16950', 'LPD1', 'Dihydrolipoyl dehydrogenase 1, chloroplastic ', 'K14A17.6', '820951', '?NM_001084696.1?', 'NP_001078165.1?', 'A8MS68', '1.8.1.4', 623, 'Potential camalexin genes'),
	('AT3G18080', 'BGLU44', 'Beta-glucosidase 44 ', 'MRC8.20', '821333', 'NM_112690', 'NP_188436', 'Q9LV33', '3.2.1.21', 512, 'Potential GSL genes'),
	('AT3G18280', 'At3g18280', 'Bifunctional inhibitor/lipid-transfer protein/seed storage 2S albumin superfamily protein', '', '821356', 'NM_112712.2', 'NP_188456.1', 'Q9LJQ3', '', 96, 'Potential GSL genes'),
	('AT3G18830', 'ATPLT5', 'Polyol transporter 5 ', 'PMT5', '821416', 'NM_112769', 'NP_188513', 'Q8VZ80', '', 539, 'Potential GSL genes'),
	('AT3G19010', 'AT3G19010', '2-oxoglutarate ', '', '821434', 'NM_180282', 'NP_850613', 'Q9LJ65', '', 349, 'Potential GSL genes'),
	('AT3G19280', 'FUT11', 'Glycoprotein 3-alpha-L-fucosyltransferase A ', 'MVI11.20', '821462', '?NM_112815.4', 'NP_188559.1?', 'Q9LJK1', '', 501, 'Potential camalexin genes'),
	('AT3G19450', 'CAD4', 'Cinnamyl alcohol dehydrogenase 4 ', 'CAD-C', '821479', 'NM_112832.4', 'NP_188576.1', 'P48523', '1.1.1.195', 365, 'Potential GSL genes'),
	('AT3G19550', 'AT3G19550', 'Putative uncharacterized protein At3g19550 ', '', '821491', 'NM_112844', 'NP_566643', 'Q8LEN7', '', 110, 'Potential GSL genes'),
	('AT3G19710', 'BCAT4', 'Methionine aminotransferase BCAT4 ', 'MMB12_16', '821508', '?NM_112861.4', 'NP_188605.1?', 'Q9LE06', '2.6.1.42', 354, 'Potential camalexin genes'),
	('AT3G20330', 'PYRB', 'Aspartate carbamoyltransferase, chloroplastic ', 'MQC12.7', '821577', '?NM_001338476.1', 'NP_001326915.1?', 'P49077', '2.1.3.2', 390, 'Potential camalexin genes'),
	('AT3G20390', 'RIDA', 'Reactive Intermediate Deaminase A, chloroplastic ', 'MQC12.15', '821584', 'NM_112930', 'NP_188674', 'Q94JQ4', '3.5.99.10', 187, 'Potential GSL genes'),
	('AT3G21110', 'PUR7', 'Phosphoribosylaminoimidazole-succinocarboxamide synthase, chloroplastic  SAICAR synthetase', 'MSA6.15', '821663', 'NM_113005.4', 'NP_188748.1', 'P38025', '6.3.2.6', 411, 'Potential GSL genes'),
	('AT3G21230', '4CL4', '4-coumarate--CoA ligase 4 4CL 4  ', 'MXL8_9', '821677', 'NM_113018.4', 'NP_188760.3', 'Q9LU36', '6.2.1.12', 570, 'Potential GSL genes'),
	('AT3G21240', '4CL2', '4-coumarate--CoA ligase 2 4CL 2  ', 'MXL8.10', '821678', 'NM_113019.4', 'NP_188761.1', 'Q9S725', '6.2.1.12', 556, 'Potential GSL genes'),
	('AT3G22370', 'AOX1A', 'Ubiquinol oxidase 1a, mitochondrial ', 'AOX1 HSR3', '821806', '?NM_113135.4', 'NP_188876.1?', 'Q39219', '', 354, 'Potential camalexin genes'),
	('AT3G22425', 'HISN5A', 'Imidazoleglycerol-phosphate dehydratase 1, chloroplastic ', 'MCB17.17', '821812', '?NM_180293.1?', 'NP_850624.1?', 'P34047', '4.2.1.19', 270, 'Potential camalexin genes'),
	('AT3G22740', 'HMT3', 'Homocysteine S-methyltransferase 3 ', 'MWI23.11', '821845', 'NM_113173', 'NP_566715', 'Q8LAX0', '2.1.1.10', 347, 'Potential GSL genes'),
	('AT3G22850', 'At3g22850', 'Aluminum induced protein with YGL and LRDR motifs', '', '821857', 'NM_113185.4', 'NP_188925.1', 'Q9LIL3', '', 248, 'Potential GSL genes'),
	('AT3G22890', 'APS1', 'ATP sulfurylase 1, chloroplastic ', 'F5N5.6', '821861', '?NM_113189.5', 'NP_188929.1?', 'Q9LIK9', '2.7.7.4', 463, 'Potential camalexin genes'),
	('AT3G23400', 'PAP6', 'Plastid-lipid-associated protein 6, chloroplastic ', 'FBN4', '821921', 'NM_113243.4', 'NP_566728.1', 'Q9LW57', '', 284, 'Potential GSL genes'),
	('AT3G23430', 'PHO1', 'Phosphate transporter PHO1 ', 'ATPHO1', '821924', 'NM_113246', 'NP_188985', 'Q8S403', '', 782, 'Potential GSL genes'),
	('AT3G23570', 'MDB19.5', 'Dienelactone hydrolase-like protein Putative uncharacterized protein MDB19.5', '', '821936', 'NM_113260', 'NP_566731', 'Q94JY3', '', 239, 'Potential GSL genes'),
	('AT3G23600', 'At3g23600', 'Alpha/beta-Hydrolases superfamily protein', '', '821939', 'NM_113263.4', 'NP_566732.1', 'Q9LUG8', '', 239, 'Potential GSL genes'),
	('AT3G23940', 'DHAD', 'Dihydroxy-acid dehydratase, chloroplastic ', 'ILVD', '821977', 'NM_113299', 'NP_189036', 'Q9LIR4', '4.2.1.9', 608, 'Potential GSL genes'),
	('AT3G24350', 'SYP32', 'Syntaxin-32', 'At3g24350', '822024', 'NM_113342.4', 'NP_189078.2', 'Q9LK09', '', 347, 'Potential GSL genes'),
	('AT3G24503', 'ALDH2C4', 'Aldehyde dehydrogenase family 2 member C4  ', 'REF1', '822042', 'NM_113359.4', 'NP_566749.1', 'Q56YU0', '1.2.1.3', 501, 'Potential GSL genes'),
	('AT3G25180', 'CYP82G1', 'Cytochrome P450 82G1 ', 'MJL12.5', '822110', '?NM_113423.4?', 'NP_189154.1?', 'Q9LSF8', '', 515, 'Potential camalexin genes'),
	('AT3G25780', 'AOC3', 'Allene oxide cyclase 3, chloroplastic ', 'K13N2.12', '822169', '?NM_113477.5', 'NP_566777.1?', 'Q9LS01', '5.3.99.6', 258, 'Potential camalexin genes'),
	('AT3G25860', 'LTA2', 'Dihydrolipoyllysine-residue acetyltransferase component 4 of pyruvate dehydrogenase complex, chloroplastic ', 'MPE11.1', '822181', '?NM_113489.3', 'NP_189215.1?', 'Q9SQI8', '', 480, 'Potential camalexin genes'),
	('AT3G26290', 'CYP71B26', 'Cytochrome P450 71B26 ', 'MTC11.22', '822232', '?NM_113536.3', 'NP_189260.1?', 'Q9LTL0', '', 500, 'Potential camalexin genes'),
	('AT3G26300', 'CYP71B34', 'Cytochrome P450 71B34 ', 'F20C19.2', '822234', '?NM_113537.2?', 'NP_189261.1?', 'Q9LIP6', '', 500, 'Potential camalexin genes'),
	('AT3G26320', 'CYP71B36', 'Cytochrome P450 71B36 ', 'F20C19.4', '822236', '?NM_113539.2', 'NP_189263.1?', 'Q9LIP4', '', 500, 'Potential camalexin genes'),
	('AT3G26330', 'CYP71B37', 'Cytochrome P450 71B37 ', 'F20C19.5', '822237', '?NM_113540.5', 'NP_189264.3?', 'Q9LIP3', '', 500, 'Potential camalexin genes'),
	('AT3G26450', '', '', '', '822251', 'NM_113553.3', 'NP_189277.1', 'Q9LIM9', '', 0, 'Potential GSL genes'),
	('AT3G26460', 'At3g26460', 'Polyketide cyclase/dehydrase and lipid transport superfamily protein', '', '822267', 'NM_113567.4', 'NP_189291.1', 'Q38956', '', 152, 'Potential GSL genes'),
	('AT3G26590', 'DTX29', 'Protein DETOXIFICATION 29 ', 'MFE16.12', '822411', 'NM_113705.4', 'NP_189427.1', 'Q9LK88', '', 500, 'Potential GSL genes'),
	('AT3G26830', 'PAD3', 'Bifunctional dihydrocamalexate synthase/camalexin synthase ', 'CYP71B15', '822298', 'NM_113595', 'NP_189318', 'Q9LW27', '1.3.1.n2', 490, 'Potential GSL genes'),
	('AT3G27190', 'UKL2', 'Uridine kinase-like protein 2, chloroplastic [Includes: Uridine kinase ', 'K17E12.1', '822338', '?NM_113633.6', 'NP_189355.1?', 'Q9LK34', '2.4.2.9, 2.7.1.48', 483, 'Potential camalexin genes'),
	('AT3G27400', 'AT3G27400', 'Putative pectate lyase 11 ', 'K1G2.11', '822361', 'NM_113655', 'NP_189376', 'Q9LTZ0', '4.2.2.2', 412, 'Potential GSL genes'),
	('AT3G27440', 'UKL5', 'Uridine kinase-like protein 5 [Includes: Probable uridine kinase ', 'K1G2.27', '822365', '?NM_113659.2', 'NP_189380.1?', 'Q9LTY6', '2.7.1.48', 465, 'Potential camalexin genes'),
	('AT3G27890', 'NQR', 'NADPH:quinone oxidoreductase ', 'K16N12.13', '822530', 'NM_113815.4', 'NP_566840.1', 'Q9MBH2', '1.6.5.2', 196, 'Potential GSL genes'),
	('AT3G28740', 'CYP81D11', 'Cytochrome P450 81D11 ', 'T19N8.3', '822506', '?NM_113795.2', 'NP_189516.1?', 'Q9LHA1', '', 509, 'Potential camalexin genes'),
	('AT3G28930', 'AIG2', 'Protein AIG2 ', 'K5K13.3', '822529', 'NM_113814', 'NP_189535', 'P54121', '2.3.2.-', 170, 'Potential GSL genes'),
	('AT3G28940', 'AIG2B', 'Avirulence-induced gene 2 protein B', 'K5K13.2', '823491', 'NM_114248.4', 'NP_189966.1', 'Q9LZG7', '2.3.2.-', 169, 'Potential GSL genes'),
	('AT3G43800', 'GSTU27', 'Glutathione S-transferase U27 ', 'T28A8.90', '823634', 'NM_114368.3', 'NP_190085.1', 'P93046', '2.5.1.18', 227, 'Potential GSL genes'),
	('AT3G44720', 'ADT4', 'Arogenate dehydratase 4, chloroplastic ', 'T32N15.11', '823601', 'NM_114340', 'NP_190058', 'O22241', '4.2.1.91', 424, 'Potential GSL genes'),
	('AT3G44990', 'XTH31', 'Xyloglucan endotransglucosylase/hydrolase protein 31 ', 'ATXG', '823650', 'NM_114383.3', 'NP_566875.1', 'P38418', '2.4.1.207\n3.2.1.151', 293, 'Potential GSL genes'),
	('AT3G45140', 'LOX2', 'Lipoxygenase 2, chloroplastic AtLOX2', 'T14D3.80', '824120', 'NM_114818.4', 'NP_190527.1', 'Q9SCK1', '1.13.11.12', 896, 'Potential GSL genes'),
	('AT3G45640', 'MPK3', 'Mitogen-activated protein kinase 3 ', 'F9K21.220', '823706', '?NM_114433.3', 'NP_190150.1?', 'Q39023', '2.7.11.24', 370, 'Potential camalexin genes'),
	('AT3G46130', 'MYB48 ', 'Transcription factor MYB48 ', 'F12M12.100', '823756', 'NM_114482', 'NP_190199', 'Q9LX82', '', 256, 'Potential GSL genes TF'),
	('AT3G46660', 'UGT76E12', 'UDP-glycosyltransferase 76E12 ', 'F12A12.180', '823819', '?NM_114533.2', 'NP_566885.1?', 'Q94AB5', '', 458, 'Potential camalexin genes'),
	('AT3G47340', 'ASN1', 'Asparagine synthetase [glutamine-hydrolyzing] 1 ', 'DIN6', '823888', '?NM_114602.4?', 'NP_190318.1?', 'P49078', '6.3.5.4', 584, 'Potential camalexin genes'),
	('AT3G47540', 'F1P2.90', 'Chitinase family protein ', '', '823908', 'NM_114622', 'NP_190338', 'Q9SN84', '', 214, 'Potential GSL genes'),
	('AT3G48560', 'CSR1', 'Acetolactate synthase, chloroplastic ', 'TZP5', '824015', 'NM_114714', 'NP_190425', 'P17597', '2.2.1.6', 670, 'Potential GSL genes'),
	('AT3G49580', 'LSU1', 'Protein RESPONSE TO LOW SULFUR 1', 'T9C5.170', '824240', 'NM_114936.5', 'NP_190645.3', 'Q9S7G2', '', 94, 'Potential GSL genes'),
	('AT3G49620', 'DIN11', 'Probable 2-oxoglutarate-dependent dioxygenase DIN11 ', 'T9C5.210', '824124', 'NM_114822', 'NP_190531', 'Q8H113', '1.14.11.-', 357, 'Potential GSL genes'),
	('AT3G50480', 'HR4', 'RPW8-like protein 4 ', 'T20E23.80', '824212', '?NM_114908.5', 'NP_566933.1?', 'Q9SCS6', '', 200, 'Potential camalexin genes'),
	('AT3G50760', 'GATL2', 'Probable galacturonosyltransferase-like 2 ', 'F18B3.40', '824402', 'NM_115097.3', 'NP_190805.1', 'Q9FT45', '2.4.1.-', 341, 'Potential GSL genes'),
	('AT3G51450', 'SSL7', 'Protein STRICTOSIDINE SYNTHASE-LIKE 7 ', 'F26O13.90', '824308', 'NM_115004', 'NP_190713', 'Q9SD04', '', 371, 'Potential GSL genes'),
	('AT3G51920', 'CML9', 'Calmodulin-like protein 9 ', 'CAM9', '824355', '?NM_115051.3', 'NP_190760.1?', 'Q9S744', '', 151, 'Potential camalexin genes'),
	('AT3G52370', 'FLA15', 'Fasciclin-like arabinogalactan protein 15', 'T25B15_140', '824412', 'NM_115107.4', 'NP_190815.1', 'Q9SVC8', '', 436, 'Potential GSL genes'),
	('AT3G52470', 'F22O6_150', 'Late embryogenesis abundant ', 'At3g52470', '824453', 'NM_115147.4', 'NP_190855.1', 'Q9LFA4', '', 208, 'Potential GSL genes'),
	('AT3G52870', 'IQM3', 'IQ domain-containing protein IQM3 ', 'F8J2_40', '824493', 'NM_115186.4', 'NP_190894.1', 'P45724', '', 456, 'Potential GSL genes'),
	('AT3G53260', 'PAL2', 'Phenylalanine ammonia-lyase 2', 'T4D2.190', '824563', 'NM_115256.4', 'NP_190964.2', 'Q9M331', '4.3.1.24', 717, 'Potential GSL genes'),
	('AT3G53960', 'NPF5.7', 'Protein NRT1/ PTR FAMILY 5.7 AtNPF5.7', 'F5K20.260', '824565', 'NM_180369.3', 'NP_850700.1', 'Q9M329', '', 602, 'Potential GSL genes'),
	('AT3G53980', 'F5K20_280', 'Bifunctional inhibitor/lipid-transfer protein/seed storage 2S albumin superfamily protein', 'At3g53980', '824771', 'NM_115463.4', 'NP_191164.1', 'Q9LYN6', '', 114, 'Potential GSL genes'),
	('AT3G54640', 'AT3G54640', 'Tryptophan synthase alpha chain, chloroplastic/ Indole-3-glycerol-phosphate lyase, chloroplastic', 'TRP3', '824629', 'NM_115321', 'NP_567004', 'Q42529', '4.2.1.20\n4.1.2.8', 312, 'Potential GSL genes'),
	('AT3G54660', 'EMB2360', 'Glutathione reductase, chloroplastic ', 'T5N23_20', '824631', '?NM_115323.4', 'NP_191026.1?', 'P42770', '1.8.1.7', 565, 'Potential camalexin genes'),
	('AT3G55870', 'F27K19_50', 'AT3g55870/F27K19_50 At3g55870/F27K19_50', '', '824753', 'NM_115445', 'NP_567028', 'Q944Q5', '', 492, 'Potential GSL genes'),
	('AT3G56050', 'At3g56050', 'Probable inactive receptor-like protein kinase ', 'F18O21.10', '824790', 'NM_115482.4', 'NP_191183.1', 'O82089', '', 499, 'Potential GSL genes'),
	('AT3G56200', 'F18O21_160', 'AT3g56200/F18O21_160 ', '', '824786', 'NM_115478', 'NP_191179', 'Q9LYM2', '', 435, 'Potential GSL genes'),
	('AT3G56240', 'CCH', 'Copper transport protein CCH ', 'F18O21.200', '824803', 'NM_115494.3', 'NP_191195.1', 'Q9LY04', '', 121, 'Potential GSL genes'),
	('AT3G56360', 'T5P19_10', 'At3g56360', 'At3g56360', '824932', 'NM_115623.6', 'NP_191322.3', 'Q6NKR6', '', 233, 'Potential GSL genes'),
	('AT3G57050', 'CBL', 'Cystathionine beta-lyase, chloroplastic ', 'F24I3.130', '824872', 'NM_180382', 'NP_850713', 'P53780', '4.4.1.8', 464, 'Potential GSL genes'),
	('AT3G57550', 'AGK2', 'Guanylate kinase 2 ', 'AGK2', '824922', '?NM_001339877.1?', 'NP_001325466.1?', 'Q9M682', '2.7.4.8', 389, 'Potential camalexin genes'),
	('AT3G57560', 'NAGK', 'Acetylglutamate kinase, chloroplastic ', 'T8H10.160', '824923', '?NM_115616.3', 'NP_191315.1?', 'Q9SCL7', '2.7.2.8', 347, 'Potential camalexin genes'),
	('AT3G57630', 'At3g57630', 'Exostosin family protein', 'AT3G57630', '824986', 'NM_115679.4', 'NP_191376.1', 'Q9M2J9', '', 793, 'Potential GSL genes'),
	('AT3G58170', 'BET11', 'Bet1-like SNARE 1-1 ', 'F9D24.80', '825030', 'NM_115723.4', 'NP_191420.1', 'Q05758', '', 122, 'Potential GSL genes'),
	('AT3G58610', 'At3g58610', 'Ketol-acid reductoisomerase, chloroplastic ', 'F14P22.200', '825372', 'NM_116064.5', 'NP_191758.1', 'Q9M266', '1.1.1.86 ', 591, 'Potential GSL genes'),
	('AT3G58740', 'CSY1', 'Citrate synthase 1, peroxisomal ', 'T20N10.90', '825043', '?NM_115736.2', 'NP_191433.1?', 'Q9LXS7', '', 480, 'Potential camalexin genes'),
	('AT3G58750', 'CSY2', 'Citrate synthase 2, peroxisomal ', 'T20N10.100', '825044', '?NM_115737.3', 'NP_191434.1?', 'Q9LXS6', '', 514, 'Potential camalexin genes'),
	('AT3G58790', 'GAUT15', 'Probable galacturonosyltransferase 15 ', 'T20N10.140', '825048', 'NM_115741', 'NP_191438', 'Q8L4B0', '2.4.1.-', 540, 'Potential GSL genes'),
	('AT3G58990', 'IPMI1', '3-isopropylmalate dehydratase small subunit 2 ', 'F17J16.40', '825068', '?NM_115761.3', 'NP_191458.1?', 'Q9LYT7', '4.2.1.33', 253, 'Potential camalexin genes'),
	('AT3G59000', 'AT3G59000', 'F-box protein At3g59000', 'F17J16.50', '825069', 'NM_115762', 'NP_191459', 'Q2V3N5', '', 491, 'Potential GSL genes'),
	('AT3G59760', 'OASC', 'Cysteine synthase, mitochondrial ', 'ATCS-C', '825145', 'NM_180692', 'NP_851023', 'Q43725', '2.5.1.47', 430, 'Potential GSL genes'),
	('AT3G60100', 'CSY5', 'Citrate synthase 5, mitochondrial ', 'T2O9.80', '825180', '?NM_115873.3', 'NP_191569.2?', 'Q9M1D3', '', 464, 'Potential camalexin genes'),
	('AT3G61400', 'F2A19.2 ', '1-aminocyclopropane-1-carboxylate oxidase homolog 8 ', 'At3g61400', '825312', 'NM_116004.2', 'NP_191699.1', 'Q9M2C4', '1.14.-.-', 370, 'Potential GSL genes'),
	('AT3G61820', 'F15G16.210', 'Aspartyl protease Putative uncharacterized protein F15G16.210', '', '825355', 'NM_116047', 'NP_191741', 'Q9M356', '', 483, 'Potential GSL genes'),
	('AT3G61990', 'OMTF3', 'S-adenosyl-L-methionine-dependent methyltransferases superfamily protein', 'F21F14.160', '825432', 'NM_116123.4', 'NP_567130.1', 'F4IYB7', '', 290, 'Potential GSL genes'),
	('AT3G62580', 'At3g62580', 'Late embryogenesis abundant protein LEA family protein', '', '825451', 'NM_116141.2', 'NP_191835.1', 'Q9LZI9', '', 213, 'Potential GSL genes'),
	('AT3G62760', 'GSTF13', 'Glutathione S-transferase F13', 'F26K9.190', '828009', 'NM_116304.4', 'NP_567187.1', 'Q8VZ38', '2.5.1.18', 219, 'Potential GSL genes'),
	('AT3G63110', 'IPT3', 'Adenylate isopentenyltransferase 3, chloroplastic ', 'T20O10.210', '825486', 'NM_116176', 'NP_567138', 'Q93WC9', '2.5.1.112', 336, 'Potential GSL genes'),
	('AT3G63520', 'CCD1', 'Carotenoid 9,10', 'NC1', '825527', '?NM_116217.3', 'NP_191911.1?', 'O65572', '', 538, 'Potential camalexin genes'),
	('AT4G00330', 'CRCK2', 'Calmodulin-binding receptor-like cytoplasmic kinase 2 ', 'F5I10.8', '828125', '?NM_001340239.1', 'NP_001329075.1?', 'Q8VZJ9', '', 411, 'Potential camalexin genes'),
	('AT4G00570', 'NAD-ME2', 'NAD-dependent malic enzyme 2, mitochondrial ', 'F6N23.16', '828222', '?NM_116281.4', 'NP_191966.2?', 'Q8L7K9', '', 607, 'Potential camalexin genes'),
	('AT4G00780', 'At4g00780', 'TRAF-like family protein', 'T18A10.3', '827912', 'NM_116337.3', 'NP_192016.1', 'Q9M156', '', 299, 'Potential GSL genes'),
	('AT4G00880', 'A_TM018A10.6', 'SAUR-like auxin-responsive protein family', '', '827989', 'NM_116314', 'NP_567196', 'O23089', '', 122, 'Potential GSL genes'),
	('AT4G01070', 'UGT72B1', 'UDP-glycosyltransferase 72B1  ', 'F2N1.15', '828075', 'NM_116369.3', 'NP_192048.2', 'F4JI18', '2.4.1.-', 480, 'Potential GSL genes'),
	('AT4G01390', 'At4g01390', 'TRAF-like family protein', 'F2N1_33', '828032', 'NM_116474.4', 'NP_567233.1', 'O81292', '', 300, 'Potential GSL genes'),
	('AT4G01430', 'AT4G01430', 'WAT1-related protein At4g01430', 'F3D13.4', '826685', 'NM_202765', 'NP_974494', 'Q9M131', '', 365, 'Potential GSL genes'),
	('AT4G01450', 'AT4G01450', 'WAT1-related protein At4g01450', 'F11O4.14', '828176', 'NM_202766', 'NP_974495', 'Q9M129', '', 361, 'Potential GSL genes'),
	('AT4G01850', 'SAM2', 'S-adenosylmethionine synthase 2 ', 'T7B11.11', '826987', '?NM_001084876.1', 'NP_001078345.1?', 'P17562', '2.5.1.6', 393, 'Potential camalexin genes'),
	('AT4G02410', 'LECRK43', 'L-type lectin-domain containing receptor kinase IV.3 LecRK-IV.3 ', 'T14P8.3', '827931', 'NM_116486.3', 'NP_192161.1', 'P46422', '2.7.11.1', 674, 'Potential GSL genes'),
	('AT4G02520', 'GSTF2', 'Glutathione S-transferase F2 ', 'PM24.1', '828100', 'NM_116541.4', 'NP_192216.1', 'Q9ZTA3', '2.5.1.18', 212, 'Potential GSL genes'),
	('AT4G04610', 'APR1', '5\'-adenylylsulfate reductase 1, chloroplastic ', 'PRH19', '825793', '?NM_116699.3', 'NP_192370.1?', 'P92979', '1.8.4.9', 465, 'Potential camalexin genes'),
	('AT4G04830', 'MSRB5', 'Peptide methionine sulfoxide reductase B5 ', 'ATMSRB5', '825820', 'NM_116721', 'NP_192392', 'Q9ZS91', '1.8.4.12', 139, 'Potential GSL genes'),
	('AT4G04840', 'MSRB6', 'Peptide methionine sulfoxide reductase B6 ', 'T4B21.4', '825821', '?NM_116722.4', 'NP_192393.2?', 'Q8GWF4', '', 153, 'Potential camalexin genes'),
	('AT4G05320', 'UBQ10', 'Polyubiquitin 10', 'C17L7.240', '825880', 'NM_202787.4', 'NP_974516.4', 'Q8H159', '', 457, 'Potential GSL genes'),
	('AT4G05590', 'MPC3', 'Mitochondrial pyruvate carrier 3 ', 'DiDi', '825927', 'NM_116797.4', 'NP_567306.1', 'Q8LD38', '', 108, 'Potential GSL genes'),
	('AT4G08300', 'AT4G08300', 'WAT1-related protein At4g08300', 'T12G13', '826384', 'NM_116899', 'NP_192570', 'Q501F8', '', 373, 'Potential GSL genes'),
	('AT4G09610', 'GASA2', 'Gibberellin-regulated protein 2 ', 'T25P22.50', '826546', '?NM_117029.2', 'NP_192699.1?', 'P46688', '', 99, 'Potential camalexin genes'),
	('AT4G10380', 'NIP5-1', 'Probable aquaporin NIP5-1 ', 'NLM6', '826630', 'NM_117106.3', 'NP_192776.1', 'Q9SV84', '', 304, 'Potential GSL genes'),
	('AT4G10390', 'F24G24.190', 'Probable receptor-like protein kinase', 'F7L13.4', '826631', 'NM_117107.5', 'NP_192777.1', 'Q9SV83', ' 2.7.11.1', 342, 'Potential GSL genes'),
	('AT4G11330', 'MPK5', 'Mitogen-activated protein kinase 5 ', 'F8L21.120', '826735', '?NM_117204.7', 'NP_567378.4?', 'Q39025', '2.7.11.24', 376, 'Potential camalexin genes'),
	('AT4G11640', 'SR', 'Serine racemase ', 'SR1', '826769', '?NM_117233.3', 'NP_192901.2?', 'Q2PGG3', '', 331, 'Potential camalexin genes'),
	('AT4G11960', 'PGRL1B', 'PGR5-like protein 1B, chloroplastic ', 'F16J13.30', '826803', '?NM_117266.4?', 'NP_192933.2?', 'Q8GYC7', '', 313, 'Potential camalexin genes'),
	('AT4G12030', 'BASS5', 'Probable sodium/metabolite cotransporter BASS5, chloroplastic ', 'BAT5', '826811', '?NM_001340768.1?', 'NP_001319909.1?', 'F4JPW1', '', 407, 'Potential camalexin genes'),
	('AT4G12390', 'PME1', 'Pectin methylesterase inhibitor 1 ', 'T4C9.230', '826848', 'NM_117309', 'NP_192976', 'Q9STH2', '', 206, 'Potential GSL genes'),
	('AT4G12440', 'APT4', 'Adenine phosphoribosyltransferase 4 ', 'T1P17.30', '826856', '?NM_001340773.1?', 'NP_001319911.1?', 'Q9SU38', '2.4.2.7', 182, 'Potential camalexin genes'),
	('AT4G13430', 'IIL1', '3-isopropylmalate dehydratase large subunit, chloroplastic ', 'T9E8.170', '826975', '?NM_117417.4', 'NP_567405.1?', 'Q94AR8', '4.2.1.33', 509, 'Potential camalexin genes'),
	('AT4G14630', 'GLP9', 'Germin-like protein subfamily 1 member 8', 'dl3355w', '827113', '?NM_117545.4', 'NP_193199.1?', 'Q9LEA7', '', 222, 'Potential camalexin genes'),
	('AT4G14680', 'APS3', 'ATP-sulfurylase 3, chloroplastic ', 'FCAALL.128', '827118', '?NM_117550.5', 'NP_193204.1?', 'O23324', '2.7.7.4', 465, 'Potential camalexin genes'),
	('AT4G14910', 'HISN5B', 'Imidazoleglycerol-phosphate dehydratase 2, chloroplastic ', 'dl3495c', '827149', '?NM_117577.4?', 'NP_567448.1?', 'O23346', '4.2.1.19', 272, 'Potential camalexin genes'),
	('AT4G15210', 'BAM5', 'Beta-amylase 5 AtBeta-Amy ', 'BMY1', '827185', 'NM_179058.1', 'NP_849389.1', 'P25853', ' 3.2.1.2', 498, 'Potential GSL genes'),
	('AT4G15310', 'CYP702A3', 'Cytochrome P450, family 702, subfamily A, polypeptide 3', 'FCAALL.266', '827197', '?NM_117619.3', 'NP_193266.2?', 'F4JJG4', '', 475, 'Potential camalexin genes'),
	('AT4G15330', 'CYP705A1', 'Cytochrome P450 like protein ', 'FCAALL.270', '827199', '?NM_117621.5', 'NP_193268.3?', 'Q0WQ07', '', 513, 'Potential camalexin genes'),
	('AT4G15440', 'CYP74B2', 'Probable inactive linolenate hydroperoxide lyase ', 'HPL1', '827215', 'NM_117633', 'NP_193279', 'B3LF83', '', 384, 'Potential GSL genes'),
	('AT4G15490', 'UGT84A3', 'UDP-glycosyltransferase 84A3 ', 'FCAALL.17', '827221', '?NM_117639.3', 'NP_193284.1?', 'O23401', '', 479, 'Potential camalexin genes'),
	('AT4G15530', 'PPDK', 'Pyruvate, phosphate dikinase 1, chloroplastic ', 'FCAALL.325', '827226', '?NM_001036570.1?', 'NP_001031647.1?', 'O23404', '2.7.9.1', 963, 'Potential camalexin genes'),
	('AT4G15920', 'SWEET17', 'Bidirectional sugar transporter SWEET17 ', 'AtSWEET17', '827274', 'NM_117684', 'NP_193327', 'Q84WN3', '', 241, 'Potential GSL genes'),
	('AT4G16740', 'TPS03', 'Tricyclene synthase, chloroplastic ', 'FCAALL.18', '827377', '?NM_001036574.1?', 'NP_001031651.1?', 'A4FVP2', '', 565, 'Potential camalexin genes'),
	('AT4G16765', 'AT4G16765', 'Iron ion binding / oxidoreductase Oxidoreductase, 2OG-FeII oxygenase family protein', '', '827383', 'NM_179213', 'NP_849544', 'F4JML1', '', 247, 'Potential GSL genes'),
	('AT4G16860', 'RPP4', 'Disease resistance protein RPP4 ', 'CHS2', '827395', '?NM_117790.4', 'NP_193420.2?', 'F4JNA9', '', 1147, 'Potential camalexin genes'),
	('AT4G16890', 'SNC1', 'Protein SUPPRESSOR OF npr1-1, CONSTITUTIVE 1 ', 'BAL', '827397', '?NM_001341145.1?', 'NP_001319970.1?', 'O23530', '', 1437, 'Potential camalexin genes'),
	('AT4G17340', 'TIP2-2', 'Probable aquaporin TIP2-2 ', 'FCAALL.412', '827446', 'NM_117838.4', 'NP_193465.1', 'Q41975', '', 250, 'Potential GSL genes'),
	('AT4G17470', 'AT4G17470', 'Alpha/beta-Hydrolases superfamily protein ', '', '827458', 'NM_117850', 'NP_193477', 'Q501G7', '', 308, 'Potential GSL genes'),
	('AT4G19170', 'CCD4', 'Probable carotenoid cleavage dioxygenase 4, chloroplastic ', 'NCED4', '827655', '?NM_118036.3', 'NP_193652.1?', 'O49675', '', 595, 'Potential camalexin genes'),
	('AT4G19450', 'T5K18.230', 'Major facilitator superfamily protein', 'T5K18_230', '827686', 'NM_118065.4', 'NP_567588.1', 'Q8H132', '', 572, 'Potential GSL genes'),
	('AT4G19810', 'ChiC', 'Class V chitinase ', 'T16H5.170', '827725', '?NM_001341373.1?', 'NP_001319999.1?', 'O81862', '', 379, 'Potential camalexin genes'),
	('AT4G19840', 'PP2A1', 'Protein PHLOEM PROTEIN 2-LIKE A1 ', 'At4g19840', '827728', 'NM_118104.5', 'NP_193719.1', 'O81865', '', 246, 'Potential GSL genes'),
	('AT4G20170', 'GALS3', 'Galactan beta-1,4-galactosyltransferase GALS3 ', 'F1C12.90', '827763', 'NM_118136', 'NP_193750', 'O65431', '2.4.1.-', 504, 'Potential GSL genes'),
	('AT4G20860', 'FAD-OXR', 'Berberine bridge enzyme-like 22 ', 'T13K14.20', '827834', '?NM_118204.2', 'NP_193818.1?', 'Q9SUC6', '', 530, 'Potential camalexin genes'),
	('AT4G21390', 'B120', 'G-type lectin S-receptor-like serine/threonine-protein kinase B120 ', 'F18E5.10', '827891', '?NM_118259.4', 'NP_193870.1?', 'O81906', '2.7.11.1', 849, 'Potential camalexin genes'),
	('AT4G21670', 'CPL1', 'RNA polymerase II C-terminal domain phosphatase-like 1 ', 'FRY2', '828254', '?NM_118287.5', 'NP_193898.3?', 'Q5YDB6', '', 967, 'Potential camalexin genes'),
	('AT4G21760', 'BGLU47', 'Beta-glucosidase 47 ', 'F17L22.220', '828264', 'NM_118296', 'NP_193907', 'Q9SVS1', '3.2.1.21', 535, 'Potential GSL genes'),
	('AT4G21830', 'MSRB7', 'Peptide methionine sulfoxide reductase B7 ', 'T8O5.40', '828271', '?NM_001084953.1?', 'NP_001078422.1?', 'Q8VY86', '', 144, 'Potential camalexin genes'),
	('AT4G21850', 'ATMSRB9', 'Peptide methionine sulfoxide reductase B9 ', 'MSRB9', '828273', 'NM_179087', 'NP_849418', 'Q84JT6', '1.8.4.12', 143, 'Potential GSL genes'),
	('AT4G21960', 'PER42', 'Peroxidase 42 ', 'P42', '828285', 'NM_118317.4', 'NP_567641.1', 'Q9SB81', '1.11.1.7', 330, 'Potential GSL genes'),
	('AT4G21980', 'APG8A', 'Autophagy-related protein 8a ', 'APG8A', '828287', '?NM_118319.4?', 'NP_567642.1?', 'Q8LEM4', '', 122, 'Potential camalexin genes'),
	('AT4G22570', 'APT3', 'Adenine phosphoribosyltransferase 3 ', 'F7K2.150', '828353', '?NM_118383.4', 'NP_193988.1?', 'Q9SUW2', '2.4.2.7', 183, 'Potential camalexin genes'),
	('AT4G22710', 'CYP706A2', 'Cytochrome P450 - like protein ', 'F25I18.3', '828367', '?NM_118397.4', 'NP_194002.1?', 'O49652', '', 526, 'Potential camalexin genes'),
	('AT4G22790', 'DTX56', 'Protein DETOXIFICATION 56 ', 'T12H17.180', '828378', 'NM_118408', 'NP_194010', 'O49660', '', 491, 'Potential GSL genes'),
	('AT4G23100', 'GSH1', 'Glutamate--cysteine ligase, chloroplastic ', 'CAD2', '828409', '?NM_001203879.2?', 'NP_001190808.1?', 'P46309', '6.3.2.2', 522, 'Potential camalexin genes'),
	('AT4G23190', 'CRK11', 'Cysteine-rich receptor-like protein kinase 11 ', 'RLK3', '828418', '?NM_118448.4', 'NP_194050.2?', 'Q9ZP16', '', 667, 'Potential camalexin genes'),
	('AT4G23270', 'CRK19', 'Cysteine-rich receptor-like protein kinase 19 ', 'F21P8.160', '828426', '?NM_001341593.1?', 'NP_001329528.1?', 'Q8GWJ7', '', 645, 'Potential camalexin genes'),
	('AT4G23600', 'CORI3', 'Cystine lyase CORI3 ', 'JR2', '828460', 'NM_179099', 'NP_849430', 'Q9SUR6', '4.4.1.-', 422, 'Potential GSL genes'),
	('AT4G23670', 'At4g23670', 'Polyketide cyclase/dehydrase and lipid transport superfamily protein', 'F9D16.140', '828467', 'NM_118498.4', 'NP_194098.1', 'Q9SUR0', '', 151, 'Potential GSL genes'),
	('AT4G23730', 'F9D16.200', 'Apospory-associated protein C ', '', '828473', 'NM_118504', 'NP_194104', 'Q9SUQ4', '', 306, 'Potential GSL genes'),
	('AT4G23810', 'WRKY53', 'Probable WRKY transcription factor 53 ', 'F9D16.280', '828481', '?NM_118512.3', 'NP_194112.1?', 'Q9SUP6', '', 324, 'Potential camalexin genes TF'),
	('AT4G24350', 'T22A6.180', 'Phosphorylase family protein ', '', '828538', 'NM_118568', 'NP_194166', 'Q94K59', '', 336, 'Potential GSL genes'),
	('AT4G24520', 'ATR1', 'NADPH--cytochrome P450 reductase 1 ', 'AR1', '828554', 'NM_118585.4', 'NP_194183.1', 'Q9SB48', '1.6.2.4', 692, 'Potential GSL genes'),
	('AT4G25100', 'FSD1', 'Superoxide dismutase [Fe] 1, chloroplastic ', 'SODB', '828613', 'NM_179110.2', 'NP_849441.1', 'P21276', '1.15.1.1', 212, 'Potential GSL genes'),
	('AT4G26510', 'UKL4', 'Uridine kinase-like protein 4 [Includes: Uridine kinase ', 'UPT1', '828757', '?NM_001341804.1', 'NP_001320072.1?', 'O65583', '2.7.1.48', 469, 'Potential camalexin genes'),
	('AT4G26900', 'HISN4', 'Imidazole glycerol phosphate synthase hisHF, chloroplastic ', 'F10M23.240', '828797', '?NM_118824.4', 'NP_194420.1?', 'Q9SZ30', '', 592, 'Potential camalexin genes'),
	('AT4G26970', 'ACO3', 'Aconitate hydratase 3, mitochondrial ', 'F10M23.310', '828805', 'NM_118831', 'NP_567763', 'Q94A28', '4.2.1.3', 995, 'Potential GSL genes'),
	('AT4G27070', 'TSB2', 'Tryptophan synthase beta chain 2, chloroplastic ', 'T24A18.20', '828815', 'NM_118841', 'NP_194437', 'P25269', '4.2.1.20', 475, 'Potential GSL genes'),
	('AT4G27710', 'CYP709B3', 'Cytochrome P450 709B3 ', '', '828885', '?NM_118910.4', 'NP_194501.1?', 'Q9T093', '', 518, 'Potential camalexin genes'),
	('AT4G27830', 'BGLU10', 'Beta-glucosidase 10 ', 'T27E11.70', '828896', 'NM_118921', 'NP_567787', 'Q93ZI4', '3.2.1.21', 508, 'Potential GSL genes'),
	('AT4G27860', 'MEB1', 'Membrane protein of ER body 1', 'T27E11.100', '828899', 'NM_118924', 'NP_567788', 'Q8W4P8', '', 611, 'Potential GSL genes'),
	('AT4G28410', 'RSA1 ', 'Tyrosine transaminase family protein', 'At4g28410', '828958', 'NM_118983.4. ', 'NP_194570.2', 'F4JL94', '', 447, 'Potential GSL genes'),
	('AT4G28420', 'F20O9.100', 'Probable aminotransferase TAT1', 'At4g28420 ', '828959', ' NM_001036662.2', 'NP_001031739.1', 'Q67Y55', '2.6.1.-', 449, 'Potential GSL genes'),
	('AT4G29210', 'GGT3', 'Gamma-glutamyltranspeptidase 3 ', 'GGT4', '829042', 'NM_202907', 'NP_974636', 'Q9M0G0', '2.3.2.23\n4.19.13', 637, 'Potential GSL genes'),
	('AT4G29220', 'PFK1', 'ATP-dependent 6-phosphofructokinase 1', 'At4g29220', '829043', 'NM_119066.3', 'NP_194651.1', 'Q9M0F9', '', 473, 'Potential GSL genes'),
	('AT4G29690', 'T16L4.200', 'Alkaline-phosphatase-like protein ', '', '829090', 'NM_119114', 'NP_194698', 'Q9SU82', '3.6.1.9', 457, 'Potential GSL genes'),
	('AT4G29700', 'AT4G29700', 'Alkaline-phosphatase-like protein ', 'T16L4.210', '829091', 'NM_119115', 'NP_194699', 'Q9SU81', '3.6.1.9', 461, 'Potential GSL genes'),
	('AT4G30110', 'HMA2', 'Cadmium/zinc-transporting ATPase HMA2', 'F6G3.140', '829134', 'NM_119157', 'NP_194740', 'Q9SZW4', '3.6.3.3\n3.6.3.5', 951, 'Potential GSL genes'),
	('AT4G30210', 'AR2', 'NADPH--cytochrome P450 reductase 2 ', 'F9N11.60', '829144', 'NM_179141', 'NP_849472', 'Q9SUM3', '1.6.2.4', 711, 'Potential GSL genes'),
	('AT4G30540', 'GGP2 ', 'Gamma-glutamyl peptidase 2 ', 'At4g30540', '829177', 'NM_119200.3', 'NP_194783.1', 'Q9M0A6', '3.4.19.-', 248, 'Potential GSL genes'),
	('AT4G30550', 'GGP3', 'Gamma-glutamyl peptidase 3', 'At4g30550', '829178', 'NM_119201.3', 'NP_194784.1', 'Q9M0A5', '3.4.19.-', 249, 'Potential GSL genes'),
	('AT4G31800', 'WRKY18', 'WRKY transcription factor 18 ', 'F28M20.10', '829308', 'NM_119329', 'NP_567882', 'Q9C5T4', '', 310, 'Potential GSL genes TF'),
	('AT4G31940', 'CYP82C4', 'Cytochrome P450 82C4 ', 'F10N7.250', '829324', '?NM_119345.3', 'NP_194922.1?', 'Q9SZ46', '', 524, 'Potential camalexin genes'),
	('AT4G32980', 'ATH1', 'Homeobox protein ATH1', 'F26P21.100', '829435', 'NM_119452', 'NP_195024', 'P48731', '', 473, 'Potential GSL genes TF'),
	('AT4G33010', 'GLDP1', 'Glycine dehydrogenase ', 'GDP1', '829438', '?NM_119455.3?', 'NP_195027.1?', 'Q94B78', '1.4.4.2', 1037, 'Potential camalexin genes'),
	('AT4G33050', 'IQM1', 'IQ domain-containing protein IQM1 ', 'EDA39', '829442', 'NM_202944', 'NP_974673', 'O82645', '', 488, 'Potential GSL genes'),
	('AT4G33150', '', 'Alpha-aminoadipic semialdehyde synthase ', 'LKR SDH', '829452', '?NM_001160811.2?', 'NP_001154283.1?', 'Q9SMZ4', '', 1064, 'Potential camalexin genes'),
	('AT4G33680', 'DAP', 'LL-diaminopimelate aminotransferase, chloroplastic ', 'AGD2', '829510', '?NM_119526.4', 'NP_567934.1?', 'Q93ZN9', '2.6.1.83', 461, 'Potential camalexin genes'),
	('AT4G34230', 'CAD5', 'Cinnamyl alcohol dehydrogenase 5', 'CAD-D', '829572', 'NM_119587.4', 'NP_195149.1', 'O49482', '1.1.1.195', 357, 'Potential GSL genes'),
	('AT4G34740', 'ASE2', 'Amidophosphoribosyltransferase 2, chloroplastic ', 'CIA1', '829626', '?NM_119640.3', 'NP_195200.1?', 'Q9STG9', '2.4.2.14', 561, 'Potential camalexin genes'),
	('AT4G34950', 'AT4G34950', 'Major facilitator family protein ', 'T11I11.190', '829647', 'NM_119661', 'NP_195221', 'Q9SW40', '', 567, 'Potential GSL genes'),
	('AT4G35260', 'IDH1', 'Isocitrate dehydrogenase [NAD] regulatory subunit 1, mitochondrial ', 'F23E12.180', '829679', '?NM_119692.3', 'NP_195252.1?', 'Q8LFC0', '', 367, 'Potential camalexin genes'),
	('AT4G35630', 'PSAT', 'Phosphoserine aminotransferase 1, chloroplastic ', 'F8D20.140', '829715', 'NM_119728', 'NP_195288', 'Q96255', '2.6.1.52', 430, 'Potential GSL genes'),
	('AT4G35830', 'ACO1', 'Aconitate hydratase 1 ', 'F4B14.100', '829737', 'NM_119749', 'NP_195308', 'Q42560', '4.2.1.3', 898, 'Potential GSL genes'),
	('AT4G36220', 'CYP84A1', 'Cytochrome P450 84A1', 'FAH1', '829779', 'NM_119790.3', 'NP_195345.1', 'Q42600', '1.14.-.- ', 520, 'Potential GSL genes'),
	('AT4G36500', 'C7A10.860', 'Putative uncharacterized protein AT4g36500 ', '', '829802', 'NM_119813', 'NP_195368', 'O23231', '', 122, 'Potential GSL genes'),
	('AT4G36640', 'C7A10.720', 'Sec14p-like phosphatidylinositol transfer family protein', 'AP22.47', '829816', 'NM_119827.4', 'NP_195382.1', 'O23217', '', 294, 'Potential GSL genes'),
	('AT4G37150', 'MES9', 'Methylesterase 9 ', 'AP22.78', '829869', '?NM_119878.5', 'NP_195432.1?', 'O23171', '', 256, 'Potential camalexin genes'),
	('AT4G37310', 'C7A10.50', 'Cytochrome P450, family 81, subfamily H, polypeptide 1', 'P450', '829886', 'NM_119895.4', 'NP_568024.2', 'Q9SW67', '', 518, 'Potential GSL genes'),
	('AT4G37320', 'C7A10.40 ', 'Cytochrome P450, family 81, subfamily D, polypeptide 5', 'At4g37320 ', '829887', 'NM_119896.4', 'NP_195449.1', 'O23156', '', 495, 'Potential GSL genes'),
	('AT4G37360', 'CYP81D2', 'Cytochrome P450, family 81, subfamily D, polypeptide 2 ', 'F6G17.10', '829890', '?NM_119899.1', 'NP_195452.1?', 'Q9SZT6', '', 499, 'Potential camalexin genes'),
	('AT4G37370', 'CYP81D8', 'Cytochrome P450, family 81, subfamily D, polypeptide 8 ', 'F6G17.20', '829891', '?NM_119900.3', 'NP_195453.1?', 'Q9SZT7', '', 497, 'Potential camalexin genes'),
	('AT4G37970', 'CAD6', 'Probable cinnamyl alcohol dehydrogenase 6 ', 'CADA', '829953', 'NM_119958.4', 'NP_195510.1', 'O65621', '1.1.1.195', 363, 'Potential GSL genes'),
	('AT4G38550', 'AT4G38550', 'Phospholipase like protein ', '', '830012', 'NM_120016', 'NP_195567', 'Q9C5F6', '', 612, 'Potential GSL genes'),
	('AT4G38740', 'CYP18-3', 'Peptidyl-prolyl cis-trans isomerase CYP18-3 ', 'At4g38740', '830029', 'NM_120034.2', 'NP_195585.1', 'P34790', '5.2.1.8 ', 172, 'Potential GSL genes'),
	('AT4G39030', 'EDS5', 'Protein DETOXIFICATION 47, chloroplastic ', 'SID1', '830058', 'NM_120063', 'NP_195614', 'Q945F0', '', 543, 'Potential GSL genes'),
	('AT4G39230', 'PCBER1', 'Isoflavone reductase homolog PCBER1 ', 'T22F8.130', '830078', '?NM_120083.5', 'NP_195634.1?', 'Q9T030', '', 308, 'Potential camalexin genes'),
	('AT4G39320', 'T22F8.220', 'Microtubule-associated protein-like protein Putative uncharacterized protein AT4g39320', '', '830087', 'NM_120092', 'NP_568057', 'Q9T038', '', 166, 'Potential GSL genes'),
	('AT4G39540', 'SK2', 'Shikimate kinase 2, chloroplastic AtSK2', 'F23K16.170', '830108', 'NM_202986.2', 'NP_974715.1', 'Q8GY88', '2.7.1.71', 300, 'Potential GSL genes'),
	('AT4G39730', 'PLAT1', 'PLAT domain-containing protein 1 ', '', '830128', 'NM_120134.3', 'NP_195683.1', 'O65660', '', 181, 'Potential GSL genes'),
	('AT4G39940', 'APK2', 'Adenylyl-sulfate kinase 2, chloroplastic ', 'AKN2', '830153', '?NM_120157.4', 'NP_195704.1?', 'O49196', '2.7.1.25', 293, 'Potential camalexin genes'),
	('AT4G39980', 'DHS1', 'Phospho-2-dehydro-3-deoxyheptonate aldolase 1, chloroplastic ', 'T5J17.150', '830159', 'NM_120162', 'NP_195708', 'P29976', '2.5.1.54', 525, 'Potential GSL genes'),
	('AT5G01500', 'TAAC', 'Thylakoid ADP,ATP carrier protein, chloroplastic', 'F7A7.20', '831861', 'NM_120228', 'NP_195770', 'Q9M024', '', 415, 'Potential GSL genes'),
	('AT5G02230', 'At5g02230', 'Haloacid dehalogenase-like hydrolase HAD superfamily protein', 'T7H20_280', '831784', 'NM_180423.3', 'NP_850754.1', 'Q9LZK9', '', 280, 'Potential GSL genes'),
	('AT5G02290', 'PBL11', 'Probable serine/threonine-protein kinase PBL11 ', 'NAK', '831880', '?NM_120307.4', 'NP_195849.1?', 'P43293', '', 389, 'Potential camalexin genes'),
	('AT5G02490', 'MED37D', 'Probable mediator of RNA polymerase II transcription subunit 37c ', 'HSC70-G8', '831856', 'NM_120327.5', 'NP_195869.1', 'P22954', '', 653, 'Potential GSL genes'),
	('AT5G02500', 'MED37E', 'Probable mediator of RNA polymerase II transcription subunit 37e', 'HSC70-1', '831020', 'NM_120328.5', 'NP_195870.1', 'P22953', '', 651, 'Potential GSL genes'),
	('AT5G03290', 'IDH-V', 'Isocitrate dehydrogenase [NAD] catalytic subunit 5, mitochondrial ', 'F12E4_20', '831884', 'NM_120407', 'NP_568113', 'Q945K7', '1.1.1.41', 374, 'Potential GSL genes'),
	('AT5G03630', 'MDAR2', 'Monodehydroascorbate reductase 2 AtMDAR2 ', 'F17C15.50', '831774', 'NM_120444.5', 'NP_568125.1', 'Q93WJ8', '1.6.5.4', 435, 'Potential GSL genes'),
	('AT5G04140', 'GLU1', 'Ferredoxin-dependent glutamate synthase 1, chloroplastic/mitochondrial ', 'GLS1', '830292', '?NM_120496.3?', 'NP_568134.1?', 'Q9ZNZ7', '', 1622, 'Potential camalexin genes'),
	('AT5G04240', 'ELF6', 'Probable lysine-specific demethylase ELF6 ', 'JMJ11', '830303', '?NM_120506.5', 'NP_196044.2?', 'Q6BDA0', '', 1340, 'Potential camalexin genes'),
	('AT5G04590', 'SIR', 'Assimilatory sulfite reductase ferredoxin, chloroplastic', 'T32M21.190', '830336', 'NM_120541', 'NP_196079', 'Q9LZ66', '1.8.7.1', 642, 'Potential GSL genes'),
	('AT5G04950', 'NAS1', 'Nicotianamine synthase 1 ', 'MUG13.19', '830377', 'NM_120577', 'NP_196114', 'Q9FF79', '2.5.1.43', 320, 'Potential GSL genes'),
	('AT5G05410', 'DREB2A', 'Dehydration-responsive element-binding protein 2A ', 'ERF045', '830424', '?NM_120623.3?', 'NP_196160.1?', 'O82132', '', 335, 'Potential camalexin genes'),
	('AT5G05590', 'PAI2', 'PHOSPHORIBOSYLANTHRANILATE ISOMERASE 2', 'MOP10.13', '830442', 'NM_203005', 'NP_974734', 'Q42527', '5.3.1.24', 275, 'Potential GSL genes'),
	('AT5G05600', 'At5g05600', 'Probable 2-oxoglutarate-dependent dioxygenase At5g05600 ', 'MOP10.14', '830443', 'NM_120642.3', 'NP_196179.1', 'Q9FFF6', '1.14.11.-', 371, 'Potential GSL genes'),
	('AT5G05730', 'ASA1', 'Anthranilate synthase alpha subunit 1, chloroplastic ', 'AMT1', '830457', '?NM_120655.4?', 'NP_196192.1?', 'P32068', '4.1.3.27', 595, 'Potential camalexin genes'),
	('AT5G05960', 'At5g05960', 'Bifunctional inhibitor/lipid-transfer protein/seed storage 2S albumin superfamily protein', 'K18J17.13', '830481', 'NM_120678.3', 'NP_568160.1', 'Q8LBY9', '', 116, 'Potential GSL genes'),
	('AT5G06870', 'PGIP2', 'Polygalacturonase inhibitor 2 ', 'MOJ9.4', '830578', '?NM_120770.4', 'NP_196305.1?', 'Q9M5J8', '', 330, 'Potential camalexin genes'),
	('AT5G07000', 'SOT14', 'Cytosolic sulfotransferase 14 ', 'ST2B', '830591', 'NM_120782.4', 'NP_196317.2', 'Q8GZ53', '2.8.2.-', 347, 'Potential GSL genes'),
	('AT5G07010', 'SOT15', 'Cytosolic sulfotransferase 15 ', 'ST2A', '830592', 'NM_120783.4', 'NP_568177.1', 'Q8L5A7', '2.8.2.39 ', 359, 'Potential GSL genes'),
	('AT5G07440', 'GDH2', 'Glutamate dehydrogenase 2 ', 'T2I1_150', '830635', '?NM_001125711.2?', 'NP_001119183.1?', 'Q38946', '', 411, 'Potential camalexin genes'),
	('AT5G07460', 'PMSR2', 'Peptide methionine sulfoxide reductase A2', 'ATMSRA2', '830637', 'NM_120828', 'NP_196363', 'Q9LY15', '1.8.4.11', 218, 'Potential GSL genes'),
	('AT5G07690', 'MYB29', 'Transcription factor MYB29 ', 'HAG3 PMG2', '830662', '?NM_120851.2', 'NP_196386.1?', 'Q9FLR1', '', 336, 'Potential camalexin genes TF'),
	('AT5G07700', 'MYB76', 'Transcription factor MYB76 ', 'HAG2', '830663', '?NM_001342956.1', 'NP_001318501.1?', 'Q9SPG5', '', 338, 'Potential camalexin genes TF'),
	('AT5G07800', 'MXM12.4', 'Flavin-containing monooxygenase FMO GS-OX-like 9 ', 'At5g07800 ', '830673', 'NM_120862.4', 'NP_196397.1', 'Q9FF12', '1.8.-.-', 460, 'Potential GSL genes'),
	('AT5G08170', 'EMB1873', 'Agmatine deiminase', 'ATAIH', '830713', 'NM_120900', 'NP_196434', 'Q8GWW7', '3.5.3.12', 383, 'Potential GSL genes'),
	('AT5G09220', 'AAP2', 'Amino acid permease 2 ', 'T2K12.6 ', '830781', 'NM_120958', 'NP_196484', 'Q38967', '', 493, 'Potential GSL genes'),
	('AT5G09650', 'AtPPa6', 'Soluble inorganic pyrophosphatase 6, chloroplastic ', 'PPa6', '830824', 'NM_121002', 'NP_196527', 'Q9LXC9', '3.6.1.1', 300, 'Potential GSL genes'),
	('AT5G09660', 'PMDH2', 'Malate dehydrogenase 2, peroxisomal ', 'MTH16.8', '830825', '?NM_121003.4?', 'NP_196528.1?', 'Q9ZP05', '1.1.1.37', 354, 'Potential camalexin genes'),
	('AT5G10170', 'ATMIPS3', 'Probable inositol 3-phosphate synthase isozyme 3 ', 'MIPS3', '830881', 'NM_121055', 'NP_196579', 'Q9LX12', '5.5.1.4', 510, 'Potential GSL genes'),
	('AT5G10180', 'AST68', 'Sulfate transporter 2.1', 'AST68', '830882', 'NM_121056', 'NP_196580', 'O04722', '', 677, 'Potential GSL genes'),
	('AT5G10240', 'ASN3', 'Asparagine synthetase [glutamine-hydrolyzing] 3', 'F18D22.10', '830888', 'NM_121062.5', 'NP_196586.1', 'Q9LFU1', '6.3.5.4', 578, 'Potential GSL genes'),
	('AT5G10300', 'HNL', 'Alpha-hydroxynitrile lyase ', 'MES5', '830894', '?NM_121068.4', 'NP_196592.1?', 'Q9LFT6', '', 258, 'Potential camalexin genes'),
	('AT5G10520', 'RBK1', 'Receptor-like cytosolic serine/threonine-protein kinase RBK1 ', 'F12B17.130', '830917', '?NM_121090.4', 'NP_568231.1?', 'Q8H1D6', '', 467, 'Potential camalexin genes'),
	('AT5G11160', 'APT5', 'Adenine phosphoribosyltransferase 5 ', 'F2I11.50', '830985', '?NM_121154.4', 'NP_196677.1?', 'Q9LFP0', '2.4.2.7', 191, 'Potential camalexin genes'),
	('AT5G11410', 'F2I11_300', 'Protein kinase family protein ', '', '831012', 'NM_121179', 'NP_196702', 'Q9LFL6', '', 336, 'Potential GSL genes'),
	('AT5G11520', 'ASP3', 'Aspartate aminotransferase 3, chloroplastic ', 'YLS4', '831024', '?NM_121190.3', 'NP_196713.1?', 'P46644', '2.6.1.1', 449, 'Potential camalexin genes'),
	('AT5G11610', 'F15N18_200', 'Exostosin family protein ', '', '831033', 'NM_203037', 'NP_974766', 'Q9LYD1', '', 546, 'Potential GSL genes'),
	('AT5G11670', 'NADP-ME2', 'NADP-dependent malic enzyme 2 ', 'T22P22.60', '831039', 'NM_121205', 'NP_196728', 'Q9LYG3', '1.1.1.40', 588, 'Potential GSL genes'),
	('AT5G12040', 'NLP3', 'Omega-amidase, chloroplastic ', 'F14F18_210', '831077', 'NM_203040', 'NP_974769', 'Q8RUF8', '3.5.1.3', 369, 'Potential GSL genes'),
	('AT5G13220', 'JAZ10', 'Protein TIFY 9 (Jasmonate ZIM domain-containing protein 10) ', 'JAS1', '831162', '?NM_001161241.2?', 'NP_001154713.1?', 'Q93ZM9', '', 197, 'Potential camalexin genes'),
	('AT5G13280', 'AK1', 'Aspartokinase 1, chloroplastic ', 'AK AK-LYS1', '831169', '?NM_121331.3', 'NP_196832.1?', 'Q9LYU8', '2.7.2.4', 569, 'Potential camalexin genes'),
	('AT5G13450', 'ATP5', 'ATP synthase subunit O, mitochondrial ', 'T22N19.100', '831186', '?NM_121348.4?', 'NP_196849.1?', 'Q96251', '', 238, 'Potential camalexin genes'),
	('AT5G13550', 'SULTR4;1', 'Sulfate transporter 4.1, chloroplastic ', 'MSH12.1', '831199', 'NM_121358', 'NP_196859', 'Q9FY46', '', 685, 'Potential GSL genes'),
	('AT5G14200', 'IMDH3', '3-isopropylmalate dehydrogenase 3, chloroplastic ', 'MUA22.20', '831270', '?NM_121424.6?', 'NP_196924.1?', 'Q9FMT1', '1.1.1.85', 409, 'Potential camalexin genes'),
	('AT5G14400', 'CYP724A1', 'Cytochrome P450, family 724, subfamily A, polypeptide 1', 'F18O22.190', '831291', '?NM_121444.4', 'NP_196944.3?', 'F4K6S3', '', 367, 'Potential camalexin genes'),
	('AT5G14700', 'T15N1_190', 'Cinnamoyl CoA reductase-like protein NADP-binding Rossmann-fold superfamily protein', 'T9L3.2', '831322', 'NM_121474.3', 'NP_196974.1', 'Q9LYJ0', '', 368, 'Potential GSL genes'),
	('AT5G14940', 'NPF5.8', 'Protein NRT1/ PTR FAMILY 5.8 ', 'F2G14.60', '831346', 'NM_121498', 'NP_196998', 'Q9LFR1', '', 552, 'Potential GSL genes'),
	('AT5G16010', 'At5g16010', '3-oxo-5-alpha-steroid 4-dehydrogenase family protein ', 'F1N13_150', '831458', 'NM_121606.2', 'NP_197105.1', 'Q9LFS3', '', 268, 'Potential GSL genes'),
	('AT5G16290', 'VAT1', 'Acetolactate synthase small subunit 1, chloroplastic ', 'MQK4.1', '831490', '?NM_121634.4', 'NP_197133.1?', 'Q9FFF4', '2.2.1.6', 477, 'Potential camalexin genes'),
	('AT5G17220', 'GSTF12', 'Glutathione S-transferase F12', 'TT19', '831586', 'NM_121728.4', 'NP_197224.1', 'Q9FE46', '2.5.1.18', 214, 'Potential GSL genes'),
	('AT5G17380', 'HACL', '2-hydroxyacyl-CoA lyase ', 'OCD', '831604', 'NM_121744', 'NP_197240', 'Q9LF46', '4.1.-.-', 572, 'Potential GSL genes'),
	('AT5G17450', 'HIPP21', 'Heavy metal-associated isoprenylated plant protein 21 ', 'K3M16_20', '831611', 'NM_203066', 'NP_974795', 'Q9LF57', '', 149, 'Potential GSL genes'),
	('AT5G17990', 'TRP1', 'Anthranilate phosphoribosyltransferase, chloroplastic ', 'MCM23.6', '831666', 'NM_121804', 'NP_197300', 'Q02166', '2.4.2.18', 444, 'Potential GSL genes'),
	('AT5G18170', 'GDH1', 'Glutamate dehydrogenase 1 ', 'MRG7.13', '831935', '?NM_121822.4', 'NP_197318.1?', 'Q43314', '', 411, 'Potential camalexin genes'),
	('AT5G19140', 'ATAILP1', 'Aluminum induced protein with YGL and LRDR motifs ', 'ATAILP1', '832034', '?NM_121919.3', 'NP_197415.1?', 'Q94BR2', '', 234, 'Potential camalexin genes'),
	('AT5G19240', 'At5g19240', 'Uncharacterized GPI-anchored protein', 'T24G5.140', '832044', 'NM_121929.3', 'NP_197425.1', 'Q84VZ5', '', 199, 'Potential GSL genes'),
	('AT5G19360', 'CPK34', 'Calcium-dependent protein kinase 34 ', 'F7K24.110', '832056', '?NM_121941.2', 'NP_197437.1?', 'Q3E9C0', '', 523, 'Potential camalexin genes'),
	('AT5G19600', 'SULTR3;5', 'Probable sulfate transporter 3.5', 'T29J13.20', '832080', 'NM_121965', 'NP_568377', 'Q94LW6', '', 634, 'Potential GSL genes'),
	('AT5G19990', 'RPT6A', '26S proteasome regulatory subunit 8 homolog A ', 'SUG1', '832121', '?NM_001343633.1', 'NP_001318606.1?', 'Q9C5U3', '', 419, 'Potential camalexin genes'),
	('AT5G20620', 'UBQ4', 'Polyubiquitin 4 [Cleaved into: Ubiquitin]', 'T1M15.20', '832184', 'NM_122069.4', 'NP_568397.1', 'P0CH32', '', 382, 'Potential GSL genes'),
	('AT5G20720', 'CPN20', '20 kDa chaperonin, chloroplastic ', 'CHCPN10', '832195', '?NM_001343684.1', 'NP_001318614.1?', 'O65282', '', 253, 'Potential camalexin genes'),
	('AT5G20960', 'AAO1', 'Indole-3-acetaldehyde oxidase ', 'ATAO', '832221', 'NM_180718', 'NP_851049', 'Q7G193', '1.2.3.7', 1368, 'Potential GSL genes'),
	('AT5G20980', 'MS3', '5-methyltetrahydropteroyltriglutamate--homocysteine methyltransferase 3, chloroplastic ', 'F22D1', '832223', 'NM_122107.4', 'NP_197598.2', 'Q0WNZ5', '2.1.1.14 ', 812, 'Potential GSL genes'),
	('AT5G22630', 'ADT5', 'Arogenate dehydratase 5, chloroplastic ', 'MDJ22.5', '832326', 'NM_122169.3', 'NP_197655.1', 'Q9FNJ8', '4.2.1.91', 425, 'Potential GSL genes'),
	('AT5G23820', 'UQI3 ', 'MD2-RELATED LIPID RECOGNITION 3', 'AT5G23820', '832447', 'NM_122287', 'NP_197771', 'Q9FF98', '', 164, 'Potential GSL genes'),
	('AT5G24110', 'WRKY30', 'Probable WRKY transcription factor 30 ', 'MLE8.3', '832476', '?NM_122316.3', 'NP_568439.1?', 'Q9FL62', '', 303, 'Potential camalexin genes TF'),
	('AT5G24160', 'SQE6', 'Squalene epoxidase 6 ', 'SQP1,2', '832482', 'NM_122321.5', 'NP_197804.1', 'O65402', '1.14.14.17', 517, 'Potential GSL genes'),
	('AT5G24290', 'MEB2', 'Membrane protein of ER body 2', 'MOP9.11', '832496', 'NM_180736', 'NP_851067', 'F4KFS7', '', 550, 'Potential GSL genes'),
	('AT5G24420', 'PGL5', 'Probable 6-phosphogluconolactonase 3 ', '', '832513', 'NM_122350', 'NP_197830', 'Q8LEV7', '3.1.1.31', 252, 'Potential GSL genes'),
	('AT5G24660', 'LSU2', 'RESPONSE TO LOW SULFUR 2 ', 'MXC17_2', '832538', 'NM_122375', 'NP_197854', 'Q9FIR9', '', 94, 'Potential GSL genes'),
	('AT5G25120', 'CYP71B11', 'Cytochrome P450 71B11 ', 'T11H3.130', '832583', '?NM_122421.3', 'NP_197894.1?', 'P58049', '', 496, 'Potential camalexin genes'),
	('AT5G25130', 'CYP71B12', 'Cytochrome P450 71B12 ', 'F21J6.2', '832584', '?NM_122422.4', 'NP_197895.1?', 'Q9ZU07', '', 496, 'Potential camalexin genes'),
	('AT5G25190', 'ERF003', 'Ethylene-responsive transcription factor ERF003', 'F21J6.103', '832590', 'NM_122428', 'NP_197901', 'Q94AW5', '', 181, 'Potential GSL genes TF'),
	('AT5G25880', 'NADP-ME3', 'NADP-dependent malic enzyme 3 ', 'T1N24.25', '832657', '?NM_122489.3', 'NP_197960.1?', 'Q9XGZ0', '', 588, 'Potential camalexin genes'),
	('AT5G26220', 'GGCT2;1 ', 'Gamma-glutamylcyclotransferase 2-1 ', 'T19G15_70', '832691', 'NM_122523', 'NP_197994', 'Q8GY54', '2.3.2.4', 216, 'Potential GSL genes'),
	('AT5G26920', 'CBP60G', 'Calmodulin-binding protein 60 G', 'F2P16.9', '832750', '?NM_001203479.1?', 'NP_001190408.1?', 'F4K2R6', '', 563, 'Potential camalexin genes'),
	('AT5G27350', 'SFP1', 'Sugar transporter ERD6-like 17 ', 'F21A20.60', '832794', 'NM_122617', 'NP_568493', 'Q94CI7', '', 474, 'Potential GSL genes'),
	('AT5G27380', 'GSH2', 'Glutathione synthetase, chloroplastic ', 'GSHII', '832797', '?NM_122620.4', 'NP_568495.2?', 'P46416', '6.3.2.3', 539, 'Potential camalexin genes'),
	('AT5G27520', 'PNC2', 'Peroxisomal adenine nucleotide carrier 2', 'F15A18', '832812', '?NM_122634.4', 'NP_198104.1?', 'Q8VZS0', '', 321, 'Potential camalexin genes'),
	('AT5G28020', 'CYSD2', 'Bifunctional L-3-cyanoalanine synthase/cysteine synthase D2 ', 'OAS6', '832872', 'NM_180756.3', 'NP_851087.1', 'Q9SXS7', '2.5.1.47 \n4.4.1.9', 323, 'Potential GSL genes'),
	('AT5G28030', 'DES1', 'Bifunctional cystathionine gamma-lyase/cysteine synthase ', 'F15F15.100', '832873', 'NM_203114.2', 'NP_974843.1', 'F4K5T2', '2.5.1.47 \n4.4.1.1', 323, 'Potential GSL genes'),
	('AT5G28237', 'AT5G28237', 'Pyridoxal-5\'-phosphate-dependent enzyme family protein', '', '2746023', 'NM_203115', 'NP_974844', 'Q8GWQ8', '', 465, 'Potential GSL genes'),
	('AT5G33290', 'XGD1', 'Xylogalacturonan beta-1,3-xylosyltransferase ', 'F19N2.10', '833302', 'NM_122853', 'NP_198314', 'Q94AA9', '2.4.2.41', 500, 'Potential GSL genes'),
	('AT5G35735', 'AT5G35735', 'Cytochrome b561 and DOMON domain-containing protein At5g35735 ', 'F28J9_6', '833550', 'NM_122964', 'NP_568531', 'Q9FKH6', '', 404, 'Potential GSL genes'),
	('AT5G36160', 'TAT', 'Tyrosine aminotransferase ', 'MAB16.11', '833613', 'NM_123007.6', 'NP_198465.3', 'Q9LVY1', '2.6.1.5 ', 420, 'Potential GSL genes'),
	('AT5G36220', 'CYP81D1', 'Cytochrome P450 81D1 ', 'CYP91A1', '833619', 'NM_123013', 'NP_568533', 'Q9FG65', '1.14.-.-', 502, 'Potential GSL genes'),
	('AT5G36880', 'ACS', 'Acetyl-coenzyme A synthetase, chloroplastic/glyoxysomal ', 'F5H8.15', '833655', '?NM_001036897.3?', 'NP_001031974.2?', 'B9DGD6', '6.2.1.1', 743, 'Potential camalexin genes'),
	('AT5G36940', 'CAT3', 'Cationic amino acid transporter 3, mitochondrial', 'MLF18.60', '833664', 'NM_123052.5', 'NP_198510.2', 'Q8GYB4', '', 609, 'Potential GSL genes'),
	('AT5G37170', 'MJG14.10', 'O-methyltransferase family protein', 'At5g37170', '833690', 'NM_123076.2', 'NP_198533.1', 'F4K5W7', '', 334, 'Potential GSL genes'),
	('AT5G37600', 'ATGSR1', 'Glutamine synthetase cytosolic isozyme 1-1 ', 'ATGLN1', '833738', 'NM_123119', 'NP_198576', 'Q56WN1', '6.3.1.2', 356, 'Potential GSL genes'),
	('AT5G38530', 'TSBtype2', 'Tryptophan synthase beta chain', '', '833841', 'NM_123214', 'NP_198669', 'Q9FFW8', '', 506, 'Potential GSL genes'),
	('AT5G40170', 'AtRLP54', 'Receptor-like protein 54 ', 'MSN9.7', '834015', '?NM_123381.3', 'NP_198833.1?', 'F4KHA2', '', 792, 'Potential camalexin genes'),
	('AT5G40360', 'MYB115', 'Transcription factor MYB115 ', 'MPO12.8', '834034', '?NM_123400.2', 'NP_568581.1?', 'Q1PDP9', '', 359, 'Potential camalexin genes TF'),
	('AT5G40370', 'GRXC2', 'Glutaredoxin-C2', 'GRX370', '834035', 'NM_123401.4', 'NP_198853.1', 'Q9FNE2', '', 111, 'Potential GSL genes'),
	('AT5G40850', 'UPM1', 'Urophorphyrin III methylase', 'MHK7_8', '834085', 'NM_123450', 'NP_198901', 'Q42606', '2.1.1.107', 369, 'Potential GSL genes'),
	('AT5G40870', 'UKL1', 'Uridine kinase-like protein 1, chloroplastic [Includes: Uridine kinase ', 'UK/UPRT1', '834088', '?NM_123452.5', 'NP_198903.1?', 'Q9FKS0', '2.4.2.9,2.7.1.48', 486, 'Potential camalexin genes'),
	('AT5G40990', 'GLIP1', 'GDSL esterase/lipase 1 ', 'MEE6.6', '834101', '?NM_123464.2', 'NP_198915.1?', 'Q9FLN0', '', 374, 'Potential camalexin genes'),
	('AT5G42580', 'CYP705A12', 'Cytochrome P450 ', 'K16E1.5', '834265', '?NM_123622.2', 'NP_199072.1?', 'Q9FH67', '', 499, 'Potential camalexin genes'),
	('AT5G42650', 'AOS', 'Allene oxide synthase, chloroplastic ', 'DDE2', '834273', 'NM_123629', 'NP_199079', 'Q96242', '4.2.1.92', 518, 'Potential GSL genes '),
	('AT5G42800', 'DFRA', 'Dihydroflavonol 4-reductase ', 'DFR', '834291', 'NM_123645.4', 'NP_199094.1', 'P51102', '1.1.1.219 \n1.1.1.234 ', 382, 'Potential GSL genes'),
	('AT5G42980', 'TRX3', 'Thioredoxin H3', 'MBD2.18', '834313', 'NM_123664.4', 'NP_199112.1', 'Q42403', '', 118, 'Potential GSL genes'),
	('AT5G43440', 'MWF20.15', '1-aminocyclopropane-1-carboxylate oxidase homolog 9 ', 'At5g43440 ', '834364', 'NM_001085231.2', 'NP_001078700.1', 'Q9LSW7', '1.14.-.-', 365, 'Potential GSL genes'),
	('AT5G43450', 'MWF20.16', '1-aminocyclopropane-1-carboxylate oxidase homolog 10 ', 'At5g43450 ', '834365', 'NM_123711.4', ' NP_199158.1', 'Q9LSW6', '1.14.-.-', 362, 'Potential GSL genes'),
	('AT5G43710', 'MNS4', 'Alpha-mannosidase I MNS4 ', 'MQD19.4', '834391', 'NM_123737', 'NP_199184', 'Q9FG93', '3.2.1.-', 624, 'Potential GSL genes'),
	('AT5G43780', 'APS4', 'ATP sulfurylase 4, chloroplastic', 'MQD19.13', '834400', 'NM_123745', 'NP_199191', 'Q9S7D8', '2.7.7.4', 469, 'Potential GSL genes'),
	('AT5G44050', 'DTX28', 'Protein DETOXIFICATION 28 ', 'MRH10.16', '834428', 'NM_123772.3', 'NP_199218.1', 'Q9FNC1', '', 491, 'Potential GSL genes'),
	('AT5G44070', 'PCS1', 'Glutathione gamma-glutamylcysteinyltransferase 1 ', 'ARA8 CAD1', '834430', '?NM_123774.4', 'NP_199220.1?', 'Q9S7Z3', '', 485, 'Potential camalexin genes'),
	('AT5G44400', 'AT5G44400', 'Berberine bridge enzyme ', '', '834466', 'NM_123807', 'NP_199253', 'Q9FKU8', '', 537, 'Potential GSL genes'),
	('AT5G44420', 'PDF1.2A', 'Defensin-like protein 16', 'LCR77', '834469', 'NM_123809.4', 'NP_199255.1', 'Q9FI23', '', 80, 'Potential GSL genes'),
	('AT5G44720', 'T19K24.17', 'Molybdenum cofactor sulfurase family protein', '', '834501', 'NM_203154', 'NP_974883', 'O48588', '', 308, 'Potential GSL genes'),
	('AT5G47220', 'ERF2', 'Ethylene-responsive transcription factor 2 ', 'ERF-2 ERF101', '834768', '?NM_124093.3', 'NP_199533.1?', 'O80338', '', 243, 'Potential camalexin genes TF'),
	('AT5G47240', 'NUDT8', 'Nudix hydrolase 8', 'NUDX8', '834771', 'NM_124095.4', 'NP_568680.1', 'Q8L7W2', '3.6.1.-', 369, 'Potential GSL genes'),
	('AT5G47910', 'RBOHD', 'Respiratory burst oxidase homolog protein D ', 'ATRBOHD', '834842', 'NM_124165', 'NP_199602', 'Q9FIJ0', '1.11.1.-\n1.6.3.-', 921, 'Potential GSL genes'),
	('AT5G47990', 'CYP705A5', 'Cytochrome P450 705A5 ', 'THAD', '834850', '?NM_124173.3', 'NP_199610.1?', 'Q9FI39', '', 511, 'Potential camalexin genes'),
	('AT5G48000', 'CYP708A2', 'Cytochrome P450 708A2 ', 'THAH', '834851', '?NM_001036953.1?', 'NP_001032030.1?', 'Q8L7D5', '', 477, 'Potential camalexin genes'),
	('AT5G48220', 'MIF21.11', 'Aldolase-type TIM barrel family protein', 'MIF21_11', '834875', 'NM_124197.3', 'NP_199633.1', 'Q9LUB2', '', 379, 'Potential GSL genes'),
	('AT5G48810', 'CYTB5-D', 'Cytochrome B5 isoform D ', 'B5-B', '834939', 'NM_124258.4', 'NP_199692.1', 'Q9ZWT2', '', 140, 'Potential GSL genes'),
	('AT5G48880', 'KAT5', '3-ketoacyl-CoA thiolase 5, peroxisomal ', 'K24G6.22', '834946', '?NM_001036960.2?', 'NP_001032037.1?', 'Q570C8', '', 457, 'Potential camalexin genes'),
	('AT5G48930', 'HST', 'Shikimate O-hydroxycinnamoyltransferase', 'HCT', '834951', 'NM_124270.4', 'NP_199704.1', 'Q9FI78', '2.3.1.133 ', 433, 'Potential GSL genes'),
	('AT5G49460', 'ACLB-2', 'ATP-citrate synthase beta chain protein 2 ', 'K7J8.14', '835006', '?NM_001344844.1', 'NP_001332247.1?', 'Q9FGX1', '6.2.1.5', 608, 'Potential camalexin genes'),
	('AT5G49630', 'AAP6', 'Amino acid permease 6', 'MNI5.1', '835025', 'NM_124341.4', 'NP_199774.1', 'P92934', '', 481, 'Potential GSL genes'),
	('AT5G49660', 'CEPR1', 'Receptor protein-tyrosine kinase CEPR1 ', 'XIP1', '835028', 'NM_124344.3', 'NP_199777.1', 'Q9FGL5', '2.7.10.1', 966, 'Potential GSL genes'),
	('AT5G52320', 'CYP96A4', 'Cytochrome P450, family 96, subfamily A, polypeptide 4', '', '835308', 'NM_124611.3', 'NP_200045.1', 'Q9FHC8', '', 502, 'Potential GSL genes'),
	('AT5G52640', 'HSP90-1', 'Heat shock protein 90-1', 'HSP81-1', '835341', 'NM_124642.4', 'NP_200076.2', 'P27323', '', 700, 'Potential GSL genes'),
	('AT5G53370', 'PME61', 'Probable pectinesterase/pectinesterase inhibitor 61', 'ARATH61', '835418', 'NM_124716.3', 'NP_200149.1', 'Q9FK05', '3.1.1.11', 587, 'Potential GSL genes'),
	('AT5G53420', 'MYN8.3', 'CCT motif family protein', 'MYN8_3', '835423', 'NM_124721.4', 'NP_568793.1', 'Q8L602', '', 264, 'Potential GSL genes'),
	('AT5G53460', 'GLT1', 'Glutamate synthase 1 [NADH], chloroplastic ', 'MYN8.7', '835427', '?NM_001203600.1', 'NP_001190529.1?', 'Q9LV03', '1.4.1.14', 2208, 'Potential camalexin genes'),
	('AT5G53560', 'CYTB5-E', 'Cytochrome b5 isoform E ', 'CB5-A', '835438', 'NM_124736.4', 'NP_200168.1', 'Q42342', '', 134, 'Potential GSL genes'),
	('AT5G53810', 'MGN6.20 ', 'Caffeic acid 3-O-methyltransferase-like protein ', 'At5g53810', '835462', 'NM_124760.3', 'NP_200192.1', 'Q9FHZ5', '', 378, 'Potential GSL genes'),
	('AT5G53880', 'AT5G53880', 'Putative uncharacterized protein At5g53880 ', '', '835469', 'NM_124767', 'NP_568802', 'Q9FN38', '', 66, 'Potential GSL genes'),
	('AT5G53990', 'UGT79B9', 'UDP-glycosyltransferase 79B9 ', '', '835482', 'NM_124778', 'NP_200210', 'Q9FN28', '2.4.1.-', 447, 'Potential GSL genes'),
	('AT5G54080', 'HGO', 'Homogentisate 1,2-dioxygenase ', 'MJP23.6', '835494', '?NM_124787.4', 'NP_200219.1?', 'Q9ZRA2', '1.13.11.5', 461, 'Potential camalexin genes'),
	('AT5G54160', 'OMT1', 'Flavone 3\'-O-methyltransferase 1', 'COMT1', '835504', 'NM_124796.4', 'NP_200227.1', 'Q9FK25', '2.1.1.42 \n2.1.1.4 \n2.1.1.68', 363, 'Potential GSL genes'),
	('AT5G54390', 'AHL', 'PAP-specific phosphatase HAL2-like ', 'HL', '835527', 'NM_124819', 'NP_200250', 'Q38945', '3.1.3.7', 373, 'Potential GSL genes'),
	('AT5G54660', 'HSP21.7', '21.7 kDa class VI heat shock protein ', 'MRB17.16', '835555', 'NM_124847', 'NP_568810', 'Q9FIT9', '', 192, 'Potential GSL genes'),
	('AT5G54810', 'TSB1', 'Tryptophan synthase beta chain 1, chloroplastic ', 'MBG8.7', '835571', '?NM_124862.5', 'NP_200292.1?', 'P14671', '4.2.1.20', 470, 'Potential camalexin genes'),
	('AT5G54960', 'PDC2', 'Pyruvate decarboxylase 2 ', 'MBG8.23', '835587', 'NM_124878', 'NP_200307', 'Q9FFT4', '4.1.1.1', 607, 'Potential GSL genes'),
	('AT5G55120', 'VTC5', 'GDP-L-galactose phosphorylase 2 ', 'VTC2L', '835603', 'NM_124894', 'NP_200323', 'Q9FLP9', '2.7.7.69', 431, 'Potential GSL genes'),
	('AT5G56000', 'HSP90-4', 'Heat shock protein 90-4 ', 'HSP81-4', '835698', 'NM_124982.3', 'NP_200411.1', 'O03986', '', 699, 'Potential GSL genes'),
	('AT5G56010', 'HSP90-3', 'Heat shock protein 90-3 ', 'HSP81-3', '835699', 'NM_124983.4', 'NP_200412.1', 'P51818', '', 699, 'Potential GSL genes'),
	('AT5G56030', 'HSP81-2', 'Heat shock protein 90-2 ', 'ERD8', '835701', 'NM_124985.5', 'NP_200414.1', 'P55737', '', 699, 'Potential GSL genes'),
	('AT5G56760', 'SAT5', 'Serine acetyltransferase 5 ', 'SAT52', '835778', '?NM_125059.3', 'NP_200487.1?', 'Q42538', '2.3.1.30', 312, 'Potential camalexin genes'),
	('AT5G57630', 'CIPK21', 'SnRK3.4', 'PKS23', '835868', 'NM_125144', 'NP_568860', 'Q94CG0', '2.7.11.1', 416, 'Potential GSL genes'),
	('AT5G57850', 'DAAT', 'D-amino-acid transaminase, chloroplastic  ', 'BCAL3', '835895', 'NM_125170.5', 'NP_200593.2', 'Q8L493', '2.6.1.21 \n4.1.3.38', 373, 'Potential GSL genes'),
	('AT5G58150', 'MCK7.2', 'Probably inactive leucine-rich repeat receptor-like protein kinase At5g58150', 'AT5G58150', '835927', '', '', 'Q9LVN2', '', 785, 'Potential GSL genes'),
	('AT5G58390', 'PER67', 'Peroxidase 67 ', 'P67', '835952', 'NM_125225', 'NP_200647', 'Q9LVL2', '1.11.1.7', 316, 'Potential GSL genes'),
	('AT5G58670', 'PLC1', 'Phosphoinositide phospholipase C 1 ', 'MZN1.12', '835981', 'NM_125254', 'NP_568881', 'Q39032', '3.1.4.11', 561, 'Potential GSL genes'),
	('AT5G59130', 'SBT4.11', 'Subtilisin-like protease SBT4.11 ', 'MNC17.4', '836031', 'NM_125303', 'NP_568899', 'Q9FIG1', '3.4.21.-', 736, 'Potential GSL genes'),
	('AT5G59530', 'F2O15.26', '1-aminocyclopropane-1-carboxylate oxidase homolog 11', 'At5g59530 ', '836072', 'NM_125345.5', ' NP_200761.1', 'Q9LTH8', '1.14.-.-', 364, 'Potential GSL genes'),
	('AT5G59540', 'At5g59540', '1-aminocyclopropane-1-carboxylate oxidase homolog 12 ', 'F2O15.6', '836073', 'NM_125346.3', 'NP_200762.1', 'Q9LTH7', '1.14.-.-', 366, 'Potential GSL genes'),
	('AT5G59590', 'UGT76E2', 'UDP-glycosyltransferase 76E2 ', 'F2O15.19', '836078', '?NM_125351.3', 'NP_200767.1?', 'Q9LTH2', '', 449, 'Potential camalexin genes'),
	('AT5G59730', 'EXO70H7', 'Exocyst subunit exo70 family protein H7', 'ATEXO70H7', '836094', 'NM_125365.2', 'NP_200781.1', 'Q9FN91', '', 634, 'Potential GSL genes'),
	('AT5G59780', 'MYB59', 'Transcription factor MYB59 ', 'MTH12.19', '836099', 'NM_180895', 'NP_851226', 'Q4JL84', '', 235, 'Potential GSL genes TF'),
	('AT5G60300', 'LECRK19', 'L-type lectin-domain containing receptor kinase I.9 ', 'DORN1', '836152', 'NM_180899', 'NP_851230', 'Q9LSR8', '2.7.11.1', 766, 'Potential GSL genes'),
	('AT5G60890', 'MYB34', 'Transcription factor MYB34 ', 'ATR1', '836210', '?NM_125482.3', 'NP_200897.1?', 'O64399', '', 295, 'Potential camalexin genes TF'),
	('AT5G61290', 'MFB13.9', 'Flavin-containing monooxygenase FMO GS-OX-like 8', 'At5g61290 ', '836250', 'NM_125522.4', 'NP_200937.1', 'Q9FLK4', '1.8.-.-', 461, 'Potential GSL genes'),
	('AT5G61420', 'MYB28', 'Transcription factor MYB28 ', 'HAG1 PMG1', '836263', '?NM_125535.4?', 'NP_200950.1?', 'Q9SPG2', '', 366, 'Potential camalexin genes TF'),
	('AT5G61660', 'AT5G61660', 'Glycine-rich protein ', '', '836288', 'NM_125560', 'NP_568938', 'Q9FKF5', '', 134, 'Potential GSL genes'),
	('AT5G63180', 'AT5G63180', 'Probable pectate lyase 22 ', 'MDC12_15', '836439', 'NM_125713', 'NP_568967', 'Q93Z25', '4.2.2.2', 432, 'Potential GSL genes'),
	('AT5G63600', 'FLS5', 'Probable flavonol synthase 5 ', 'MBK5.7', '836480', '?NM_125755.4?', 'NP_201165.1?', 'Q9FFQ4', '', 325, 'Potential camalexin genes'),
	('AT5G63710', 'At5g63710', 'Probable LRR receptor-like serine/threonine-protein kinase At5g63710 ', 'MBK5.19', '836491', 'NM_125766.3', 'NP_568977.1', 'Q8W4S5', '2.7.11.1', 614, 'Potential GSL genes'),
	('AT5G63850', 'AAP4', 'Amino acid permease 4 ', 'MGI19.5', '836505', 'NM_125780.3', 'NP_201190.1', 'Q9FN04', '', 466, 'Potential GSL genes'),
	('AT5G63890', 'HISN8', 'Histidinol dehydrogenase, chloroplastic ', 'HDH', '836509', '?NM_125784.3?', 'NP_568981.2?', 'Q9C5U8', '1.1.1.23', 466, 'Potential camalexin genes'),
	('AT5G63980', 'SAL1', 'SAL1 phosphatase 3\'2\',5\'-bisphosphate nucleotidase 1 ', 'FRY1', '836519', 'NM_125794', 'NP_201203', 'Q42546', '3.1.3.7', 353, 'Potential GSL genes'),
	('AT5G63990', 'SAL3', 'Probable SAL3 phosphatase ', 'MBM17.9', '836520', 'NM_203259', 'NP_974988', 'Q8GY63', '3.1.3.7\n3.1.3.57', 357, 'Potential GSL genes'),
	('AT5G64370', 'BETA-UP', 'Beta-ureidopropionase ', 'PYD3', '836558', 'NM_125833', 'NP_201242', 'Q8H183', '3.5.1.6', 408, 'Potential GSL genes'),
	('AT5G64900', 'PEP1', 'Elicitor peptide 1', 'PROPEP1', '836613', '?NM_125888.4', 'NP_569001.1?', 'Q9LV87', '', 92, 'Potential camalexin genes'),
	('AT5G65010', 'ASN2', 'Asparagine synthetase [glutamine-hydrolyzing] 2', 'MXK3.25', '836625', 'NM_180941.3', 'NP_851272.1', 'Q9LV77', '6.3.5.4', 578, 'Potential GSL genes'),
	('AT5G65780', 'BCAT5', 'Branched-chain-amino-acid aminotransferase 5, chloroplastic ', 'F6H11.110', '836707', 'NM_125975', 'NP_201379', 'Q9FYA6', '2.6.1.42', 415, 'Potential GSL genes'),
	('AT5G65870', 'PSK5', 'Phytosulfokines 5 AtPSK5', 'K14B20.4', '836716', 'NM_125984.4', 'NP_201388.1', 'Q9FEB4', '', 77, 'Potential GSL genes'),
	('AT5G65930', 'ZWI', 'Kinesin-like protein KIN-14E ', 'KCBP', '836723', '?NM_125990.4?', 'NP_569022.2?', 'Q9FHN8', '', 1260, 'Potential camalexin genes'),
	('AT5G66120', 'DHQS', '3-dehydroquinate synthase, chloroplastic ', 'AROB', '836744', 'NM_180948.2', 'NP_851279.1', 'Q8VYV7', '4.2.3.4', 442, 'Potential GSL genes'),
	('AT5G66420', 'At5g66420', 'TIM-barrel signal transduction protein', 'K1F13.7', '836774', 'NM_126040.4', 'NP_569034.1', 'Q94JM0', '', 655, 'Potential GSL genes'),
	('AT5G66760', 'SDH1-1', 'Succinate dehydrogenase [ubiquinone] flavoprotein subunit 1, mitochondrial ', 'MSN2.16', '836809', '?NM_126074.3', 'NP_201477.1?', 'O82663', '1.3.5.1', 634, 'Potential camalexin genes'),
	('AT5G67030', 'ZEP', 'Zeaxanthin epoxidase, chloroplastic ', 'ABA1', '836838', '?NM_126103.2?', 'NP_201504.2?', 'Q9FGC7', '1.14.15.21', 667, 'Potential camalexin genes'),
	('AT5G67150', 'AT5G67150', 'Anthranilate N-hydroxycinnamoyl/benzoyltransferase-like protein ', '', '836850', 'NM_126115', 'NP_201516', 'Q9FH98', '', 448, 'Potential GSL genes'),
	('AT5G67160', 'EPS1', 'Anthranilate N-hydroxycinnamoyl/benzoyltransferase-like protein ', '', '836851', 'NM_126116', 'NP_201517', 'Q9FH97', '', 434, 'Potential GSL genes'),
	('AT5G67210', 'IRX15-L', 'Protein IRX15-LIKE', 'K21H1.17', '836856', 'NM_126121.2', 'NP_201522.1', 'Q9FH92', '', 317, 'Potential GSL genes'),
	('AT5G67310', 'CYP81G1 ', 'Cytochrome P450, family 81, subfamily G, polypeptide 1', 'At5g67310', '836866', 'NM_126131.4', 'NP_201532.2', 'Q8GZ20', '', 507, 'Potential GSL genes'),
	('AT5G67520', 'APK4', 'Adenylyl-sulfate kinase 4, chloroplastic', 'K9I9.8', '836888', 'NM_126152', 'NP_569050', 'Q84JF0', '2.7.1.25', 310, 'Potential GSL genes');
/*!40000 ALTER TABLE `coexpressions` ENABLE KEYS */;

-- Dumping structure for table gslbase.coexpressions_databases
CREATE TABLE IF NOT EXISTS `coexpressions_databases` (
  `agi_id` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  `score` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  `database` int(11) DEFAULT NULL,
  KEY `Index 1` (`agi_id`,`database`)
) ENGINE=InnoDB DEFAULT CHARSET=utf8 COLLATE=utf8_unicode_ci;

-- Dumping data for table gslbase.coexpressions_databases: ~650 rows (approximately)
/*!40000 ALTER TABLE `coexpressions_databases` DISABLE KEYS */;
INSERT INTO `coexpressions_databases` (`agi_id`, `score`, `database`) VALUES
	('AT1G01120', '0.09', 3),
	('AT1G01390', '28.9', 1),
	('AT1G01470', '0.08', 3),
	('AT1G02920', '41.11', 1),
	('AT1G02930', '41.19', 1),
	('AT1G02940', '36.56', 1),
	('AT1G02950', '34.48', 1),
	('AT1G03820', '0.009217073', 2),
	('AT1G03980', '0.012880596', 2),
	('AT1G04710', '25.98', 1),
	('AT1G04770', '0.009849897', 2),
	('AT1G04770', '0.1', 3),
	('AT1G06000', '0.12', 3),
	('AT1G06160', '0.007946367', 2),
	('AT1G06640', '0.011351318', 2),
	('AT1G06640', '0.13', 3),
	('AT1G06830', '0.013840156', 2),
	('AT1G07260', '0.007848023', 2),
	('AT1G07610', '0.11', 3),
	('AT1G07780', '0.008608057', 2),
	('AT1G07890', '0.13', 3),
	('AT1G07920', '32.85', 1),
	('AT1G07930', '32.85', 1),
	('AT1G07940', '32.85', 1),
	('AT1G08920', '0.007813939', 2),
	('AT1G08930', '0.007683566', 2),
	('AT1G10060', '43.05', 1),
	('AT1G10060', '0.012931243', 2),
	('AT1G10070', '28.67', 1),
	('AT1G10070', '0.014816208', 2),
	('AT1G10900', '0.1', 3),
	('AT1G11580', '0.01325139', 2),
	('AT1G11580', '0.17', 3),
	('AT1G11840', '0.16', 3),
	('AT1G11860', '28.5', 1),
	('AT1G12110', '0.11', 3),
	('AT1G12140', '0.14', 3),
	('AT1G12200', '0.013567281', 2),
	('AT1G12200', '0.11', 3),
	('AT1G13430', '24.73', 1),
	('AT1G14120', '0.11', 3),
	('AT1G14130', '0.007465988', 2),
	('AT1G15950', '0.12', 3),
	('AT1G16030', '35.55', 1),
	('AT1G16060', '0.008852183', 2),
	('AT1G17380', '0.11', 3),
	('AT1G17420', '0.1', 3),
	('AT1G17745', '0.15', 3),
	('AT1G18500', '45.14', 1),
	('AT1G18500', '0.01276834', 2),
	('AT1G18590', '0.3', 3),
	('AT1G18880', '0.13', 3),
	('AT1G19180', '0.12', 3),
	('AT1G19300', '0.1', 3),
	('AT1G19670', '0.010315066', 2),
	('AT1G19670', '0.15', 3),
	('AT1G19920', '41.01', 1),
	('AT1G19920', '0.011872762', 2),
	('AT1G20160', '0.1', 3),
	('AT1G20510', '0.009526769', 2),
	('AT1G20510', '0.16', 3),
	('AT1G20560', '26.08', 1),
	('AT1G20620', '0.008388977', 2),
	('AT1G20823', '0.08', 3),
	('AT1G21130', '0.009991929', 2),
	('AT1G21250', '0.1', 3),
	('AT1G21440', '57.45', 1),
	('AT1G21440', '0.038527335', 2),
	('AT1G21440', '0.21', 3),
	('AT1G21590', '0.11', 3),
	('AT1G22360', '0.007500064', 2),
	('AT1G22410', '0.007472499', 2),
	('AT1G22410', '0.13', 3),
	('AT1G22710', '0.1', 3),
	('AT1G23800', '0.09', 3),
	('AT1G23850', '0.011697611', 2),
	('AT1G24100', '0.28', 3),
	('AT1G24575', '0.11', 3),
	('AT1G25220', '29.42', 1),
	('AT1G27030', '0.009202314', 2),
	('AT1G27030', '0.12', 3),
	('AT1G27130', '0.011029434', 2),
	('AT1G27130', '0.14', 3),
	('AT1G28600', '0.13', 3),
	('AT1G28610', '0.009313683', 2),
	('AT1G28680', '0.14', 3),
	('AT1G29410', '0.007398439', 2),
	('AT1G31180', '122.8', 1),
	('AT1G31230', '39.07', 1),
	('AT1G31230', '0.025622383', 2),
	('AT1G31550', '0.14', 3),
	('AT1G31710', '0.011022622', 2),
	('AT1G31710', '0.16', 3),
	('AT1G31770', '0.009548151', 2),
	('AT1G32480', '0.009689005', 2),
	('AT1G32640', '0.14', 3),
	('AT1G33260', '0.1', 3),
	('AT1G35260', '0.008002023', 2),
	('AT1G35260', '0.11', 3),
	('AT1G35720', '0.1', 3),
	('AT1G36160', '29.8', 1),
	('AT1G37130', '0.008680259', 2),
	('AT1G37130', '0.11', 3),
	('AT1G43160', '0.009632884', 2),
	('AT1G44100', '0.12', 3),
	('AT1G44170', '0.11', 3),
	('AT1G44350', '0.007701489', 2),
	('AT1G44800', '0.007937126', 2),
	('AT1G44800', '0.15', 3),
	('AT1G48850', '0.00802201', 2),
	('AT1G49230', '0.01998176', 2),
	('AT1G49470', '0.015892832', 2),
	('AT1G49470', '0.11', 3),
	('AT1G49860', '30.79', 1),
	('AT1G50090', '56.73', 1),
	('AT1G50090', '0.01284748', 2),
	('AT1G51680', '0.16', 3),
	('AT1G52000', '0.12', 3),
	('AT1G52400', '0.008971776', 2),
	('AT1G52410', '0.009038827', 2),
	('AT1G52410', '0.13', 3),
	('AT1G53440', '0.007320246', 2),
	('AT1G54030', '0.011990791', 2),
	('AT1G54030', '0.12', 3),
	('AT1G54340', '0.007733707', 2),
	('AT1G54350', '41.47', 1),
	('AT1G55020', '0.1', 3),
	('AT1G55090', '0.007579347', 2),
	('AT1G55210', '0.13', 3),
	('AT1G55450', '0.007545121', 2),
	('AT1G55920', '28.09', 1),
	('AT1G55920', '0.008728159', 2),
	('AT1G55920', '0.11', 3),
	('AT1G56160', '0.008060972', 2),
	('AT1G56430', '0.009587159', 2),
	('AT1G59740', '0.08', 3),
	('AT1G61610', '0.00754617', 2),
	('AT1G61660', '0.1', 3),
	('AT1G61820', '0.007920402', 2),
	('AT1G62180', '0.13', 3),
	('AT1G62560', '0.24', 3),
	('AT1G62660', '0.007168551', 2),
	('AT1G62660', '0.13', 3),
	('AT1G62800', '0.017323725', 2),
	('AT1G62800', '0.19', 3),
	('AT1G62810', '0.00934691', 2),
	('AT1G63010', '0.09', 3),
	('AT1G64370', '0.14', 3),
	('AT1G64400', '0.1', 3),
	('AT1G65860', '0.24', 3),
	('AT1G66200', '0.008447937', 2),
	('AT1G66200', '0.14', 3),
	('AT1G67870', '0.008511902', 2),
	('AT1G67870', '0.14', 3),
	('AT1G70700', '0.09', 3),
	('AT1G70810', '0.12', 3),
	('AT1G70890', '0.13', 3),
	('AT1G72450', '0.15', 3),
	('AT1G72810', '0.015489334', 2),
	('AT1G72900', '0.008880038', 2),
	('AT1G72920', '0.09', 3),
	('AT1G73330', '0.008058273', 2),
	('AT1G73330', '0.13', 3),
	('AT1G74030', '27.57', 1),
	('AT1G74040', '49.17', 1),
	('AT1G74040', '0.012314181', 2),
	('AT1G74090', '0.27', 3),
	('AT1G74100', '0.24', 3),
	('AT1G74640', '0.1', 3),
	('AT1G74950', '0.11', 3),
	('AT1G75280', '0.13', 3),
	('AT1G76360', '0.11', 3),
	('AT1G76790', '0.01520347', 2),
	('AT1G76790', '0.15', 3),
	('AT1G76800', '0.010916041', 2),
	('AT1G77420', '0.1', 3),
	('AT1G77760', '0.08', 3),
	('AT1G77920', '0.11', 3),
	('AT1G77990', '28.85', 1),
	('AT1G78320', '0.007674419', 2),
	('AT1G78370', '0.22', 3),
	('AT1G78380', '0.00732902', 2),
	('AT1G78490', '0.009866072', 2),
	('AT1G78670', '0.12', 3),
	('AT1G78680', '0.14', 3),
	('AT1G79010', '27.22', 1),
	('AT1G80555', '0.012710439', 2),
	('AT1G80560', '97.96', 1),
	('AT1G80760', '0.009543835', 2),
	('AT2G02930', '41.52', 1),
	('AT2G03760', '25.46', 1),
	('AT2G03760', '0.00789325', 2),
	('AT2G03770', '25.46', 1),
	('AT2G04350', '25.06', 1),
	('AT2G04400', '38.1', 1),
	('AT2G04400', '0.019139764', 2),
	('AT2G04400', '0.17', 3),
	('AT2G05710', '31.56', 1),
	('AT2G05710', '0.008948262', 2),
	('AT2G05940', '0.13', 3),
	('AT2G06050', '0.007443637', 2),
	('AT2G06050', '0.16', 3),
	('AT2G14750', '0.27', 3),
	('AT2G14920', '25.46', 1),
	('AT2G15620', '0.013151983', 2),
	('AT2G15620', '0.13', 3),
	('AT2G16660', '0.013870348', 2),
	('AT2G16740', '0.007355211', 2),
	('AT2G16740', '0.13', 3),
	('AT2G16890', '0.007447992', 2),
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/*!40000 ALTER TABLE `coexpressions_databases` ENABLE KEYS */;

-- Dumping structure for table gslbase.compounds
CREATE TABLE IF NOT EXISTS `compounds` (
  `compound_id` int(11) NOT NULL,
  `compound_name` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  `common_name` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  `knapsack_id` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  `formula` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  `GSL_type` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  `result_type_id` int(11) DEFAULT NULL,
  PRIMARY KEY (`compound_id`)
) ENGINE=InnoDB DEFAULT CHARSET=utf8 COLLATE=utf8_unicode_ci;

-- Dumping data for table gslbase.compounds: ~84 rows (approximately)
/*!40000 ALTER TABLE `compounds` DISABLE KEYS */;
INSERT INTO `compounds` (`compound_id`, `compound_name`, `common_name`, `knapsack_id`, `formula`, `GSL_type`, `result_type_id`) VALUES
	(1, '2-Phenylethyl glucosinolate', 'Gluconasturtiin', 'C00007350', 'C15H21NO9S2', 'Homo-phenylalanine derived glucosinolates; Benzyl glucosinolates', 4),
	(2, '3-Indolylmethylglucosinolate (I3M)', 'Glucobrassicin', 'C00000125', 'C16H20N2O9S2', 'Tryptophan derived glucosinolates; Indolylmethyl glucosinolates', 4),
	(3, '3-Indolylmethyl desulfoglucosinolate', '', 'C00007398', 'C16H20N2O6S2', 'Tryptophan derived glucosinolates; Indolylmethyl desulfo glucosinolates', 4),
	(4, '1-Methoxy-3-indolylmethyl glucosinolate', 'Neoglucobrassicin', 'C00000126', 'C17H22N2O10S2', 'Tryptophan derived glucosinolates; Indolylmethyl glucosinolates', 4),
	(5, '1-Methylethyl glucosinolate', 'Glucoputranjivin', '', 'C10H19NO9S2', 'Valine-derived glucosinolates; Methyl alkyl glucosinolates ', 4),
	(6, '1-Methylpropyl glucosinolate', '', '', '', 'Isoleucine-derived glucosinolates', 4),
	(7, '4-Hydroxy-3-indolylmethyl glucosinolate', '4-Hydroxyglucobrassicin', '', 'C16H20N2O10S2', 'Tryptophan derived glucosinolates; Indolylmethyl glucosinolates', 4),
	(8, '4-Methoxy-3-indolylmethyl glucosinolate', '4-Methoxyglucobrassicin', 'C00000128', 'C17H22N2O10S2', 'Tryptophan derived glucosinolates; Metoxy indolylmethyl glucosinolates', 4),
	(9, 'Benzyl glucosinolate', 'Glucotropaeolin', 'C00007346', 'C14H19NO9S2', 'Phenylalanine derived glucosinolates; Benzyl glucosinolates', 4),
	(10, '(2R)-2-Hydroxy 3-butenyl glucosinolate', 'Progoitrin', 'C00001486', 'C11H19NO10S2', 'Methionine-derived glucosinolates; Hydroxy alkenyl glucosinolates ', 4),
	(11, '(2S)-2-Hydroxy 3-butenyl glucosinolate', 'Epiprogoitrin', '', 'C11H19NO10S2', 'Methionine-derived glucosinolates; Hydroxy alkenyl glucosinolates ', 4),
	(12, '(2S)-2-Benzoyloxy 3-butenyl glucosinolate', '', 'C00007669', 'C18H23NO11S2', 'Methionine-derived glucosinolates; Benzoyloxy alkenyl glucosinolates ', 4),
	(13, '2-Methylsulfinylethyl glucosinolate', '', 'C00007341', 'C10H19NO10S3', 'Methionine-derived glucosinolates; Methylsulfinyl alkyl glucosinolates', 4),
	(14, '2-Propenyl glucosinolate', 'Sinigrin', 'C00001488', 'C10H17NO9S2', 'Methionine-derived glucosinolates; Alkenyl glucosinolates', 4),
	(15, '2-Methylthioethyl glucosinolate', 'Glucoviorylin', '', '', 'Methionine-derived glucosinolates; Methylthio alkyl glucosinolates', 4),
	(16, '2-Methylpropyl glucosinolate', 'Isobutyl?glucosinolate', '', 'C11H21NO9S2', 'Leucine-derived glucosinolates', 4),
	(17, '2-Hydroxyethyl glucosinolate', '', '', '', 'Methionine-derived glucosinolates; Hydroxy alkyl glucosinolates', 4),
	(18, '2-Hydroxy-4-pentenyl glucosinolate', 'Gluconapoleiferin', '', 'C12H21NO10S2', 'Methionine-derived glucosinolates; Hydroxy alkyl glucosinolates', 4),
	(19, '3-Methylthiopropyl glucosinolate', 'Glucoiberverin', '', 'C11H20NO9S3', 'Methionine-derived glucosinolates; Methylthio alkyl glucosinolates', 4),
	(20, '3-Methylsulfinylpropyl glucosinolate', 'Glucoiberin', 'C00007343', 'C11H20NO10S3', 'Methionine-derived glucosinolates; Methylsulfinyl alkyl glucosinolates', 4),
	(21, '3-Butenyl glucosinolate', 'Gluconapin', 'C00007586', 'C11H18NO9S2', 'Methionine-derived glucosinolates; Alkenyl glucosinolates', 4),
	(22, '3-Hydroxypropyl glucosinolate', '', 'C00007340', 'C10H19NO10S2', 'Methionine-derived glucosinolates; Hydroxy alkyl glucosinolates ', 4),
	(23, '3-Benzoyloxypropyl glucosinolate', 'Glucomalcomiin', 'C00007358', 'C17H22NO11S2', 'Methionine-derived glucosinolates; Benzoyloxy alkyl glucosinolates ', 4),
	(24, '4-Methylthiobutyl glucosinolate', 'Glucoerucin', 'C00007344', 'C12H22NO9S3', 'Methionine-derived glucosinolates; Methylthio alkyl glucosinolates', 4),
	(25, '4-Methylsulphinylbutyl glucosinolate', 'Glucoraphanin', 'C00007545', 'C12H22NO10S3', 'Methionine-derived glucosinolates; Methylsulfinyl alkyl glucosinolates', 4),
	(26, '4-Hydroxybutyl glucosinolate', '', 'C00007342', 'C11H21NO10S2', 'Methionine-derived glucosinolates; Hydroxy alkyl glucosinolates ', 4),
	(27, '4-Benzoyloxybutyl glucosinolate', '', 'C00007359', 'C18H25NO11S2', 'Methionine-derived glucosinolates; Benzoyloxy alkyl glucosinolates ', 4),
	(28, '4-Pentenyl glucosinolate', 'Glucobrassicanapin', '', 'C12H21NO9S2', 'Methionine-derived glucosinolates; Alkenyl glucosinolates', 4),
	(29, '5-Methylsulfinylpentyl glucosinolate', 'Glucoalyssin', 'C00007345', 'C13H24NO10S3', 'Methionine-derived glucosinolates; Methylsulfinyl alkyl glucosinolates', 4),
	(30, '5-Methylthiopentyl glucosinolate', 'Glucoberteroin', 'C00007593', 'C13H24NO9S3', 'Methionine-derived glucosinolates; Methylthio alkyl glucosinolates', 4),
	(31, '5-Methylthiopentyldesulfo glucosinolate', '', 'C00007624', 'C13H25NO6S2', 'Methionine-derived glucosinolates; Methylthio alkyl glucosinolates', 4),
	(32, '6-Methylthiohexyl glucosinolate', 'Glucolesquerellin', '', 'C14H26NO9S3', 'Methionine-derived glucosinolates; Methylthio alkyl glucosinolates', 4),
	(33, '6-Methylsulfinylhexyl glucosinolate', 'Glucohesperin', 'C00007348', 'C14H26NO10S3', 'Methionine-derived glucosinolates; Methylsulfinyl alkyl glucosinolates', 4),
	(34, '7-Methylsulfinylheptyl glucosinolate', 'Glucoibarin', 'C00007352', 'C15H28NO10S3', 'Methionine-derived glucosinolates; Methylsulfinyl alkyl glucosinolates', 4),
	(35, '7-Methylthioheptyl glucosinolate', '', 'C00007353', 'C15H28NO9S3', 'Methionine-derived glucosinolates; Methylthio alkyl glucosinolates', 4),
	(36, '8-Methylthio-octyl glucosinolate', '', 'C00007356', 'C16H30NO9S3', 'Methionine-derived glucosinolates; Methylthio alkyl glucosinolates', 4),
	(37, '8-Methylsulfinyl-octyl glucosinolate', 'Glucohirsutin', 'C00007355', 'C16H30NO10S3', 'Methionine-derived glucosinolates; Methylsulfinyl alkyl glucosinolates', 4),
	(38, '8-Benzoyloxy-octyl glucosinolate', '', '', '', 'Methionine-derived glucosinolates; Benzoyloxy alkyl glucosinolates', 4),
	(39, '3-Methylbutyl glucosinolate', '', '', '', 'Leucine-derived glucosinolates; Methylalkyl glucosinolates', 4),
	(40, '4-Methylpentyl glucosinolate', '', '', '', 'Leucine-derived glucosinolates; Methylalkyl glucosinolates', 4),
	(41, '5-Benzoyloxypentyl glucosinolate', '', '', '', 'Methionine-derived glucosinolates; Benzoyloxy alkyl glucosinolates ', 4),
	(42, '6-Benzoyloxyhexyl glucosinolate ', '', '', '', 'Methionine-derived glucosinolates; Benzoyloxy alkyl glucosinolates ', 4),
	(43, '2-Phenylethyl glucosinolate', 'Gluconasturtiin', 'C00007350', 'C15H21NO9S2', 'Homo-phenylalanine derived glucosinolates; Benzyl glucosinolates', 2),
	(44, '3-Indolylmethylglucosinolate (I3M)', 'Glucobrassicin', 'C00000125', 'C16H20N2O9S2', 'Tryptophan derived glucosinolates; Indolylmethyl glucosinolates', 2),
	(45, '1-Methoxy-3-indolylmethyl glucosinolate', 'Neoglucobrassicin', 'C00000126', 'C17H22N2O10S2', 'Tryptophan derived glucosinolates; Indolylmethyl glucosinolates', 2),
	(46, '4-Hydroxy-3-indolylmethyl glucosinolate', '4-Hydroxyglucobrassicin', 'C00000127', 'C16H20N2O10S2', 'Tryptophan derived glucosinolates; Indolylmethyl glucosinolates', 2),
	(47, '4-Methoxy-3-indolylmethyl glucosinolate', '4-Methoxyglucobrassicin', 'C00000128', 'C17H22N2O10S2', 'Tryptophan derived glucosinolates; Metoxy indolylmethyl glucosinolates', 2),
	(48, '(2R)-2-Hydroxy 3-butenyl glucosinolate', 'Progoitrin', 'C00001486', 'C11H19NO10S2', 'Methionine-derived glucosinolates; Hydroxy alkenyl glucosinolates ', 2),
	(49, '(2S)-2-Hydroxy 3-butenyl glucosinolate', 'Epiprogoitrin', 'C00007864', 'C11H19NO10S2', 'Methionine-derived glucosinolates; Hydroxy alkenyl glucosinolates ', 2),
	(50, '2-Propenyl glucosinolate', 'Sinigrin', '', 'C10H17NO9S2', 'Methionine-derived glucosinolates; Alkenyl glucosinolates', 2),
	(51, '2-Hydroxy-4-pentenyl glucosinolate', 'Gluconapoleiferin', 'C00001477', 'C12H21NO10S2', 'Methionine-derived glucosinolates; Hydroxy alkyl glucosinolates', 2),
	(52, '3-Methylthiopropyl glucosinolate', 'Glucoiberverin', 'C00001473', 'C11H20NO9S3', 'Methionine-derived glucosinolates; Methylthio alkyl glucosinolates', 2),
	(53, '3-Methylsulfinylpropyl glucosinolate', 'Glucoiberin', 'C00007343', 'C11H20NO10S3', 'Methionine-derived glucosinolates; Methylsulfinyl alkyl glucosinolates', 2),
	(54, '3-Butenyl glucosinolate', 'Gluconapin', 'C00007586', 'C11H18NO9S2', 'Methionine-derived glucosinolates; Alkenyl glucosinolates', 2),
	(55, '4-Methylthiobutyl glucosinolate', 'Glucoerucin', 'C00007344', 'C12H22NO9S3', 'Methionine-derived glucosinolates; Methylthio alkyl glucosinolates', 2),
	(56, '4-Methylsulphinylbutyl glucosinolate', 'Glucoraphanin', 'C00007545', 'C12H22NO10S3', 'Methionine-derived glucosinolates; Methylsulfinyl alkyl glucosinolates', 2),
	(57, '4-Pentenyl glucosinolate', 'Glucobrassicanapin', 'C00001463', 'C12H21NO9S2', 'Methionine-derived glucosinolates; Alkenyl glucosinolates', 2),
	(58, '5-Methylsulfinylpentyl glucosinolate', 'Glucoalyssin', 'C00007345', 'C13H24NO10S3', 'Methionine-derived glucosinolates; Methylsulfinyl alkyl glucosinolates', 2),
	(59, '2-Phenylethyl glucosinolate', 'Gluconasturtiin', 'C00007350', 'C15H21NO9S2', 'Homo-phenylalanine derived glucosinolates; Benzyl glucosinolates', 3),
	(60, '3-Indolylmethylglucosinolate (I3M)', 'Glucobrassicin', 'C00000125', 'C16H20N2O9S2', 'Tryptophan derived glucosinolates; Indolylmethyl glucosinolates', 3),
	(61, '1-Methoxy-3-indolylmethyl glucosinolate', 'Neoglucobrassicin', 'C00000126', 'C17H22N2O10S2', 'Tryptophan derived glucosinolates; Indolylmethyl glucosinolates', 3),
	(62, '1-Methylethyl glucosinolate', 'Glucoputranjivin', 'C00001479', 'C10H19NO9S2', 'Methionine-derived glucosinolates; Methyl alkyl glucosinolates ', 3),
	(63, '4-Hydroxy-3-indolylmethyl glucosinolate', '4-Hydroxyglucobrassicin', 'C00000127', 'C16H20N2O10S2', 'Tryptophan derived glucosinolates; Indolylmethyl glucosinolates', 3),
	(64, '4-Methoxy-3-indolylmethyl glucosinolate', '4-Methoxyglucobrassicin', '', 'C17H22N2O10S2', 'Tryptophan derived glucosinolates; Metoxy indolylmethyl glucosinolates', 3),
	(65, '5-Methoxy-3-indolylmethyl glucosinolate', '5-Methoxyglucobrassicin', 'C00000131', 'C17H22N2O10S2', 'Tryptophan derived glucosinolates; Metoxy indolylmethyl glucosinolates', 3),
	(66, '5-Hydroxy-3-indolylmethyl glucosinolate', '5-Hydroxyglucobrassicin', 'C00000130', 'C16H20N2O10S2', 'Tryptophan derived glucosinolates; Hydroxy indolylmethyl glucosinolates', 3),
	(67, '(2R)-2-Hydroxy 3-butenyl glucosinolate', 'Progoitrin', 'C00001486', 'C11H19NO10S2', 'Methionine-derived glucosinolates; Hydroxy alkenyl glucosinolates ', 3),
	(68, '(2S)-2-Hydroxy 3-butenyl?glucosinolate', 'Epiprogoitrin', 'C00007864', 'C11H19NO10S2', 'Methionine-derived glucosinolates; Hydroxy alkenyl glucosinolates ', 3),
	(69, '2-Propenyl glucosinolate', 'Sinigrin', 'C00001488', 'C10H17NO9S2', 'Methionine-derived glucosinolates; Alkenyl glucosinolates', 3),
	(70, '2-Hydroxy-4-pentenyl glucosinolate', 'Gluconapoleiferin', '', 'C12H21NO10S2', 'Methionine-derived glucosinolates; Hydroxy alkyl glucosinolates', 3),
	(71, '3-Methylthiopropyl glucosinolate', 'Glucoiberverin', 'C00001473', 'C11H20NO9S3', 'Methionine-derived glucosinolates; Methylthio alkyl glucosinolates', 3),
	(72, '3-Methylsulfinylpropyl glucosinolate', 'Glucoiberin', 'C00007343', 'C11H20NO10S3', 'Methionine-derived glucosinolates; Methylsulfinyl alkyl glucosinolates', 3),
	(73, '3-Butenyl glucosinolate', 'Gluconapin', 'C00007586', 'C11H18NO9S2', 'Methionine-derived glucosinolates; Alkenyl glucosinolates', 3),
	(74, '4-Methylthiobutyl glucosinolate', 'Glucoerucin', 'C00007344', 'C12H22NO9S3', 'Methionine-derived glucosinolates; Methylthio alkyl glucosinolates', 3),
	(75, '4-Methylsulphinylbutyl glucosinolate', 'Glucoraphanin', 'C00007545', 'C12H22NO10S3', 'Methionine-derived glucosinolates; Methylsulfinyl alkyl glucosinolates', 3),
	(76, '4-Methylsulphinyl-3-butenyl glucosinolate', 'Glucoraphenin', '', 'C12H21NO10S3', 'Methionine-derived glucosinolates; Methylsulfinyl alkenyl glucosinolates', 3),
	(77, '4-Pentenyl glucosinolate', 'Glucobrassicanapin', 'C00001463', 'C12H21NO9S2', 'Methionine-derived glucosinolates; Alkenyl glucosinolates', 3),
	(78, '5-Methylsulfinylpentyl glucosinolate', 'Glucoalyssin', 'C00007345', 'C13H24NO10S3', 'Methionine-derived glucosinolates; Methylsulfinyl alkyl glucosinolates', 3),
	(79, '5-Methylthiopentyl glucosinolate', 'Glucoberteroin', '', 'C13H24NO9S3', 'Methionine-derived glucosinolates; Methylthio alkyl glucosinolates', 3),
	(80, 'Benzyl glucosinolate', 'Glucotropaeolin', 'C00007346', 'C14H19NO9S2', 'Phenylalanine derived glucosinolates; Benzyl glucosinolates', 1),
	(81, '3-(1,3-thiazol-2-yl)-1H-indole', 'Camalexin', 'C00007330', 'C11H8N2S', 'Camalexin', 1),
	(82, '6-Methoxy-3-(2-thiazolyl)-1H-indole', '6-methoxycamalexin', 'C00036628', 'C12H10N2OS', 'Camalexin', 1),
	(83, '6-(O-beta-D-glucopyranosyl) camalexin', 'Camalexin', '', 'C17H18N2O5S', 'Camalexin', 1),
	(84, '2-(1H-indol-3-yl)-4,5-dihydro-1,3-thiazole-4-carboxylic acid', 'Dihydrocamalexic Acid', '', 'C12H10N2O2S', 'Camalexin', 1);
/*!40000 ALTER TABLE `compounds` ENABLE KEYS */;

-- Dumping structure for table gslbase.compounds_references
CREATE TABLE IF NOT EXISTS `compounds_references` (
  `compound_name` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  `reference_id` int(11) DEFAULT NULL,
  `description_source` longtext COLLATE utf8_unicode_ci
) ENGINE=InnoDB DEFAULT CHARSET=utf8 COLLATE=utf8_unicode_ci;

-- Dumping data for table gslbase.compounds_references: ~144 rows (approximately)
/*!40000 ALTER TABLE `compounds_references` DISABLE KEYS */;
INSERT INTO `compounds_references` (`compound_name`, `reference_id`, `description_source`) VALUES
	('1', 11, 'Individual glucosinolates in various organs of the Columbia ecotype of A. thaliana during development with special emphasis on changes occurring during seedling germination and leaf development. 2-Phenylethyl glucosinolate and compounds with benzoyloxy substituents glucosinolates were most abundant in the seed (Brown et al. 2003)'),
	('2', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('2', 11, 'The only indole glucosinolates detected in the A. thaliana seeds were indol-3-ylmethyl glucosinolate (I3M) and trace amounts of its 4-hydroxyl derivative; which in total comprised only 2% of the seed glucosinolate content. In the leaves proportion of aliphatic glucosinolates declined with age resulting in the predominance of indole glucosinolates; mostly indol-3-ylmethyl glucosinolate (I3M) and its 1-methoxyl derivative (1MOI3M); by the time of senescence (Brown et al. 2003)'),
	('3', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('4', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('4', 11, 'The 16 most abundant glucosinolates showed divergent patterns of change during this time course. During the first two days after planting; there was a general increase in all glucosinolates causing total concentration to rise to almost 1.60 nmol (seedling) 1; approximately 3.3% of dry weight. After this point; specific increases were observed for glucosinolates associated with vegetative tissues. Increases of at least 6-fold were detected for 4MSOB; 5-methylsulfinylpentyl-; 1MOI3M and 4-methoxyindol-3-ylmethyl- glucosinolate; while 6-methylsulfinylhexyl-; 7-methylsulfinylheptyl-glucosinolate and I3M increased about 2-fold (Brown et al. 2003)'),
	('5', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('5', 94, 'In Arabidopsis; constitutive expression of the cassava CYP79D2 (CYP79D2 plants) leads to accumulation of valine-derived isopropyl-GS (IPGS) and isoleucine-derived 1-methylpropyl-GS (MPGS) (Mikkelsen and Halkier; 2003)'),
	('6', 94, 'In Arabidopsis; constitutive expression of the cassava CYP79D2 (CYP79D2 plants) leads to accumulation of valine-derived isopropyl-GS (IPGS) and isoleucine-derived 1-methylpropyl-GS (MPGS) (Mikkelsen and Halkier; 2003)'),
	('7', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('7', 72, 'Glucosinolates were extracted from seeds of Columbia (Col-0) and identified 12 glucosinolates; including five novel compounds (Reichelt et al. 2002)'),
	('7', 11, 'Glucosinolates that predominate in the seed; including 3-hydroxypropyl-; 4-hydroxybutyl-; 3-benzoyloxypropyl-; 4-benzoyloxybutyl-; 4-methylthiobutyl-;7-methylthioheptyl-; 8 methylsulfinyoctyl-; 8-methylthiooctyl-; and 4-hydroxyindol-3-ylmethyl- glucosinolate remained constant or showed a decrease upon seedling germination  (Brown et al. 2003)'),
	('8', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('8', 72, 'Glucosinolates were extracted from seeds of Columbia (Col-0) and identified 12 glucosinolates; including five novel compounds (Reichelt et al. 2002)'),
	('8', 11, 'The 16 most abundant glucosinolates showed divergent patterns of change during this time course. During the first two days after planting; there was a general increase in all glucosinolates causing total concentration to rise to almost 1.60 nmol (seedling) 1; approximately 3.3% of dry weight. After this point; specific increases were observed for glucosinolates associated with vegetative tissues. Increases of at least 6-fold were detected for 4MSOB; 5-methylsulfinylpentyl-; 1MOI3M and 4-methoxyindol-3-ylmethyl- glucosinolate; while 6-methylsulfinylhexyl-; 7-methylsulfinylheptyl-glucosinolate and I3M increased about 2-fold (Brown et al. 2003)'),
	('9', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('9', 72, 'Glucosinolates were extracted from seeds of Columbia (Col-0) and identified 12 glucosinolates; including five novel compounds. Seven other glucosinolates that have been previously described in the literature; but not yet reported from this species; including allyl (2-propenyl); 4-pentenyl; (2R)-2-hydroxy-3-butenyl; (2S)-2-hydroxy-3-butenyl; benzyl; 3-methylbutyl and 4-methylpentyl glucosinolate (isolated from ecotypes other than Columbia) (Reichelt et al. 2002)'),
	('10', 44, 'The Kas and Sorbo ecotypes contain significant amounts of 2-hydroxy-3-butenyl glucosinolate in the seeds (Kliebenstein et al. 2001)'),
	('10', 72, 'Glucosinolates were extracted from seeds of Columbia (Col-0) and identified 12 glucosinolates; including five novel compounds. Seven other glucosinolates that have been previously described in the literature; but not yet reported from this species; including allyl (2-propenyl); 4-pentenyl; (2R)-2-hydroxy-3-butenyl; (2S)-2-hydroxy-3-butenyl; benzyl; 3-methylbutyl and 4-methylpentyl glucosinolate (isolated from ecotypes other than Columbia) (Reichelt et al. 2002)'),
	('11', 72, 'Glucosinolates were extracted from seeds of Columbia (Col-0) and identified 12 glucosinolates; including five novel compounds. Seven other glucosinolates that have been previously described in the literature; but not yet reported from this species; including allyl (2-propenyl); 4-pentenyl; (2R)-2-hydroxy-3-butenyl; (2S)-2-hydroxy-3-butenyl; benzyl; 3-methylbutyl and 4-methylpentyl glucosinolate (isolated from ecotypes other than Columbia) (Reichelt et al. 2002)'),
	('12', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('13', 72, 'Glucosinolates were extracted from seeds of Columbia (Col-0) and identified 12 glucosinolates; including five novel compounds. 2-methylsulfinylethyl glucosinolate; the first non-chain elongated methionine-derived glucosinolate to be isolated from A. thaliana (Reichelt et al. 2002)'),
	('14', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('14', 72, 'Glucosinolates were extracted from seeds of Columbia (Col-0) and identified 12 glucosinolates; including five novel compounds. Seven other glucosinolates that have been previously described in the literature; but not yet reported from this species; including allyl (2-propenyl); 4-pentenyl; (2R)-2-hydroxy-3-butenyl; (2S)-2-hydroxy-3-butenyl; benzyl; 3-methylbutyl and 4-methylpentyl glucosinolate (Reichelt et al. 2002)'),
	('14', 11, 'Individual glucosinolates in various organs of the Columbia ecotype of A. thaliana during development with special emphasis on changes occurring during seedling germination and leaf development (Brown et al. 2003)'),
	('15', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('15', 72, 'Glucosinolates were extracted from seeds of Columbia (Col-0) and identified 12 glucosinolates; including five novel compounds (Reichelt et al. 2002)'),
	('16', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('17', 72, 'Glucosinolates were extracted from seeds of Columbia (Col-0) and identified 12 glucosinolates; including five novel compounds (Reichelt et al. 2002)'),
	('18', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('19', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('19', 72, 'Glucosinolates were extracted from seeds of Columbia (Col-0) and identified 12 glucosinolates; including five novel compounds (Reichelt et al. 2002)'),
	('19', 11, 'Individual glucosinolates in various organs of the Columbia ecotype of A. thaliana during development with special emphasis on changes occurring during seedling germination and leaf development (Brown et al. 2003)'),
	('20', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('20', 72, 'Glucosinolates were extracted from seeds of Columbia (Col-0) and identified 12 glucosinolates; including five novel compounds (Reichelt et al. 2002)'),
	('20', 11, 'Individual glucosinolates in various organs of the Columbia ecotype of\nA. thaliana during development with special emphasis on changes occurring during seedling germination and leaf development (Brown et al. 2003)'),
	('20', 82, 'Seven 3-week-old A. thaliana were challenged for 48 h with two neonate S. littoralis larvae per plant. Unchallenged plants were used as controls. Glucosinolates analyzed by UHPLC-QTOFMS (Schweizer et al. 2013)'),
	('21', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('21', 72, 'Glucosinolates were extracted from seeds of Columbia (Col-0) and identified 12 glucosinolates; including five novel compounds (Reichelt et al. 2002)'),
	('22', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('22', 72, 'Glucosinolates were extracted from seeds of Columbia (Col-0) and identified 12 glucosinolates; including five novel compounds (Reichelt et al. 2002)'),
	('22', 11, 'Seeds contained six novel glucosinolates relative to the vegetative tissues; including 7-methylthioheptyl-; 8-methylthiooctyl-; 3-hydroxypropyl-; 4-hydroxybutyl-; 3-benzoyloxypropyl- and 4-benzoyloxybutyl- glucosinolates. On the other hand; glucosinolates that predominate in the seed; including 3-hydroxypropyl-; 4-hydroxybutyl-; 3-benzoyloxypropyl-; 4-benzoyloxybutyl-; 4-methylthiobutyl-; 7-methylthioheptyl-; 8-methylsulfinyoctyl-; 8-methylthiooctyl-; and 4-hydroxyindol-3-ylmethyl- glucosinolate remained constant or showed a decrease upon seedling germination (Brown et al. 2003)'),
	('23', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('23', 72, 'Especially prominent; were compounds with benzoyloxy substituents; The most abundant of this group were desulfo-3-benzoyloxypropyl and desulfo-4-benzoyloxybutyl (Reichelt et al. 2002)'),
	('23', 11, 'Seeds contained six novel glucosinolates relative to the vegetative tissues; including 7-methylthioheptyl-; 8-methylthiooctyl-; 3-hydroxypropyl-; 4-hydroxybutyl-; 3-benzoyloxypropyl- and 4-benzoyloxybutyl- glucosinolates. On the other hand; glucosinolates that predominate in the seed; including 3-hydroxypropyl-; 4-hydroxybutyl-; 3-benzoyloxypropyl-; 4-benzoyloxybutyl-; 4-methylthiobutyl-; 7-methylthioheptyl-; 8-methylsulfinyoctyl-; 8-methylthiooctyl-; and 4-hydroxyindol-3-ylmethyl- glucosinolate remained constant or showed a decrease upon seedling germination (Brown et al. 2003)'),
	('23', 46, 'Seeds have the highest overall glucosinolate levels; up to 3% of total seed weight; and also contain benzoyloxyglucosinolates; which do not accumulate in vegetative tissue (Kliebenstein et al. 2007)'),
	('24', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('24', 72, 'Glucosinolates were extracted from seeds of Columbia (Col-0) and identified 12 glucosinolates; including five novel compounds (Reichelt et al. 2002)'),
	('24', 11, 'Individual glucosinolates in various organs of the Columbia ecotype of A. thaliana during development with special emphasis on changes occurring during seedling germination and leaf development. The leaves of the oldest plants also contained typical seed glucosinolates; such as 4-methylthiobutyl-; 4-hydroxybutyl- and 4-benzoyloxybutyl-glucosinolates. On the other hand; glucosinolates that predominate in the seed; including 3-hydroxypropyl-; 4-hydroxybutyl-; 3-benzoyloxypropyl-; 4-benzoyloxybutyl-; 4-methylthiobutyl-; 7-methylthioheptyl-; 8-methylsulfinyoctyl-; 8-methylthiooctyl-; and 4-hydroxyindol-3-ylmethyl- glucosinolate remained constant or showed a decrease upon seedling germination (Brown et al. 2003)'),
	('25', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('25', 72, 'Glucosinolates were extracted from seeds of Columbia (Col-0) and identified 12 glucosinolates; including five novel compounds (Reichelt et al. 2002)'),
	('25', 11, 'Individual glucosinolates in various organs of the Columbia ecotype of A. thaliana during development with special emphasis on changes occurring during seedling germination and leaf development. The major class of glucosinolates in the rosette leaves depended on their age. In the vegetative stage; 4-methylsulfinylbutyl glucosinolate (4MSOB) and other aliphatic glucosinolates contributed more than 80% of the total; with indole glucosinolates contributing the balance. However; the proportion of aliphatic glucosinolates declined withage resulting in the predominance of indole glucosinolates; mostly indol-3-ylmethyl glucosinolate (I3M) and its 1-methoxyl derivative (1MOI3M); by the time of senescence (Brown et al. 2003)'),
	('26', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('26', 72, 'Glucosinolates were extracted from seeds of Columbia (Col-0) and identified 12 glucosinolates; including five novel compounds (Reichelt et al. 2002)'),
	('26', 11, 'Individual glucosinolates in various organs of the Columbia ecotype of A. thaliana during development with special emphasis on changes occurring during seedling germination and leaf development. The leaves of the oldest plants also contained typical seed glucosinolates; such as 4-methylthiobutyl-; 4-hydroxybutyl- and 4-benzoyloxybutyl-glucosinolates (Brown et al. 2003)'),
	('27', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('27', 72, 'Especially prominent; were compounds with benzoyloxy substituents; The most abundant of this group were desulfo-3-benzoyloxypropyl and desulfo-4-benzoyloxybutyl (Reichelt et al. 2002)'),
	('27', 11, 'Individual glucosinolates in various organs of the Columbia ecotype of A. thaliana during development with special emphasis on changes occurring during seedling germination and leaf development. The leaves of the oldest plants also contained typical seed glucosinolates; such as 4-methylthiobutyl-; 4-hydroxybutyl- and 4-benzoyloxybutyl-glucosinolates (Brown et al. 2003)'),
	('28', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('28', 72, 'Glucosinolates were extracted from seeds of Columbia (Col-0) and identified 12 glucosinolates; including five novel compounds. Seven other glucosinolates that have been previously described in the literature; but not yet reported from this species; including allyl (2-propenyl); 4-pentenyl; (2R)-2-hydroxy-3-butenyl; (2S)-2-hydroxy-3-butenyl; benzyl; 3-methylbutyl and 4-methylpentyl glucosinolate (Reichelt et al. 2002)'),
	('29', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('29', 72, 'Glucosinolates were extracted from seeds of Columbia (Col-0) and identified 12 glucosinolates; including five novel compounds (Reichelt et al. 2002)'),
	('29', 11, 'Individual glucosinolates in various organs of the Columbia ecotype of A. thaliana during development with special emphasis on changes occurring during seedling germination and leaf development. The 16 most abundant glucosinolates showed divergent patterns of change during this time course. During the first two days after planting; there was a general increase in all glucosinolates causing total concentration to rise to almost 1.60 nmol (seedling); approximately 3.3% of dry weight. After this point; specific increases were observed for glucosinolates associated with vegetative tissues. Increases of at least 6-fold were detected for 4MSOB; 5-methylsulfinylpentyl-; 1MOI3M and 4-methoxyindol-3-ylmethyl- glucosinolate; while 6 methylsulfinylhexyl-; 7-methylsulfinylheptyl-glucosinolate and I3M increased about 2-fold (Brown et al. 2003)'),
	('30', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('30', 72, 'Glucosinolates were extracted from seeds of Columbia (Col-0) and identified 12 glucosinolates; including five novel compounds (Reichelt et al. 2002)'),
	('30', 11, 'Individual glucosinolates in various organs of the Columbia ecotype of A. thaliana during development with special emphasis on changes occurring during seedling germination and leaf development. The 16 most abundant glucosinolates showed divergent patterns of change during this time course (Brown et al. 2003)'),
	('31', 70, 'Extraction of GSLs from plant material and purification as desulfoGSLs were performed as described by Brown et al. (2003). For quantification; benzylGSL were added as an internal standard at the beginning of the extraction procedure. desulfoGSLs were separated by HPLC (Piotrowski et al. 2004)'),
	('32', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('32', 72, 'Glucosinolates were extracted from seeds of Columbia (Col-0) and identified 12 glucosinolates; including five novel compounds (Reichelt et al. 2002)'),
	('33', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('33', 72, 'Glucosinolates were extracted from seeds of Columbia (Col-0) and identified 12 glucosinolates; including five novel compounds (Reichelt et al. 2002)'),
	('33', 11, 'Individual glucosinolates in various organs of the Columbia ecotype of A. thaliana during development with special emphasis on changes occurring during seedling germination and leaf development. The 16 most abundant glucosinolates showed divergent patterns of change during this time course. During the first two days after planting; there was a general increase in all glucosinolates causing total concentration to rise to almost 1.60 nmol (seedling); approximately 3.3% of dry weight. After this point; specific increases were observed for glucosinolates associated with vegetative tissues. Increases of at least 6-fold were detected for 4MSOB; 5-methylsulfinylpentyl-; 1MOI3M and 4-methoxyindol-3-ylmethyl- glucosinolate; while 6 methylsulfinylhexyl-; 7-methylsulfinylheptyl-glucosinolate and I3M increased about 2-fold (Brown et al. 2003)'),
	('34', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('34', 72, 'Glucosinolates were extracted from seeds of Columbia (Col-0) and identified 12 glucosinolates; including five novel compounds (Reichelt et al. 2002)'),
	('34', 11, 'Individual glucosinolates in various organs of the Columbia ecotype of A. thaliana during development with special emphasis on changes occurring during seedling germination and leaf development. The predominant seed glucosinolate; representing 41% of the total; has an aliphatic; butylbased side chain with a sulfur atom; but is not 4MSOB; the main glucosinolate found in the vegetative parts of the plant; but rather its reduced counterpart; 4 methylthiobutyl glucosinolate (4MTB). The seeds also contain greater amounts of the longer-chain aliphatic glucosinolates; such as 7-methylsulfinylheptyl- and 8-methylsulfinyloctyl- glucosinolate; than are found in the vegetative tissues. The 16 most abundant glucosinolates showed divergent patterns of change during this time course. During the first two days after planting; there was a general increase in all glucosinolates causing total concentration to rise to almost 1.60 nmol (seedling); approximately 3.3% of dry weight. After this point; specific increases were observed for glucosinolates associated with vegetative tissues. Increases of at least 6-fold were detected for 4MSOB; 5-methylsulfinylpentyl-; 1MOI3M and 4-methoxyindol-3-ylmethyl- glucosinolate; while 6 methylsulfinylhexyl-; 7-methylsulfinylheptyl-glucosinolate and I3M increased about 2-fold (Brown et al. 2003)'),
	('35', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('35', 72, 'Glucosinolates were extracted from seeds of Columbia (Col-0) and identified 12 glucosinolates; including five novel compounds (Reichelt et al. 2002)'),
	('35', 11, 'Seeds contained six novel glucosinolates relative to the vegetative tissues; including 7-methylthioheptyl-; 8-methylthiooctyl-; 3-hydroxypropyl-; 4-hydroxybutyl-; 3-benzoyloxypropyl- and 4-benzoyloxybutyl- glucosinolates. On the other hand; glucosinolates that predominate in the seed; including 3-hydroxypropyl-; 4-hydroxybutyl-; 3-benzoyloxypropyl-; 4-benzoyloxybutyl-; 4-methylthiobutyl-; 7-methylthioheptyl-; 8-methylsulfinyoctyl-; 8-methylthiooctyl-; and 4-hydroxyindol-3-ylmethyl- glucosinolate remained constant or showed a decrease upon seedling germination (Brown et al. 2003)'),
	('36', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('36', 72, 'Glucosinolates were extracted from seeds of Columbia (Col-0) and identified 12 glucosinolates; including five novel compounds (Reichelt et al. 2002)'),
	('36', 11, 'Seeds contained six novel glucosinolates relative to the vegetative tissues; including 7-methylthioheptyl-; 8-methylthiooctyl-; 3-hydroxypropyl-; 4-hydroxybutyl-; 3-benzoyloxypropyl- and 4-benzoyloxybutyl- glucosinolates. On the other hand; glucosinolates that predominate in the seed; including 3-hydroxypropyl-; 4-hydroxybutyl-; 3-benzoyloxypropyl-; 4-benzoyloxybutyl-; 4-methylthiobutyl-; 7-methylthioheptyl-; 8-methylsulfinyoctyl-; 8-methylthiooctyl-; and 4-hydroxyindol-3-ylmethyl- glucosinolate remained constant or showed a decrease upon seedling germination (Brown et al. 2003)'),
	('37', 72, 'Glucosinolates were extracted from seeds of Columbia (Col-0) and identified 12 glucosinolates; including five novel compounds (Reichelt et al. 2002)'),
	('37', 11, 'The predominant seed glucosinolate; representing 41% of the total; has an aliphatic; butylbased side chain with a sulfur atom; but is not 4MSOB; the main glucosinolate found in the vegetative parts of the plant; but rather its reduced counterpart; 4-methylthiobutyl glucosinolate (4MTB). The seeds also contain greater amounts of the longer-chain aliphatic glucosinolates; such as 7-methylsulfinylheptyl- and 8-methylsulfinyloctyl- glucosinolate; than are found in the vegetative tissues (Brown et al. 2003)'),
	('38', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('39', 72, 'Glucosinolates were extracted from seeds of Columbia (Col-0) and identified 12 glucosinolates; including five novel compounds. Seven other glucosinolates that have been previously described in the literature; but not yet reported from this species; including allyl (2-propenyl); 4-pentenyl; (2R)-2-hydroxy-3-butenyl; (2S)-2-hydroxy-3-butenyl; benzyl; 3-methylbutyl and 4-methylpentyl glucosinolate (isolated from ecotypes other than Columbia) (Reichelt et al. 2002)'),
	('40', 72, 'Glucosinolates were extracted from seeds of Columbia (Col-0) and identified 12 glucosinolates; including five novel compounds. Seven other glucosinolates that have been previously described in the literature; but not yet reported from this species; including allyl (2-propenyl); 4-pentenyl; (2R)-2-hydroxy-3-butenyl; (2S)-2-hydroxy-3-butenyl; benzyl; 3-methylbutyl and 4-methylpentyl glucosinolate (isolated from ecotypes other than Columbia) (Reichelt et al. 2002)'),
	('41', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('41', 72, 'Especially prominent; were compounds with benzoyloxy substituents; The most abundant of this group were desulfo-3-benzoyloxypropyl and desulfo-4-benzoyloxybutyl (Reichelt et al. 2002)'),
	('42', 44, '34 different glucosinolates found from the leaves and seeds of 39 different Arabidopsis ecotypes (Kliebenstein et al. 2001)'),
	('42', 72, 'The benzoyloxy substituents were also prominent; The most abundant of this group were desulfo-3-benzoyloxypropyl and desulfo-4-benzoyloxybutyl (Reichelt et al. 2002)'),
	('43', 96, 'Glucosinolate levels in leaves were determined in a collection of 113 varieties of turnip greens (Brassica rapa L.) from northwestern Spain grown at two sites. Sixteen glucosinolates; belonging to the three chemical classes; were detected in the whole collection. Three glucosinolates were detected in all varieties: glucobrassicanapin; glucobrassicin; and gluconasturtiin and four more were detected in about 90% of the varieties: gluconapin; progoitrin; glucoiberin; and neoglucobrassicin (Padilla et al. 2007)'),
	('43', 95, 'Individual GSLs (glucoallysin; glucobrassicanapin; gluconasturtiin; glucobrassicin; 4-methoxyglucobrassicin; neoglucobrassicin and 4-hydroxyglucobrassicin) contents increased in transgenic hairy roots compared to that in non-transgenic roots in turnip (Brassica rapa ssp. rapa) (Chung et al. 2010)'),
	('44', 96, 'Glucosinolate levels in leaves were determined in a collection of 113 varieties of turnip greens (Brassica rapa L.) from northwestern Spain grown at two sites. Sixteen glucosinolates; belonging to the three chemical classes; were detected in the whole collection. Three glucosinolates were detected in all varieties: glucobrassicanapin; glucobrassicin; and gluconasturtiin and four more were detected in about 90% of the varieties: gluconapin; progoitrin; glucoiberin; and neoglucobrassicin (Padilla et al. 2007)'),
	('44', 31, 'The indolyl glucosinolate glucobrassicin is present in Savoy cabbage; Brussels sprouts and cauliflower (Hayes et al. 2008)'),
	('44', 95, 'Individual GSLs (glucoallysin; glucobrassicanapin; gluconasturtiin; glucobrassicin; 4-methoxyglucobrassicin; neoglucobrassicin and 4-hydroxyglucobrassicin) contents increased in transgenic hairy roots compared to that in non-transgenic roots in turnip (Brassica rapa ssp. rapa) (Chung et al. 2016)'),
	('45', 96, 'Glucosinolate levels in leaves were determined in a collection of 113 varieties of turnip greens (Brassica rapa L.) from northwestern Spain grown at two sites. Sixteen glucosinolates; belonging to the three chemical classes; were detected in the whole collection. Three glucosinolates were detected in all varieties: glucobrassicanapin; glucobrassicin; and gluconasturtiin and four more were detected in about 90% of the varieties: gluconapin; progoitrin; glucoiberin; and neoglucobrassicin (Padilla et al. 2007)'),
	('45', 95, 'Individual GSLs (glucoallysin; glucobrassicanapin; gluconasturtiin; glucobrassicin; 4-methoxyglucobrassicin; neoglucobrassicin and 4-hydroxyglucobrassicin) contents increased in transgenic hairy roots compared to that in non-transgenic roots in turnip (Brassica rapa ssp. rapa) (Chung et al. 2016)'),
	('46', 96, 'Glucosinolate levels in leaves were determined in a collection of 113 varieties of turnip greens (Brassica rapa L.) from northwestern Spain grown at two sites. Sixteen glucosinolates; belonging to the three chemical classes; were detected in the whole collection. For gluconapoleiferin; glucoalyssin; 4-\nhydroxyglucobrassicin; and glucoiberverin; analyses of variance showed significant differences among varieties (Padilla et al. 2007)'),
	('47', 96, 'Glucosinolate levels in leaves were determined in a collection of 113 varieties of turnip greens (Brassica rapa L.) from northwestern Spain grown at two sites. Sixteen glucosinolates; belonging to the three chemical classes; were detected in the whole collection. Epiprogoitrin; glucoraphanin; glucoerucin; and 4-methoxyglucobrassicin were present in a few varieties and no statistical differences in concentrations among varieties were found (Padilla et al. 2007)'),
	('47', 95, 'Individual GSLs (glucoallysin; glucobrassicanapin; gluconasturtiin; glucobrassicin; 4-methoxyglucobrassicin; neoglucobrassicin and 4-hydroxyglucobrassicin) contents increased in transgenic hairy roots compared to that in non-transgenic roots in turnip (Brassica rapa ssp. rapa) (Chung et al. 2016)'),
	('48', 96, 'Glucosinolate levels in leaves were determined in a collection of 113 varieties of turnip greens (Brassica rapa L.) from northwestern Spain grown at two sites. Sixteen glucosinolates; belonging to the three chemical classes; were detected in the whole collection. Three glucosinolates were detected in all varieties: glucobrassicanapin; glucobrassicin; and gluconasturtiin and four more were detected in about 90% of the varieties: gluconapin; progoitrin; glucoiberin; and neoglucobrassicin (Padilla et al. 2007)'),
	('48', 95, 'Gluconapin; progoitrin; and sinigrin levels decreased in hairy roots compared to non-transformed roots in turnip (Brassica rapa ssp. rapa) (Chung et al. 2016)'),
	('49', 96, 'Glucosinolate levels in leaves were determined in a collection of 113 varieties of turnip greens (Brassica rapa L.) from northwestern Spain grown at two sites. Sixteen glucosinolates; belonging to the three chemical classes; were detected in the whole collection. Epiprogoitrin; glucoraphanin; glucoerucin; and 4-methoxyglucobrassicin were present in a few varieties and no statistical differences in concentrations among varieties were found (Padilla et al. 2007).'),
	('50', 95, 'Gluconapin; progoitrin; and sinigrin levels decreased in hairy roots compared to non-transformed roots in turnip (Brassica rapa ssp. rapa) (Chung et al. 2016)'),
	('51', 96, 'Glucosinolate levels in leaves were determined in a collection of 113 varieties of turnip greens (Brassica rapa L.) from northwestern Spain grown at two sites. Sixteen glucosinolates were identified; being the aliphatic glucosinolates; gluconapin and glucobrassicanapin the most abundant. Other aliphatic glucosinolates; such as progoitrin; glucoalyssin; and gluconapoleiferin were relatively abundant in varieties with a different glucosinolate profile (Padilla et al. 2007).'),
	('52', 96, 'Glucosinolate levels in leaves were determined in a collection of 113 varieties of turnip greens (Brassica rapa L.) from northwestern Spain grown at two sites. Sixteen glucosinolates; belonging to the three chemical classes; were detected in the whole collection; being the aliphatic glucosinolates; gluconapin and glucobrassicanapin the most abundant. For gluconapoleiferin; glucoalyssin; 4- hydroxyglucobrassicin; and glucoiberverin; analyses of variance showed significant differences among varieties (Padilla et al. 2007)'),
	('53', 96, 'Glucosinolate levels in leaves were determined in a collection of 113 varieties of turnip greens (Brassica rapa L.) from northwestern Spain grown at two sites. Sixteen glucosinolates; belonging to the three chemical classes; were detected in the whole collection; being the aliphatic glucosinolates; gluconapin and glucobrassicanapin the most abundant. Three glucosinolates were detected in all varieties: glucobrassicanapin; glucobrassicin; and gluconasturtiin and four more were detected in about 90% of the varieties: gluconapin; progoitrin; glucoiberin; and neoglucobrassicin (Padilla et al. 2007)'),
	('54', 96, 'Glucosinolate levels in leaves were determined in a collection of 113 varieties of turnip greens (Brassica rapa L.) from northwestern Spain grown at two sites. Sixteen glucosinolates; belonging to the three chemical classes; were detected in the whole collection; being the aliphatic glucosinolates; gluconapin and glucobrassicanapin the most abundant. Three glucosinolates were detected in all varieties: glucobrassicanapin; glucobrassicin; and gluconasturtiin and four more were detected in about 90% of the varieties: gluconapin; progoitrin; glucoiberin; and neoglucobrassicin (Padilla et al. 2007)'),
	('54', 95, 'Gluconapin; progoitrin; and sinigrin levels decreased in hairy roots compared to non-transformed roots in turnip (Brassica rapa ssp. rapa) (Chung et al. 2016)'),
	('55', 96, 'Glucosinolate levels in leaves were determined in a collection of 113 varieties of turnip greens (Brassica rapa L.) from northwestern Spain grown at two sites. Sixteen glucosinolates; belonging to the three chemical classes; were detected in the whole collection. Epiprogoitrin; glucoraphanin; glucoerucin; and 4-methoxyglucobrassicin were present in a few varieties and no statistical differences in concentrations among varieties were found (Padilla et al. 2007)'),
	('56', 96, 'Glucosinolate levels in leaves were determined in a collection of 113 varieties of turnip greens (Brassica rapa L.) from northwestern Spain grown at two sites. Sixteen glucosinolates; belonging to the three chemical classes; were detected in the whole collection; being the aliphatic glucosinolates; gluconapin and glucobrassicanapin the most abundant. Three glucosinolates were detected in all varieties: glucobrassicanapin; glucobrassicin; and gluconasturtiin and four more were detected in about 90% of the varieties: gluconapin; progoitrin; glucoiberin; and neoglucobrassicin. The presence of glucoraphanin in 27 varieties should be studied more exhaustively since this aliphatic glucosinolate is the precursor of sulforaphane; a potent anti-cancer isothiocyanate (Padilla et al. 2007)'),
	('57', 96, 'Glucosinolate levels in leaves were determined in a collection of 113 varieties of turnip greens (Brassica rapa L.) from northwestern Spain grown at two sites. Sixteen glucosinolates; belonging to the three chemical classes; were detected in the whole collection; being the aliphatic glucosinolates; gluconapin and glucobrassicanapin the most abundant. Three glucosinolates were detected in all varieties: glucobrassicanapin; glucobrassicin; and gluconasturtiin and four more were detected in about 90% of the varieties: gluconapin; progoitrin; glucoiberin; and neoglucobrassicin (Padilla et al. 2007)'),
	('58', 96, 'Glucosinolate levels in leaves were determined in a collection of 113 varieties of turnip greens (Brassica rapa L.) from northwestern Spain grown at two sites. Sixteen glucosinolates; belonging to the three chemical classes; were detected in the whole collection. For gluconapoleiferin; glucoalyssin; 4-\nhydroxyglucobrassicin; and glucoiberverin; analyses of variance showed significant differences among varieties (Padilla et al. 2007)'),
	('58', 95, 'Individual GSLs (glucoallysin; glucobrassicanapin; gluconasturtiin; glucobrassicin; 4-methoxyglucobrassicin; neoglucobrassicin and 4-hydroxyglucobrassicin) contents increased in transgenic hairy roots compared to that in non-transgenic roots in turnip (Brassica rapa ssp. rapa) (Chung et al. 2016)'),
	('59', 90, 'HPLC analysis revealed the presence of 16 different types of glucosinolates in three different edible\norgans of four different subspecies of B. oleracea. In this study; other glucosinolates such as glucoraphanin; progoitrin; glucobrassicin; methoxyglucobrassicin; neoglucobrassicin and gluconasturtiin were also expressed in all three types of edible organs; such as in the leaves; stems and florets (Yi et al. 2015)'),
	('59', 16, 'The GSLs found in 10 cultivars of cabbage (Brassica oleracea var. capitata) popularly cultivated in Korea and China were identified and quantified. Three GSL classes (6 aliphatic; 1 aromatic; and 3 indolyl) were identified and quantified using high-performance liquid chromatography mass spectrometry (HPLC-MS) and HPLC. The concentration of these GSLs varied by season (spring- and fall-sown); leaf position (inside and outside); and cabbage color (green and red). The gluconasturtiin content was very low in all the cabbage varieties analyzed in this study (Choi et al. 2014)'),
	('60', 90, 'HPLC analysis revealed the presence of 16 different types of glucosinolates in three different edible\norgans of four different subspecies of B. oleracea. In this study; other glucosinolates such as glucoraphanin; progoitrin; glucobrassicin; methoxyglucobrassicin; neoglucobrassicin and gluconasturtiin were also expressed in all three types of edible organs; such as in the leaves; stems and florets (Yi et al. 2015)'),
	('61', 90, 'HPLC analysis revealed the presence of 16 different types of glucosinolates in three different edible\norgans of four different subspecies of B. oleracea. In this study; other glucosinolates such as glucoraphanin; progoitrin; glucobrassicin; methoxyglucobrassicin; neoglucobrassicin and gluconasturtiin were also expressed in all three types of edible organs; such as in the leaves; stems and florets (Yi et al. 2015)'),
	('61', 73, 'HPLC analysis detected a total of eight types of glucosinolate molecules in four cabbage\ninbred lines. Those were progoitrin; glucoraphanin; sinigrin; gluconapin; glucoerucin;\n4-hydroxy-glucobrassicin (4HGBS); methoxy-glucobrassicin (MGBS) and neoglucobrassicin (NGBS) (Robin et al. 2016)'),
	('63', 95, 'Individual GSLs (glucoallysin; glucobrassicanapin; gluconasturtiin; glucobrassicin; 4-methoxyglucobrassicin; neoglucobrassicin and 4-hydroxyglucobrassicin) contents increased in transgenic hairy roots compared to that in non-transgenic roots in turnip (Brassica rapa ssp. rapa) (Chung et al. 2016)'),
	('63', 90, 'HPLC analysis revealed the presence of 16 different types of glucosinolates in three different edible\norgans of four different subspecies of B. oleracea. Cabbage leaves contained 12 glucosinolates; kale leaves contained 10; kohlrabi stems contained 11 and the cauliflower florets contained 14. Gluconapin; glucoalyssin; gluconapoleiferin and 4-hydroxy glucobrassicin were identified only the florets of cauliflower (Yi et al. 2015)'),
	('63', 73, 'HPLC analysis detected a total of eight types of glucosinolate molecules in four cabbage inbred lines. Those were progoitrin; glucoraphanin; sinigrin; gluconapin; glucoerucin; 4-hydroxy-glucobrassicin (4HGBS); methoxy-glucobrassicin (MGBS) and neoglucobrassicin (NGBS) (Robin et al. 2016)'),
	('64', 90, 'HPLC analysis revealed the presence of 16 different types of glucosinolates in three different edible\norgans of four different subspecies of B. oleracea. In this study; other glucosinolates such as glucoraphanin; progoitrin; glucobrassicin; methoxyglucobrassicin; neoglucobrassicin and gluconasturtiin were also expressed in all three types of edible organs; such as in the leaves; stems and florets (Yi et al. 2015)'),
	('64', 73, 'HPLC analysis detected a total of eight types of glucosinolate molecules in four cabbage inbred lines. Those were progoitrin; glucoraphanin; sinigrin; gluconapin; glucoerucin; 4-hydroxy-glucobrassicin (4HGBS); methoxy-glucobrassicin (MGBS) and neoglucobrassicin (NGBS) (Robin et al. 2016)'),
	('67', 90, 'HPLC analysis revealed the presence of 16 different types of glucosinolates in three different edible\norgans of four different subspecies of B. oleracea. In this study; other glucosinolates such as glucoraphanin; progoitrin; glucobrassicin; methoxyglucobrassicin; neoglucobrassicin and gluconasturtiin were also expressed in all three types of edible organs; such as in the leaves; stems and florets (Yi et al. 2015)'),
	('67', 73, 'HPLC analysis detected a total of eight types of glucosinolate molecules in four cabbage inbred lines. Those were progoitrin; glucoraphanin; sinigrin; gluconapin; glucoerucin; 4-hydroxy-glucobrassicin (4HGBS); methoxy-glucobrassicin (MGBS) and neoglucobrassicin (NGBS) (Robin et al. 2016)'),
	('69', 90, 'HPLC analysis revealed the presence of 16 different types of glucosinolates in three different edible\norgans of four different subspecies of B. oleracea. In this study; we measured glucosinolate concentration only at one time point. Similar to our study; the presence of glucoiberin; sinigrin and glucobrassicin was previously reported in all different subspecies of B. oleracea (Yi et al. 2015)'),
	('69', 73, 'HPLC analysis detected a total of eight types of glucosinolate molecules in four cabbage inbred lines. Those were progoitrin; glucoraphanin; sinigrin; gluconapin; glucoerucin; 4-hydroxy-glucobrassicin (4HGBS); methoxy-glucobrassicin (MGBS) and neoglucobrassicin (NGBS) (Robin et al. 2016)'),
	('70', 90, 'HPLC analysis revealed the presence of 16 different types of glucosinolates in three different edible\norgans of four different subspecies of B. oleracea. Out of 11 aliphatic glucosinolates identified in three types of edible organs in 12 genotypes of four B. oleracea subspecies; only gluconapin; glucoalyssin and gluconapoleiferin were expressed in the florets of cauliflower (Yi et al. 2015)'),
	('71', 90, 'HPLC analysis revealed the presence of 16 different types of glucosinolates in three different edible\norgans of four different subspecies of B. oleracea. Glucoerucin was only found in the cabbage leaves;\nand glucoiberverin was identified in the cabbage leaves and kohlrabi stems (Yi et al. 2015)'),
	('72', 90, 'HPLC analysis revealed the presence of 16 different types of glucosinolates in three different edible\norgans of four different subspecies of B. oleracea. In this study; we measured glucosinolate concentration only at one time point. Similar to our study; the presence of glucoiberin; sinigrin and glucobrassicin was previously reported in all different subspecies of B. oleracea (Yi et al. 2015)'),
	('73', 73, 'HPLC analysis detected a total of eight types of glucosinolate molecules in four cabbage inbred lines. Those were progoitrin; glucoraphanin; sinigrin; gluconapin; glucoerucin; 4-hydroxy-glucobrassicin (4HGBS); methoxy-glucobrassicin (MGBS) and neoglucobrassicin (NGBS) (Robin et al. 2016)'),
	('74', 90, 'HPLC analysis revealed the presence of 16 different types of glucosinolates in three different edible\norgans of four different subspecies of B. oleracea. Glucoerucin was only found in the cabbage leaves;\nand glucoiberverin was identified in the cabbage leaves and kohlrabi stems (Yi et al. 2015)'),
	('74', 73, 'HPLC analysis detected a total of eight types of glucosinolate molecules in four cabbage inbred lines. Those were progoitrin; glucoraphanin; sinigrin; gluconapin; glucoerucin; 4-hydroxy-glucobrassicin (4HGBS); methoxy-glucobrassicin (MGBS) and neoglucobrassicin (NGBS) (Robin et al. 2016)'),
	('75', 90, 'HPLC analysis revealed the presence of 16 different types of glucosinolates in three different edible\norgans of four different subspecies of B. oleracea. In this study; other glucosinolates such as glucoraphanin; progoitrin; glucobrassicin; methoxyglucobrassicin; neoglucobrassicin and gluconasturtiin were also expressed in all three types of edible organs; such as in the leaves; stems and florets (Yi et al. 2015)'),
	('76', 90, 'HPLC analysis revealed the presence of 16 different types of glucosinolates in three different edible\norgans of four different subspecies of B. oleracea (Yi et al. 2015)'),
	('77', 90, 'HPLC analysis revealed the presence of 16 different types of glucosinolates in three different edible\norgans of four different subspecies of B. oleracea. Stems of kohlrabi contained the most\nglucoiberverin and glucobrassicanapin while the florets of cauliflower contained the highest gluconapin\ncontent compared to other edible organs (Yi et al. 2015)'),
	('78', 90, 'HPLC analysis revealed the presence of 16 different types of glucosinolates in three different edible\norgans of four different subspecies of B. oleracea. Cabbage leaves contained 12 glucosinolates; kale leaves contained 10; kohlrabi stems contained 11 and the cauliflower florets contained 14. Gluconapin; glucoalyssin; gluconapoleiferin and 4-hydroxy glucobrassicin were identified only the florets of cauliflower (Yi et al. 2015)'),
	('79', 73, 'HPLC analysis detected a total of eight types of glucosinolate molecules in four cabbage inbred lines. Those were progoitrin; glucoraphanin; sinigrin; gluconapin; glucoerucin; 4-hydroxy-glucobrassicin (4HGBS); methoxy-glucobrassicin (MGBS) and neoglucobrassicin (NGBS) (Robin et al. 2016)'),
	('80', 99, 'Benzylglucosinolate was detected in all of the tissues of Carica papaya (pawpaw). No other glucosinolates were detected in any tissue of C. papaya. Previous suggestions that indolyl-3-methylglucosinolate might be present could not be confirmed. The highest concentrations of benzylglucosinolate were found in the youngest leaves; but the compound was also detected in leaf stalks; stem internodes and roots. The presence of benzylglucosinolate in shoots was developmentally regulated?high concentrations in young tissues; declining as they matured (Bennet et al. 1997)'),
	('83', 195, 'Brassilexin was the most antifungal of the phytoalexins, followed by camalexin, cyclobrassinin and brassinin. Although B. cinerea is a species phylogenetically related to the phytopathogenic fungus Sclerotinia sclerotiorum (Lib) de Bary, contrary to S. sclerotiorum, detoxification of strongly antifungal phytoalexins occurred via either oxidative degradation or hydrolysis but not through glucosylation, suggesting that glucosyl transferases are not involved (Pedras et al. 2011)'),
	('82', 196, '6-Methoxy-3-(2-thiazolyl)-1H-indole is found in fats and oils. 6-Methoxy-3-(2-thiazolyl)-1H-indole is from Camelina sativa (false flax) infected with Alternaria brassicae'),
	('84', 173, 'CYP71B15 also catalyzed thiazoline ring closure, DHCA formation, and cyanide release with Cys(IAN) as substrate.  in the camalexin biosynthetic pathway, IAN is derivatized to the intermediate Cys(IAN), which serves as substrate of the multifunctional cytochrome P450 enzyme CYP71B15 (B?ttcher et al. 2009)'),
	('81', 175, 'ARF1 and ARF9 negatively regulate glucosinolate accumulation, and that ARF9 positively regulates camalexin accumulation. The action of miR393 on auxin signalling triggers two complementary responses. First, it prevents suppression of SA levels by auxin. Second, it stabilizes ARF1 and ARF9 in inactive complexes (Robert-Seilaniantz et al. 2011)');
/*!40000 ALTER TABLE `compounds_references` ENABLE KEYS */;

-- Dumping structure for table gslbase.databases
CREATE TABLE IF NOT EXISTS `databases` (
  `id` int(11) NOT NULL,
  `database` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  PRIMARY KEY (`id`)
) ENGINE=InnoDB DEFAULT CHARSET=utf8 COLLATE=utf8_unicode_ci;

-- Dumping data for table gslbase.databases: ~3 rows (approximately)
/*!40000 ALTER TABLE `databases` DISABLE KEYS */;
INSERT INTO `databases` (`id`, `database`) VALUES
	(1, 'AraNet'),
	(2, 'GeneMANIA'),
	(3, 'ATTED');
/*!40000 ALTER TABLE `databases` ENABLE KEYS */;

-- Dumping structure for table gslbase.genes
CREATE TABLE IF NOT EXISTS `genes` (
  `agi_id` varchar(255) COLLATE utf8_unicode_ci NOT NULL DEFAULT '',
  `gene_name` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  `protein_name` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  `synonym` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  `entrez_gene` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  `refseq_mrna` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  `refseq_protein` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  `uniprot` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  `protein_sequence` text COLLATE utf8_unicode_ci NOT NULL,
  `length` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  `ec_number` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  `AraCyc` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  `KEGG` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  `function` mediumtext COLLATE utf8_unicode_ci,
  `group` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  `reference` varchar(255) COLLATE utf8_unicode_ci DEFAULT NULL,
  PRIMARY KEY (`agi_id`)
) ENGINE=InnoDB DEFAULT CHARSET=utf8 COLLATE=utf8_unicode_ci;

-- Dumping data for table gslbase.genes: ~147 rows (approximately)
/*!40000 ALTER TABLE `genes` DISABLE KEYS */;
INSERT INTO `genes` (`agi_id`, `gene_name`, `protein_name`, `synonym`, `entrez_gene`, `refseq_mrna`, `refseq_protein`, `uniprot`, `protein_sequence`, `length`, `ec_number`, `AraCyc`, `KEGG`, `function`, `group`, `reference`) VALUES
	('AT1G02930', 'GSTF6', 'Glutathione S-transferase F6', 'ERD11, GST1, GSTF3', '839515', 'NM_001197964', 'NP_001184893', 'P42760', 'MAGIKVFGHPASTATRRVLIALHEKNVDFEFVHVELKDGEHKKEPFILRNPFGKVPAFEDGDFKIFESRAITQYIAHEFSDKGNNLLSTGKDMAIIAMGIEIESHEFDPVGSKLVWEQVLKPLYGMTTDKTVVEEEEAKLAKVLDVYEHRLGESKYLASDHFTLVDLHTIPVIQYLLGTPTKKLFDERPHVSAWVADITSRPSAQKVL', '208', 'EC 2.5.1.18', '', '', 'GSTF6 overexpression increased and GSTF6-knockout reduced camalexin production. Arabidopsis GSTF6 expressed in yeast cells catalyzed GSH(IAN) formation. GSH(IAN), (IAN)CysGly, and GluCys(IAN) were determined to be intermediates within the camalexin biosynthetic pathway. The expression of GSTF6, GGT1, GGT2, and PCS1 was coordinately upregulated during camalexin biosynthesis. These results suggest that GSH is the Cys derivative used during camalexin biosynthesis, that the conjugation of GSH with IAN is catalyzed by GSTF6, and that GGTs and PCS are involved in camalexin biosynthesis (Su et al. 2011).', 'Camalexin biosynthesis', 'Su et al. 2011; Zhao et al. 1998'),
	('AT1G04580', 'AAO4', 'Benzaldehyde dehydrogenase ', 'ATAO2', '839488', 'NM_100337', 'NP_563711', 'Q7G191', 'MAGDDLVFAVNGEKFEVLSVNPSTTLLEFLRSNTCFKSVKLSCGEGGCGACIVILSKYDPVLDQVEEYSINSCLTLLCSLNGCSITTSDGLGNTEKGFHPIHKRFAGFHASQCGFCTPGMCISLYSALSKAHNSQSSPDYLTALAAEKSIAGNLCRCTGYRPIADACKSFASDVDIEDLGFNSFWRKGESREEMLKKLPPYNPEKDLITFPDFLKEKIKCQHNVLDQTRYHWSTPGSVAELQEILATTNPGKDRGLIKLVVGNTGTGYYKEEKQYGRYIDISHIPEMSMIKKDDREIEIGAVVTISKVIDALMEENTSAYVFKKIGVHMEKVANHFIRNSGSIGGNLVMAQSKSFPSDITTLLLAADASVHMINAGRHEKLRMGEYLVSPPILDTKTVLLKVHIPRWIASSTTGLLFETYRAALRPIGSALPYINAAFLAVVSHDASSSGIIVDKCRLAFGSYGGYHSIRAREVEDFLTGKILSHSVLYEAVRLLKGIIVPSIDTSYSEYKKSLAVGFLFDFLYPLIESGSWDSEGKHIDGHIDPTICLPLLSSAQQVFESKEYHPVGEAIIKFGAEMQASGEAVYVDDIPSLPHCLHGAFIYSTKPLAWIKSVGFSGNVTPIGVLAVITFKDIPEVGQNIGYITMFGTGLLFADEVTISAGQIIALVVADTQKHADMAAHLAVVEYDSRNIGTPVLSVEDAVKRSSLFEVPPEYQPEPVGDISKGMAEADRKIRSVELRLGSQYFFYMETQTALALPDEDNCLVVYSSTQAPEFTQTVIATCLGIPEHNVRVITRRVGGGFGGKAIKSMPVATACALAAKKMQRPVRIYVNRKTDMIMAGGRHPLKITYSVGFRSDGKLTALDLNLFIDAGSDVDVSLVMPQNIMNSLRKYDWGALSFDIKVCKTNLPSRTSLRAPGEVQGSYIAESIIENVASSLKMDVDVVRRINLHTYESLRKFYKQAAGEPDEYTLPLLWDKLEVSADFRRRAESVKEFNRCNIWRKRGISRVPIIHLVIHRPTPGKVSILNDGSVAVEVAGIEVGQGLWTKVQQMVAYGLGMIKCEGSDDLLERIRLLQTDTLSMSQSSYTAGSTTSENCCEAVRLCCGILVERLRPTMNQILENARSVTWDMLIQQANAQSVDLSARTFYKPESSSAEYLNYGVGASEVEVDLVTGRTEIIRSDIIYDCGKSLNPAVDLGQIEGAFVQGIGFFMYEEYTTNENGLVNEEGTWDYKIPTIDTIPKQFNVQILNSGHHKNRVLSSKASGEPPLLVAASVHCATRSAIREARKQYLSWNCIDDDHRERCDLGFELPVPATMPVVKQLCGLESIEKYLEWKTYP', '1337', 'EC 1.2.1.28', '', '', 'A. thaliana siliques produce high levels of benzoic acid (BA) that also include GSL compounds such as 3-benzoyloxypropylGSL (3BZO) and 4-benzoyloxybutylGSL (4BZO). T-DNA insertions that eliminate functional transcripts of At1g04580 (AAO4) cause decreases in the levels of total benzoic acid (BA) and in the levels of benzoylated GSLs in seeds (Ibdah et al. 2009)', 'GSL Side chain modification', 'Ibdah et al. 2009'),
	('AT1G04770', 'SDI2', 'Protein SULFUR DEFICIENCY-INDUCED 2', 'F13M7.24', '839418', 'NM_100355.4. ', 'NP_171969.2', 'Q8L730', 'MMMMIQRRGGERQDSSAAAYNVVHKLPHGDSPYVRAKHVQLVEKDAEAAIELFWIAIKARDRVDSALKDMALLMKQQNRAEEAIDAIQSFRDLCSRQAQESLDNVLIDLYKKCGRIEEQVELLKQKLWMIYQGEAFNGKPTKTARSHGKKFQVTVEKETSRILGNLGWAYMQLMDYTAAEAVYRKAQLIEPDANKACNLCTCLIKQGKHDEARSILFRDVLMENKEGSGDPRLMARVQELLSELKPQEEEAAASVSVECEVGIDEIAVVEGLDEFVKEWRRPYRTRRLPIFEEILPLRDQLAC', '303', '', '', '', 'Sulfur deficiency induced 1 (SD1) and SD2 are -S marker genes sulfur deficiency that act as major repressors controlling GSL biosynthesis in Arabidopsis under -S condition. SDI1 and SDI2 expression negatively correlated with GSL biosynthesis in both transcript and metabolite levels. Principal components analysis of transcriptome data indicated that SDI1 regulates aliphatic GSL biosynthesis as part of -S response. SDI1 was localized to the nucleus and interacted with MYB28 a major transcription factor that promotes aliphatic GSL biosynthesis in both yeast and plant cells (Aarabi et al. 2016)', 'GSL core structure synthesis', 'Aarabi et al. 2016'),
	('AT1G07640', 'OBP2', 'Dof zinc finger protein DOF1.1 ', 'DOF1.1', '837277', 'NM_180607', 'NP_850938', 'Q8L9V6', 'MPTNSNHQHHLQHQLNENGSIISGHGLVLSHQLPPLQANPNPNHHHVATSAGLPSRMGGSMAERARQANIPPLAGPLKCPRCDSSNTKFCYYNNYNLTQPRHFCKGCRRYWTQGGALRNVPVGGGCRRNNKKGKNGNLKSSSSSSKQSSSVNAQSPSSGQLRTNHQFPFSPTLYNLTQLGGIGLNLAATNGNNQAHQIGSSLMMSDLGFLHGRNTSTPMTGNIHENNNNNNNENNLMASVGSLSPFALFDPTTGLYAFQNDGNIGNNVGISGSSTSMVDSRVYQTPPVKMEEQPNLANLSRPVSGLTSPGNQTNQYFWPGSDFSGPSNDLL', '331', '', '', '', 'OBP2 is expressed in the vasculature of all Arabidopsis organs; including leaves; roots; flower stalks and petals. OBP2 expression is induced in response to a generalist herbivore; Spodoptera littoralis and by treatment with the plant signalling molecule methyl jasmonate both of which also trigger indolic GSL accumulation (Skirycz et al. 2006)', 'GSL transcription factor', 'Skirycz et al. 2006  '),
	('AT1G11610', 'CYP71A18', 'Cytochrome P450 71A18', 'F25C20.24', '837705', 'NM_101034', 'NP_172627', 'Q9SAB6', 'MEMTLMVSLCLTTLLTLLLLKKFLKRTAKKVNLPPSPWRIPVIGNLHQLSLHPHRSLHSLSLRYGPLMLLHFGRVPILVVSSSEAAHEILKTHDLKFANRPKSKAVHGLMNGGRDVVFGPYGEYWRQMKSVCILNLLTNKMVASFEKVREEEVNAMMEKLEKASCSSSAENLSELFVTLTSDVTSRVSLGKKYWEDETAGGLKKRVRQIMELLREFPIGDYVPALAWIDRINGFNSKIVEVSRAYSDLMEKVVQEHLEAGEHKADFVNILLSIEKEKNNGFKVQRNDIKFMILDMFIGGISTSSTLLEWIMTELIRNPECMKKLQNEIRSTIRPHGSYIKEKEVENMRYLKAVIKEVFRVHPPLPLILPRLLTEDVKVKGYDIAAGTEVLINAWSIHRDPAIWGPDAEEFKPERHLDSTLDYHGQDLKYIPFGSGRRICPGINLAMGLVEVTLANLVGRFDWSVDPGPNGDQPDLAEDFGLDIPKKVFINNLPRIRFECIDFKI', '497', 'EC 1.14.-.- ', 'AraCyc', '', 'Camalexin originates from tryptophan and its biosynthesis involves the cytochrome P450 enzymes CYP79B2 and CYP71B15 (PAD3). Camalexin induction is a complex process, for which triggering by reactive oxygen species (ROS), salicylic acid signalling, and the glutathione status are important. Targets of the signalling cascade are the tryptophan and camalexin biosynthetic genes, which are strongly transcriptionally upregulated at the sites of pathogen infection (Glawischnig et al. 2004) .', 'Camalexin biosynthesis', 'Glawischnig et al. 2004'),
	('AT1G12130', 'FMOGS-OX6', 'Flavin-containing monooxygenase FMO GS-OX6', 'T28K15.13', '837765', 'NM_101085', 'NP_172677', 'Q9FWW3', 'MTPPPNSISSRNVAVIGAGAAGLVAARELRREGHTVTIFERQKQVGGLWVCTPNVEPDLLSIDPDRTVVHSSVYQSLRTNLPRECMGYSDFPFVTRPDDESRDPRRYPDHREVMRYLQDFAKEFKIEEMIRFETEVFRVEPTAENSCKWRVQFRSSSGVSGEDIFDAVVICNGHFTEPRLAHIPGIESWPGKQIHSHNYRVSDPFKGQVVIVIGYQSSGSDISRDIAILAKEVHIAAKSDAYAKESSIYSNLHFHPTIDRVYEDGSVVFQDGKLIFADAIVHCTGYKYCFPFLETKGYVNVEDNRVGPLYKHVFPPALAPGLSFIGLPSMALQFFMFEIQSRWVASVLSGRVKLPSEEQMMEDVIAFYAKLKSLGIPKRFTHFLTDPQWTPMFEKLKPHEAVLISQSEYFNWIAEQCGCSSIERWREEQYNIAIKKDDDNFRDEWDDDDQIIQEAYRDFAKFKPSKVWST', '470', '', '', '', 'Two additional FMOGS-OX enzymes; FMOGS-OX6 and FMOGS-OX7 encoded by At1g12130 and At1g12160 respectively. The overexpression of both FMOGS-OX6 and FMOGS-OX7 decreased the ratio of methylthioalkyl GSLs to the sum of methylthioalkyl and methylsulfinylalkyl GSLs suggesting that the introduction of the two genes converted methylthioalkyl GSLs into methylsulfinylalkyl GSLs (Kong et al. 2016)', 'GSL side chain modificatian', 'Kong et al. 2016  '),
	('AT1G12140', 'FMOGS-OX5 ', 'Flavin-containing monooxygenase FMO GS-OX5 ', 'T28K15.12', '88657', 'NM_101086', 'NP_172678', 'A8MRX0', 'MAPARTRVNSLNVAVIGAGAAGLVAARELRRENHTVVVFERDSKVGGLWVYTPNSEPDPLSLDPNRTIVHSSVYDSLRTNLPRECMGYRDFPFVPRPEDDESRDSRRYPSHREVLAYLEDFAREFKLVEMVRFKTEVVLVEPEDKKWRVQSKNSDGISKDEIFDAVVVCNGHYTEPRVAHVPDSWPGKQIHSHNYRVPDQFKDQVVVVIGNFASGADISRDITGVAKEVHIASRSNPSKTYSKLPGSNNLWLHSMIESVHEDGTIVFQNGKVVQADTIVHCTGYKYHFPFLNTNGYITVEDNCVGPLYEHVFPPALAPGLSFIGLPWMTLQFFMFELQSKWVAAALSGRVTLPSEEKMMEDVTAYYAKREAFGQPKRYTHRLGGGQVDYLNWIAEQIGAPPGEQWRYQEINGGYYRLATQSDTFRDKWDDDHLIVEAYEDFLRQKLISSLPSQLLES', '459', 'EC 1.8.-.-', '', '', 'Four uncharacterized FMOs designated FMOGS-OX2 to FMOGS-OX5 were found to involve in biosynthesis aliphatic GSL. Biochemical characterization of the recombinant protein combined with the analysis of GSL content in knockout mutants and overexpression lines show that FMOGS-OX2; FMOGS-OX3; and FMOGS-OX4 have broad substrate specificity and catalyze the conversion from methylthioalkyl GSL to the corresponding methylsulfinylalkyl GSL independent of chain length. In contrast; FMOGS-OX5 shows substrate specificity toward the long-chain 8-methylthiooctyl GSL. Identification of the FMOGS-OX subclade will generate better understanding of the evolution of biosynthetic activities and specificities in secondary metabolism and provides an important tool for breeding plants with improved cancer prevention characteristics as provided by the methylsulfinylalkyl GSL (Li et al. 2008)', 'GSL side chain modificatian', 'Li et al. 2008; Li et al. 2011  '),
	('AT1G12160', 'FMOGS-OX7', 'Flavin-containing monooxygenase FMO GS-OX7', 'T28K15.10', '837768', 'NM_101088', 'NP_172680', 'Q9FWW6', 'MTSVITSRARHVAVIGLGAAGLVAVRELRREGHTVIGFEREKHVGGLWVYTDRVDSDSVSVDPDRTIVHSSIYQSLRTNLPRECMGYSDFPFVTRSSDGDPRRYPDHREVLMYLQDFAKEFKIEDMIRFETEVLCVEPSPENNRKWRVQFKSSNGVSGEEIFDAVVVCNGHFTEPRLAHIPGIESWPGKQIHSHNYRIPDPFKDEVVIVIGSQASGNDISTDIATIAKEVHISSKMVASDSYGCYDNLRIHPTIYRAREDGSVVFRNGKVVFADAIVHCTGYKYHFPFLKTSGYVTVEDNRVGPLYKHVFPPALAPGISFIGLPFMGLQFFMFEIQSKWVASVLSGRVKLPAEDKMMEEAVAFYSKLEDLGIPKRYTHFLTDPRGNPMLGTFKPEDAVVISQSDYFNWIAKQCGCTSIERWRERLYNVAIKKVFFGGDSYRDRWDDDQLIEEVYREFAKLKPNQDCSS', '468', '', '', '', 'Two additional FMOGS-OX enzymes; FMOGS-OX6 and FMOGS-OX7 encoded by At1g12130 and At1g12160 respectively. The overexpression of both FMOGS-OX6 and FMOGS-OX7 decreased the ratio of methylthioalkyl GSLs to the sum of methylthioalkyl and methylsulfinylalkyl GSLs suggesting that the introduction of the two genes converted methylthioalkyl GSLs into methylsulfinylalkyl GSLs (Kong et al. 2016)', 'GSL side chain modificatian', 'Kong et al. 2016  '),
	('AT1G12200', 'FMO', 'Flavin-containing monooxygenase FMO GS-OX-like 2', 'T28K15.7', '837773', 'NM_101092', 'NM_101092', 'Q9FWW9', 'MATSHPDPTTSRHVAVIGAGAAGLVAARELRREGHSVVVLERGSQIGGVWAYTSQVEPDPLSLDPTRPVVHSSLYRSLRTNIPRECMGFTDFPFATRPHDGSRDPRRHPAHTEVLAYLRDFAKEFDIEEMVRFETEVVKAEQVAAEGEERGKWRVESRSSDGVVDEIYDAVVVCNGHYTEPRHALITGIDSWPGKQIHSHNYRVPDQFKDQVVIVIGSSASGVDICRDIAQVAKEVHVSSRSTSPDTYEKLTGYENLWLHSTIQIAREDGSVVFENGKTIYADTIMHCTGYKYYFPFLDTKGEVTVDDNRVGPLYKHVFPPALAPSLSFIGLPWQITPFPMFELQSKWVAAVLSGRVSLPSQDEMMEDTKAFYDKLEASGIPKRYTHLMPDDSQFEYDNWLADQCEYPRIEKWREQMFYIGFKRIYAQSSTYRDNWDDDHLIVEAYDDFVKFMSSYQELLPMLKT', '465', 'EC 1.8.-.-', 'AraCyc', '', 'FMO convert 4-methylthioalkyl to 4-meth-ylsulfinylalkyl GSLs and is pathogen-induced independent of COI1. Simultaneous induction of methionine, tryptophan,camalexin, and GSL biosynthetic genes provided evidence for coordinated regulation of primary and secondary metabolism (Stotz et al. 2011)', 'GSL side chain modification / Camalexin biosynthesis', 'Stotz et al. 2011'),
	('AT1G13110', 'CYP71B7', 'Cytochrome P450 71B7', 'F3F19.13', '837868', 'NM_101181', 'NP_172770', 'Q96514', 'MSILLCFLCLLPVFLVSLSILSKRLKPSKWKLPPGPKTLPIIGNLHNLTGLPHTCFRNLSQKFGPVMLLHFGFVPVVVISSKEGAEEALKTQDLECCSRPETVATRMISYNFKDIGFAPYGEEWKALRKLVVMELLNTKKFQSFRYIREEENDLLIKKLTESALKKSPVNLKKTLFTLVASIVCRLAFGVNIHKCEFVDEDNVADLVNKFEMLVAGVAFTDFFPGVGWLVDRISGQNKTLNNVFSELDTFFQNVLDDHIKPGRQVSENPDVVDVMLDLMKKQEKDGESFKLTTDHLKGIISDIFLAGVNTSAVTLNWAMAELIRNPRVMKKVQDEIRTTLGDKKQRITEQDLSQVHYFKLVVKEIFRLHPAAPLLLPRETMSHVKIQGYDIPVKTQMMINIYSIARDPKLWTNPDEFNPDRFLDSSIDYRGLNFELLPFGSGRRICPGMTLGITTVELGLLNLLYFFDWVVPVGKNVKDINLEETGSIIISKKTTLELVPLVHH', '504', 'EC 1.14.-.- ', 'AraCyc', '', 'Camalexin originates from tryptophan and its biosynthesis involves the cytochrome P450 enzymes CYP79B2 and CYP71B15 (PAD3). Camalexin induction is a complex process, for which triggering by reactive oxygen species (ROS), salicylic acid signalling, and the glutathione status are important. Targets of the signalling cascade are the tryptophan and camalexin biosynthetic genes, which are strongly transcriptionally upregulated at the sites of pathogen infection (Glawischnig et al. 2004) .', 'Camalexin biosynthesis', 'Glawischnig et al. 2004'),
	('AT1G16400', 'CYP79F2', 'Hexahomomethionine N-hydroxylase ', 'F3O9.20', '838210', 'NM_101506', 'NP_563995', 'Q9FUY7', 'MMMKISFNTCFQILLGFIVFIASITLLGRIFSRPSKTKDRCRQLPPGRPGWPILGNLPELIMTRPRSKYFHLAMKELKTDIACFNFAGTHTITINSDEIAREAFRERDADLADRPQLSIVESIGDNYKTMGTSSYGEHFMKMKKVITTEIMSVKTLNMLEAARTIEADNLIAYIHSMYQRSETVDVRELSRVYGYAVTMRMLFGRRHVTKENMFSDDGRLGKAEKHHLEVIFNTLNCLPGFSPVDYVDRWLGGWNIDGEEERAKVNVNLVRSYNNPIIDERVEIWREKGGKAAVEDWLDTFITLKDQNGNYLVTPDEIKAQCVEFCIAAIDNPANNMEWTLGEMLKNPEILRKALKELDEVVGKDRLVQESDIRNLNYLKACCRETFRIHPSAHYVPPHVARQDTTLGGYFIPKGSHIHVCRPGLGRNPKIWKDPLAYEPERHLQGDGITKEVTLVETEMRFVSFSTGRRGCVGVKVGTIMMAMMLARFLQGFNWKLHRDFGPLSLEEDDASLLMAKPLLLSVEPRLASNLYPKFRP', '537', 'EC 1.14.13.n6', 'AraCyc', 'KEGG', 'CYP79F1 and CYP79F2 are two important genes whose products catalyse accumulation of long-chain aliphatic GSLs; while the product of CYP79F1 also functions in the biosynthesis of short-chain aliphatic GSLs (Chen et al. 2003)', 'GSL core structure synthesis', 'Chen et al. 2003; Hansen et al. 2001; Miao et al. 2013  '),
	('AT1G16410', 'CYP79F1', 'Dihomomethionine N-hydroxylase ', 'BUS1', '838211', 'NM_202111', 'NP_973840', 'Q949U1', 'MMSFTTSLPYPFHILLVFILSMASITLLGRILSRPTKTKDRSCQLPPGPPGWPILGNLPELFMTRPRSKYFRLAMKELKTDIACFNFAGIRAITINSDEIAREAFRERDADLADRPQLFIMETIGDNYKSMGISPYGEQFMKMKRVITTEIMSVKTLKMLEAARTIEADNLIAYVHSMYQRSETVDVRELSRVYGYAVTMRMLFGRRHVTKENVFSDDGRLGNAEKHHLEVIFNTLNCLPSFSPADYVERWLRGWNVDGQEKRVTENCNIVRSYNNPIIDERVQLWREEGGKAAVEDWLDTFITLKDQNGKYLVTPDEIKAQCVEFCIAAIDNPANNMEWTLGEMLKNPEILRKALKELDEVVGRDRLVQESDIPNLNYLKACCRETFRIHPSAHYVPSHLARQDTTLGGYFIPKGKKKKKKR', '538', 'EC 1.14.13.n5', 'AraCyc', 'KEGG', 'CYP79F1 and CYP79F2 are two important genes whose products catalyse accumulation of long-chain aliphatic GSLs; while the product of CYP79F1 also functions in the biosynthesis of short-chain aliphatic GSLs (Chen et al. 2003)', 'GSL core structure synthesis', 'Chen et al. 2003; Miao et al. 2013; Zang et al. 2009  '),
	('AT1G18570', 'MYB51', 'Transcription factor MYB51 ', 'HIG1', '838438', 'NM_101715', 'NP_173292', 'O49782', 'MVRTPCCKAELGLKKGAWTPEEDQKLLSYLNRHGEGGWRTLPEKAGLKRCGKSCRLRWANYLRPDIKRGEFTEDEERSIISLHALHGNKWSAIARGLPGRTDNEIKNYWNTHIKKRLIKKGIDPVTHKGITSGTDKSENLPEKQNVNLTTSDHDLDNDKAKKNNKNFGLSSASFLNKVANRFGKRINQSVLSEIIGSGGPLASTSHTTNTTTTSVSVDSESVKSTSSSFAPTSNLLCHGTVATTPVSSNFDVDGNVNLTCSSSTFSDSSVNNPLMYCDNFVGNNNVDDEDTIGFSTFLNDEDFMMLEESCVENTAFMKELTRFLHEDENDVVDVTPVYERQDLFDEIDNYFG', '352', '', '', '', 'MYB34; MYB51 and MYB122 act together to control the biosynthesis of indole-3-ylmethyl-GSL (I3M) in shoots and roots with MYB34 controlling biosynthesis of indolic GSLs (IGs) mainly in the roots. MYB51 regulating biosynthesis in shoots and MYB122 having an accessory role in the biosynthesis of IGs (Frerigmann & Gigolashvili 2014)', 'GSL transcription factor / Camalexin biosynthesis', 'Frerigmann & Gigolashvili 2014; Frerigmann et al. 2015'),
	('AT1G18590', 'SOT17', 'Cytosolic sulfotransferase 17 ', 'ATST5C', '838440', 'NM_101717', 'NP_173294', 'Q9FZ80', 'MESKTINDVVVSESNHELASSSPSEFEKNQKHYQEIIATLPHKDGWRPKDPFVEYGGHWWLQPLLEGLLHAQKFFKARPNDFFVCSYPKTGTTWLKALTFAIANRSKFDVSTNPLLKRNPHEFVPYIEIDFPFFPSVDVLKDEGNTLFSTHIPYDLLPESVVKSGCKIVYIWRDPKDTFVSMWTFAHKERSQQGPVVSIEEAFDKYCQGLSAYGPYLDHVLGYWKAYQANPDQILFLKYETMRADPLPYVKRLAEFMGYGFTKEEEEGNVVEKVVKLCSFETLKNLEANKGEKDREDRPAVYANSAYFRKGKVGDWQNYLTPEMVARIDGLMEEKFKGTGFLSSKS', '346', 'EC 2.8.2.-', 'AraCyc', 'KEGG', 'The three enzymes were shown to catalyze the final step in the biosynthesis of the GSL core structure; the sulfation of desulfoGSLs (dsGSs). They accept a broad range of desulfoGSLs as substrates. In a competitive situation; AtST5a (SOT16) clearly prefers tryptophan and phenylalanine-derived desulfoGSLs whereas long chain desulfoGSLs derived from methionine are the preferred substrates of SOT17 and SOT18 (Piotrowski et al. 2004)', 'GSL core structure synthesis', 'Hirschmann & Papenbrock 2015; Piotrowski et al. 2004'),
	('AT1G21100', 'IGMT1', 'Indole glucosinolate O-methyltransferase 1 ', 'T22I11.7', '838706', 'NM_101964', 'NP_173534', 'Q9LPU5', 'MGYLFQETLSSNPKTPIVVDDDNELGLMAVRLANAAAFPMVLKAALELGVFDTLYAAASRTDSFLSPYEIASKLPTTPRNPEAPVLLDRMLRLLASYSMVKCGKALSGKGERVYRAEPICRFFLKDNIQDIGSLASQVIVNFDSVFLNTWAQLKDVVLEGGDAFGRAHGGMKLFDYMGTDERFSKLFNQTGFTIAVVKKALEVYEGFKGVKVLVDVGGGVGNTLGVVTSKYPNIKGINFDLTCALAQAPSYPGVEHVAGDMFVDVPTGDAMILKRILHDWTDEDCVKILKNCWKSLPENGKVVVIELVTPDEAENGDINANIAFDMDMLMFTQCSGGKERSRAEFEALAAASGFTHCKFVCQAYHCWIIEFCK', '373', 'EC 2.1.1.-', '', '', 'Arabidopsis O-methyl-transferase genes were found to coexpressed with CYP81F genes are fairly specific for the biosynthesis of modified indole GSLs which are IGMT1 and IGMT2. IGMT1 and 2 form a small gene cluster of O-MT genes on Arabidopsis chromosome 1 (Pfalz et al. 2011)', 'GSL side chain modification', 'Pfalz et al. 2011  '),
	('AT1G21120', 'IGMT2', 'Indole glucosinolate O-methyltransferase 2 ', 'T22I11.5', '838708', 'NM_101966', 'NP_173536', 'Q9LPU7', 'MGYLFEETLSSNPKTPIVVDDDNELGLMAVRLANAAAFPMVLKASLELGVFDTLYAEASRTDSFLSPSEIASKLPTTPRNPGAPVLLDRMLRLLASYSMVKCEKVSVGKGERVYRAEPICRFFLKNNIQDIGSLASQVIVNFDSVFLNTWAQLKDVVLEGGDAFGRAHGGMKLFDYMGTDERFSKLFNQTGFTIAVVKKALEVYQGFKGVNVLVDVGGGVGNTLGVVTSKYPNIKGINFDLTCALAQAPSYPGVEHVAGDMFVDVPTGDAMILKRILHDWTDEDCVKILKNCWKSLPENGKVVVIELVTPDEAENGDINANIAFDMDMLMFTQCSGGKERSRAEFEALAAASCFTHCKFVCQAYHCWIIEFCK', '373', 'EC 2.1.1.-', '', '', 'Arabidopsis O-methyl-transferase genes were found to coexpressed with CYP81F genes are fairly specific for the biosynthesis of modified indole GSLs which are IGMT1 and IGMT2. IGMT1 and 2 form a small gene cluster of O-MT genes on Arabidopsis chromosome 1 (Pfalz et al. 2011)', 'GSL side chain modification', 'Pfalz et al. 2011  '),
	('AT1G24100', 'UGT74B1', 'UDP-glycosyltransferase 74B1 ', '', '839022', 'NM_102256', 'NP_173820', 'O48676', 'MAETTPKVKGHVVILPYPVQGHLNPMVQFAKRLVSKNVKVTIATTTYTASSITTPSLSVEPISDGFDFIPIGIPGFSVDTYSESFKLNGSETLTLLIEKFKSTDSPIDCLIYDSFLPWGLEVARSMELSAASFFTNNLTVCSVLRKFSNGDFPLPADPNSAPFRIRGLPSLSYDELPSFVGRHWLTHPEHGRVLLNQFPNHENADWLFVNGFEGLEETQDCENGESDAMKATLIGPMIPSAYLDDRMEDDKDYGASLLKPISKECMEWLETKQAQSVAFVSFGSFGILFEKQLAEVAIALQESDLNFLWVIKEAHIAKLPEGFVESTKDRALLVSWCNQLEVLAHESIGCFLTHCGWNSTLEGLSLGVPMVGVPQWSDQMNDAKFVEEVWKVGYRAKEEAGEVIVKSEELVRCLKGVMEGESSVKIRESSKKWKDLAVKAMSEGGSSDRSINEFIESLGK', '460', 'EC 2.4.1.- EC 2.4.1.195', 'AraCyc', 'KEGG', 'Analysis of UGT74B1 promoter activity during plant development reveals expression patterns consistent with GSL metabolism and induction by auxin treatment. The results are discussed in the context of known mutations in GSL pathway genes and their effects on auxin homeostasis. This research provides complementary in vitro and in vivo evidence for a primary role of UGT74B1 in GSL biosynthesis (Grubb et al. 2004)', 'GSL core structure synthesis', 'Douglas Grubb et al. 2004'),
	('AT1G32640', 'MYC2', 'Transcription factor MYC2', 'AtbHLH6', '840158', 'NM_102998.4', 'NP_174541.1', 'Q39204', 'MTDYRLQPTMNLWTTDDNASMMEAFMSSSDISTLWPPASTTTTTATTETTPTPAMEIPAQAGFNQETLQQRLQALIEGTHEGWTYAIFWQPSYDFSGASVLGWGDGYYKGEEDKANPRRRSSSPPFSTPADQEYRKKVLRELNSLISGGVAPSDDAVDEEVTDTEWFFLVSMTQSFACGAGLAGKAFATGNAVWVSGSDQLSGSGCERAKQGGVFGMHTIACIPSANGVVEVGSTEPIRQSSDLINKVRILFNFDGGAGDLSGLNWNLDPDQGENDPSMWINDPIGTPGSNEPGNGAPSSSSQLFSKSIQFENGSSSTITENPNLDPTPSPVHSQTQNPKFNNTFSRELNFSTSSSTLVKPRSGEILNFGDEGKRSSGNPDPSSYSGQTQFENKRKRSMVLNEDKVLSFGDKTAGESDHSDLEASVVKEVAVEKRPKKRGRKPANGREEPLNHVEAERQRREKLNQRFYALRAVVPNVSKMDKASLLGDAIAYINELKSKVVKTESEKLQIKNQLEEVKLELAGRKASASGGDMSSSCSSIKPVGMEIEVKIIGWDAMIRVESSKRNHPAARLMSALMDLELEVNHASMSVVNDLMIQQATVKMGFRIYTQEQLRASLISKIG', '623', '', '', '', 'The myc2 myc3 myc4 (myc234) triple mutant was almost completely devoid of GSL and was extremely susceptible to the generalist herbivore Spodoptera littoralis. On the contrary the specialist Pieris brassicae was unaffected by the presence of GSL and preferred to feed on wild-type plants. In addition lack of GSL in myc234 drastically modified S. littoralis feeding behavior. Surprisingly the expression of MYB factors known to regulate GS biosynthesis genes was not altered in myc234; suggesting that MYC2/MYC3/MYC4 are necessary for direct transcriptional activation of GS biosynthesis genes. Yeast two-hybrid and pull-down experiments indicated that MYC2/MYC3/MYC4 interact directly with GS-related MYBs. This specific MYC?MYB interaction plays a crucial role in the regulation of defense secondary metabolite production and underlines the importance of GSL in shaping plant interactions with adapted and nonadapted herbivores (Schweizer et al. 2013)', 'GSL transcription factor', 'Schweizer et al. 2013'),
	('AT1G47600', 'TGG4', 'Myrosinase 4 ', 'BGLU34', '841169', 'NM_103653', 'NP_175191', 'Q8GRX1', 'MAIPKAHYSLAVLVLLFVVVSSSQKVCNPECKAKEPFHCDNTHAFNRTGFPRNFTFGAATSAYQIEGAAHRALNGWDYFTHRYPEKVPDRSSGDLACDSYDLYKDDVKLLKRMNVQAYRLSIAWSRVLPKGRLTGGVDENGITYYNNLINELKANGIEPYVTIFHWDVPQTLEDEYGGFLSTRIVEDYTNYAELLFQRFGDRVKFWITLNQPFSLATKGYGDGSYPPGRCTGCELGGDSGVEPYTVAHNQLLAHAKTVSLYRKRYQKFQGGKIGTTLIGRWFAPLNEFSELDKAAAKRAFDFFVGWFLDPLVYGKYPTIMREMVGDRLPEFTPEQSALVKGSLDFLGLNYYVTQYATDAPPPTQLNAITDARVTLGFYRNGVPIGVVAPSFVYYPPGFRQILNYIKDNYKNPLTYITENGVADLDLGNVTLATALADNGRIQNHCSHLSCLKCAMKDGCNVAGYFAWSLMDNYEFGNGYTLRFGMNWVNFTNPADRKEKASGKWFSKFLAK', '511', 'EC 3.2.1.147', '', '', 'Different myrosinases in A. thaliana were compared: cDNAs corresponding to TGG1 from leaves and TGG4 and TGG5 from roots were cloned and overexpressed in Pichia pastoris. The His-tagged recombinant proteins were purified using affinity chromatography and the preparations were homogenous according to SDS?PAGE analysis. Myrosinase activity was confirmed for all forms and compared with respect to catalytic activity towards the allyl-GSL sinigrin (Andersson et al. 2009)', 'GSL degradation', 'Wittstock & Burow 2010'),
	('AT1G50110', 'BCAT6', 'Branched-chain-amino-acid aminotransferase 6 ', 'F2J10.4', '841433', 'NM_103897', 'NP_175431', 'Q9LPM9', 'MAPSSSPLRTTSETDEKYANVKWEELGFALTPIDYMYVAKCRQGESFTQGKIVPYGDISISPCSPILNYGQGLFEGLKAYRTEDDRIRIFRPDQNALRMQTGAERLCMTPPTLEQFVEAVKQTVLANKKWVPPPGKGTLYIRPLLLGSGATLGVAPAPEYTFLIYASPVGDYHKVSSGLNLKVDHKYHRAHSGGTGGVKSCTNYSPVVKSLLEAKSAGFSDVLFLDAATGRNIEELTACNIFIVKGNIVSTPPTSGTILPGVTRKSISELAHDIGYQVEERDVSVDELLEAEEVFCTGTAVVVKAVETVTFHDKKVKYRTGEAALSTKLHSMLTNIQMGVVEDKKGWMVDIDPCQG', '356', 'EC 2.6.1.42', '', '', 'The activity with Met and 4-methylthio-2-oxobutanoate (MTOB) suggests a potential function of BCAT6 in the Met chain elongation pathway (Lachler et al. 2015)', 'GSL side chain elongation', 'Lachler et al. 2015'),
	('AT1G51470', 'TGG5', 'Myrosinase 5 ', 'BGLU35', '841572', 'NM_104025', 'NP_175558', 'Q3ECS3', 'MAIPKAHYSLAVLVLLFVVVSSSQKVCNPECKAKEPFHCDNTHAFNRSGFPKNFTFGAATSAYQIEGAAHRALNGWDYFTHRYPEKVPDRSSADLACDSYDLYKDDVKLLKRMNVQAYRLSIAWSRVLPKGRLTGGVDENGITYYNNLINELKANGIEPYVTIFHWDVPQTLEDEYGGFLSTRIVEDYTNYAELLFQRFGDRVKFWITLNQPLSLALKGYGNGSYPPGRCTGCELGGDSGVEPYTVAHNQLLAHAKTVSLYRKRYQKFQGGKIGTTLIGRWFVPLNEFSELDKAAAKRAFDFFVGWFLDPLVYGKYPTIMREMVGDRLPEFTPEESALVKGSLDFLGLNYYVSQYATDAPPPTQPNAITDARVTLGFYRNGSPIGVVASSFVYYPPGFRQILNYIKDNYKNPLTYITENGVADLDLGNVTLATALADNGRIQNHCSHLSCLKCAMKDGCNVAGYFAWSLMDNYEFGNGYTLRFGMNWVNFTNPADRKEKASGKWFSKFLAK', '511', 'EC 3.2.1.147', '', '', 'Different myrosinases in A. thaliana were compared: cDNAs corresponding to TGG1 from leaves and TGG4 and TGG5 from roots were cloned and overexpressed in Pichia pastoris. The His-tagged recombinant proteins were purified using affinity chromatography and the preparations were homogenous according to SDS?PAGE analysis. Myrosinase activity was confirmed for all forms and compared with respect to catalytic activity towards the allyl-GSL sinigrin (Andersson et al. 2009)', 'GSL degradation', 'Wittstock & Burow 2010'),
	('AT1G54040', 'ESP', 'Epithiospecifier protein ', 'TASTY', '841842', 'NM_180632', 'NP_850963', 'Q8RY71', 'MAPTLQGQWIKVGQKGGTGPGPRSSHGIAAVGDKLYSFGGELTPNKHIDKDLYVFDFNTQTWSIAQPKGDAPTVSCLGVRMVAVGTKIYIFGGRDENRNFENFRSYDTVTSEWTFLTKLDEVGGPEARTFHSMASDENHVYVFGGVSKGGTMNTPTRFRTIEAYNIADGKWAQLPDPGDNFEKRGGAGFAVVQGKIWVVYGFATSIVPGGKDDYESNAVQFYDPASKKWTEVETTGAKPSARSVFAHAVVGKYIIIFAGEVWPDLNGHYGPGTLSNEGYALDTETLVWEKLGEEGAPAIPRGWTAYTAATVDGKNGLLMHGGKLPTNERTDDLYFYAVNSA', '341', '', '', '', 'Myrosinase is not sufficient for indol-3-acetonitrile production from indol-3-ylmethyl GSL and requires the presence of functional epithospecifier protein (ESP) in planta and in vitro to produce significant levels of indol-3-acetonitrile (Burow et al. 2008)', 'GSL degradation', 'Burow et al. 2008  '),
	('AT1G59750', 'ARF1', 'Auxin response factor 1', 'F23H11.7', '842268', 'NM_104668', 'NP_176184', 'Q8L7G0', 'MAASNHSSGKPGGVLSDALCRELWHACAGPLVTLPREGERVYYFPEGHMEQLEASMHQGLEQQMPSFNLPSKILCKVINIQRRAEPETDEVYAQITLLPELDQSEPTSPDAPVQEPEKCTVHSFCKTLTASDTSTHGGFSVLRRHADDCLPPLDMSQQPPWQELVATDLHNSEWHFRHIFRGQPRRHLLTTGWSVFVSSKKLVAGDAFIFLRGENEELRVGVRRHMRQQTNIPSSVISSHSMHIGVLATAAHAITTGTIFSVFYKPRTSRSEFIVSVNRYLEAKTQKLSVGMRFKMRFEGEEAPEKRFSGTIVGVQENKSSVWHDSEWRSLKVQWDEPSSVFRPERVSPWELEPLVANSTPSSQPQPPQRNKRPRPPGLPSPATGPSGPDGVWKSPADTPSSVPLFSPPAKAATFGHGGNKSFGVSIGSAFWPTNADSAAESFASAFNNESTEKKQTNGNVCRLFGFELVENVNVDECFSAASVSGAVAVDQPVPSNEFDSGQQSEPLNINQSDIPSGSGDPEKSSLRSPQESQSRQIRSCTKVHMQGSAVGRAIDLTRSECYEDLFKKLEEMFDIKGELLESTKKWQVVYTDDEDDMMMVGDDPWNEFCGMVRKIFIYTPEEVKKLSPKNKLAVNARMQLKADAEENGNTEGRSSSMAGSR', '665', '', '', '', 'ARF1 and ARF9 negatively regulate glucosinolate accumulation, and that ARF9 positively regulates camalexin accumulation. The action of miR393 on auxin signalling triggers two complementary responses. First, it prevents suppression of SA levels by auxin. Second, it stabilizes ARF1 and ARF9 in inactive complexes (Robert-Seilaniantz et al. 2011)', 'Camalexin biosynthesis', 'Robert-Seilaniantz et al. 2011'),
	('AT1G59870', 'PEN3', 'ABC transporter G family member 36 ', 'ABCG36', '842281', 'NM_104680', 'NP_176196', 'Q9XIE2', 'MDYNPNLPPLGGGGVSMRRSISRSVSRASRNIEDIFSSGSRRTQSVNDDEEALKWAAIEKLPTYSRLRTTLMNAVVEDDVYGNQLMSKEVDVTKLDGEDRQKFIDMVFKVAEQDNERILTKLRNRIDRVGIKLPTVEVRYEHLTIKADCYTGNRSLPTLLNVVRNMGESALGMIGIQFAKKAQLTILKDISGVIKPGRMTLLLGPPSSGKTTLLLALAGKLDKSLQVSGDITYNGYQLDEFVPRKTSAYISQNDLHVGIMTVKETLDFSARCQGVGTRYDLLNELARREKDAGIFPEADVDLFMKASAAQGVKNSLVTDYTLKILGLDICKDTIVGDDMMRGISGGQKKRVTTGEMIVGPTKTLFMDEISTGLDSSTTFQIVKCLQQIVHLNEATVLMSLLQPAPETFDLFDDIILVSEGQIVYQGPRDNILEFFESFGFKCPERKGTADFLQEVTSKKDQEQYWVNPNRPYHYIPVSEFASRYKSFHVGTKMSNELAVPFDKSRGHKAALVFDKYSVSKRELLKSCWDKEWLLMQRNAFFYVFKTVQIVIIAAITSTLFLRTEMNTRNEGDANLYIGALLFGMIINMFNGFAEMAMMVSRLPVFYKQRDLLFYPSWTFSLPTFLLGIPSSILESTAWMVVTYYSIGFAPDASRFFKQFLLVFLIQQMAASLFRLIASVCRTMMIANTGGALTLLLVFLLGGFLLPKGKIPDWWGWAYWVSPLTYAFNGLVVNEMFAPRWMNKMASSNSTIKLGTMVLNTWDVYHQKNWYWISVGALLCFTALFNILFTLALTYLNPLGKKAGLLPEEENEDADQGKDPMRRSLSTADGNRRGEVAMGRMSRDSAAEASGGAGNKKGMVLPFTPLAMSFDDVKYFVDMPGEMRDQGVTETRLQLLKGVTGAFRPGVLTALMGVSGAGKTTLMDVLAGRKTGGYIEGDVRISGFPKVQETFARISGYCEQTDIHSPQVTVRESLIFSAFLRLPKEVGKDEKMMFVDQVMELVELDSLRDSIVGLPGVTGLSTEQRKRLTIAVELVANPSIIFMDEPTSGLDARAAAIVMRAVRNTVDTGRTVVCTIHQPSIDIFEAFDELMLMKRGGQVIYAGPLGQNSHKVVEYFESFPGVSKIPEKYNPATWMLEASSLAAELKLSVDFAELYNQSALHQRNKALVKELSVPPAGASDLYFATQFSQNTWGQFKSCLWKQWWTYWRSPDYNLVRFIFTLATSLLIGTVFWQIGGNRSNAGDLTMVIGALYAAIIFVGINNCSTVQPMVAVERTVFYRERAAGMYSAMPYAISQVTCELPYVLIQTVYYSLIVYAMVGFEWKAEKFFWFVFVSYFSFLYWTYYGMMTVSLTPNQQVASIFASAFYGIFNLFSGFFIPRPKIPKWWIWYYWICPVAWTVYGLIVSQYGDVETRIQVLGGAPDLTVKQYIEDHYGFQSDFMGPVAAVLIAFTVFFAFIFAFCIRTLNFQTR', '1469', '', '', '', 'Two genes; PEN2 and PEN3 are also necessary for resistance to pathogens and are required for both callose deposition and GSL activation suggesting that the pathogen-triggered callose response is required for resistance to microbial pathogens. The study shows that well- studied plant metabolites previously identified as important in avoiding damage by herbivores are also required as a component of the plant defense response against microbial pathogens (Clay et al. 2009)', 'GSL degradation', 'Bednarek et al. 2009; Clay et al. 2009'),
	('AT1G62180', 'APR2', '5\'-adenylylsulfate reductase 2 chloroplastic', 'PRH43', '842514', 'NM_104899', 'NP_176409', 'P92981', 'MALAVTSSSTAISGSSFSRSGASSESKALQICSIRLSDRTHLSQRRYSMKPLNAESHSRSESWVTRASTLIAPEVEDFEQLAKKLEDASPLEIMDKALERFGDQIAIAFSGAEDVALIEYARLTGKPFRVFSLDTGRLNPETYRLFDAVEKQYGIRIEYMFPDAVEVQALVRNKGLFSFYEDGHQECCRVRKVRPLRRALKGLKAWITGQRKDQSPGTRSEIPIVQVDPVFEGLDGGVGSLVKWNPLANVEGADVWNFLRTMDVPVNALHAQGYVSIGCEPCTRPVLPGQHEREGRWWWEDAKAKECGLHKGNIKEEDGAADSKPAAVQEIFESNNVVALSKGGVENLLKLENRKEAWLVVLYAPWCPFCQAMEASYIELAEKLAGKGVKVAKFRADGEQKEFAKQELQLGSFPTILLFPKRAPRAIKYPSEHRDVDSLMSFVNLLR', '454', 'EC 1.8.4.9', '', '', 'Using trans-activation assays two isoforms of APK; APK1 and APK2 are regulated by both classes of GSL MYB transcription factors; whereas two ATPS genes; ATPS1 and ATPS3 are differentially regulated by these two groups of MYB factors. The adenosine 5-phosphosulfate reductases APR1; APR2; and APR3 which participate in primary sulfate reduction are also activated by the MYB factors (Yatusevich et al. 2010)  ', 'GSL core structure synthesis', 'Yatusevich et al. 2010'),
	('AT1G62540', 'FMOGS-OX2', 'Flavin-containing monooxygenase FMO GS-OX2 ', 'T3P18.10', '88716', 'NM_104933', 'NP_564796', 'Q94K43', 'MAPAQNPISSQHVVVIGAGAAGLVAARELSREGHTVVVLEREKEVGGLWIYSPKAESDPLSLDPTRSIVHSSVYESLRTNLPRECMGFTDFPFVPRFDDESRDSRRYPSHMEVLAYLQDFAREFNLEEMVRFEIEVVRVEPVNGKWRVWSKTSGGVSHDEIFDAVVVCSGHYTEPNVAHIPGIKSWPGKQIHSHNYRVPGPFENEVVVVIGNFASGADISRDIAKVAKEVHIASRASEFDTYEKLPVPRNNLWIHSEIDTAYEDGSIVFKNGKVVYADSIVYCTGYKYRFTFLETNGYMNIDENRVEHLYKHVFPPALSPGLSFVGLPSMGIQFVMFEIQSKWVAAVLSRRVTLPTEDKMMEDISAWYASLDAVGIPKRYTHKLGKIQSEYLNWVAEECGCPLVEHWRNQQIVRGYQRLVSHPETYRDEWDDNDLMEEAYEDFARKKLISFHPSHIL', '457', 'EC 1.8.-.-', '', '', 'Four uncharacterized FMOs designated FMOGS-OX2 to FMOGS-OX5 were found to involve in biosynthesis aliphatic GSL. Biochemical characterization of the recombinant protein combined with the analysis of GSL content in knockout mutants and overexpression lines show that FMOGS-OX2; FMOGS-OX3; and FMOGS-OX4 have broad substrate specificity and catalyze the conversion from methylthioalkyl GSL to the corresponding methylsulfinylalkyl GSL independent of chain length. In contrast; FMOGS-OX5 shows substrate specificity toward the long-chain 8-methylthiooctyl GSL. Identification of the FMOGS-OX subclade will generate better understanding of the evolution of biosynthetic activities and specificities in secondary metabolism and provides an important tool for breeding plants with improved cancer prevention characteristics as provided by the methylsulfinylalkyl GSL (Li et al. 2008)', 'GSL side chain modificatian', 'Hansen et al. 2007;  Li et al. 2008'),
	('AT1G62560', 'FMOGS-OX3', 'Flavin-containing monooxygenase FMO GS-OX3 ', 'T3P18.12', '88718', 'NM_104934', 'NP_176444', 'Q9SXE1', 'MAPAQNQITSKHVAVIGAGPAGLITSRELRREGHSVVVFEREKQVGGLWVYTPKSDSDPLSLDPTRSKVHSSIYESLRTNVPRESMGVRDFPFLPRFDDESRDARRYPNHREVLAYIQDFAREFKIEEMIRFETEVVRVEPVDNGNWRVQSKNSGGFLEDEIYDAVVVCNGHYTEPNIAHIPGIKSWPGKQIHSHNYRVPDPFENEVVVVIGNFASGADISRDIAKVAKEVHIASRAREPHTYEKISVPQNNLWMHSEIDTTHEDGSIVFKNGKVIFADSIVYCTGYKYNFPFLETNGYLRIDEKRVEPLYKHVFPPALAPGLAFVGLPAMGIVFVMFEIQSKWVAAVLSGRVTLPSTDKMMEDINAWYASLDALGIPKRHTHTIGRIQSEYLNWVAKESGCELVERWRGQEVDGGYLRLVAHPETYRDEWDDDELIEEAYNDFSRKKLISVDPSYYLENGR', '462', 'EC 1.8.-.-', '', '', 'Four uncharacterized FMOs. designated FMOGS-OX2 to FMOGS-OX5 were found to involve in biosynthesis aliphatic GSL. Biochemical characterization of the recombinant protein combined with the analysis of GSL content in knockout mutants and overexpression lines show that FMOGS-OX2. FMOGS-OX3. and FMOGS-OX4 have broad substrate specificity and catalyze the conversion from methylthioalkyl GSL to the corresponding methylsulfinylalkyl GSL independent of chain length. In contrast. FMOGS-OX5 shows substrate specificity toward the long-chain 8-methylthiooctyl GSL. Identification of the FMOGS-OX subclade will generate better understanding of the evolution of biosynthetic activities and specificities in secondary metabolism and provides an important tool for breeding plants with improved cancer prevention characteristics as provided by the methylsulfinylalkyl GSL (Li et al. 2008)', 'GSL side chain modificatian', 'Li et al. 2008; Li et al. 2011  '),
	('AT1G62570', 'FMOGS-OX4', 'Flavin-containing monooxygenase FMO GS-OX4 ', 'T3P18.13', '88719', 'NM_104935', 'NP_564797', 'Q93Y23', 'MAPAPSPINSQHVAVIGAGAAGLVAARELRREGHTVVVLDREKQVGGLWVYTPETESDELGLDPTRPIVHSSVYKSLRTNLPRECMGYKDFPFVPRGDDPSRDSRRYPSHREVLAYLQDFATEFNIEEMIRFETEVLRVEPVNGKWRVQSKTGGGFSNDEIYDAVVMCCGHFAEPNIAQIPGIESWPGRQTHSHSYRVPDPFKDEVVVVIGNFASGADISRDISKVAKEVHIASRASKSNTFEKRPVPNNNLWMHSEIDTAHEDGTIVFKNGKVVHADTIVHCTGYKYYFPFLETNNYMRVDDNRVEPLYKHIFPPALAPGLSFIGLPAMGLQFYMFEVQSKWVAAVLSGRVTLPSVDEMMDDLKLSYETQEALGIPKRYTHKLGKSQCEYLDWIADLCGFPHVEHWRDQEVTRGYQRLGNQPETFRDEWDDDDLMEEAYEDFARLNLINFHPSRFLESGR', '461', 'EC 1.8.-.-', '', '', 'Four uncharacterized FMOs. designated FMOGS-OX2 to FMOGS-OX5 were found to involve in biosynthesis aliphatic GSL. Biochemical characterization of the recombinant protein combined with the analysis of GSL content in knockout mutants and overexpression lines show that FMOGS-OX2. FMOGS-OX3. and FMOGS-OX4 have broad substrate specificity and catalyze the conversion from methylthioalkyl GSL to the corresponding methylsulfinylalkyl GSL independent of chain length. In contrast. FMOGS-OX5 shows substrate specificity toward the long-chain 8-methylthiooctyl GSL. Identification of the FMOGS-OX subclade will generate better understanding of the evolution of biosynthetic activities and specificities in secondary metabolism and provides an important tool for breeding plants with improved cancer prevention characteristics as provided by the methylsulfinylalkyl GSL (Li et al. 2008)', 'GSL side chain modificatian', 'Li et al. 2008; Li et al. 2011  '),
	('AT1G64070', 'RLM1A', 'Disease resistance protein RML1A', 'F22C12.17', '842711', 'NM_105080', 'NP_176590', 'F4I594', 'MASSSSSASRTWRYRVFTSFHGSDVRTSFLSHFRKQFNNNGITMFDDQRILRGETISPALTQAIRESRISIVLLSKNYASSGWCLDELLEILKCKDDMGQIVMTVFYGVDPSDVRKQTGEFGIAFNETCACRTEEERQKWSQALNYVGNIAGEHLLNWDNEAKMIEKIARDVSEKLNVTPCRDFDGMVGIEAHLRKIQSLLDLDNDEVKMVAISGPAGIGKSTIGRALHSLLSNRFHHTCFVDNLRGSHPIGLDEYGLKLRLQEQLLSKILNQDGSRICHLGAIKERLCDMKVFIILDDVNDVKQLEALANESNWFGPGSRIIVTTENKELLKQHGINNTYYVGFPSDEEAIKILCRYAFRQSSSRHGFKKLTRSVTELCGKLPLGLRVVGSSLHGKNEEEWEYVIRRLETIIDRDIEQVLRVGYESLHENEQSLFLHIAIFFNYEDGDLVKAMLAENDLDIEHELNILVNKSLIYISTDGRIRMHKLLQLVGRQANQREEPWKRRILIDAQEICHVLENDIGTGAVSGILFDTSGINEVSISNKALRRMCNLRFLSVYKTKHDGYNRMDIPEDMEFPPRLRLLHWDAYPSKCLPLKFRAENLVELDMKDSRLEYLWPGTQLLTKLKKLNLEGSYNLKELPDLSNATNLEMLDLSVCLALAELPSSIKNLHKLDVIYMDLCESLHMIPTNINLASLETMYMTGCPQLKTFPAFSTKIKRLYLVRTGVEEVPASITHCSRLLKIDLSGSRNLKSITHLPSSLQTLDLSSTDIEMIADSCIKDLQRLDHLRLCRCRKLKSLPELPASLRLLTAEDCESLERVTYPLNTPTGQLNFTNCLKLGEEAQRVIIQQSLVKHACFPGSVMPSEFNHRARGNSLKILVKSSASFAFKACVLISPRQLQCERNQRRVKIRCRVTDGRGRFVGSKVVSLEHPNHSTGIRTKHLCFFNGVLTEVSCDALCFVFKISAYNPLDNYEISECAVQILTNEPERRSCDGGSE', '997', '', '', '', 'Analyses of mutants defective in hormone signaling in the camalexin-free rlm1(Ler)pad3 background revealed a significant influence of JA and ET on symptom development and pathogen colonization. The overall results indicate that the defense responses of primary importance induced by RLM1 are all associated with physical barriers, and that responses of secondary importance involve complex cross-talk among SA, JA and ET (Persson et al. 2009)', 'Camalexin biosynthesis', 'Persson et al. 2009'),
	('AT1G64280', 'NPR1', 'Regulatory protein NPR1', 'NIM1, SAI1', '842733', 'NM_105102', 'NP_176610', 'P93002', 'MDTTIDGFADSYEISSTSFVATDNTDSSIVYLAAEQVLTGPDVSALQLLSNSFESVFDSPDDFYSDAKLVLSDGREVSFHRCVLSARSSFFKSALAAAKKEKDSNNTAAVKLELKEIAKDYEVGFDSVVTVLAYVYSSRVRPPPKGVSECADENCCHVACRPAVDFMLEVLYLAFIFKIPELITLYQRHLLDVVDKVVIEDTLVILKLANICGKACMKLLDRCKEIIVKSNVDMVSLEKSLPEELVKEIIDRRKELGLEVPKVKKHVSNVHKALDSDDIELVKLLLKEDHTNLDDACALHFAVAYCNVKTATDLLKLDLADVNHRNPRGYTVLHVAAMRKEPQLILSLLEKGASASEATLEGRTALMIAKQATMAVECNNIPEQCKHSLKGRLCVEILEQEDKREQIPRDVPPSFAVAADELKMTLLDLENRVALAQRLFPTEAQAAMEIAEMKGTCEFIVTSLEPDRLTGTKRTSPGVKIAPFRILEEHQSRLKALSKTVELGKRFFPRCSAVLDQIMNCEDLTQLACGEDDTAEKRLQKKQRYMEIQETLKKAFSEDNLELGNSSLTDSTSSTSKSTGGKRSNRKLSHRRR', '593', '', '', '', 'Decreasing camalexin levels by mutation of the camalexin synthetase gene?PAD3?or the camalexin synthesis regulator?AtWRKY33?compromised the powdery mildew resistance in these mutants (Liu et al. 2016)', 'Camalexin biosynthesis', 'Liu et al. 2016; Bohman et al. 2003; Ferrari et al. 2003'),
	('AT1G65860', 'FMOGS-OX1 ', 'Flavin-containing monooxygenase FMO GS-OX1 ', 'F12P19.2', '88765', 'NM_105258', 'NP_176761', 'Q9SS04', 'MAPTQNTICSKHVAVIGAGAAGLVTARELRREGHTVVVFDREKQVGGLWNYSSKADSDPLSLDTTRTIVHTSIYESLRTNLPRECMGFTDFPFVPRIHDISRDSRRYPSHREVLAYLQDFAREFKIEEMVRFETEVVCVEPVNGKWSVRSKNSVGFAAHEIFDAVVVCSGHFTEPNVAHIPGIKSWPGKQIHSHNYRVPGPFNNEVVVVIGNYASGADISRDIAKVAKEVHIASRASESDTYQKLPVPQNNLWVHSEIDFAHQDGSILFKNGKVVYADTIVHCTGYKYYFPFLETNGYININENRVEPLYKHVFLPALAPSLSFIGLPGMAIQFVMFEIQSKWVAAVLSGRVILPSQDKMMEDIIEWYATLDVLGIPKRHTHKLGKISCEYLNWIAEECHCSPVENWRIQEVERGFQRMVSHPEIYRDEWDDDDLMEEAYKDFARKKLISSHPSYFLES', '457', 'EC 1.8.-.-', '', '', 'Flavin-monooxygenase (FMO) enzyme; FMOGS-OX1 catalyzes the conversion of methylthioalkyl GSLs into methylsulfinylalkyl GSLs. This is evidenced by biochemical characterization of the recombinant protein and analyses of the GSL content in FMOGS-OX1 overexpression lines and an FMOGS-OX1 knock-out mutant of Arabidopsis. The FMOGS-OX1 overexpression lines show almost complete conversion of methylthioalkyl into methylsulfinylalkyl GSLs with an approximately fivefold increase in 4-methylsulfinylbutyl GSL in seeds. Identification of FMOGS-OX1 provides a molecular tool for breeding of Brassica vegetable crops with increased levels of this important GSL which has implications for production of functional foods enriched with the cancer-preventive sulforaphane (Hansen et al. 2007)', 'GSL side chain modificatian', 'Hansen et al. 2007;  Li et al. 2008; Li et al. 2011  '),
	('AT1G65880', 'BZO1', 'Benzoate--CoA ligase peroxisomal', 'AAE20  ', '842900', 'NM_105260', 'NP_176763', 'Q9SS01', 'MDDLALCEANNVPLTPMTFLKRASECYPNRTSIIYGKTRFTWPQTYDRCCRLAASLISLNISKNDVVSVMAPNTPALYEMHFAVPMAGAVLNPINTRLDATSIAAILRHAKPKILFLDRSFEALARESLHLLSSEDSNLNLPVIFIHENDFPKRASFEELDYECLIQRGEPTPSMVARMFRIQDEHDPISLNYTSGTTADPKGVVISHRGAYLCTLSAIIGWEMGTCPVYLWTLPMFHCNGWTFTWGTAARGGTSVCMRHVTAPEIYKNIEMHNVTHMCCVPTVFNILLKGNSLDLSPRSGPVHVLTGGSPPPAALVKKVQRLGFQVMHAYGQTEATGPILFCEWQDEWNRLPENQQMELKARQGISILGLADVDVKNKETQKSAPRDGKTMGEILIKGSSIMKGYLKNPKATFEAFKHGWLNTGDVGVIHPDGHVEIKDRSKDIIISGGENISSVEVENVLYKYPKVLETAVVAMPHPTWGETPCAFVVLEKSETTIKEDRVDKFQTRERNLIEYCRENLPHFMCPRKVVFLEELPKNGNGKILKPKLRDIAKGLVVEDEINVIAKEVKRPVGHFISRL', '580', 'EC 6.2.1.25', '', '', 'Genetic mapping and analysis of T-DNA insertions in candidate genes identified BZO1 (At1g65880) which encodes an enzyme with benzoyl-CoA ligase activity as being required for the accumulation of benzoyloxyGSLs. Long-chain aliphatic GSLs are elevated in bzo1 mutants suggesting substrate competition for the common short-chain aliphatic GSL precursors. Whereas bzo1 mutations have seed-specific effects on benzoyloxyGSL accumulation the relative abundance of 3-benzoyloxypropyl- and 4-benzoyloxy-butylGSLs depends on the maternal genotype (Kliebenstein et al. 2007)', 'GSL side chain modification', 'Lee et al. 2012; Zhang et al. 2015'),
	('AT1G73500', 'MKK9', 'Mitogen-activated protein kinase kinase 9', 'MAP2K9', '843685', 'NM_106009', 'NP_177492', 'Q9FX43', 'MALVRERRQLNLRLPLPPISDRRFSTSSSSATTTTVAGCNGISACDLEKLNVLGCGNGGIVYKVRHKTTSEIYALKTVNGDMDPIFTRQLMREMEILRRTDSPYVVKCHGIFEKPVVGEVSILMEYMDGGTLESLRGGVTEQKLAGFAKQILKGLSYLHALKIVHRDIKPANLLLNSKNEVKIADFGVSKILVRSLDSCNSYVGTCAYMSPERFDSESSGGSSDIYAGDIWSFGLMMLELLVGHFPLLPPGQRPDWATLMCAVCFGEPPRAPEGCSEEFRSFVECCLRKDSSKRWTAPQLLAHPFLREDL', '310', 'EC 2.7.12.2', '', '', 'MKK9, an MKK, is an upstream activator of the MPKs MPK3 and MPK6 both in vitro and in planta. Expression of active MKK9 protein in transgenic plants induces the synthesis of ethylene and camalexin through the activation of the endogenous MPK3 and MPK6 kinases. MKK9-MPK3/MPK6 cascade participates in the regulation of the biosynthesis of ethylene and camalexin and may be an important axis in the stress responses of Arabidopsis (Xu et al. 2008).', 'Camalexin biosynthesis', 'Xu et al. 2008'),
	('AT1G73730', 'SLIM1', 'ETHYLENE INSENSITIVE 3-like 3 protein', 'EIL3', '843708', 'NM_106032', 'NP_177514', 'O23116', 'MGDLAMSVADIRMENEPDDLASDNVAEIDVSDEEIDADDLERRMWKDRVRLKRIKERQKAGSQGAQTKETPKKISDQAQRKKMSRAQDGILKYMLKLMEVCKVRGFVYGIIPEKGKPVSGSSDNIRAWWKEKVKFDKNGPAAIAKYEEECLAFGKSDGNRNSQFVLQDLQDATLGSLLSSLMQHCDPPQRKYPLEKGTPPPWWPTGNEEWWVKLGLPKSQSPPYRKPHDLKKMWKVGVLTAVINHMLPDIAKIKRHVRQSKCLQDKMTAKESAIWLAVLNQEESLIQQPSSDNGNSNVTETHRRGNNADRRKPVVNSDSDYDVDGTEEASGSVSSKDSRRNQIQKEQPTAISHSVRDQDKAEKHRRRKRPRIRSGTVNRQEEEQPEAQQRNILPDMNHVDAPLLEYNINGTHQEDDVVDPNIALGPEDNGLELVVPEFNNNYTYLPLVNEQTMMPVDERPMLYGPNPNQELQFGSGYNFYNPSAVFVHNQEDDILHTQIEMNTQAPPHNSGFEEAPGGVLQPLGLLGNEDGVTGSELPQYQSGILSPLTDLDFDYGGFGDDFSWFGA', '567', '', '', '', 'SLIM1 functioned as a central transcriptional regulator which controlled both the activation of sulfate acquisition and degradation of GSLs under ?S conditions. Metabolite analysis indicated stable accumulation of GSLs in slim1 mutants; even under ?S conditions; particularly in the molecular species with methylsulfinylalkyl side chains beneficial to human health (Maruyama-Nakashita et al. 2006)', 'GSL transcription factor', 'Maruyama-Nakashita et al. 2006'),
	('AT1G74080', 'MYB122', 'Transcription factor MYB122 ', 'ATMYB122', '843748', 'NM_106068', 'NP_177548', 'Q9C9C8', 'MVRTPCCRAEGLKKGAWTQEEDQKLIAYVQRHGEGGWRTLPDKAGLKRCGKSCRLRWANYLRPDIKRGEFSQDEEDSIINLHAIHGNKWSAIARKIPRRTDNEIKNHWNTHIKKCLVKKGIDPLTHKSLLDGAGKSSDHSAHPEKSSVHDDKDDQNSNNKKLSGSSSARFLNRVANRFGHRINHNVLSDIIGSNGLLTSHTTPTTSVSEGERSTSSSSTHTSSNLPINRSITVDATSLSSSTFSDSPDPCLYEEIVGDIEDMTRFSSRCLSHVLSHEDLLMSVESCLENTSFMREITMIFQEDKIETTSFNDSYVTPINEVDDSCEGIDNYFG', '333', '', '', '', 'MYB34; MYB51 and MYB122 act together to control the biosynthesis of indole-3-ylmethyl-GSL (I3M) in shoots and roots with MYB34 controlling biosynthesis of indolic GSLs (IGs) mainly in the roots. MYB51 regulating biosynthesis in shoots and MYB122 having an accessory role in the biosynthesis of IGs (Frerigmann & Gigolashvili 2014)', 'GSL transcription factor / Camalexin biosynthesis', 'Frerigmann & Gigolashvili 2014; Gigolashvili et al 2007; Frerigmann et al. 2015'),
	('AT1G74090', 'SOT18', 'Cytosolic sulfotransferase 18 ', 'ATST5B', '843749', 'NM_106069', 'NP_177549', 'Q9C9C9', 'MESETLTAKATITTTTLPSHDETKTESTEFEKNQKRYQDLISTFPHEKGWRPKEPLIEYGGYWWLPSLLEGCIHAQEFFQARPSDFLVCSYPKTGTTWLKALTFAIANRSRFDDSSNPLLKRNPHEFVPYIEIDFPFFPEVDVLKDKGNTLFSTHIPYELLPDSVVKSGCKMVYIWREPKDTFISMWTFLHKERTELGPVSNLEESFDMFCRGLSGYGPYLNHILAYWKAYQENPDRILFLKYETMRADPLPYVKSLAEFMGHGFTAEEEEKGVVEKVVNLCSFETLKNLEANKGEKDREDRPGVYANSAYFRKGKVGDWSNYLTPEMAARIDGLMEEKFKGTGLLEHGK', '344', 'EC 2.8.2.-', 'AraCyc', 'KEGG', 'The three enzymes were shown to catalyze the final step in the biosynthesis of the GSL core structure; the sulfation of desulfoGSLs (dsGSs). They accept a broad range of desulfoGSLs as substrates. In a competitive situation; AtST5a (SOT16) clearly prefers tryptophan and phenylalanine-derived desulfoGSLs whereas long chain desulfoGSLs derived from methionine are the preferred substrates of SOT17 and SOT18 (Piotrowski et al. 2004)', 'GSL core structure synthesis', 'Hirschmann & Papenbrock 2015; Piotrowski et al. 2004'),
	('AT1G74100', 'SOT16', 'Cytosolic sulfotransferase 16 ', 'CORI-7', '843750', 'NM_106070', 'NP_177550', 'Q9C9D0', 'MESKTTQNGSEVVELTEFEKTQKKYQDFIATLPKSKGWRPDEILTQYGGHWWQECLLEGLFHAKDHFEARPTDFLVCSYPKTGTTWLKALTYAIVNRSRYDDAANPLLKRNPHEFVPYVEIDFAFYPTVDVLQDRKNPLFSTHIPNGLLPDSIVNSGCKMVYIWRDPKDTFISMWTFLHKEKSQEGQLASLEDSFDMFCKGLSVYGPYLDHVLGYWKAYQENPDRILFLRYETMRANPLPFVKRLAEFMGYGFTDEEEENGVAEKVVKLCSFETLKNLEANKGDKEREDRPAVYANSAYFRKGKVGDWANYLTPEMAARIDGLVEEKFKDTGLLQHDN', '338', 'EC 2.8.2.-', 'AraCyc', 'KEGG', 'The three enzymes were shown to catalyze the final step in the biosynthesis of the GSL core structure; the sulfation of desulfoGSLs (dsGSs). They accept a broad range of desulfoGSLs as substrates. In a competitive situation; AtST5a (SOT16) clearly prefers tryptophan and phenylalanine-derived desulfoGSLs whereas long chain desulfoGSLs derived from methionine are the preferred substrates of SOT17 and SOT18 (Piotrowski et al. 2004)', 'GSL core structure synthesis', 'Hirschmann & Papenbrock 2015; Piotrowski et al. 2004'),
	('AT1G74710', 'ICS1', 'Isochorismate synthase 1, chloroplastic', 'EDS16', '843810', 'NM_106129', 'NP_565090', 'Q9S7H8', 'MASLQFSSQFLGSNTKTHSSIISISRSYSPTPFTRFSRKKYESCSMSMNGCDGDFKTPLGTVETRTMTAVLSPAAATERLISAVSELKSQPPSFSSGVVRLQVPIDQQIGAIDWLQAQNEIQPRCFFSRRSDVGRPDLLLDLANENGNGNGNGTVSSDRNLVSVAGIGSAVFFRDLDPFSHDDWRSIRRFLSSTSPLIRAYGGMRFDPNGKIAVEWEPFGAFYFSVPQVEFNEFGGSSMLAATIAWDDELSWTLENAIEALQETMLQVSSVVMKLRNRSLGVSVLSKNHVPTKGAYFPAVEKALEMINQKSSPLNKVVLARNSRIITDTDIDPIAWLAQLQREGHDAYQFCLQPPGAPAFIGNTPERLFQRTQLGVCSEALAATRPRAASSARDMEIERDLLTSPKDDLEFSIVRENIREKLNGICDRVVVKPQKTVRKLARVQHLYSQLAGRLTKEDDEYKILAALHPTPAVCGLPAEEARLLIKEIESFDRGMYAGPIGFFGGEESEFAVGIRSALVEKGLGALIYAGTGIVAGSDPSSEWNELDLKISQVRAFVQKMFSDIMVLCYQNPNFYSLFCCCFCSSPSQLNMKQQHLYRRLIEERVTFVFDCFVCMGDKGFSQ', '524', 'EC 5.4.4.2', '', '', 'Decreasing camalexin levels by mutation of the camalexin synthetase gene?PAD3?or the camalexin synthesis regulator?AtWRKY33?compromised the powdery mildew resistance in these mutants (Liu et al. 2016)', 'Camalexin biosynthesis', 'Liu et al. 2016'),
	('AT1G76790', 'IGMT5', 'Indole glucosinolate O-methyltransferase 5 ', 'F28O16.16', '844013', 'NM_106329', 'NP_177805', 'Q9SRD4', 'MGHLIPQTGDEETELGLAAVRLANCAAFPMVFKAAIELGVIDTLYLAARDDVTGSSSFLTPSEIAIRLPTKPSNPEAPALLDRILRLLASYSMVKCQIIDGNRVYKAEPICRYFLKDNVDEELGTLASQLIVTLDTVFLNTWGELKNVVLEGGVAFGRANGGLKLFDYISKDERLSKLFNRTGFSVAVLKKILQVYSGFEGVNVLVDVGGGVGDTLGFVTSKYPNIKGINFDLTCALTQAPSYPNVEHVAGDMFVDVPKGDAILLKRILHDWTDEDCEKILKNCWKALPENGKVIVMEVVTPDEADNRDVISNIAFDMDLLMLTQLSGGKERSRAEYVAMAANSGFPRCNFVCSAYHLWVIELTKQA', '367', 'EC 2.1.1.-', '', '', 'Biosynthesis of 1-methoxyindol-3-ylmethyl GSL (1MOI3M) from I3M involves the predicted instable intermediate 1-hydroxyindol-3-ylmethyl GSL (1OHI3M) and that IGMT5; a gene with moderate similarity to previously characterized IGMTs encodes the methyltransferase that is responsible for the conversion of 1OHI3M to 1MOI3M. Disruption of IGMT5 function increases resistance against the root-knot nematode Meloidogyne javanica and suggests a potential role for the 1-IG-modification pathway in Arabidopsis below-ground defense (Pfalz et al. 2016)', 'GSL side chain modification', 'Pfalz et al. 2016'),
	('AT1G78000', 'SULTR1;2', 'Sulfate transporter 1.2', 'SEL1', '844135', 'NM_179568', 'NP_849899', 'Q9MAX3', 'MSSRAHPVDGSPATDGGHVPMKPSPTRHKVGIPPKQNMFKDFMYTFKETFFHDDPLRDFKDQPKSKQFMLGLQSVFPVFDWGRNYTFKKFRGDLISGLTIASLCIPQDIGYAKLANLDPKYGLYSSFVPPLVYACMGSSRDIAIGPVAVVSLLLGTLLRAEIDPNTSPDEYLRLAFTATFFAGITEAALGFFRLGFLIDFLSHAAVVGFMGGAAITIALQQLKGFLGIKKFTKKTDIISVLESVFKAAHHGWNWQTILIGASFLTFLLTSKIIGKKSKKLFWVPAIAPLISVIVSTFFVYITRADKQGVQIVKHLDQGINPSSFHLIYFTGDNLAKGIRIGVVAGMVALTEAVAIGRTFAAMKDYQIDGNKEMVALGMMNVVGSMSSCYVATGSFSRSAVNFMAGCQTAVSNIIMSIVVLLTLLFLTPLFKYTPNAILAAIIINAVIPLIDIQAAILIFKVDKLDFIACIGAFFGVIFVSVEIGLLIAVSISFAKILLQVTRPRTAVLGNIPRTSVYRNIQQYPEATMVPGVLTIRVDSAIYFSNSNYVRERIQRWLHEEEEKVKAASLPRIQFLIIEMSPVTDIDTSGIHALEDLYKSLQKRDIQLILANPGPLVIGKLHLSHFADMLGQDNIYLTVADAVEACCPKLSNEV', '653', '', '', '', 'SLIM1 is required for the -S-responsive induction of the high-affinity sulfate transport system facilitated by SULTR1;2 sulfate transporter in Arabidopsis roots (Maruyama-Nakashita et al. 2006)', 'GSL core structure synthesis', 'Maruyama-Nakashita et al. 2006'),
	('AT1G78370', 'GSTU20', 'Glutathione S-transferase U20 ', 'ATGSTU20', '844173', 'NM_106484', 'NP_177958', 'Q8L7C9', 'MANLPILLDYWPSMFGMRARVALREKGVEFEYREEDFSNKSPLLLQSNPIHKKIPVLVHNGKPVCESLNVVQYVDEAWPEKNPFFPSDPYGRAQARFWADFVDKKFTDAQFKVWGKKGEEQEAGKKEFIEAVKILESELGDKPYFGGDSFGYVDISLITFSSWFQAYEKFGNFSIESESPKLIAWAKRCMEKESVSKSLPDSEKIVAYAAEYRKNNL', '217', 'EC 2.5.1.18', '', '', 'GST-type enzymes may be involved in an enzyme complex formed by CYP83s and C-S lyase. The S-alkylthiohydroximate formed after CYP83-catalyzed aldoxime oxidation and spontaneous conjugation to cysteine is cyclized in vitro to form a dead-end product. Hence metabolic channeling aided by GST-type enzymes is postulated in vivo to avoid this consequence the dead-end product. The two putative GST genes (At3g03190 and At1g78370) could be candidates coding for such an activity (Hirai et al. 2005)', 'GSL core structure synthesis', 'Hirai et al. 2005; Hirai et al. 2007  '),
	('AT2G03590', 'UPS1', 'Ureide permease 1', 'F19B11.4', '814888', 'NM_126409', 'NP_565303', 'Q9ZPR7', 'MYMIESKGGAIACMLLALLFLGTWPAIMTLTERRGRLPQHTYLDYTLTNLLAAVIIALTLGEIGPSRPNFFTQLSQDNWQSVMFAMAGGIVLSLGNLATQYAWAYVGLSVTEVITASITVVIGTTLNYFLDDRINRAEVLFPGVACFLIAVCFGSAVHKSNAADNKTKLQNFKSLETTSSFEMETISASNGLTKGKAKEGTAAFLIELEKQRAIKVFGKSTIIGLVITFFAGICFSLFSPAFNLATNDQWHTLKHGVPKLNVYTAFFYFSISAFVVALILNIRFLYWPILGLPRSSFKAYLNDWNGRGWSFLAGFLCGFGNGLQFMGGQAAGYAAADAVQALPLVSTFWGILLFGEYRRSSRKTYTLLISMLLMFIVAVAVLMASSGHRK', '390', '', '', '', 'Pre-treatment of A. thaliana with UV-C leads to increased camalexin accumulation and substantial resistance to B. cinerea. UV-C-induced resistance was not seen in the camalexin-deficient mutants cyp79B2/B3, cyp71A13, pad3 or pad2, and was strongly reduced in ups1.  ABC transporter demonstrates as a virulence factor that increases tolerance of the pathogen towards a phytoalexin, and the complete restoration of virulence on host plants lacking this phytoalexin (Stefanato et al 2009).', 'Camalexin biosynthesis', 'Stefanato et al. 2009; Denby et al. 2005'),
	('AT2G14750', 'APK1', 'Adenylyl-sulfate kinase 1 chloroplastic', 'ATAKN1', '815963', 'NM_127039', 'NP_179082', 'Q43295', 'MIAAGAKSLLGLSMASPKGIFDSNSMSNSRSVVVVRACVSMDGSQTLSHNKNGSIPEVKSINGHTGQKQGPLSTVGNSTNIKWHECSVEKVDRQRLLDQKGCVIWVTGLSGSGKSTLACALNQMLYQKGKLCYILDGDNVRHGLNRDLSFKAEDRAENIRRVGEVAKLFADAGIICIASLISPYRTDRDACRSLLPEGDFVEVFMDVPLSVCEARDPKGLYKLARAGKIKGFTGIDDPYEPPLNCEISLGREGGTSPIEMAEKVVGYLDNKGYLQA', '276', 'EC 2.7.1.25', '', '', 'The levels of GSLs and the sulfated 12-hydroxyjasmonate were reduced approximately fivefold in apk1 apk2 plants. The reduction in GSLs resulted in increased transcript levels for genes involved in GSL biosynthesis and accumulation of desulfated precursors (Mugford et al. 2009)', 'GSL core structure synthesis', 'Badenes-Perez et al. 2013'),
	('AT2G20610', 'SUR1', 'S-alkyl-thiohydroximate lyase SUR1 ', 'RTY1', '816585', 'NM_201760', 'NP_973489', 'Q9SIV0', 'MSEEQPHANLAVPAFKTEKEPITQTRNGQSSVWRFGGSDKAAKASTVTLRGVIYMLFDNCGKDVNKTILPLGHGDPSVYPCFRTCIEAEDAVVDVLRSGKGNSYGPGAGILPARRAVADYMNRDLPHKLTPEDIFLTAGCNQGIEIVFESLARPNANILLPRPGFPHYDARAAYSGLEVRKFDLLPEKEWEIDLEGIEAIADENTVAMVVINPNNPCGNVYSHDHLKKVAETARKLGIMVISDEVYDRTIFGDNPFVSMGKFASIVPVLTLAGISKGWVVPGWKIGWIALNDPEGVFETTKVLQSIKQNLDVTPDPATIIQAALPAILEKADKNFFAKKNKILKHNVDLVCDRLKDIPCVVCPKKPESCTYLLTKLELSLMDNIKDDIDFCVKLAREENLVFLPGKIMKLSSMSLDLSFDTKMGFVGNVLQGMLWV', '462', 'EC 4.4.1.-', 'AraCyc', 'KEGG', 'SUPERROOT1 (SUR1) was characterized as the C-S lyase in GSL biosynthesis. This is supported by selective metabolite profiling of sur1 which is completely devoid of aliphatic and indolic GSLs (Mikkelsen et al. 2004)', 'GSL core structure synthesis / Camalexin biosynthesis', 'Kong et al. 2015; Mikkelsen et al. 2004; Glawischnig et al. 2004'),
	('AT2G22300', 'CAMTA3', 'Calmodulin-binding transcription activator 3 ', 'SARD3', '816762', 'NM_179692', 'NP_850023', 'Q8GSA7', 'MAEARRFSPVHELDVGQILSEARHRWLRPPEICEILQNYQRFQISTEPPTTPSSGSVFMFDRKVLRYFRKDGHNWRKKKDGKTVKEAHERLKAGSVDVLHCYYAHGQDNENFQRRSYWLLQEELSHIVFVHYLEVKGSRVSTSFNRMQRTEDAARSPQETGDALTSEHDGYASCSFNQNDHSNHSQTTDSASVNGFHSPELEDAESAYNQHGSSTAYSHQELQQPATGGNLTGFDPYYQISLTPRDSYQKELRTIPVTDSSIMVDKSKTINSPGVTNGLKNRKSIDSQTWEEILGNCGSGVEALPLQPNSEHEVLDQILESSFTMQDFASLQESMVKSQNQELNSGLTSDRTVWFQGQDMELNAISNLASNEKAPYLSTMKQHLLHGALGEEGLKKMDSFNRWMSKELGDVGVIADANESFTQSSSRTYWEEVESEDGSNGHNSRRDMDGYVMSPSLSKEQLFSINDFSPSWAYVGCEVVVFVTGKFLKTREETEIGEWSCMFGQTEVPADVISNGILQCVAPMHEAGRVPFYVTCSNRLACSEVREFEYKVAESQVFDREADDESTIDILEARFVKLLCSKSENTSPVSGNDSDLSQLSEKISLLLFENDDQLDQMLMNEISQENMKNNLLQEFLKESLHSWLLQKIAEGGKGPSVLDEGGQGVLHFAASLGYNWALEPTIIAGVSVDFRDVNGWTALHWAAFFGRERIIGSLIALGAAPGTLTDPNPDFPSGSTPSDLAYANGHKGIAGYLSEYALRAHVSLLSLNDKNAETVEMAPSPSSSSLTDSLTAVRNATQAAARIHQVFRAQSFQKKQLKEFGDKKLGMSEERALSMLAPKTHKSGRAHSDDSVQAAAIRIQNKFRGYKGRKDYLITRQRIIKIQAHVRGYQFRKNYRKIIWSVGVLEKVILRWRRKGAGLRGFKSEALVEKMQDGTEKEEDDDFFKQGRKQTEDRLQKALARVKSMVQYPEARDQYRRLLNVVNDIQESKVEKALENSEATCFDDDDDLIDIEALLEDDDTLMLPMSSSLWTS', '1032', '', '', '', 'AtSR1/CAMTA3 is an important component of plant resistance to insect herbivory as well as one of the proteins involved in Ca2+/CaM-dependent signaling to function in the regulation of GSL metabolism (Laluk et al. 2012)', 'GSL transcription factor', 'Laluk et al. 2012  '),
	('AT2G22330', 'CYP79B3', 'Tryptophan N-monooxygenase 2 ', 'T26C19.1', '816765', 'NM_127798', 'NP_179820', 'Q501D8', 'MDTLASNSSDLTTKSSLGMSSFTNMYLLTTLQALAALCFLMILNKIKSSSRNKKLHPLPPGPTGFPIVGMIPAMLKNRPVFRWLHSLMKELNTEIACVRLGNTHVIPVTCPKIAREIFKQQDALFASRPLTYAQKILSNGYKTCVITPFGEQFKKMRKVIMTEIVCPARHRWLHDNRAEETDHLTAWLYNMVKNSEPVDLRFVTRHYCGNAIKRLMFGTRTFSEKTEADGGPTLEDIEHMDAMFEGLGFTFAFCISDYLPMLTGLDLNGHEKIMRESSAIMDKYHDPIIDERIKMWREGKRTQIEDFLDIFISIKDEAGQPLLTADEIKPTIKELVMAAPDNPSNAVEWAIAEMINKPEILHKAMEEIDRVVGKERFVQESDIPKLNYVKAIIREAFRLHPVAAFNLPHVALSDTTVAGYHIPKGSQVLLSRYGLGRNPKVWSDPLSFKPERHLNECSEVTLTENDLRFISFSTGKRGCAAPALGTAITTMMLARLLQGFKWKLAGSETRVELMESSHDMFLSKPLVLVGELRLSEDLYPMVK', '543', 'EC 1.14.13.125', 'AraCyc', 'KEGG', 'Two Arabidopsis cytochrome P450s (CYP79B2 and CYP79B3) are able to convert Trp to indole-3-acetaldoxime (IAOx); a precursor to indole-3-acetic acid (IAA) and indole GSLs (Hull et al. 2000)', 'GSL core structure synthesis / Camalexin biosynthesis', 'Hull et al. 2000; Mikkelsen et al. 2000; Zhao et al. 2015; Kettles et al. 2013; Su et al. 2011; B?ttcher et al. 2009; Nafisi et al. 2007; Schuhegger et al. 2006; Glawischnig 2006; Schlaeppi et al. 2010; Glawischnig et al. 2004;'),
	('AT2G25450', 'GSL-OH', 'Probable 2-oxoacid dependent dioxygenase ', 'F13B15.11', '817083', 'NM_128102', 'NP_180115', 'Q9SKK4', 'MAENYDRASELKAFDEMKIGVKGLVDAGVTKVPRIFHNPHVNVANPKPTSTVVMIPTIDLGGVFESTVVRESVVAKVKDAMEKFGFFQAINHGVPLDVMEKMINGIRRFHDQDPEVRKMFYTRDKTKKLKYHSNADLYESPAASWRDTLSCVMAPDVPKAQDLPEVCGEIMLEYSKEVMKLAELMFEILSEALGLSPNHLKEMDCAKGLWMLCHCFPPCPEPNRTFGGAQHTDRSFLTILLNDNNGGLQVLYDGYWIDVPPNPEALIFNVGDFLQLISNDKFVSMEHRILANGGEEPRISVACFFVHTFTSPSSRVYGPIKELLSELNPPKYRDTTSESSNHYVARKPNGNSSLDHLRI', '359', 'EC 1.14.-.-', '', '', 'Arabidopsis thaliana contain three different patterns of 2-hydroxybut-3-enyl GSL accumulation (present in leaves and seeds; seeds only; or absent) corresponding to three different alleles at a single locus GSL-OH. Fine-scale mapping of the GSL-OH locus identified a 2-oxoacid-dependent dioxygenase encoded by At2g25450 required for the formation of both 2R- and 2S-2-hydroxybut-3-enyl GSL from the precursor 3-butenyl GSL precursor. Naturally occurring null mutations and T-DNA insertional mutations in At2g25450 exhibit a complete absence of 2-hydroxybut-3-enyl GSL accumulation. Analysis of herbivory by the generalist lepidopteran Trichoplusia ni showed that production of 2-hydroxybut-3-enyl GSL provides increased resistance. These results show that At2g25450 is necessary for the hydroxylation of but-3-enyl GSL to 2-hydroxybut-3-enyl GSL in planta and that this metabolite increases resistance to generalist herbivory (Hansen et al. 2008)', 'GSL side chain modification', 'Hansen et al. 2008  '),
	('AT2G29090', 'CYP707A2', 'Abscisic acid 8\'-hydroxylase 2', 'T9I4.17', '817457', 'NM_128466', 'NP_180473', 'O81077', 'MQISSSSSSNFFSSLYADEPALITLTIVVVVVVLLFKWWLHWKEQRLRLPPGSMGLPYIGETLRLYTENPNSFFATRQNKYGDIFKTHILGCPCVMISSPEAARMVLVSKAHLFKPTYPPSKERMIGPEALFFHQGPYHSTLKRLVQSSFMPSALRPTVSHIELLVLQTLSSWTSQKSINTLEYMKRYAFDVAIMSAFGDKEEPTTIDVIKLLYQRLERGYNSMPLDLPGTLFHKSMKARIELSEELRKVIEKRRENGREEGGLLGVLLGAKDQKRNGLSDSQIADNIIGVIFAATDTTASVLTWLLKYLHDHPNLLQEVSREQFSIRQKIKKENRRISWEDTRKMPLTTRVIQETLRAASVLSFTFREAVQDVEYDGYLIPKGWKVLPLFRRIHHSSEFFPDPEKFDPSRFEVAPKPYTYMPFGNGVHSCPGSELAKLEMLILLHHLTTSFRWEVIGDEEGIQYGPFPVPKKGLPIRVTPI', '482', 'EC 1.14.13.93', '', '', 'Camalexin originates from tryptophan and its biosynthesis involves the cytochrome P450 enzymes CYP79B2 and CYP71B15 (PAD3). Camalexin induction is a complex process, for which triggering by reactive oxygen species (ROS), salicylic acid signalling, and the glutathione status are important. Targets of the signalling cascade are the tryptophan and camalexin biosynthetic genes, which are strongly transcriptionally upregulated at the sites of pathogen infection (Glawischnig et al. 2004) .', 'Camalexin biosynthesis', 'Glawischnig et al. 2004'),
	('AT2G30750', 'CYP71A12', 'Cytochrome P450 71A12', 'T11J7.14', '817626', 'NM_128628', 'NP_180633', 'O49340', 'MSNIQEMEMILMVSLCLTTLITLFLLKQFLKRTANKVNLPPSPWRLPLIGNLHQLSLHPHRSLHSLSLRYGPLMLLHFGRVPILVVSSGEAAQEVLKTHDLKFANRPRSKAVHGLMNGGRDVVFGPYGEYWRQMKSVCILNLLTNKMVASFEKIREEELNEMIKKLEKASSSSSSENLSELFVTLPSDVTSRIALGRKHSEDETARDLKKRVRQIMELLGEFPIGDYVPALAWIDRINGFNARIKEVSQGFSDLMDKVVQEHLEAGNHKEDFVDILLSIESEKSIGFQAQRDDIKFMILDMFIGGTSTSSTLLEWIMTELIRNPNVMKKLQDEIRSTIRPHGSYIKEKDVENMKYLKAVIKEVFRVHPPLPLILPRLLSEDVKVKGYNIAAGTEVIINAWAIQRDPAIWGPDAEEFKPERHLDSTLDYHGKDLNFIPFGSGRRICPGINLALGLVEVTVANLVGRFDWRAEAGPNGDQPDLTEAFGLDVCRKFPLIAFPSSVI', '497', 'EC 1.14.-.-', 'AraCyc', '', 'Camalexin biosynthesis was induced in infected roots of both Col-0 (susceptible) and Bur-0 (partially resistant) accessions during the secondary phase of infection. However, the level of accumulation was four-to-seven times higher in Bur-0 than Col-0. This was associated with the enhanced transcription of a set of camalexin biosynthetic P450 genes in Bur-0: CYP71A13, CYP71A12, and CYP79B2 (Lemari? et al 2015)', 'Camalexin biosynthesis', 'Lemari? et al. 2015; Wang et al. 2012; Saga et al. 2012; Nafisi et al. 2007; Glawischnig et al. 2004; M?ller et al. 2015; M?ldrup?et al. 2013'),
	('AT2G30770', 'CYP71A13', 'Indoleacetaldoxime dehydratase', 'T11J7.16', '817628', 'NM_128630', 'NP_180635', 'O49342', 'MSNIQEMEMILSISLCLTTLITLLLLRRFLKRTATKVNLPPSPWRLPVIGNLHQLSLHPHRSLRSLSLRYGPLMLLHFGRVPILVVSSGEAAQEVLKTHDHKFANRPRSKAVHGLMNGGRDVVFAPYGEYWRQMKSVCILNLLTNKMVESFEKVREDEVNAMIEKLEKASSSSSSENLSELFITLPSDVTSRVALGRKHSEDETARDLKKRVRQIMELLGEFPIGEYVPILAWIDGIRGFNNKIKEVSRGFSDLMDKVVQEHLEASNDKADFVDILLSIEKDKNSGFQVQRNDIKFMILDMFIGGTSTTSTLLEWTMTELIRSPKSMKKLQDEIRSTIRPHGSYIKEKEVENMKYLKAVIKEVLRLHPSLPMILPRLLSEDVKVKGYNIAAGTEVIINAWAIQRDTAIWGPDAEEFKPERHLDSGLDYHGKNLNYIPFGSGRRICPGINLALGLAEVTVANLVGRFDWRVEAGPNGDQPDLTEAIGIDVCRKFPLIAFPSSVV', '497', 'EC 4.99.1.6', 'AraCyc', '', 'Camalexin biosynthesis was induced in infected roots of both Col-0 (susceptible) and Bur-0 (partially resistant) accessions during the secondary phase of infection. However, the level of accumulation was four-to-seven times higher in Bur-0 than Col-0. This was associated with the enhanced transcription of a set of camalexin biosynthetic P450 genes in Bur-0: CYP71A13, CYP71A12, and CYP79B2 (Lemari? et al 2015)', 'Camalexin biosynthesis', 'Lemari? et al. 2015; Frerigmann et al. 2015; Wang et al. 2012; Saga et al. 2012; Su et al. 2011; Stefanato et al. 2009; B?ttcher et al. 2009; Nafisi et al. 2007; M?ller et al. 2015; Klein et al. 2013; M?ldrup?et al. 2013; Xu et al. 2008;'),
	('AT2G30860', 'GSTF9', 'Glutathione S-transferase F9 ', 'ATGSTF9', '817636', 'NM_128638', 'NP_180643', 'O80852', 'MVLKVYGPHFASPKRALVTLIEKGVAFETIPVDLMKGEHKQPAYLALQPFGTVPAVVDGDYKIFESRAVMRYVAEKYRSQGPDLLGKTVEDRGQVEQWLDVEATTYHPPLLNLTLHIMFASVMGFPSDEKLIKESEEKLAGVLDVYEAHLSKSKYLAGDFVSLADLAHLPFTDYLVGPIGKAYMIKDRKHVSAWWDDISSRPAWKETVAKYSFPA', '215', 'EC 2.5.1.18', '', '', 'An analysis of candidate genes for QTL-controlling GSL networks of transcripts and metabolites suggested that the controlling factors are a mix of enzymes and regulatory factors that include GSTF9 and GSTF10 (Wentzell et al. 2007)', 'GSL core structure synthesis', 'Wentzell et al. 2007  '),
	('AT2G30870', 'GSTF10', 'Glutathione S-transferase F10 ', 'ATGSTF10', '817637', 'NM_128639', 'NP_180644', 'P42761', 'MVLTIYAPLFASSKRAVVTLVEKGVSFETVNVDLMKGEQRQPEYLAIQPFGKIPVLVDGDYKIFESRAIMRYIAEKYRSQGPDLLGKTIEERGQVEQWLDVEATSYHPPLLALTLNIVFAPLMGFPADEKVIKESEEKLAEVLDVYEAQLSKNEYLAGDFVSLADLAHLPFTEYLVGPIGKAHLIKDRKHVSAWWDKISSRAAWKEVSAKYSLPV', '215', '', '', '', 'An analysis of candidate genes for QTL-controlling GSL networks of transcripts and metabolites suggested that the controlling factors are a mix of enzymes and regulatory factors that include GSTF9 and GSTF10 (Wentzell et al. 2007)', 'GSL core structure synthesis', 'Wentzell et al. 2007  '),
	('AT2G31790', 'UGT74C1', 'UDP-glycosyltransferase 74C1 ', '', '817736', 'NM_128737', 'NP_180738', 'Q9SKC1', 'MSEAKKGHVLFFPYPLQGHINPMIQLAKRLSKKGITSTLIIASKDHREPYTSDDYSITVHTIHDGFFPHEHPHAKFVDLDRFHNSTSRSLTDFISSAKLSDNPPKALIYDPFMPFALDIAKDLDLYVVAYFTQPWLASLVYYHINEGTYDVPVDRHENPTLASFPGFPLLSQDDLPSFACEKGSYPLLHEFVVRQFSNLLQADCILCNTFDQLEPKVVKWMNDQWPVKNIGPVVPSKFLDNRLPEDKDYELENSKTEPDESVLKWLGNRPAKSVVYVAFGTLVALSEKQMKEIAMAISQTGYHFLWSVRESERSKLPSGFIEEAEEKDSGLVAKWVPQLEVLAHESIGCFVSHCGWNSTLEALCLGVPMVGVPQWTDQPTNAKFIEDVWKIGVRVRTDGEGLSSKEEIARCIVEVMEGERGKEIRKNVEKLKVLAREAISEGGSSDKKIDEFVALLT', '457', 'EC 2.4.1.-', '', '', 'UGT74C1 complement phenotypes and chemotypes of the ugt74b1-2 knockout mutant and was able to express thiohydroximate UGT activity in planta provides conclusive evidence for UGT74C1 being an accessory enzyme in GSL biosynthesis with a potential function during plant adaptation to environmental challenge (Grubb et al. 2014)', 'GSL core structure synthesis', 'Gachon et al. 2005'),
	('AT2G33070', 'NSP2', 'Nitrile-specifier protein 2 ', 'JAL21', '817869', 'NM_128867', 'NP_180866', 'O49326', 'MVQKVEARGGEIGDVWDDGAYDGVRKVYVGQGEDGIAFVKFEYVNGSQEVVGDERGKKTLLGAEEFEVDPDDYIVYVEGYHEKVFGVTTKEIISTLTFKTYKGKTSPPFGIVSGTKFVLQGGKIVGFHGRSTDVLHSLGAYISSPATPKLRGKWIKVVVEQKGEGPGPRCSHDIAQVGNKIFSFGGELTPNQPIDKHLYVFDLETRTWSISPATGDVPNLSCLGVRMVSIGSSLYVFGGRDASRKYNGFYSFDTTKNEWKLLTPVEQGPTPRSFHSMTADENNVYVFGGVSATVRLKTLDAYNIVDHKWVQCSTPGGSCSVRGGAGLEVVQGKVWVVYGFNGCEVDDVHCYDPAQDKWTQVETFGEKPCARSVFASAVVGKHILVFGGEIAMDPKAHEGPGQLSGGTFALDTETLKWEKLDKLGEEEETPSIRGWSASTTGTIDGKKGLVMFGGKAQTNDRFGDLFFYGVDSA', '471', '', '', '', 'Nitrile formation by NSP2 is evident from GSL hydrolysis product profiles in homogenates of Arabidopsis expressing NSP2 under control of the CaMV35S-promoter (Kissen & Bones 2009)', 'GSL degradation', 'Kissen & Bones 2009; Wittstock & Burow 2010; Wittstock et al. 2016 '),
	('AT2G36380?', 'ABCG34', 'ABC transporter G family member 34', 'PDR6', '818211', 'NM_129195', 'NP_181179', 'Q7PC87', 'MLGRDEDLVRTMSGRGSLGSTSHRSLAGAASKSFRDVFAPPTDDVFGRSDRREEDDVELR\nWAALERLPTYDRLRKGMLPQTMVNGKIGLEDVDVTNLAPKEKKHLMEMILKFVEEDNEKF\nLRRLRERTDRVGIEVPKIEVRYENLSVEGDVRSASRALPTLFNVTLNTIESILGLFHLLP\nSKKRKIEILKDISGIIKPSRMTLLLGPPSSGKTTLLQALAGKLDDTLQMSGRITYCGHEF\nREFVPQKTCAYISQHDLHFGEMTVRESLDFSGRCLGVGTRYQLLTELSRREREAGIKPDP\nEIDAFMKSIAISGQETSLVTDYVLKLLGLDICADTLVGDVMRRGISGGQRKRLTTGEMLV\nGPATALFMDEISTGLDSSTTFQICKFMRQLVHIADVTMVISLLQPAPETFELFDDIILLS\nEGQIVYQGSRDNVLEFFEYMGFKCPERKGIADFLQEVTSKKDQEQYWNRREHPYSYVSVH\nDFSSGFNSFHAGQQLASEFRVPYDKAKTHPAALVTQKYGISNKDLFKACFDREWLLMKRN\nSFVYVFKTVQITIMSLIAMTVYFRTEMHVGTVQDGQKFYGALFFSLINLMFNGMAELAFT\nVMRLPVFFKQRDFLFYPPWAFALPGFLLKIPLSLIESVIWIALTYYTIGFAPSAARFFRQ\nLLAYFCVNQMALSLFRFLGALGRTEVIANSGGTLALLVVFVLGGFIISKDDIPSWLTWCY\nYTSPMMYGQTALVINEFLDERWGSPNNDTRINAKTVGEVLLKSRGFFTEPYWFWICIGAL\nLGFTVLFNFCYIIALMYLNPLGNSKATTVVEEGKDKHKGSHSGTGGSVVELTSTSSHGPK\nKGMVLPFQPLSLAFNNVNYYVDMPAEMKAQGVEGDRLQLLRDVGGAFRPGVLTALVGVSG\nAGKTTLMDVLAGRKTGGYVEGSINISGYPKNQATFARVSGYCEQNDIHSPHVTVYESLIY\nSAWLRLSADIDTKTREMFVEEVMELVELKPLRNSIVGLPGVDGLSTEQRKRLTIAVELVA\nNPSIIFMDEPTSGLDARAAAIVMRTVRNTVDTGRTVVCTIHQPSIDIFESFDELLLMKRG\nGQVIYAGTLGHHSQKLVEYFEAIEGVPKIKDGYNPATWMLDVTTPSMESQMSVDFAQIFV\nNSSVNRRNQELIKELSTPPPGSNDLYFRTKYAQPFSTQTKACFWKMYWSNWRYPQYNAIR\nFLMTVVIGVLFGLLFWQTGTKIEKEQDLNNFFGAMYAAVLFLGATNAATVQPAVAIERTV\nFYREKAAGMYSAIPYAISQVAVEIMYNTIQTGVYTLILYSMIGYDWTVVKFFWFYYYMLT\nCFVYFTLYGMMLVALTPNYQIAGICLSFFLSFWNLFSGFLIPRPQIPIWWRWYYWASPVA\nWTLYGIITSQVGDRDSIVHITGVGDMSLKTLLKNGFGFDYDFLPVVAVVHIAWILIFLFA\nFAYGIKFLNFQRR', '1453', '', '', '', 'Mediates the secretion of camalexin from the epidermal cells to the surface of leaves and thereby confers resistance to?A.?brassicicola?infection (Khare et al. 2017)', 'Camalexin biosynthesis', 'Khare et al. 2017'),
	('AT2G38470', 'WRKY33', 'Probable WRKY transcription factor 33', 'T19C21.4', '818429', 'NM_129404', 'NP_181381', 'Q8S8P5', 'MAASFLTMDNSRTRQNMNGSANWSQQSGRTSTSSLEDLEIPKFRSFAPSSISISPSLVSPSTCFSPSLFLDSPAFVSSSANVLASPTTGALITNVTNQKGINEGDKSNNNNFNLFDFSFHTQSSGVSAPTTTTTTTTTTTTTNSSIFQSQEQQKKNQSEQWSQTETRPNNQAVSYNGREQRKGEDGYNWRKYGQKQVKGSENPRSYYKCTFPNCPTKKKVERSLEGQITEIVYKGSHNHPKPQSTRRSSSSSSTFHSAVYNASLDHNRQASSDQPNSNNSFHQSDSFGMQQEDNTTSDSVGDDEFEQGSSIVSRDEEDCGSEPEAKRWKGDNETNGGNGGGSKTVREPRIVVQTTSDIDILDDGYRWRKYGQKVVKGNPNPRSYYKCTTIGCPVRKHVERASHDMRAVITTYEGKHNHDVPAARGSGYATNRAPQDSSSVPIRPAAIAGHSNYTTSSQAPYTLQMLHNNNTNTGPFGYAMNNNNNNSNLQTQQNFVGGGFSRAKEEPNEETSFFDSFMP', '519', '', '', '', 'Decreasing camalexin levels by mutation of the camalexin synthetase gene?PAD3?or the camalexin synthesis regulator?AtWRKY33?compromised the powdery mildew resistance in these mutants (Liu et al. 2016)', 'Camalexin biosynthesis', 'Liu et al. 2016'),
	('AT2G39940', 'COI1', 'Coronatine-insensitive protein 1', 'FBL2', '818581', 'NM_129552', 'NP_565919', 'O04197', 'MEDPDIKRCKLSCVATVDDVIEQVMTYITDPKDRDSASLVCRRWFKIDSETREHVTMALCYTATPDRLSRRFPNLRSLKLKGKPRAAMFNLIPENWGGYVTPWVTEISNNLRQLKSVHFRRMIVSDLDLDRLAKARADDLETLKLDKCSGFTTDGLLSIVTHCRKIKTLLMEESSFSEKDGKWLHELAQHNTSLEVLNFYMTEFAKISPKDLETIARNCRSLVSVKVGDFEILELVGFFKAAANLEEFCGGSLNEDIGMPEKYMNLVFPRKLCRLGLSYMGPNEMPILFPFAAQIRKLDLLYALLETEDHCTLIQKCPNLEVLETRNVIGDRGLEVLAQYCKQLKRLRIERGADEQGMEDEEGLVSQRGLIALAQGCQELEYMAVYVSDITNESLESIGTYLKNLCDFRLVLLDREERITDLPLDNGVRSLLIGCKKLRRFAFYLRQGGLTDLGLSYIGQYSPNVRWMLLGYVGESDEGLMEFSRGCPNLQKLEMRGCCFSERAIAAAVTKLPSLRYLWVQGYRASMTGQDLMQMARPYWNIELIPSRRVPEVNQQGEIREMEHPAHILAYYSLAGQRTDCPTTVRVLKEPI', '592', '', '', '', 'FMO convert 4-methylthioalkyl to 4-meth-ylsulfinylalkyl GSLs and is pathogen-induced independent of COI1. Simultaneous induction of methionine, tryptophan,camalexin, and GSL biosynthetic genes provided evidence for coordinated regulation of primary and secondary metabolism (Stotz et al. 2011)', 'GSL side chain modification / Camalexin biosynthesis', 'Stotz et al. 2011'),
	('AT2G43000', 'JUB1', 'Transcription factor JUNGBRUNNEN 1', 'NAC042', '818902', 'NM_129861', 'NP_181828', 'Q9SK55', 'MSGEGNLGKDHEEENEAPLPGFRFHPTDEELLGYYLRRKVENKTIKLELIKQIDIYKYDPWDLPRVSSVGEKEWYFFCMRGRKYRNSVRPNRVTGSGFWKATGIDKPVYSNLDCVGLKKSLVYYLGSAGKGTKTDWMMHEFRLPSTTKTDSPAQQAEVWTLCRIFKRVTSQRNPTILPPNRKPVITLTDTCSKTSSLDSDHTSHRTVDSMSHEPPLPQPQNPYWNQHIVGFNQPTYTGNDNNLLMSFWNGNGGDFIGDSASWDELRSVIDGNTKP', '275', '', '', '', 'ANAC042, a member of the NAM, ATAF1/2, and CUC2 (NAC) transcription factor family genes, is involved in camalexin biosynthesis induction. ANAC042 as a key transcription factor involved in previously unknown regulatory mechanisms to induce phytoalexin biosynthesis in Arabidopsis (Saga et al. 2012)', 'Camalexin biosynthesis', 'Saga et al. 2012'),
	('AT2G43100', 'IPMI2', '3-isopropylmalate dehydratase small subunit 1 ', 'ATLEUD1', '818912', 'NM_129871', 'NP_181838', 'Q9ZW84', 'MAYSLPTFPQALPCSSTKTSSSLATFRSPFLRFNGSTSLIPSSISITSRGTSSPTIIPRAAASESDSNEALANTTFHGLCYVLKDNIDTDQIIPAGAACTFPSNQQERDEIAAHALSGLPDFHKTRFIEPGENRSKYSIIIGGENFGCGSSREHAPVCLGAAGAKAIVAESYARIFFRNSVATGEVFPLESEVRVCEECKTGDTVTIELSDSGGLLTNHTTGKNYKLKSIGDAGPVIDAGGIFAYARMMGMIPSLA', '256', 'EC 4.2.1.33', 'AraCyc', '', 'Two isopropylmalate isomerases genes; IPMI1 and IPMI2 and the isopropylmalate dehydrogenase gene; IPMDH1 were identified as targets of HAG1/MYB28 and the corresponding proteins localized to plastids suggesting a role in plastidic chain elongation reactions (Gigolashvili et al. 2009)', 'GSL side chain elongation', 'Beekwilder et al. 2008; 23; He et al. 2010; Sawada& Kuwahara et al. 2009  '),
	('AT2G43790', 'MPK6', 'Mitogen-activated protein kinase 6', 'F18O19.10', '818982', 'NM_129941', 'NP_181907', 'Q39026', 'MDGGSGQPAADTEMTEAPGGFPAAAPSPQMPGIENIPATLSHGGRFIQYNIFGNIFEVTAKYKPPIMPIGKGAYGIVCSAMNSETNESVAIKKIANAFDNKIDAKRTLREIKLLRHMDHENIVAIRDIIPPPLRNAFNDVYIAYELMDTDLHQIIRSNQALSEEHCQYFLYQILRGLKYIHSANVLHRDLKPSNLLLNANCDLKICDFGLARVTSESDFMTEYVVTRWYRAPELLLNSSDYTAAIDVWSVGCIFMELMDRKPLFPGRDHVHQLRLLMELIGTPSEEELEFLNENAKRYIRQLPPYPRQSITDKFPTVHPLAIDLIEKMLTFDPRRRITVLDALAHPYLNSLHDISDEPECTIPFNFDFENHALSEEQMKELIYREALAFNPEYQQ', '395', 'EC 2.7.11.24', '', '', 'MKK9, an MKK, is an upstream activator of the MPKs MPK3 and MPK6 both in vitro and in planta. Expression of active MKK9 protein in transgenic plants induces the synthesis of ethylene and camalexin through the activation of the endogenous MPK3 and MPK6 kinases. MKK9-MPK3/MPK6 cascade participates in the regulation of the biosynthesis of ethylene and camalexin and may be an important axis in the stress responses of Arabidopsis (Xu et al. 2008).', 'Camalexin biosynthesis', 'Xu et al. 2008'),
	('AT2G44490', 'PEN2', 'Beta-glucosidase 26 peroxisomal ', 'BGLU26', '819056', 'NM_130012', 'NP_181977', 'O64883', 'MAHLQRTFPTEMSKGRASFPKGFLFGTASSSYQYEGAVNEGARGQSVWDHFSNRFPHRISDSSDGNVAVDFYHRYKEDIKRMKDINMDSFRLSIAWPRVLPYGKRDRGVSEEGIKFYNDVIDELLANEITPLVTIFHWDIPQDLEDEYGGFLSEQIIDDFRDYASLCFERFGDRVSLWCTMNEPWVYSVAGYDTGRKAPGRCSKYVNGASVAGMSGYEAYIVSHNMLLAHAEAVEVFRKCDHIKNGQIGIAHNPLWYEPYDPSDPDDVEGCNRAMDFMLGWHQHPTACGDYPETMKKSVGDRLPSFTPEQSKKLIGSCDYVGINYYSSLFVKSIKHVDPTQPTWRTDQGVDWMKTNIDGKQIAKQGGSEWSFTYPTGLRNILKYVKKTYGNPPILITENGYGEVAEQSQSLYMYNPSIDTERLEYIEGHIHAIHQAIHEDGVRVEGYYVWSLLDNFEWNSGYGVRYGLYYIDYKDGLRRYPKMSALWLKEFLRFDQEDDSSTSKKEEKKESYGKQLLHSVQDSQFVHSIKDSGALPAVLGSLFVVSATVGTSLFFKGANN', '560', 'EC 3.2.1.21', '', '', 'The Arabidopsis CYP81F2 gene encodes a P450 monooxygenase that is essential for the pathogen-induced accumulation of 4-methoxyindol-3-ylmethylGSL which in turn is activated by the atypical PEN2 myrosinase (a type of b-thioglucoside glucohydrolase) for antifungal defense (Bednarek et al. 2009)', 'GSL degradation / Camalexin biosynthesis', 'Bednarek et al. 2009;  Zhao et al. 2015; Cargnel et al. 2014'),
	('AT2G45970', 'CYP86A8', 'Cytochrome P450 86A8', 'LCR', '819205', 'NM_130160', 'NP_182121', 'O80823', 'MEISTALMILSAITAYFLWLTFISRCLKGPRVWPILGSLPGLIENCERMHDWISDNLRACSGTYQTCICAIPFLAKKQGLVTVTCDPRNLEHILKNRFDNYPKGPTWQAVFHDLLGQGIFNSDGDTWLFQRKTAALEFTTRTLRQAMARWVNRAIKLRFLPILENARLGSEPIDLQDLLLRLTFDNICGLTFGKDPRTCAPGLPVNTFAVAFDRATEASLQRFILPEILWKFKRWLRLGLEVSLTRSLVQVDNYLSEIITTRKEEMMTQHNNGKHHDDLLSRFIKKKESYSDETLQRVALNFILAGRDTSSVALSWFFWLITQHPAIEDKILREICTVLVETRGDDVALWTDEPLSCEELDRLVFLKAALSETLRLYPSVPEDSKRAVKDDVLPDGTFVPAGSSITYSIYSAGRMKSTWGEDCLEFKPERWISQSDGGRFINHDPFKFVAFNAGPRICLGKDLAYLQMKSIASAVLLRHRLTVVTGHKVEQKMSLTLFMKYGLLVNVHERDLTAIAADLRECKSNVVNDGVGNGVSS', '537', 'EC 1.14.14.1', '', '', 'Camalexin originates from tryptophan and its biosynthesis involves the cytochrome P450 enzymes CYP79B2 and CYP71B15 (PAD3). Camalexin induction is a complex process, for which triggering by reactive oxygen species (ROS), salicylic acid signalling, and the glutathione status are important. Targets of the signalling cascade are the tryptophan and camalexin biosynthetic genes, which are strongly transcriptionally upregulated at the sites of pathogen infection (Glawischnig et al. 2004) .', 'Camalexin biosynthesis', 'Glawischnig et al. 2004'),
	('AT2G46070', 'MPK12', 'Mitogen-activated protein kinase 12', 'T3F17.28', '819215', 'NM_130170', 'NP_182131', 'Q8GYQ5', 'MSGESSSGSTEHCIKVVPTHGGRYVQYNVYGQLFEVSRKYVPPIRPIGRGACGIVCAAVNSVTGEKVAIKKIGNAFDNIIDAKRTLREIKLLRHMDHENVITIKDIVRPPQRDIFNDVYIVYELMDTDLQRILRSNQTLTSDQCRFLVYQLLRGLKYVHSANILHRDLRPSNVLLNSKNELKIGDFGLARTTSDTDFMTEYVVTRWYRAPELLLNCSEYTAAIDIWSVGCILGEIMTGQPLFPGKDYVHQLRLITELVGSPDNSSLGFLRSDNARRYVRQLPRYPKQQFAARFPKMPTTAIDLLERMLVFDPNRRISDLHVLCV', '372', 'EC 2.7.11.24', '', '', 'MKK9, an MKK, is an upstream activator of the MPKs MPK3 and MPK6 both in vitro and in planta. Expression of active MKK9 protein in transgenic plants induces the synthesis of ethylene and camalexin through the activation of the endogenous MPK3 and MPK6 kinases. MKK9-MPK3/MPK6 cascade participates in the regulation of the biosynthesis of ethylene and camalexin and may be an important axis in the stress responses of Arabidopsis (Xu et al. 2008).', 'Camalexin biosynthesis', 'Xu et al. 2008'),
	('AT2G46370', 'JAR1', 'Jasmonic acid-amido synthetase JAR1', 'FIN219', '819244', 'NM_130200', 'NP_566071', 'Q9SKE2', 'MVDGDTSPILTGHPVPAISLSSGTSQGRPKFIPFTDELMENTLQLFRTAFAFRNRDFPIDDNGKALQFIFSSKQYISTGGVPVGTATTNVYRNPNFKAGMKSITSPSCSPDEVIFSPDVHQALYCHLLSGILFRDQVQYVFAVFAHGLVHAFRTFEQVWEEIVTDIKDGVLSNRITVPSVRTAMSKLLTPNPELAETIRTKCMSLSNWYGLIPALFPNAKYVYGIMTGSMEPYVPKLRHYAGDLPLVSHDYGSSEGWIAANVTPRLSPEEATFAVIPNLGYFEFLPVSETGEGEEKPVGLTQVKIGEEYEVVITNYAGLYRYRLGDVVKVIGFYNNTPQLKFICRRNLILSINIDKNTERDLQLSVESAAKRLSEEKIEVIDFSSYIDVSTDPGHYAIFWEISGETNEDVLQDCCNCLDRAFIDAGYVSSRKCKTIGALELRVVAKGTFRKIQEHFLGLGSSAGQFKMPRCVKPSNAKVLQILCENVVSSYFSTAF', '575', 'EC 6.3.2.-', '', '', 'The rate of development of B. cinerea disease symptoms on primary infected leaves was affected by responses mediated by the genes EIN2, JAR1, EDS4, PAD2, and PAD3, but was largely independent of EDS5, SID2/ICS1, and PAD4. a double ein2 npr1 mutant was significantly more susceptible than ein2 plants, and exogenous application of SA decreased B. cinerea lesion size through an NPR1-dependent mechanism that could be mimicked by the cpr1 mutation. These data indicate that local resistance to B. cinerea requires ethylene-, jasmonate-, and SA-mediated signaling, that the SA affecting this resistance does not require ICS1 and is likely synthesized via PAL, and that camalexin limits lesion development (Ferrari et al. 2003)', 'Camalexin biosynthesis', 'Ferrari et al. 2003'),
	('AT2G46650', 'CYTB5-C', 'Cytochrome B5 isoform C', 'CB5-C', '819277', 'NM_130230', 'NP_182188', 'Q9ZNV4', 'MANLISFHDVAKHKCKNDCWILIHGKVYDISTFMDEHPGGDNVLLAVTGKDASIDFEDVNHSKDAKELMKKYCIGDVDQSTVPVTQQYIPPWEKESTAAETTKEESGKKLLIYLIPLLILGVAFALRFYNNK', '132', '', '', '', 'The roles of the many CB5 isoforms in plants remain unknown. CB5 proteins was predicted to support the cytochrome P450 enzymes of plant specialized metabolism and found CB5C from Arabidopsis thaliana to co-express with GSL biosynthetic genes. GSL profiles of 2 T-DNA insertion mutants of CB5C were characterized and found that long-chained aliphatic glucosinolates were reduced in one of the mutant lines ? a phenotype that was exaggerated upon methyl-jasmonate treatment. These results support the hypothesis that CB5C influences glucosinolate biosynthesis however; the mode of action remains unknown (Vik et al. 2016)', 'GSL core structure synthesis', 'Vik et al. 2016'),
	('AT3G03190', 'GSTF11', 'Glutathione S-transferase F11 ', 'ATGSTF11', '821227', 'NM_111189', 'NP_186969', 'Q96324', 'MVVKVYGQIKAANPQRVLLCFLEKDIEFEVIHVDLDKLEQKKPQHLLRQPFGQVPAIEDGYLKLFESRAIARYYATKYADQGTDLLGKTLEGRAIVDQWVEVENNYFYAVALPLVMNVVFKPKSGKPCDVALVEELKVKFDKVLDVYENRLATNRYLGGDEFTLADLSHMPGMRYIMNETSLSGLVTSRENLNRWWNEISARPAWKKLMELAAY', '214', 'EC 2.5.1.18', '', '', 'GST-type enzymes may be involved in an enzyme complex formed by CYP83s and C-S lyase. The S-alkylthiohydroximate formed after CYP83-catalyzed aldoxime oxidation and spontaneous conjugation to cysteine is cyclized in vitro to form a dead-end product. Hence metabolic channeling aided by GST-type enzymes is postulated in vivo to avoid this consequence the dead-end product. The two putative GST genes (At3g03190 and At1g78370) could be candidates coding for such an activity (Hirai et al. 2005)', 'GSL core structure synthesis', 'Hirai et al. 2005; Hirai et al. 2007; Wentzell et al. 2007  '),
	('AT3G09710', 'IQD1', 'Protein IQ-DOMAIN 1', 'F11F8.30', '820128', 'NM_111805', 'NP_187582', 'Q9SF32', 'MVKKAKWLKNVKKAFSPDSKKLKHESVECQDSVISYPVLIATSRSSSPQFEVRVDEVNYEQKKNLYPPSSDSVTATVAHVLVDSPPSSPESVHQAIVVNRFAGKSKEEAAAILIQSTFRGHLARRESQVMRGQERLKLLMEGSVVQRQAAITLKCMQTLSRVQSQIRSRRIRMSEENQARHKQLLQKHAKELGGLKNGGNWNYSNQSKEQVEAGMLHKYEATMRRERALAYAFTHQQNLKSFSKTANPMFMDPSNPTWGWSWLERWMAGRPWESSEKEQNTTNNDNSSVKNSTNRNSQGGETAKSSNRNKLNSSTKPNTPSASSTATRNPRKKRPIPSSIKSKSSDDEAKSSERNRRPSIARPSVSDDETLSSSTARRSSNLIPTTKSARGKPKSQTSSRVAVTTSTTEESSILPEKAPAKKRLSTSASPAPKPRRSSAPPKVEKGVLKAERTP', '454', '', '', '', 'Analysis of steady-state messenger RNA levels of GSL pathway genes indicates that IQD1 affects expression of multiple genes with roles in GSL metabolism. Histochemical analysis of tissue-specific IQD1::GUS expression reveals IQD1 promoter activity mainly in vascular tissues of all organs. consistent with the expression patterns of several GSL-related genes. Interestingly overexpression of IQD1 reduces insect herbivory which is demonstrated in dual-choice assays with the generalist phloem-feeding green peach aphid (Myzus persicae) and in weight-gain assays with the cabbage looper (Trichoplusia ni); a generalist-chewing lepidopteran (Levy et al. 2005)', 'GSL transcription factor', 'Laluk et al. 2012; Levy et al. 2005  '),
	('AT3G12203', 'SCPL17', 'Serine carboxypeptidase-like 17 ', 'F28J15.16', '820399', 'NM_112056', 'NP_187828', 'Q9C7D6', 'MGKECYYLSWILKFHLLLVLIQLVDSGSTIRFLPGFQGPLPFELETGYIGVGEAEKDQMFYYFIKSESNPEKDPLLLWLSGGPFCSSFTALIYENGPIAFKAEEYNGSIPSLVSTTYAWTKVASILYLDQPVGTGFSYSRNPLADIPSDTGVAKPVNEFLHKWLDKHPEFLSNPLYVAGNSYSGIVIPTIVQEISNGNHLDSKPQINLQGFVLGNPATDTDIDLNSRIPFAHGKALISDEHYESLKRSCQGNYISVNPRNTKCLKLLEDFKKCVSGISEEYILKPDCMWLYSCMANLHSLSEYWANEKSVRKALLVNEGTVRKWIRCNTEIAYNKDIRSSVPYHKYISIEGYRSLVFSGDHDMLVPFLGTQAWIRSLNYSIVDDWRPWMVQNQVAGYTRTYANKMTFATVKGGGHTSEYKPVETYIMIKRWLSGQPL', '437', 'EC 3.4.16.-', '', '', 'SCPL17 is the acyltransferase involved in transferring the benzoyl moiety from benzoylglucose (BG) to hydroxylated GSLs (OH-GSLs) (Lee et al. 2012)', 'GSL side chain modification', 'Lee et al. 2012; Zhang et al. 2015'),
	('AT3G14210', 'ESM1', 'GDSL esterase/lipase ESM1 ', 'MAG2.6', '820639', 'NM_112278', 'NP_188037', 'Q9LJG3', 'MADNLNLVSVLGVLLVLTIFHNPIIVYAGEGVPNVALFTFGDSYYDAGNKVFLSQRKDLPQTYWPYGKSRDYPNGKFSDGHIVPDFIADFISIPNGVLPPVLKPGVDISRGVSFAVADASILGAPVESMTLNQQVVKFKNMKSNWNDSYIEKSLFMIYIGTEDYLNFTKANPNADASAQQAFVTNVINRLKNDIKLLYSLGASKFVVQLLAPLGCLPIVRQEYKTGNECYELLNDLAKQHNGKIGPMLNEFAKISTSPYGFQFTVFDFYNAVLRRIATGRSLNYRFFVTNTSCCGVGTHNAYGCGKGNVHSKLCEYQRSYFFFDGRHNTEKAQEEMAHLLYGADPDVVQPMTVRELIVYPTGETMREYWEPNNLAIRRRPSRDFYLGLAAYY', '392', 'EC 3.1.1.-', '', '', 'Following tissue disruption; indol-3-acetonitrile (IACN) can be generated from indole GSLs through the action of ESP and myrosinase; and that its production is regulated by ESM1 (Burow et al. 2008)', 'GSL degradation', 'Burow et al. 2008  '),
	('AT3G16390', 'NSP3', 'Nitrile-specifier protein 3 ', 'JAL27', '820886', 'NM_112510', 'NP_566545', 'O04318', 'MAQKLVAQGGETGDVWDDGVYDNVTKVYVGQGQYGIAFVKFEYANGSEVVVGDEHGEKTELGVEEFEIDSDDYIVYVEGYREKVSDMTSEMITFLSFKTSKGKTSQPIVKKPGVKFVLHGGKIVGFHGRSTDVLHSLGAYVSLPSTPKLLGNWIKVEQNGEGPGLRCSHGIAQVGNKIYSFGGELIPNQPIDKHLYVFDLETRTWSIAPATGDVPHLSCLGVRMVSVGSTLYTFGGRDFSRQYNGFYSFDTTTNEWKLLTPVEEGPTPRSFHSMAADEENVYVFGGVGAMDRIKTLDSYNIVDKTWFHCSNPGDSFSIRGGAGLEVVQGKVWIVYGFNGCEVDDVHFYDPAEDKWTQVETFGVKPNERSVFASAAIGKHIVIFGGEIAMDPRAHVGPGQLIDGTFALDTETLQWERLDKFEGTPSSRGWTASTTGTIDGKKGLVMHGGKAPTNDRFDDLFFYGIDSV', '467', '', '', '', 'Besides NSP2; 3-butenylnitrile was also detected upon incubation with NSP1 and NSP3 showing that these proteins also possess nitrile-specifier activity (Kissen & Bones 2009)', 'GSL degradation', 'Kissen & Bones 2009'),
	('AT3G16400', 'NSP1', 'Nitrile-specifier protein 1 ', 'JAL28', '820887', 'NM_112511', 'NP_566546', 'Q9SDM9', 'MAQKLEAKGGEMGDVWDDGVYENVRKVYVGQAQYGIAFVKFEYVNGSQVVVGDEHGKKTELGVEEFEIDADDYIVYVEGYREKVNDMTSEMITFLSIKTFKGKTSHPIEKRPGVKFVLHGGKIVGFHGRSTDVLHSLGAYVSLSSTIKLLGKWIKVEQKGEGPGLRCSHGIAQVGNKIYSFGGEFTPNQPIDKHLYVFDLETRTWSISPATGDVPHLSCLGVRMVSVGSTLYVFGGRDASRQYNGFYSFDTTTNEWKLLTPVEEGPTPRSFHSMAADEENVYVFGGVSATARLNTLDSYNIVDKKWFHCSTPGDSLTARGGAGLEVVQGKVWVVYGFNGCEVDDVHYYDPVQDKWTQVETFGVRPSERSVFASAAIGKHIVIFGGEIAMDPLAHVGPGQLTDGTFALDTETLQWERLDKFGGEEETPSSRGWTASTTATIDGKKGLVMHGGKAPTNDRFDDLFFYGIDSA', '470', '', '', '', 'Product formation by ESP and NSP1 from different GSLs as substrates for myrosinase has been analyzed using purified proteins expressed in E. coli (Burow et al. 2008)', 'GSL degradation', 'Burow et al. 2008; Wittstock & Burow 2010; Wittstock et al. 2016 '),
	('AT3G16410', 'NSP4', 'Nitrile-specifier protein 4 ', 'JAL29', '820888', 'NM_112512', 'NP_188262', 'O04316', 'MAQKVEAQGGNGGNQWDDGSEYDAVTKIQVAAGGNGIEYVKFTYVKNGQTEEAPLRGVKGRSFEADPFVINHPEEHLVSVEGRYNPEGLILGLTFKSNKKTSDLIGYEDGTPFTLQVQDKKIVGFYGFAGNNLHSLGAYFAPLTNVTPLNAKKLEAKGGDTGDIWDDGVYDNVRKVYVGQAQYGIAFVKFEYVNGSQVVVGDEHGKKTELGVEEFEIDADDYIVYVEGYREKVNGMTSEMITFLSFKTYKGKTSQPIEQRPGIKFVLQGGKIVGFHGRSTDVLDSLGAYISLSPTPNLHGKWTKVDENGDGPGLRCSHDIAQVGNKIYSFGGEFTPNQPIDKHLYVFDIESRTWSISPATGDIPTLSCLGVCMVSIGSTLYVFGGRDASRQYNGFYSFDTTTNEWKLLTPVEEGPTPRSFHSMAADEENVYVFGGVSATARLNTLDSYNIVDKKWFHCSTPGDSLTARGGAGLEVVQGKVWVVYGFNGCEVDDVHYYDPVQDKWTQVETFGVRPSERSVFASAALGKHIVIFGGEIAMDPLAHVGPGQLTDGTFALDTETLQWERLDKFGGEEETPSSRGWTASTTATIGGKKGLVMHGGKAPTNDRFDDLFFYGIDSA', '619', '', '', '', 'The seed content of the precursor GSL; 4-methylthiobutylGSL was consistently reduced in nsp3-2; nsp4-1 and nsp5-1 relative to WT (Wittstock et al. 2016)', 'GSL degradation', 'Wittstock & Burow 2010'),
	('AT3G19710', 'BCAT4', 'Methionine aminotransferase BCAT4 ', 'MMB12_16', '821508', 'NM_112861', 'NP_188605', 'Q9LE06', 'MAPSAQPLPVSVSDEKYANVKWEELAFKFVRTDYMYVAKCNHGESFQEGKILPFADLQLNPCAAVLQYGQGLYEGLKAYRTEDGRILLFRPDQNGLRLQAGADRLYMPYPSVDQFVSAIKQVALANKKWIPPPGKGTLYIRPILFGSGPILGSFPIPETTFTAFACPVGRYHKDNSGLNLKIEDQFRRAFPSGTGGVKSITNYCPVWIPLAEAKKQGFSDILFLDAATGKNIEELFAANVFMLKGNVVSTPTIAGTILPGVTRNCVMELCRDFGYQVEERTIPLVDFLDADEAFCTGTASIVTSIASVTFKDKKTGFKTGEETLAAKLYETLSDIQTGRVEDTKGWTVEIDRQG', '354', 'EC 2.6.1.88 ', 'AraCyc', 'KEGG', 'Recombinant BCAT4 showed high efficiency with Met and its derivatives and the corresponding 2-oxo acids suggesting its participation in the chain elongation pathway of Met-derived GSL biosynthesis. This was substantiated by in vivo analysis of two BCAT4 T-DNA knockout mutants in which Met-derived aliphatic GSL accumulation is reduced by nearly 50% (Schuster et al. 2006)', 'GSL side chain elongation', 'Schuster et al. 2006'),
	('AT3G20960', 'CYP705A33', 'At3g20960', '', '821646', 'NM_112988', 'NP_188732', 'Q8GYY9', 'MNISSRGAAAIDESLVFGSSGVVYAPYGDYLKFVKKIIATKLLRPQVLERSRGLRAEELQRLYNRILDKAKMNENVEIGKEATMLMNNIFCRMSMGRSFSEENGEAERVRGLVAESYALAKKIFFASVLRRLLKKLRIPLFKKDIMDVSNRFNELLEKILVEHNEKLDEEHKDTDMMDVLLAAYADENAEYKITRNHIKSFFVELFVGGTDTSVQTTQWTMAEIINNSDVLERLREEIDSVVGTSRMIQETDIPNLPYLQAVVKEGLRLHPPFPLLTRKFEERCEIKGFYIPEKTFLIINAYAWMRDPDSWEDPNEFKPERFLGSSRLGQVDEREEAQKYIPFGGGRRGCPGANLASIFVGTAIGVMVQCFDWGIKGDKINMEETFEGLTLTMVHPIKCTPIPRTLPFVTSNLQSPSS', '418', '', '', '', 'Camalexin originates from tryptophan and its biosynthesis involves the cytochrome P450 enzymes CYP79B2 and CYP71B15 (PAD3). Camalexin induction is a complex process, for which triggering by reactive oxygen species (ROS), salicylic acid signalling, and the glutathione status are important. Targets of the signalling cascade are the tryptophan and camalexin biosynthetic genes, which are strongly transcriptionally upregulated at the sites of pathogen infection (Glawischnig et al. 2004) .', 'Camalexin biosynthesis', 'Glawischnig et al. 2004'),
	('AT3G22890', 'APS1', 'ATP sulfurylase 1 chloroplastic', 'F5N5.6', '821861', 'NM_113189', 'NP_188929', 'Q9LIK9', 'MASMAAVLSKTPFLSQPLTKSSPNSDLPFAAVSFPSKSLRRRVGSIRAGLIAPDGGKLVELIVEEPKRREKKHEAADLPRVELTAIDLQWMHVLSEGWASPLGGFMRESEFLQTLHFNSLRLDDGSVVNMSVPIVLAIDDEQKARIGESTRVALFNSDGNPVAILSDIEIYKHPKEERIARTWGTTAPGLPYVDEAITNAGNWLIGGDLEVLEPVKYNDGLDRFRLSPAELRKELEKRNADAVFAFQLRNPVHNGHALLMTDTRRRLLEMGYKNPILLLHPLGGFTKADDVPLDWRMKQHEKVLEDGVLDPETTVVSIFPSPMHYAGPTEVQWHAKARINAGANFYIVGRDPAGMGHPVEKRDLYDADHGKKVLSMAPGLERLNILPFRVAAYDKTQGKMAFFDPSRPQDFLFISGTKMRTLAKNNENPPDGFMCPGGWKVLVDYYESLTPAGNGRLPEVVPV', '463', 'EC 2.7.7.4', '', '', 'Using trans-activation assays two isoforms of APK; APK1 and APK2 are regulated by both classes of GSL MYB transcription factors; whereas two ATPS genes; ATPS1 and ATPS3 are differentially regulated by these two groups of MYB factors. The adenosine 5-phosphosulfate reductases APR1; APR2; and APR3 which participate in primary sulfate reduction are also activated by the MYB factors (Yatusevich et al. 2010)  ', 'GSL core structure synthesis', 'Yatusevich et al. 2010'),
	('AT3G25180', 'CYP82G1', 'Cytochrome P450 82G1', 'MJL12.5', '822110', 'NM_113423', 'NP_189154', 'Q9LSF8', 'MTFLFSTLQLSLFSLALVIFGYIFLRKQLSRCEVDSSTIPEPLGALPLFGHLHLLRGKKLLCKKLAAMSQKHGPIFSLKLGFYRLVVASDPKTVKDCFTTNDLATATRPNIAFGRYVGYNNASLTLAPYGDYWRELRKIVTVHLFSNHSIEMLGHIRSSEVNTLIKHLYKGNGGTSIVKIDMLFEFLTFNIILRKMVGKRIGFGEVNSDEWRYKEALKHCEYLAVIPMIGDVIPWLGWLDFAKNSQMKRLFKELDSVNTKWLHEHLKKRSRNEKDQERTIMDLLLDILPEDIVISGHVRDVIVKATILALTLTGSDSTSITLTWAVSLLLNNPAALEAAQEEIDNSVGKGRWIEESDIQNLKYLQAIVKETHRLYPPAPLTGHKSKNLYCHYNSYFMTLLIL', '515', 'EC 1.14.-.-', '', '', 'Camalexin originates from tryptophan and its biosynthesis involves the cytochrome P450 enzymes CYP79B2 and CYP71B15 (PAD3). Camalexin induction is a complex process, for which triggering by reactive oxygen species (ROS), salicylic acid signalling, and the glutathione status are important. Targets of the signalling cascade are the tryptophan and camalexin biosynthetic genes, which are strongly transcriptionally upregulated at the sites of pathogen infection (Glawischnig et al. 2004) .', 'Camalexin biosynthesis', 'Glawischnig et al. 2004'),
	('AT3G26830', 'CYP71B15', 'Bifunctional dihydrocamalexate synthase/camalexin synthase', 'PAD3', '822298', 'NM_113595', 'NP_189318', 'Q9LW27', 'MSVFLCFLVLLPLILIFLNVLKPSKYKLPPGPKKLPIIGNLHQRRTLHPRNRRNLAEMYGPVALLQYGFVPVVAISSKEAAEEVLKINDLECCSRPEAAGMRATFYNFKDIGMAPFGDEWSLMRKLSVVELFSVKKLQSFKYIIEEENNLCVKKLSEFATRQSPVNLERAIFTLVGNIVCRIGYGINLYECDFFEADRVVDLVLKAEAVIRETVFSDFFPGRIGRFIDCISGQNRRLKNNFSVVDTFFQNVLNEHLKPGRESSTIVDLMIDMKKKQENDGDALKFTTDHLKGMISDIFVAGIGGVAGITLWGMTELIRNPRVMKKVQDEIRTTLGDKKERIKEEDLNQLHYFKLVVKETLRLHPTTPLLLPRQTMSHIKIQGYDVPAKTQILVNVYAMGRDPKLWENADEFNPDRFLDSSVDFKGKNYEFIPFGSGRRICPGMTMGTILVEMALLNLLYFFDWGLAKQEEAKEIINGEENFLAFFQVLHH', '490', 'EC 1.14.19.52', 'AraCyc', '', 'Multifunctional enzyme involved in the biosynthesis of the indole-derived phytoalexin camalexin. Catalyzes two reactions, the formation of dihydrocamalexate from indole-3-acetonitrile-cysteine conjugate and the oxidative decarboxylation of dihydrocamalexate which is the final step in camalexin biosynthesis (Ferrari et al. 2003)', 'Camalexin biosynthesis', 'Zhou et al. 1999; Ferrari et al. 2003; Bohman et al. 2003; Glawischnig 2006; Schuhegger et al. 2007; Schuhegger et al. 2006; Glawischnig 2007; Nafisi et al. 2007; B?ttcher et al. 2009; Chapman et al. 2016; Liu et al. 2016; Savatin et al. 2015; Lemari? et '),
	('AT3G27785', 'MYB118', 'Myb domain protein 118 ', 'PGA37', '822399', 'NM_113694', 'NP_189416', 'Q9LVW4', 'MEFESVFKMHYPYLAAVIYDDSSTLKDFHPSLTDDFSCVHNVHHKPSMPHTYEIPSKETIRGITPSPCTEAFEACFHGTSNDHVFFGMAYTTPPTIEPNVSHVSHDNTMWENDQNQGFIFGTESTLNQAMADSNQFNMPKPLLSANEDTIMNRRQNNQVMIKTEQIKKKNKRFQMRRICKPTKKASIIKGQWTPEEDKLLVQLVDLHGTKKWSQIAKMLQGRVGKQCRERWHNHLRPDIKKDGWTEEEDIILIKAHKEIGNRWAEIARKLPGRTENTIKNHWNATKRRQHSRRTKGKDEISLSLGSNTLQNYIRSVTYNDDPFMTANANANIGPRNMRGKGKNVMVAVSEYDEGECKYIVDGVNNLGLEDGRIKMPSLAAMSASGSASTSGSASGSGSGVTMEIDEPMTDSWMVMHGCDEVMMNEIALLEMIAHGRL', '437', '', '', '', 'Two conserved TFs; MYB115 and MYB118 were co-expressed with the key enzyme encoding genes in the newly evolved benzoyloxy GSL (GLS) pathway. These TFs interacted with the promoters of the GLS biosynthetic genes and negatively influenced their expression. Similarly the GLS profiles of these two TFs knockouts showed that they influenced the aliphatic GLS accumulation within seed; leaf and flower while they mainly expressed in seeds (Zhang et al. 2015)', 'GSL transcription factor', 'Zhang et al. 2015'),
	('AT3G44300', 'NIT2', 'Nitrilase 2 ', 'T10D17_90', '823555', 'NM_114298', 'NP_190016', 'P32962', 'MSTSENTPFNGVASSTIVRATIVQASTVYNDTPATLEKANKFIVEAASKGSELVVFPEAFIGGYPRGFRFGLGVGVHNEEGRDEFRKYHASAIKVPGPEVEKLAELAGKNNVYLVMGAIEKDGYTLYCTALFFSPQGQFLGKHRKLMPTSLERCIWGQGDGSTIPVYDTPIGKLGAAICWENRMPLYRTALYAKGIELYCAPTADGSKEWQSSMLHIAIEGGCFVLSACQFCLRKDFPDHPDYLFTDWYDDKEPDSIVSQGGSVIISPLGQVLAGPNFESEGLITADLDLGDVARAKLYFDSVGHYSRPDVLHLTVNEHPKKPVTFISKVEKAEDDSNK', '339', 'EC 3.5.5.1', '', '', 'Enzymes of the NIT1 group have a broad substrate specificity and accept nitriles with structural similarity to GSL-derived nitriles and the predominant isoform NIT1 (At3g44310) is most active on nitriles derived from GSLs (Piotrowski et al. 2008)', 'GSL degradation', 'Piotrowski et al. 2004; Wittstock & Burow 2010'),
	('AT3G44310', 'NIT1', 'Nitrilase 1 ', 'T10D17_100', '823556', 'NM_180680', 'NP_851011', 'P32961', 'MSSTKDMSTVQNATPFNGVAPSTTVRVTIVQSSTVYNDTPATIDKAEKYIVEAASKGAELVLFPEGFIGGYPRGFRFGLAVGVHNEEGRDEFRKYHASAIHVPGPEVARLADVARKNHVYLVMGAIEKEGYTLYCTVLFFSPQGQFLGKHRKLMPTSLERCIWGQGDGSTIPVYDTPIGKLGAAICWENRMPLYRTALYAKGIELYCAPTADGSKEWQSSMLHIAIEGGCFVLSACQFCQRKHFPDHPDYLFTDWYDDKEHDSIVSQGGSVIISPLGQVLAGPNFESEGLVTADIDLGDIARAKLYFDSVGHYSRPDVLHLTVNEHPRKSVTFVTKVEKAEDDSNK', '346', 'EC 3.5.5.1', '', '', 'Enzymes of the NIT1 group have a broad substrate specificity and accept nitriles with structural similarity to GSL-derived nitriles and the predominant isoform NIT1 (At3g44310) is most active on nitriles derived from GSLs (Piotrowski et al. 2008)', 'GSL degradation', 'Piotrowski et al. 2004; Wittstock & Burow 2010'),
	('AT3G44320', 'NIT3', 'Nitrilase 3 ', 'T10D17_110', '823557', 'NM_114300', 'NP_190018', 'P46010', 'MSSTEEMSSVKNTTQVIGVDPSSTVRVTIVQSSTVYNDTPATLDKAEKFIVEAASKGAKLVLFPEAFIGGYPRGFRFGLAVGVHNEEGRDEFRNYHASAIKVPGPEVERLAELAGKNNVHLVMGAIEKDGYTLYCTALFFSPQGQFLGKHRKVMPTSLERCIWGQGDGSTIPVYDTPIGKIGAAICWENRMPLYRTALYAKGIEIYCAPTADYSLEWQASMIHIAVEGGCFVLSAHQFCKRREFPEHPDYLFNDIVDTKEHDPTVSGGGSVIISPLGKVLAGPNYESEGLVTADLDLGDIARAKLYFDVVGHYSKPDIFNLTVNEHPKKPVTFMTKVEKAEDESNK', '346', 'EC 3.5.5.1', '', '', 'Enzymes of the NIT1 group have a broad substrate specificity and accept nitriles with structural similarity to GSL-derived nitriles and the predominant isoform NIT1 (At3g44310) is most active on nitriles derived from GSLs (Piotrowski et al. 2008)', 'GSL degradation / Camalexin biosynthesis', 'Piotrowski et al. 2004; Wittstock & Burow 2010; Glawischnig et al. 2004'),
	('AT3G45640', 'MPK3', 'Mitogen-activated protein kinase 3', 'F9K21.220', '823706', 'NM_114433', 'NP_190150', 'Q39023', 'MNTGGGQYTDFPAVETHGGQFISYDIFGSLFEITSKYRPPIIPIGRGAYGIVCSVLDTETNELVAMKKIANAFDNHMDAKRTLREIKLLRHLDHENIIAIRDVVPPPLRRQFSDVYISTELMDTDLHQIIRSNQSLSEEHCQYFLYQLLRGLKYIHSANIIHRDLKPSNLLLNANCDLKICDFGLARPTSENDFMTEYVVTRWYRAPELLLNSSDYTAAIDVWSVGCIFMELMNRKPLFPGKDHVHQMRLLTELLGTPTESDLGFTHNEDAKRYIRQLPNFPRQPLAKLFSHVNPMAIDLVDRMLTFDPNRRITVEQALNHQYLAKLHDPNDEPICQKPFSFEFEQQPLDEEQIKEMIYQEAIALNPTYG', '370', 'EC 2.7.11.24', '', '', 'MKK9, an MKK, is an upstream activator of the MPKs MPK3 and MPK6 both in vitro and in planta. Expression of active MKK9 protein in transgenic plants induces the synthesis of ethylene and camalexin through the activation of the endogenous MPK3 and MPK6 kinases. MKK9-MPK3/MPK6 cascade participates in the regulation of the biosynthesis of ethylene and camalexin and may be an important axis in the stress responses of Arabidopsis (Xu et al. 2008).', 'Camalexin biosynthesis', 'Xu et al. 2008'),
	('AT3G47960', 'GTR1', 'Protein NRT1/ PTR FAMILY 2.10 ', 'NPF2.10', '823951', 'NM_114665', 'NP_566896', 'Q944G5', 'MKSRVILNHRDRRDKNHNNNNTNHYTQVDTMERKPLEVEPSTTTTNTDVVDSFEEEQRKIVYRGWKVMPFIIGNETFEKLGIIGTLSNLLVYLTSVFNLKSYTAATIINAFSGTINFGTFIAAFLCDTYFGRYKTLSVAVIACFLGSFVILLTAAIPSLHPVACGNKISCEGPSVGQILFLLMGLGFLVVGAGGIRPCNLAFGADQFNPKSESGKKGINSFFNWYFFTFTFAQIISLTAVVYIQSNVSWTIGLIIPVALMFLACVIFFAGDRLYVKVKASGSPLAGIARVIAAAIKKRGLKPVKQPWVNLYNHIPSNYANTTLKYTDQFRFLDKAAIMTPEEKLNSDGTASDPWKLCTLQQVEEVKCIVRVIPIWFASTIYYLAITIQMTYPVFQALQSDRRLGSGGFRIPAATYVVFLMTGMTVFIIFYDRVLVPSLRRVTGLETGISLLQRIGAGFTFAIMSLLVSGFIEERRRNFALTKPTLGMAPRTGEISSMSALWLIPQLTLAGIAEAFAAIGQMEFYYKQFPENMKSFAGSIFYVGAGVSSYLASFLISTVHRTTAHSPSGNWLAEDLNKAKLDYFYFMLTGLMVVNMAYFLLMARWYRYKGGNDEDITEIETNEEETKQQQLQDKNSV', '636', '', '', '', 'Leaf apoplastic fluid analysis and GSL feeding experiments showed two GSL transporters. GTR1 and GTR2 were essential for long-distance transport of GSLs in Arabidopsis and also play key roles in GSL allocation within a mature leaf by effectively importing apoplastically localized GSLs into appropriate cells (Madsen et al. 2014)', 'GSL degradation', 'Nour-Eldin et al. 2012; Madsen et al. 2014'),
	('AT3G48090', 'EDS1', 'Protein EDS', 'EDS1-90, EDS1A', '823964', 'NM_001035752', 'NP_001030829', 'Q9SU72', 'MAFEALTGINGDLITRSWSASKQAYLTERYHKEEAGAVVIFAFQPSFSEKDFFDPDNKSSFGEIKLNRVQFPCMRKIGKGDVATVNEAFLKNLEAIIDPRTSFQASVEMAVRSRKQIVFTGHSSGGATAILATVWYLEKYFIRNPNVYLEPRCVTFGAPLVGDSIFSHALGREKWSRFFVNFVSRFDIVPRIMLARKASVEETLPHVLAQLDPRKSSVQESEQRITEFYTRVMRDTSTVANQAVCELTGSAEAFLETLSSFLELSPYRPAGTFVFSTEKRLVAVNNSDAILQMLFYTSQASDEQEWSLIPFRSIRDHHSYEELVQSMGKKLFNHLDGENSIESTLNDLGVSTRGRQYVQAALEEEKKRVENQKKIIQVIEQERFLKKLAWIEDEYKPKCQAHKNGYYDSFKVSNEENDFKANVKRAELAGVFDEVLGLMKKCQLPDEFEGDIDWIKLATRYRRLVEPLDIANYHRHLKNEDTGPYMKRGRPTRYIYAQRGYEHYILKPNGMIAEDVFWNKVNGLNLGLQLEEIQETLKNSGSECGSCFWAEVEELKGKPYEEVEVRVKTLEGMLGEWITDGEVDDKEIFLEGSTFRKWWITLPKNHKSHSPLRDYMMDEITDT', '622', '', '', '', 'Decreasing camalexin levels by mutation of the camalexin synthetase gene?PAD3?or the camalexin synthesis regulator?AtWRKY33?compromised the powdery mildew resistance in these mutants (Liu et al. 2016)', 'Camalexin biosynthesis', 'Liu et al. 2016'),
	('AT3G49680', 'BCAT3', 'Branched-chain-amino-acid aminotransferase 3 chloroplastic', 'ATBCAT-3', '824130', 'NM_114828', 'NP_566923', 'Q9M401', 'MERAAILPSVNQNYLLCPSRAFSTRLHSSTRNLSPPSFASIKLQHSSSSVSSNGGISLTRCNAVSSNSSSTLVTELADIDWDTVGFGLKPADYMYVMKCNIDGEFSKGELQRFGNIEISPSAGVLNYGQGLFEGLKAYRKKDGNNILLFRPEENAKRMRNGAERMCMPAPTVEQFVEAVTETVLANKRWVPPPGKGSLYVRPLLMGTGAVLGLAPAPEYTFIIYVSPVGNYFKEGVAPINLIVENEFHRATPGGTGGVKTIGNYAAVLKAQSIAKAKGYSDVLYLDCIYKRYLEEVSSCNIFIVKDNVISTPEIKGTILPGITRKSMIDVARTQGFQVEERNVTVDELLEADEVFCTGTAVVVSPVGSVTYKGKRVSYGEGTFGTVSKQLYTVLTSLQMGLIEDNMKWTVNLS', '413', 'EC 2.6.1.42 EC 2.6.1.88', 'AraCyc', 'KEGG', 'Metabolite profiling of bcat3-1 single and bcat3-1/bcat4-2 double knockout mutants showed significant alterations in the profiles of both amino acids and GSLs. The changes in GSL proportions suggest that BCAT3 most likely catalyzes the terminal steps in the chain elongation process leading to short-chain GSLs (Knill et al. 2008)', 'GSL side chain elongation', 'Knill et al. 2008'),
	('AT3G52430', 'PAD4', 'Lipase-like PAD4', 'EDS9', '824408', 'NM_115103', 'NP_190811', 'Q9S745', 'MDDCRFETSELQASVMISTPLFTDSWSSCNTANCNGSIKIHDIAGITYVAIPAVSMIQLGNLVGLPVTGDVLFPGLSSDEPLPMVDAAILKLFLQLKIKEGLELELLGKKLVVITGHSTGGALAAFTALWLLSQSSPPSFRVFCITFGSPLLGNQSLSTSISRSRLAHNFCHVVSIHDLVPRSSNEQFWPFGTYLFCSDKGGVCLDNAGSVRLMFNILNTTATQNTEEHQRYGHYVFTLSHMFLKSRSFLGGSIPDNSYQAGVALAVEALGFSNDDTSGVLVKECIETATRIVRAPILRSAELANELASVLPARLEIQWYKDRCDASEEQLGYYDFFKRYSLKRDFKVNMSRIRLAKFWDTVIKMVETNELPFDFHLGKKWIYASQFYQLLAEPLDIANFYKNRDIKTGGHYLEGNRPKRYEVIDKWQKGVKVPEECVRSRYASTTQDTCFWAKLEQAKEWLDEARKESSDPQRRSLLREKIVPFESYANTLVTKKEVSLDVKAKNSSYSVWEANLKEFKCKMGYENEIEMVVDESDAMET', '541', 'EC 2.3.1.-', '', '', 'Decreasing camalexin levels by mutation of the camalexin synthetase gene?PAD3?or the camalexin synthesis regulator?AtWRKY33?compromised the powdery mildew resistance in these mutants (Liu et al. 2016)', 'Camalexin biosynthesis', 'Liu et al. 2016; Bohman et al. 2003; Ferrari et al. 2003'),
	('AT3G58990', 'IPMI1', '3-isopropylmalate dehydratase small subunit 2 ', 'AtLEUD2', '825068', 'NM_115761', 'NP_191458', 'Q9LYT7', 'MATSQQFLNPTLFKSLASSNKNSCTLCPSPFLQLKSASTIFNYKPLTSSSATIITRVAASSSDSGESITRETFHGLCFVLKDNIDTDQIIPAEYGTLIPSIPEDREKLGSFALNGLPKFYNERFVVPGEMKSKYSVIIGGDNFGCGSSREHAPVCLGAAGAKAVVAESYARIFFRNCVATGEIFPLESEVRICDECKTGDVVTIEHKEDGSSLLINHTTRKEYKLKPLGDAGPVIDAGGIFAYARKAGMIPSA', '253', 'EC 4.2.1.33', '', '', 'Two isopropylmalate isomerases genes; IPMI1 and IPMI2 and the isopropylmalate dehydrogenase gene; IPMDH1 were identified as targets of HAG1/MYB28 and the corresponding proteins localized to plastids suggesting a role in plastidic chain elongation reactions (Gigolashvili et al. 2009)', 'GSL side chain elongation', 'Gigolashvili et al. 2009; Knill et al. 2009; Sawada & Kuwahara et al. 2009  '),
	('AT3G62250', 'RPS27AC', 'Ubiquitin-40S ribosomal protein S27a-3', 'UBQ5', '825398', 'NM_116090', 'NP_191784', 'P59233', 'MQIFVKTLTGKTITLEVESSDTIDNVKAKIQDKEGIPPDQQRLIFAGKQLEDGRTLADYNIQKESTLHLVLRLRGGAKKRKKKTYTKPKKIKHKHKKVKLAVLQFYKIDGSGKVQRLRKECPNATCGAGTFMASHFDRHYCGKCGLTYVYQKEGVEA', '157', '', '', '', 'MKK9, an MKK, is an upstream activator of the MPKs MPK3 and MPK6 both in vitro and in planta. Expression of active MKK9 protein in transgenic plants induces the synthesis of ethylene and camalexin through the activation of the endogenous MPK3 and MPK6 kinases. MKK9-MPK3/MPK6 cascade participates in the regulation of the biosynthesis of ethylene and camalexin and may be an important axis in the stress responses of Arabidopsis (Xu et al. 2008).', 'Camalexin biosynthesis', 'Xu et al. 2008'),
	('AT4G03050', 'AOP3', '2-oxoglutarate-dependent dioxygenase AOP3 ', '', '828104', 'NM_001340416', 'NP_001319854', 'Q9ZTA1', 'MIQLYAEKLAELDMMVRRLILESYGIEYFIDEHLNSTYYRMRLMKYIARPDNDITAAVGANVDNGANDNADGDANVNDDGASIGVKVNVDVGDDVNDNDSVNIGVGVDINVETNVNGDLDAEANGDATAWVVGAVSGNASVGAKEANVDAELGLPSHTDKSLTGIIYQHQIDGLEVKTKEGKWIRVKPAPNTVIVIAGDALCALMNGRIPSPYHRVRVTEKKKTRYAAALFSNPKEGYIIDSPKELVDEKHPRAFKPFDFVDLFNFYHTEAGRRAPSTLQAFCGVSAGK', '411', 'EC 1.14.11.-', '', '', 'AOP3 directs the formation of hydroxyalkyl GSLs from methylsulfinylalkyl GSLs. Absence of functional AOP2 and AOP3 leads to the accumulation of the precursor methylsulfinylalkyl GSLs (Kliebenstein et al. 2001)', 'GSL Side chain modification', 'Kliebenstein & Lambrix et al. 2001; Zhang et al. 2015'),
	('AT4G03060', 'AOP2', 'Alkenyl hydroxalkyl producing 2', '', '', '', '', 'Q9ZTA2', 'MGSCSLQLPLINLADKTLEPGSSKWAEVRSDVRKALEDFGCFEASYDKVSLELQESIMKT\nMEELFALPVETKQRNVCPKPYVGYLNHNNLSESLGISNANILENINEFTQQLWPHGDGNE\nNISKTIQLFAEKLVEIDVMVRRMVMESFGIEKYIDDHLKSTAYATDELNIVGVEPNVGVK\nVNADISDDVNANASVNAGVGANVNADTGVNDNLNVDANVAVGGGVNANTDLGVGVNVNSN\nVAVNAKTGGDDVEANDDNEEKKLGLPCHTDKNLFTVLFQHEIEGLEVKTKDEKWIRVKPS\nPNTFIVIAGDSLCALMNGRIRAPYHRVRVTEKKRTRYTAAIFTCPKPDYVIEAPKELVDE\nKHPRLFRPFDYRDLFTFYHSEAGRKIQYTLQAYCAVSEA', '399', '', '', '', 'By heterologous expression in Escherichia and the correlation of gene expression patterns to the GSL phenotype. AOP2 catalyzes the conversion of methylsulfinylalkyl GSLs to alkenyl GSLs in Arabidopsis. Absence of functional AOP2 and AOP3 leads to the accumulation of the precursor methylsulfinylalkyl GSLs (Kliebenstein et al. 2001)', 'GSL Side chain modification', 'Kliebenstein & Lambrix et al. 2001; Burow et al. 2015'),
	('AT4G03190', 'GRH1', 'GRR1-like protein 1', 'AFB1, FBL18, GER1, LRF1', '828045', 'NM_116555', 'NP_567255', 'Q9ZR12', 'MGLRFPPKVLEHILSFIDSNEDRNSVSLVCKSWFETERKTRKRVFVGNCYAVSPAAVTRRFPEMRSLTLKGKPHFADYNLVPDGWGGYAWPWIEAMAAKSSSLEEIRMKRMVVTDECLEKIAASFKDFKVLVLTSCEGFSTDGIAAIAATCRNLRVLELRECIVEDLGGDWLSYFPESSTSLVSLDFSCLDSEVKISDLERLVSRSPNLKSLKLNPAVTLDGLVSLLRCAPQLTELGTGSFAAQLKPEAFSKLSEAFSNCKQLQSLSGLWDVLPEYLPALYSVCPGLTSLNLSYATVRMPDLVELLRRCSKLQKLWVMDLIEDKGLEAVASYCKELRELRVFPSEPDLDATNIPLTEQGLVFVSKGCRKLESVLYFCVQFTNAALFTIARKRPNLKCFRLCVIEPFAPDYKTNEPLDKGFKAIAEGCRDLRRLSVSGLLSDKAFKYIGKHAKKVRMLSIAFAGDSDLMLHHLLSGCESLKKLEIRDCPFGDTALLEHAAKLETMRSLWMSSCFVSFGACKLLSQKMPRLNVEVIDEHPPESRPESSPVERIYIYRTVAGPRMDTPEFVWTIHKNPENGVSHLAIK', '585', '', '', '', 'ARF1 and ARF9 negatively regulate glucosinolate accumulation, and that ARF9 positively regulates camalexin accumulation. The action of miR393 on auxin signalling triggers two complementary responses. First, it prevents suppression of SA levels by auxin. Second, it stabilizes ARF1 and ARF9 in inactive complexes (Robert-Seilaniantz et al. 2011)', 'Camalexin biosynthesis', 'Robert-Seilaniantz et al. 2011'),
	('AT4G04610', 'APR1', '5\'-adenylylsulfate reductase 1 chloroplastic', 'PRH19', '825793', 'NM_116699', 'NP_192370', 'P92979', 'MAMSVNVSSSSSSGIINSRFGVSLEPKVSQIGSLRLLDRVHVAPVSLNLSGKRSSSVKPLNAEPKTKDSMIPLAATMVAEIAEEVEVVEIEDFEELAKKLENASPLEIMDKALEKYGNDIAIAFSGAEDVALIEYAHLTGRPFRVFSLDTGRLNPETYRFFDAVEKHYGIRIEYMFPDSVEVQGLVRSKGLFSFYEDGHQECCRVRKVRPLRRALKGLKAWITGQRKDQSPGTRSEIPVVQVDPVFEGLDGGVGSLVKWNPVANVEGNDVWNFLRTMDVPVNTLHAAGYISIGCEPCTKAVLPGQHEREGRWWWEDAKAKECGLHKGNVKENSDDAKVNGESKSAVADIFKSENLVTLSRQGIENLMKLENRKEPWIVVLYAPWCPFCQAMEASYDELADKLAGSGIKVAKFRADGDQKEFAKQELQLGSFPTILVFPKNSSRPIKYPSEKRDVESLTSFLNLVR', '465', 'EC 1.8.4.9', '', '', 'Using trans-activation assays two isoforms of APK; APK1 and APK2 are regulated by both classes of GSL MYB transcription factors; whereas two ATPS genes; ATPS1 and ATPS3 are differentially regulated by these two groups of MYB factors. The adenosine 5-phosphosulfate reductases APR1; APR2; and APR3 which participate in primary sulfate reduction are also activated by the MYB factors (Yatusevich et al. 2010)  ', 'GSL core structure synthesis', 'Yatusevich et al. 2010'),
	('AT4G08620', 'SULTR1;1', 'Sulfate transporter 1.1 ', 'HST1', '826426', 'NM_116931', 'NP_192602', 'Q9SAY1', 'MSGTINPPDGGGSGARNPPVVRQRVLAPPKAGLLKDIKSVVEETFFHDAPLRDFKGQTPAKKALLGIQAVFPIIGWAREYTLRKFRGDLIAGLTIASLCIPQDIGYAKLANVDPKYGLYSSFVPPLIYAGMGSSRDIAIGPVAVVSLLVGTLCQAVIDPKKNPEDYLRLVFTATFFAGIFQAGLGFLRLGFLIDFLSHAAVVGFMGGAAITIALQQLKGFLGIKTFTKKTDIVSVMHSVFKNAEHGWNWQTIVIGASFLTFLLVTKFIGKRNRKLFWVPAIAPLISVIISTFFVFIFRADKQGVQIVKHIDQGINPISVHKIFFSGKYFTEGIRIGGIAGMVALTEAVAIARTFAAMKDYQIDGNKEMIALGTMNVVGSMTSCYIATGSFSRSAVNFMAGVETAVSNIVMAIVVALTLEFITPLFKYTPNAILAAIIISAVLGLIDIDAAILIWRIDKLDFLACMGAFLGVIFISVEIGLLIAVVISFAKILLQVTRPRTTVLGKLPNSNVYRNTLQYPDAAQIPGILIIRVDSAIYFSNSNYVRERASRWVREEQENAKEYGMPAIRFVIIEMSPVTDIDTSGIHSIEELLKSLEKQEIQLILANPGPVVIEKLYASKFVEEIGEKNIFLTVGDAVAVCSTEVAEQQT', '649', '', '', '', 'Gene expression studies with promoter-reporter constructs indicated that both SULTR1;1 and SULTR1;2 are regulated under their ?S-responsive promoters in response to sulfur nutrition (Maruyama-Nakashita et al. 2006)', 'GSL core structure synthesis', 'Maruyama-Nakashita et al. 2006'),
	('AT4G12030', 'BAT5', 'Probable sodium/metabolite cotransporter BASS5 chloroplastic', 'BASS5', '826811', 'NM_202809', 'NP_974538', 'F4JPW1', 'MMFAVGINSNERDFLEALKRPDAIFAGYIGQYLIKPLLGYIFGVIAVSLFNLPTSIGAGIMLVSCVSGAQLSNYTTFLTDPSLAALSIVMTSISTATAVLVTPMLSLLLIGKKLPVDVFGMISSILQVVITPIAAGLLLNRLFPRLSNAIKPFLPALTVIDMSCCIGAPLALNIDSILSPFGATILFLVITFHLLAFVAGYFFTGFFFSKAPDVKALQRTISYETGMQSSLLALALATKFFQDPLVGVPPAISTVVMSLMGVSLVTIWKNRKE', '407', ' ', '', '', 'Mechanical stimuli and methyl jasmonate transiently induced BAT5 expression in inflorescences and leaves. BAT5 was identified as the first transporter component of the aliphatic GSL biosynthetic pathway (Gigolashvili et al. 2009)', 'GSL side chain elongation', 'Gigolashvili et al. 2009'),
	('AT4G12320', 'CYP706A6', 'At4g12320', 'T4C9.160', '826841', 'NM_117302', 'NP_192969', 'Q66GJ1', 'MSPISNLFAGNTINLTPYAILILIAIFSILWYLFKRSPQPHLPPGPRGLPIVGNLPFLDPDLHTYFTKLAESYGPIFKLNLGSKLTVVVNTPSLAREILKDQDINFSNHDVPLTARAVTYGGLDLVWLPYGAEWRMLRKVCVLKLLSHRTLNSFYELRRKEIRERTRYLYQKGQEESPVNVGEQVFLTMMNLTMNMLWGGSVKAEEMESVGTEFKEVISEITRLLGEPNVSDFFPRLARFDLQGLVKKMHVCARELDAILDRAIEQMQLLRTRDGDDGECKDFLQHLMKLKDQEADSEVPITVNHVKAVLVDLVVGGTDTSTNTIEFAMAELIRKPELMKRAQQELDEVVGKDNIIEESHITRLPFISAIMKETLRLYPTIPLLVPHRPSETALVGGYTIPKNTKIFINVWSIQRDPNVWEYPTEFRPERFLDKKSCDFTGTDYSYLPFGSGRRICAGIALAERMILYTLATLLHSFDWKIPEGHILDLKEKFGIVLKLKSPLVALPVPRLSNSNLYL', '518', '', '', '', 'Camalexin originates from tryptophan and its biosynthesis involves the cytochrome P450 enzymes CYP79B2 and CYP71B15 (PAD3). Camalexin induction is a complex process, for which triggering by reactive oxygen species (ROS), salicylic acid signalling, and the glutathione status are important. Targets of the signalling cascade are the tryptophan and camalexin biosynthetic genes, which are strongly transcriptionally upregulated at the sites of pathogen infection (Glawischnig et al. 2004) .', 'Camalexin biosynthesis', 'Glawischnig et al. 2004'),
	('AT4G13430', 'IIL1', '3-isopropylmalate dehydratase large subunit ', 'ATLEUC1', '826975', 'NM_117417', 'NP_567405', 'Q94AR8', 'MASVISSSPFLCKSSSKSDLGISSFPKSSQISIHRCQKKSISRKIVSVMAPQKDRSPGTTGSVKTGMTMTEKILARASEKSLVVPGDNIWVNVDVLMTHDVCGPGAFGIFKREFGEKAKVWDPEKIVVIPDHYIFTADKRANRNVDIMREHCREQNIKYFYDITDLGNFKANPDYKGVCHVALAQEGHCRPGEVLLGTDSHTCTAGAFGQFATGIGNTDAGFVLGTGKILLKVPPTMRFILDGEMPSYLQAKDLILQIIGEISVAGATYKTMEFSGTTIESLSMEERMTLCNMVVEAGGKNGVIPPDATTLNYVENRTSVPFEPVYSDGNASFVADYRFDVSKLEPVVAKPHSPDNRALARECKDVKIDRVYIGSCTGGKTEDFMAAAKLFHAAGRKVKVPTFLVPATQKVWMDVYALPVPGAGGKTCAQIFEEAGCDTPASPSCGACLGGPADTYARLNEPQVCVSTTNRNFPGRMGHKEGQIYLASPYTAAASALTGRVADPREFLQ', '509', 'EC 4.2.1.33', 'AraCyc', '', 'Knocking out either of the candidate genes; AtleuC1 (IIL1) or AtIMD1 (IMD1) would reduced the level of Met-GSLs indicating that both genes are actually involved in Met-GSL biosynthesis (Sawada & Kuwahara et al. 2009)', 'GSL side chain elongation', 'He et al. 2010; Hirai et al. 2007; Knill et al. 2009; Sawada & Kuwahara et al. 2009  '),
	('AT4G13770', 'CYP83A1', 'Cytochrome P450 83A1 ', 'REF2', '827011', 'NM_117451', 'NP_193113', 'P48421', 'MEDIIIGVVALAAVLLFFLYQKPKTKRYKLPPGPSPLPVIGNLLQLQKLNPQRFFAGWAKKYGPILSYRIGSRTMVVISSAELAKELLKTQDVNFADRPPHRGHEFISYGRRDMALNHYTPYYREIRKMGMNHLFSPTRVATFKHVREEEARRMMDKINKAADKSEVVDISELMLTFTNSVVCRQAFGKKYNEDGEEMKRFIKILYGTQSVLGKIFFSDFFPYCGFLDDLSGLTAYMKECFERQDTYIQEVVNETLDPKRVKPETESMIDLLMGIYKEQPFASEFTVDNVKAVILDIVVAGTDTAAAAVVWGMTYLMKYPQVLKKAQAEVREYMKEKGSTFVTEDDVKNLPYFRALVKETLRIEPVIPLLIPRACIQDTKIAGYDIPAGTTVNVNAWAVSRDEKEWGPNPDEFRPERFLEKEVDFKGTDYEFIPFGSGRRMCPGMRLGAAMLEVPYANLLLSFNFKLPNGMKPDDINMDVMTGLAMHKSQHLKLVPEKVNKY', '502', 'EC 1.14.-.-', 'AraCyc', 'KEGG', 'The GSL profiles of transgenic Arabidopsis overexpressing either CYP83A1 or CYP83B1 exhibited wild-type levels of indole GSLs (Naur et al. 2003)', 'GSL core structure synthesis / Camalexin biosynthesis', 'Bak et al. 2001; Naur et al. 2003; Zang et al. 2009 ;Liu et al. 2016'),
	('AT4G14680', 'APS3', 'ATP-sulfurylase 3 chloroplastic', 'FCAALL.128', '827118', 'NM_117550', 'NP_193204', 'O23324', 'MASMSTVFPKPTSFISQPLTKSHKSDSVTTSISFPSNSKTRSLRTISVRAGLIEPDGGKLVDLVVPEPRRREKKHEAADLPRVRLTAIDLQWMHVLSEGWASPLRGFMRESEFLQTLHFNLLNLDDGSVVNMSVPIVLAIDDQQKALIGESKRVSLVDSDDNPIAILNDIEIYKHPKEERIARTWGTTAPGLPYVEEAITNAGDWLIGGDLEVLEPVKYNDGLDRFRLSPFELRKELEKRGADAVFAFQLRNPVHNGHALLMTDTRRRLLEMGYKNPILLLHPLGGFTKADDVPLSWRMKQHEKVLEDGVLDPETTVVSIFPSPMLYAGPTEVQWHAKARINAGANFYIVGRDPAGMGHPVEKRDLYDADHGKKVLSMAPGLERLNILPFRVAAYDKTQGKMAFFDPSRAQDFLFISGTKMRALAKNRENPPDGFMCPGGWKVLVDYYDSLTLTGNTKLPEKIPV', '465', 'EC 2.7.7.4', '', '', 'Using trans-activation assays two isoforms of APK; APK1 and APK2 are regulated by both classes of GSL MYB transcription factors; whereas two ATPS genes; ATPS1 and ATPS3 are differentially regulated by these two groups of MYB factors. The adenosine 5-phosphosulfate reductases APR1; APR2; and APR3 which participate in primary sulfate reduction are also activated by the MYB factors (Yatusevich et al. 2010)  ', 'GSL core structure synthesis', 'Yatusevich et al. 2010'),
	('AT4G14880', 'OASA1', 'Cysteine synthase 1 ', 'OLD3', '827145', 'NM_179055', 'NP_849386', 'P47998', 'MASRIAKDVTELIGNTPLVYLNNVAEGCVGRVAAKLEMMEPCSSVKDRIGFSMISDAEKKGLIKPGESVLIEPTSGNTGVGLAFTAAAKGYKLIITMPASMSTERRIILLAFGVELVLTDPAKGMKGAIAKAEEILAKTPNGYMLQQFENPANPKIHYETTGPEIWKGTGGKIDGFVSGIGTGGTITGAGKYLKEQNANVKLYGVEPVESAILSGGKPGPHKIQGIGAGFIPSVLNVDLIDEVVQVSSDESIDMARQLALKEGLLVGISSGAAAAAAIKLAQRPENAGKLFVAIFPSFGERYLSTVLFDATRKEAEAMTFEA', '322', 'EC 2.5.1.47', '', '', 'In plants OAS has a similar direct regulatory role as its counterpart N-acetylserine in E. coli is questionable; as no clear cut correlation was found between the Arabidopsis root OAS cellular content and the mRNA levels of either SULTR1;1 and SULTR1;2 (Rouached et al. 2008)', 'GSL core structure synthesis', 'Rouached et al. 2008'),
	('AT4G15370', 'BARS1', 'Baruol synthase', 'PEN2', '827203', 'NM_117625', 'NP_193272', 'O23390', 'MWRLRIGAKAKDNTHLFTTNNYVGRQIWEFDANAGSPEELAEVEEARRNFSNNRSRFKASADLLWRMQFLREKKFEQKIPRVIVEDAEKITYEDAKTALRRGLLYFTALQADDGHWPAENAGSIFFNAPFVICLYITGHLEKIFTHEHRVELLRYMYNHQNEDGGWGLHVESPSNMFCSVINYICLRILGVEAGHDDKGSACARARKWILDHGGATYSPLIGKAWLSVLGVYDWSGCKPIPPEFWFLPSFFPVNGGTLWIYLRDIFMGLSYLYGKNFVATSTPLILQLREEIYPEPYTNISWRQARNRCAKEDLYYPQSFLQDLFWKGVHVFSENILNRWPFNNLIRQRALRTTMELVHYHDEATRYITGGSVPKVIAVFHMLACWVEDPESDYFKKHLARVPDFIWIGEDGLKIQSFGSQVWDTALSLHVFIDGFDDDVDEEIRSTLLKGYDYLEKSQVTENPPGDYMKMFRHMAKGGWTFSDQDQGWPVSDCTAESLECCLFFESMSSEFIGKKMDVEKLYDAVDFLLYLQSDNGGITAWQPADGKLVEFIEDAVVEHEYVECTGSAIVALAQFNKQFPGYKKEEVERFITKGVKYIEDLQMVDGSWYGNWGVCFIYGTFFAVRGLVAAGKCYNNCEAIRRAVRFILDTQNTEGGWGESYLSCPRKKYIPLIGNKTNVVNTGQALMVLIMGNQMKRDPLPVHRAAKVLINSQMDNGDFPQQEIMGVFKMNVMLHFPTYRNMFTLWALTHYTKALRGL', '759', 'EC 5.4.99.57', '', '', 'The effect of low R:FR increasing Arabidopsis susceptibility to B.cinerea was not present in mutants deficient in the biosynthesis of camalexin (pad3) or metabolism of iGS (pen2). In a mutant deficient in the JASMONATE ZIM DOMAIN-10 (JAZ10) protein, which does not respond to low R:FR with increased susceptibility to B. cinerea, supplemental FR failed to down-regulate iGS production. These results indicate that suppression of Arabidopsis immunity against B. cinerea by low R:FR ratios is mediated by reduced levels of Trp-derived defenses, and provide further evidence for a functional role of JAZ10 in the link between phytochrome and jasmonate signaling (Cargnel et al. 2014)', 'Camalexin biosynthesis', 'Cargnel et al. 2014'),
	('AT4G15380', 'CYP705A4', 'Cytochrome P450, family 705, subfamily A, polypeptide 4', 'FCAALL.280', '827204', 'NM_117626', 'NP_193273', 'Q8L7H7', 'MAAMNMIDFQNCFIFILLCLFSRLCYSHFFKKPKDPRLHFDLPPSPPSLPIIGHLHLLLSVLLHRSLQKLSTKYGSILYLRVFRFPVVLISSASIAYEIFRAHDLNISYRGFTPTDDSLFAGSFSFISAPYGDYWKFMKKVLVTNVFGPQAHEQSRGVRADVLERFYGNLFDKAIKKQSVEICAEALKLSNSSICKMIMGRSCSEERFRALATELDVLTKKLFFANMLRAWFKKLVVSLFKKETTVISYRFDELLESILVEHEKKLDVHHQRTDLMDALLAAYRDENAEYKITRNHIKSIIADLLFAGTENQVQTIQWAMAEIINNPNVLERLRGEIDSVVGKSRLIQETDLPKLPYLQAVVKETIRLHPPGPFFLRFTKEGCRIRGFYVPENTSVVVNVYAVMRDPDAWEDPLVFKPERFLASSRAEQEEERREKEIKYLPFGSGRRSCPGENLAYVIMGTAIGVMVQGFEWRTTEEKINMDEAVVGLSLTMAHPLKIIPVARTSNSLTSSLQKCL', '517', '', '', '', 'Camalexin originates from tryptophan and its biosynthesis involves the cytochrome P450 enzymes CYP79B2 and CYP71B15 (PAD3). Camalexin induction is a complex process, for which triggering by reactive oxygen species (ROS), salicylic acid signalling, and the glutathione status are important. Targets of the signalling cascade are the tryptophan and camalexin biosynthetic genes, which are strongly transcriptionally upregulated at the sites of pathogen infection (Glawischnig et al. 2004) .', 'Camalexin biosynthesis', 'Glawischnig et al. 2004'),
	('AT4G17490', 'ERF6', 'Ethylene-responsive transcription factor 6', 'ERF-6, ERF103', '827463', 'NM_117854', 'NP_567529', 'Q8VZ91', 'MATPNEVSALFLIKKYLLDELSPLPTTATTNRWMNDFTSFDQTGFEFSEFETKPEIIDLVTPKPEIFDFDVKSEIPSESNDSFTFQSNPPRVTVQSNRKPPLKIAPPNRTKWIQFATGNPKPELPVPVVAAEEKRHYRGVRMRPWGKFAAEIRDPTRRGTRVWLGTFETAIEAARAYDKEAFRLRGSKAILNFPLEVDKWNPRAEDGRGLYNKRKRDGEEEEVTVVEKVLKTEESYDVSGGENVESGLTAIDDWDLTEFLSMPLLSPLSPHPPFGYPQLTVV', '282', '', '', '', 'MKK9, an MKK, is an upstream activator of the MPKs MPK3 and MPK6 both in vitro and in planta. Expression of active MKK9 protein in transgenic plants induces the synthesis of ethylene and camalexin through the activation of the endogenous MPK3 and MPK6 kinases. MKK9-MPK3/MPK6 cascade participates in the regulation of the biosynthesis of ethylene and camalexin and may be an important axis in the stress responses of Arabidopsis (Xu et al. 2008).', 'Camalexin biosynthesis', 'Xu et al. 2008'),
	('AT4G17880', 'MYC4', 'Transcription factor MYC4', 'AtbHLH4', '827511', 'NM_117897.4', 'NP_193522.1', 'O49687', 'MSPTNVQVTDYHLNQSKTDTTNLWSTDDDASVMEAFIGGGSDHSSLFPPLPPPPLPQVNEDNLQQRLQALIEGANENWTYAVFWQSSHGFAGEDNNNNNTVLLGWGDGYYKGEEEKSRKKKSNPASAAEQEHRKRVIRELNSLISGGVGGGDEAGDEEVTDTEWFFLVSMTQSFVKGTGLPGQAFSNSDTIWLSGSNALAGSSCERARQGQIYGLQTMVCVATENGVVELGSSEIIHQSSDLVDKVDTFFNFNNGGGEFGSWAFNLNPDQGENDPGLWISEPNGVDSGLVAAPVMNNGGNDSTSNSDSQPISKLCNGSSVENPNPKVLKSCEMVNFKNGIENGQEEDSSNKKRSPVSNNEEGMLSFTSVLPCDSNHSDLEASVAKEAESNRVVVEPEKKPRKRGRKPANGREEPLNHVEAERQRREKLNQRFYSLRAVVPNVSKMDKASLLGDAISYISELKSKLQKAESDKEELQKQIDVMNKEAGNAKSSVKDRKCLNQESSVLIEMEVDVKIIGWDAMIRIQCSKRNHPGAKFMEALKELDLEVNHASLSVVNDLMIQQATVKMGNQFFTQDQLKVALTEKVGECP', '589', '', '', '', 'The myc2 myc3 myc4 (myc234) triple mutant was almost completely devoid of GSL and was extremely susceptible to the generalist herbivore Spodoptera littoralis. On the contrary the specialist Pieris brassicae was unaffected by the presence of GSL and preferred to feed on wild-type plants. In addition lack of GSL in myc234 drastically modified S. littoralis feeding behavior. Surprisingly the expression of MYB factors known to regulate GS biosynthesis genes was not altered in myc234; suggesting that MYC2/MYC3/MYC4 are necessary for direct transcriptional activation of GS biosynthesis genes. Yeast two-hybrid and pull-down experiments indicated that MYC2/MYC3/MYC4 interact directly with GS-related MYBs. This specific MYC?MYB interaction plays a crucial role in the regulation of defense secondary metabolite production and underlines the importance of GSL in shaping plant interactions with adapted and nonadapted herbivores (Schweizer et al. 2013)', 'GSL transcription factor', 'Schweizer et al. 2013'),
	('AT4G21990', 'APR3', '5\'-adenylylsulfate reductase 3 chloroplastic', 'PRH26', '828288', 'NM_118320', 'NP_193930', 'P92980', 'MALAINVSSSSSSAISSSSFPSSDLKVTKIGSLRLLNRTNVSAASLSLSGKRSSVKALNVQSITKESIVASEVTEKLDVVEVEDFEELAKRLENASPLEIMDKALEKFGNDIAIAFSGAEDVALIEYAHLTGRPYRVFSLDTGRLNPETYRLFDTVEKHYGIRIEYMFPDAVEVQALVRNKGLFSFYEDGHQECCRIRKVRPLRRALKGLRAWITGQRKDQSPGTRSEIPVVQVDPVFEGLDGGVGSLVKWNPVANVEGNDVWNFLRTMDVPVNTLHAAGYVSIGCEPCTRAVLPGQHEREGRWWWEDAKAKECGLHKGNIKENTNGNATANVNGTASVADIFNSENVVNLSRQGIENLMKLENRKEAWIVVLYAPWCPFCQAMEASFDELADKLGGSGVKVAKFRADGDQKDFAKKELQLGSFPTILVFPKNSSRPIKYPSEKRDVDSLTSFLNLVR', '458', 'EC 1.8.4.9', '', '', 'Using trans-activation assays two isoforms of APK; APK1 and APK2 are regulated by both classes of GSL MYB transcription factors; whereas two ATPS genes; ATPS1 and ATPS3 are differentially regulated by these two groups of MYB factors. The adenosine 5-phosphosulfate reductases APR1; APR2; and APR3 which participate in primary sulfate reduction are also activated by the MYB factors (Yatusevich et al. 2010)  ', 'GSL core structure synthesis', 'Yatusevich et al. 2010'),
	('AT4G22690', 'CYP706A1', 'Cytochrome P450, family 706, subfamily A, polypeptide 1', 'T12H17.80', '828365', 'NM_118395', 'NP_567665', 'F4JLY4', 'MSTLPLFSLHHHTTQNLQTNNQNTVRYFSLKPKMETASSNFSLSQILNIEEPYSSVMLGVAALLAVVCYFWIQGKSKSKNGPPLPPGPWPLPIVGNLPFLNSDVLHTQFQALTLKHGPLMKIHLGSKLAIVVSSPDMAREVLKTHDITFANHDLPEVGKINTYGGEDILWSPYGTHWRRLRKLCVMKMFTTPTLEASYSTRREETRQTIVHMSEMAREGSPVNLGEQIFLSIFNVVTRMMWGATVEGDERTSLGNELKTLISDISDIEGIQNYSDFFPLFSRFDFQGLVKQMKGHVKKLDLLFDRVMESHVKMVGKKSEEEEDFLQYLLRVKDDDEKAPLSMTHVKSLLMDMVLGGVDTSVNASEFAMAEIVSRPEVLNKIRLELDQVVGKDNIVEESHLPKLPYLQAVMKETLRLHPTLPLLVPHRNSETSVVAGYTVPKDSKIFINVWAIHRDPKNWDEPNEFKPERFLENSLDFNGGDFKYLPFGSGRRICAAINMAERLVLFNIASLLHSFDWKAPQGQKFEVEEKFGLVLKLKSPLVAIPVPRLSDPKLYTA', '557', '', '', '', 'Camalexin originates from tryptophan and its biosynthesis involves the cytochrome P450 enzymes CYP79B2 and CYP71B15 (PAD3). Camalexin induction is a complex process, for which triggering by reactive oxygen species (ROS), salicylic acid signalling, and the glutathione status are important. Targets of the signalling cascade are the tryptophan and camalexin biosynthetic genes, which are strongly transcriptionally upregulated at the sites of pathogen infection (Glawischnig et al. 2004) .', 'Camalexin biosynthesis', 'Glawischnig et al. 2004'),
	('AT4G23100', 'GSH1', 'Glutamate--cysteine ligase chloroplastic', 'CAD2', '828409', 'NM_118439', 'NP_194041', 'P46309', 'MALLSQAGGSYTVVPSGVCSKAGTKAVVSGGVRNLDVLRMKEAFGSSYSRSLSTKSMLLHSVKRSKRGHQLIVAASPPTEEAVVATEPLTREDLIAYLASGCKTKDKYRIGTEHEKFGFEVNTLRPMKYDQIAELLNGIAERFEWEKVMEGDKIIGLKQGKQSISLEPGGQFELSGAPLETLHQTCAEVNSHLYQVKAVAEEMGIGFLGIGFQPKWRREDIPIMPKGRYDIMRNYMPKVGTLGLDMMLRTCTVQVNLDFSSEADMIRKFRAGLALQPIATALFANSPFTEGKPNGFLSMRSHIWTDTDKDRTGMLPFVFDDSFGFEQYVDYALDVPMYFAYRKNKYIDCTGMTFRQFLAGKLPCLPGELPSYNDWENHLTTIFPEVRLKRYLEMRGADGGPWRRLCALPAFWVGLLYDDDSLQAILDLTADWTPAEREMLRNKVPVTGLKTPFRDGLLKHVAEDVLKLAKDGLERRGYKEAGFLNAVDEVVRTGVTPAEKLLEMYNGEWGQSVDPVFEELLY', '522', 'EC 6.3.2.2', '', '', 'Both gamma glutamyl cysteine ligase (GSH1) and glutathione synthetase (GSH2); which catalyse its synthesis were significantly enriched in bundle sheath (BS) cells that can be related with sulfur and GSL metabolism (Aubry et al. 2014)', 'GSL core structure synthesis / Camalexin biosynthesis', 'Aubry et al. 2014; Bednarek et al. 2009; Hiruma et al. 2013; Schlaeppi et al. 2008; Stefanato et al. 2009; Ferrari et al. 2003; Kagan et al. 2001  '),
	('AT4G23980', 'ARF9', 'Auxin response factor 9', 'T19F6.20', '828498', 'NM_118530', 'NP_194129', 'Q9XED8', 'MANRGGEYLYDELWKLCAGPLVDVPQAQERVYYFPQGHMEQLEASTQQVDLNTMKPLFVLPPKILCNVMNVSLQAEKDTDEVYAQITLIPVGTEVDEPMSPDPSPPELQRPKVHSFSKVLTASDTSTHGGFSVLRKHATECLPPLDMTQQTPTQELVAEDVHGYQWKFKHIFRGQPRRHLLTTGWSTFVTSKRLVAGDTFVFLRGENGELRVGVRRANLQQSSMPSSVISSHSMHLGVLATARHATQTKTMFIVYYKPRTSQFIISLNKYLEAMSNKFSVGMRFKMRFEGEDSPERRYSGTVIGVKDCSPHWKDSKWRCLEVHWDEPASISRPNKVSPWEIEPFVNSENVPKSVMLKNKRPRQVSEVSALDVGITASNLWSSVLTQPHEFAQSCITSQWSSPQQCHRDANEDAKKSDWLNNSYSVSNVAKDSTLNDQMVSPVEQKKPETTANYRLFGIDLMSSSLAVPEEKTAPMRPINISKPTMDSHSDPKSEISKVSEEKKQEPAEGSPKEVQSKQSSSTRSRTKVQMQGVPVGRAVDLNALKGYNELIDDIEKLFDIKGELRSRNQWEIVFTDDEGDMMLVGDDPWPEFCNMVKRIFIWSKEEVKKMTPGNQLRMLLREVETTLTTTSKTDNHSN', '638', '', '', '', 'ARF1 and ARF9 negatively regulate glucosinolate accumulation, and that ARF9 positively regulates camalexin accumulation. The action of miR393 on auxin signalling triggers two complementary responses. First, it prevents suppression of SA levels by auxin. Second, it stabilizes ARF1 and ARF9 in inactive complexes (Robert-Seilaniantz et al. 2011)', 'Camalexin biosynthesis', 'Robert-Seilaniantz et al. 2011'),
	('AT4G27260', 'WES1', 'Indole-3-acetic acid-amido synthetase', 'GH3.5', '828834', 'NM_118860', 'NP_194456', 'O81829', 'MPEAPKKESLEVFDLTLDQKNKQKLQLIEELTSNADQVQRQVLEEILTRNADVEYLRRHDLNGRTDRETFKNIMPVITYEDIEPEINRIANGDKSPILSSKPISEFLTSSGTSGGERKLMPTIEEELDRRSLLYSLLMPVMSQFVPGLENGKGMYFLFIKSESKTPGGLPARPVLTSYYKSSHFKERPYDPYTNYTSPNETILCSDSYQSMYSQMLCGLCQHQEVLRVGAVFASGFIRAIKFLEKHWIELVRDIRTGTLSSLITDPSVREAVAKILKPSPKLADFVEFECKKSSWQGIITRLWPNTKYVDVIVTGTMSQYIPTLDYYSNGLPLVCTMYASSECYFGVNLRPLCKPSEVSYTLIPSMAYFEFLPVHRNNGVTNSINLPKALTEKEQQELVDLVDVKLGQEYELVVTTYAGLCRYRVGDLLRVTGFKNKAPQFSFICRKNVVLSIDSDKTDEVELQNAVKNAVTHLVPFDASLSEYTSYADTSSIPGHYVLFWELCLDGNTPIPPSVFEDCCLAVEESFNTVYRQGRVSDKSIGPLEIKIVEPGTFDKLMDYAISLGASINQYKTPRCVKFAPIIELLNSRVVDSYFSPKCPKWVPGHKQWGSN', '612', 'EC 6.3.2.-', '', '', 'Arabidopsis GH3.5 protein, a multifunctional acetyl-amido synthetase, is involved in camalexin biosynthesis via conjugating indole-3-carboxylic acid (ICA) and cysteine (Cys) and regulating camalexin biosynthesis genes. Camalexin levels were increased in the activation-tagged mutant gh3.5-1D in both Col-0 and cyp71A13-2 mutant backgrounds after pathogen infection. The recombinant GH3.5 protein catalyzed the conjugation of ICA and Cys to form a possible intermediate indole-3-acyl-cysteinate (ICA(Cys)) in vitro. In support of the in vitro reaction, feeding with ICA and Cys increased camalexin levels in Col-0 and gh3.5-1D. Dihydrocamalexic acid (DHCA), the precursor of camalexin and the substrate for PAD3, was accumulated in gh3.5-1D/pad3-1, suggesting that ICA(Cys) could be an additional precursor of DHCA for camalexin biosynthesis (Wang et al. 2012)', 'Camalexin biosynthesis', 'Wang et al. 2012'),
	('AT4G30530', 'GGP1', 'Gamma-glutamyl peptidase 1 ', 'AT4G30530', '829176', 'NM_119199', 'NP_194782', 'Q9M0A7', 'MVEQKRYALFLATLDSEFVKKTYGGYHNVFVTTFGDEGEHWDSFRVVSGEFPDEKDLEKYDGFVISGSSHDAFENDDWILKLCDIVKKIDEMKKKILGICFGHQIIARVRGGTVGRAKKGPELKLGDITIVKDAITPGSYFGNEIPDSIAIIKCHQDEVLVLPETAKVLAYSKNYEVEMYSIEDHLFCIQGHPEYNKEILFEIVDRVLALGYVKQEFADAAKATMENRGADRKLWETICKNFLKGRVPTN', '250', 'EC 3.4.19.-', '', '', 'GGP1 is a gamma-glutamyl peptidase that cleaves off the gamma-glutamyl residue from the glutathione conjugate intermediate (S-[(Z)-phenylacetohydroximoyl]-L-glutathione; GS-B) in the benzylGSLs (BGLS) pathway (Geu-Flores et al. 2009)', 'GSL core structure synthesis', 'Geu-Flores et al. 2009; Moldrup et al. 2011  '),
	('AT4G30550', 'GGP3', 'Gamma-glutamyl peptidase 3', '', '829178', 'NM_119201', 'NP_194784', 'Q9M0A5', 'MVVIEQKKRFALFLATCDSEFVKKTYGGYFNVFVSTFGEEGEQWDLFRVIDGQFPDENDLDKYDGFVISGSPHDAFGDADWIVKLCEVCQKLDHMKKKVLGICFGHQIITRVKGGKIGRALKGADMGLRSITIAKDNEKLRGYFGDVEVPASLAIIKCHQDEVLELPESATLLASSEVCNVEMFSIGDHFFCIQGHPEYNKEILFEIVDRVLNMKLMEQEFADKAKSTMETAQPDRILWQKLCKNFLKG', '249', 'EC 3.4.19.16', 'AraCyc', '', 'Arabidopsis thaliana mutant impaired in the production of the gamma-glutamyl peptidases GGP1 and GGP3 has altered glucosinolate levels and accumulates up to 10 related GSH conjugates. The double mutant is impaired in the production of camalexin and accumulates high amounts of the camalexin intermediate GS-IAN upon induction. In addition, the cellular and subcellular localization of GGP1 and GGP3 matches that of known glucosinolate and camalexin enzymes. GSH is the sulfur donor in the biosynthesis of glucosinolates and establish an in vivo function for the only known cytosolic plant gamma-glutamyl peptidases, namely, the processing of GSH conjugates in the glucosinolate and camalexin pathways (Geu-Flores et al. 2011)', 'Camalexin biosynthesis', 'Geu-Flores et al. 2011'),
	('AT4G31500', 'CYP83B1', 'Cytochrome P450 83B1 ', 'SUR2', '829277', 'NM_119299', 'NP_194878', 'O65782', 'MDLLLIIAGLVAAAAFFFLRSTTKKSLRLPPGPKGLPIIGNLHQMEKFNPQHFLFRLSKLYGPIFTMKIGGRRLAVISSAELAKELLKTQDLNFTARPLLKGQQTMSYQGRELGFGQYTAYYREMRKMCMVNLFSPNRVASFRPVREEECQRMMDKIYKAADQSGTVDLSELLLSFTNCVVCRQAFGKRYNEYGTEMKRFIDILYETQALLGTLFFSDLFPYFGFLDNLTGLSARLKKAFKELDTYLQELLDETLDPNRPKQETESFIDLLMQIYKDQPFSIKFTHENVKAMILDIVVPGTDTAAAVVVWAMTYLIKYPEAMKKAQDEVRSVIGDKGYVSEEDIPNLPYLKAVIKESLRLEPVIPILLHRETIADAKIGGYDIPAKTIIQVNAWAVSRDTAAWGDNPNEFIPERFMNEHKGVDFKGQDFELLPFGSGRRMCPAMHLGIAMVEIPFANLLYKFDWSLPKGIKPEDIKMDVMTGLAMHKKEHLVLAPTKHI', '499', 'EC 1.14.-.-', 'AraCyc', 'KEGG', 'The GSL profiles of transgenic Arabidopsis overexpressing either CYP83A1 or CYP83B1 exhibited wild-type levels of indole GSLs (Naur et al. 2003)', 'GSL core structure synthesis', 'Bak et al. 2001; Naur et al. 2003  '),
	('AT4G37400', 'CYP81F3', 'Cytochrome P450 81F3 ', 'F6G17.50', '829894', 'NM_119903', 'NP_568025', 'Q0WTF4', 'MFYYVIVLPLALFLLAYKLFFTSKTKRFNLPPSPPYSLPILGHHNLLKPPVHRLFHRLSKTHGPIFSLQFGSRRAVVISSSSLATQCFTGQNDIILSNRPCFLTAKYVAYNYTTVGTAPYGDHWRNLRRICSLEILSSNRLTNFLHIRKDEIHRMLTRLSRDVNKEIELEPLLSDLTFNNIVRMVTGKRYYGDEVHNEEEANVFKKLVADINDCSGARHPGDYLPFMKMFGGSFEKKVKALAEAMDEILQRLLEECKRDKDGNTMVNHLLSLQQNEPEYYTDVTIKGLMLGMMIAGTDTSAVTLEWAMSSLLNHPEALEKAKLEIDEKIGQERLIDEPDIANLPYLQNIVSETFRLYPAAPLLVPRSPTEDIKVGGYDVPRGTMVMVNAWAIHRDPELWNEPEKFKPERFNGGEGGGRGEDVHKLMPFGNGRRSCPGAGLGQKIVTLALGSLIQCFDWQKVNGEAIDMTETPGMAMRKKIPLSALCQSRPIMSKLQAHLKG', '501', 'EC 1.14.-.-', 'AraCyc', '', 'All four Arabidopsis CYP81F gene products had the capacity to modify the indole GSL structure. CYP81F1; CYP81F2; and CYP81F3 but not CYP81F4 catalyzed the conversion of indol-3-yl-methyl GSL (I3M) to 4-hydroxy-indol-3-yl-methyl (4OH-I3M) and all four CYP81Fs converted I3M to 1-hydroxy-indol-3-yl-methyl GSL (1OH-I3M) (Pfalz et al. 2011)', 'GSL core structure synthesis', 'Pfalz et al. 2011  '),
	('AT4G37410', 'CYP81F4', 'Cytochrome P450 81F4 ', 'F6G17.60', '829895', 'NM_119904', 'NP_195457', 'Q9SZU1', 'MFNYVIILPLALFLLAYKFFFTSKKQRYYLPPSPSYSLPILGHHLLIKPPVHRLFHRLSNIHGPIFYLRLGSRRAVVISSSSLARECFTGQNDVIVSNRPRFLTSKYIAYNYTTIATTSYGDHWRNLRRICSLEIVSSKRLANFLHIRKEEIQRMLTRLSRDARVGKEVELESILYDLTFNNIVRMVTGKIYYGDDVSDKEEAELFKKLFTFITTNSGARHPGEYLPFMKIFGGSFEKEVKAAAKVIDEMLQRLLDECKSDKDGNTMVNHLLSLQQDDPEYYTDIIIKGLMLGIMVASSETSALTIEWAMASLLNHPKVLDKVKLEIDEIIGQDRLIEESDIANLPYLQNVVSETLRLHPAAPVLVPRSTAEDIKIGGYDVPRDTMVMVNAWAIHRDPDLWTEPERFNPERFNGGEGEKDDVRMLIAFGSGRRICPGVGLAHKIVTLALGSLIQCFDWKKVNEKEIDMSEGPGMAMRMMVPLRALCKTRPIMNKLPAYTKV', '501', 'EC 1.14.-.', 'AraCyc', '', 'All four Arabidopsis CYP81F gene products had the capacity to modify the indole GSL structure. CYP81F1; CYP81F2; and CYP81F3 but not CYP81F4 catalyzed the conversion of indol-3-yl-methyl GSL (I3M) to 4-hydroxy-indol-3-yl-methyl (4OH-I3M) and all four CYP81Fs converted I3M to 1-hydroxy-indol-3-yl-methyl GSL (1OH-I3M) (Pfalz et al. 2011)', 'GSL core structure synthesis', 'Pfalz et al. 2011  '),
	('AT4G37430', 'CYP81F1', 'Cytochrome P450 81F1 ', 'CYP91A2', '829897', 'NM_119906', 'NP_195459', 'O65790', 'MLYFILLPLLFLVISYKFLYSKTQRFNLPPGPPSRPFVGHLHLMKPPIHRLLQRYSNQYGPIFSLRFGSRRVVVITSPSLAQESFTGQNDIVLSSRPLQLTAKYVAYNHTTVGTAPYGDHWRNLRRICSQEILSSHRLINFQHIRKDEILRMLTRLSRYTQTSNESNDFTHIELEPLLSDLTFNNIVRMVTGKRYYGDDVNNKEEAELFKKLVYDIAMYSGANHSADYLPILKLFGNKFEKEVKAIGKSMDDILQRLLDECRRDKEGNTMVNHLISLQQQQPEYYTDVIIKGLMMSMMLAGTETSAVTLEWAMANLLRNPEVLEKARSEIDEKIGKDRLIDESDIAVLPYLQNVVSETFRLFPVAPFLIPRSPTDDMKIGGYDVPRDTIVMVNAWAIHRDPEIWEEPEKFNPDRYNDGCGSDYYVYKLMPFGNGRRTCPGAGLGQRIVTLALGSLIQCFEWENVKGEEMDMSESTGLGMRKMDPLRAMCRPRPIMSKLLL', '500', 'EC 1.14.-.-', 'AraCyc', '', 'All four Arabidopsis CYP81F gene products had the capacity to modify the indole GSL structure. CYP81F1; CYP81F2; and CYP81F3 but not CYP81F4 catalyzed the conversion of indol-3-yl-methyl GSL (I3M) to 4-hydroxy-indol-3-yl-methyl (4OH-I3M) and all four CYP81Fs converted I3M to 1-hydroxy-indol-3-yl-methyl GSL (1OH-I3M) (Pfalz et al. 2011)', 'GSL core structure synthesis', 'Pfalz et al. 2011  '),
	('AT4G39030', 'DTX47', 'Protein DETOXIFICATION 47, chloroplastic', 'EDS5, IAP1, SCORD3, SID1', '830058', 'NM_120063', 'NP_195614', 'Q945F0', 'MLIKSQRLTLFSPLLSKTRRIPVNSHQTLVAESVITRRTLGAITATPSFHKNPVVIRRRIKLERVTRNCVRIDREIDEEEEEEEKERGDLVKQSIWEQMKEIVKFTGPAMGMWICGPLMSLIDTVVIGQGSSIELAALGPGTVLCDHMSYVFMFLSVATSNMVATSLAKQDKKEAQHQISVLLFIGLVCGLMMLLLTRLFGPWAVTAFTRGKNIEIVPAANKYIQIRGLAWPFILVGLVAQSASLGMKNSWGPLKALAAATIINGLGDTILCLFLGQGIAGAAWATTASQIVSAYMMMDSLNKEGYNAYSFAIPSPQELWKISALAAPVFISIFSKIAFYSFIIYCATSMGTHVLAAHQVMAQTYRMCNVWGEPLSQTAQSFMPEMLYGANRNLPKARTLLKSLMIIGATLGLVLGVIGTAVPGLFPGVYTHDKVIISEMHRLLIPFFMALSALPMTVSLEGTLLAGRDLKFVSSVMSSSFIIGCLTLMFVTRSGYGLLGCWFVLVGFQWGRFGLYLRRLLSPGGILNSDGPSPYTVEKIKSI', '513', '', '', '', 'Decreasing camalexin levels by mutation of the camalexin synthetase gene?PAD3?or the camalexin synthesis regulator?AtWRKY33?compromised the powdery mildew resistance in these mutants (Liu et al. 2016)', 'Camalexin biosynthesis', 'Liu et al. 2016; Ferrari et al. 2003; Nawrath et al. 1999'),
	('AT4G39650', 'GGT2', 'Glutathione hydrolase 2', 'T19P19.40', '830119', 'NM_120125', 'NP_195675', 'Q680I5', 'MNSFMSLVRTATIALLLIAFLQNANAVKNLQSIVAYHGAVATDDGRCSAIGTNVLRQGGNAIDASVAAALCLGVVSPASSGIGGGAFTMIKLANGTEVAYDSRETAPLSATEDMYGDNPERKKKGSLSVGVPGEVAGLYTAWTQHGKLPWKQLVEPAEKLAAEGFKISKYLYMQMNATRSDILADKGLSELFVSNGELKKPGAICRNPKLADTLSQIAEYGPKAFYNGTVGFNLVSDIQKAGGIITLKDLQNYNVKVKEPLSTEILGYRLLGMPPPSSGGPAMMLILNILAQYGIPSGVSGPLGVHRLVEALKHAFAVRMNLGDPDFVPEVTNVVADMLSPKFAQDLKSKINDEKTFDPKYYGGKWGQIKDHGTSHLSIIDSERNAVSMTSTINGYFGAIMLSPSTGIVLNNEMDDFSIPTKSGGDPDVPPPAPANFIRPGKRPLSSMTPTIVLKDGKVKAALGASGGMYIIAGTTQVYLNHFFLNMDPLSSVVAPRIYHQLIPNKASYENWTTVYSDHFEIPEEIRLVLEKKGQVLTPIAGGTISQLIVEQSDGKSGGISKLVAVSDPRKGGFPSGY', '552', 'EC 3.4.19.13', '', '', 'GSTF6 overexpression increased and GSTF6-knockout reduced camalexin production. Arabidopsis GSTF6 expressed in yeast cells catalyzed GSH(IAN) formation. GSH(IAN), (IAN)CysGly, and ?GluCys(IAN) were determined to be intermediates within the camalexin biosynthetic pathway. The expression of GSTF6, GGT1, GGT2, and PCS1 was coordinately upregulated during camalexin biosynthesis. These results suggest that GSH is the Cys derivative used during camalexin biosynthesis, that the conjugation of GSH with IAN is catalyzed by GSTF6, and that GGTs and PCS are involved in camalexin biosynthesis (Su et al. 2011).', 'Camalexin biosynthesis', 'Su et al. 2011'),
	('AT4G39940', 'APK2', 'Adenylyl-sulfate kinase 2 chloroplastic ', 'AKN2', '830153', 'NM_120157', 'NP_195704', 'O49196', 'MEGLAIRASRPSVFCSIPGLGGDSHRKPPSDGFLKLPASSIPADSRKLVANSTSFHPISAVNVSAQASLTADFPALSETILKEGRNNGKEKAENIVWHESSICRCDRQQLLQQKGCVVWITGLSGSGKSTVACALSKALFERGKLTYTLDGDNVRHGLNRDLTFKAEHRTENIRRIGEVAKLFADVGVICIASLISPYRRDRDACRSLLPDGDFVEVFMDVPLHVCESRDPKGLYKLARAGKIKGFTGIDDPYEAPVNCEVVLKHTGDDESCSPRQMAENIISYLQNKGYLEG', '293', 'EC 2.7.1.25', '', '', 'The levels of GSLs and the sulfated 12-hydroxyjasmonate were reduced approximately fivefold in apk1 apk2 plants. The reduction in GSLs resulted in increased transcript levels for genes involved in GSL biosynthesis and accumulation of desulfated precursors (Mugford et al. 2009)', 'GSL core structure synthesis', 'Badenes-Perez et al. 2013'),
	('AT4G39950', 'CYP79B2', 'Tryptophan N-monooxygenase 1 ', 'T5J17.120', '830154', 'NM_120158', 'NP_195705', 'O81346', 'MNTFTSNSSDLTTTATETSSFSTLYLLSTLQAFVAITLVMLLKKLMTDPNKKKPYLPPGPTGWPIIGMIPTMLKSRPVFRWLHSIMKQLNTEIACVKLGNTHVITVTCPKIAREILKQQDALFASRPLTYAQKILSNGYKTCVITPFGDQFKKMRKVVMTELVCPARHRWLHQKRSEENDHLTAWVYNMVKNSGSVDFRFMTRHYCGNAIKKLMFGTRTFSKNTAPDGGPTVEDVEHMEAMFEALGFTFAFCISDYLPMLTGLDLNGHEKIMRESSAIMDKYHDPIIDERIKMWREGKRTQIEDFLDIFISIKDEQGNPLLTADEIKPTIKELVMAAPDNPSNAVEWAMAEMVNKPEILRKAMEEIDRVVGKERLVQESDIPKLNYVKAILREAFRLHPVAAFNLPHVALSDTTVAGYHIPKGSQVLLSRYGLGRNPKVWADPLCFKPERHLNECSEVTLTENDLRFISFSTGKRGCAAPALGTALTTMMLARLLQGFTWKLPENETRVELMESSHDMFLAKPLVMVGDLRLPEHLYPTVK', '541', 'EC 1.14.13.125', 'AraCyc', 'KEGG', 'Two Arabidopsis cytochrome P450s (CYP79B2 and CYP79B3) are able to convert Trp to indole-3-acetaldoxime (IAOx); a precursor to indole-3-acetic acid (IAA) and indole GSLs (Hull et al. 2000)', 'GSL core structure synthesis / Camalexin biosynthesis', 'Hull et al. 2000; Mikkelsen et al. 2000; Zhao et al. 2015; Savatin et al. 2015; Lemari? et al. 2015; Kettles et al. 2013; Zandalinas et al. 2012; Wang et al. 2012; Su et al. 2011; Stefanato et al. 2009; B?ttcher et al. 2009; Nafisi et al. 2007; Glawischni'),
	('AT5G03280', 'EIN2', 'Ethylene-insensitive protein 2', 'CKR1, ORE3', '831889', 'NM_120406', 'NP_195948', 'Q9S814', 'MEAEIVNVRPQLGFIQRMVPALLPVLLVSVGYIDPGKWVANIEGGARFGYDLVAITLLFNFAAILCQYVAARISVVTGKHLAQICNEEYDKWTCMFLGIQAEFSAILLDLTMVVGVAHALNLLFGVELSTGVFLAAMDAFLFPVFASFLENGMANTVSIYSAGLVLLLYVSGVLLSQSEIPLSMNGVLTRLNGESAFALMGLLGASIVPHNFYIHSYFAGESTSSSDVDKSSLCQDHLFAIFGVFSGLSLVNYVLMNAAANVFHSTGLVVLTFHDALSLMEQVFMSPLIPVVFLMLLFFSSQITALAWAFGGEVVLHDFLKIEIPAWLHRATIRILAVAPALYCVWTSGADGIYQLLIFTQVLVAMMLPCSVIPLFRIASSRQIMGVHKIPQVGEFLALTTFLGFLGLNVVFVVEMVFGSSDWAGGLRWNTVMGTSIQYTTLLVSSCASLCLILWLAATPLKSASNRAEAQIWNMDAQNALSYPSVQEEEIERTETRRNEDESIVRLESRVKDQLDTTSVTSSVYDLPENILMTDQEIRSSPPEERELDVKYSTSQVSSLKEDSDVKEQSVLQSTVVNEVSDKDLIVETKMAKIEPMSPVEKIVSMENNSKFIEKDVEGVSWETEEATKAAPTSNFTVGSDGPPSFRSLSGEGGSGTGSLSRLQGLGRAARRHLSAILDEFWGHLYDFHGQLVAEARAKKLDQLFGTDQKSASSMKADSFGKDISSGYCMSPTAKGMDSQMTSSLYDSLKQQRTPGSIDSLYGLQRGSSPSPLVNRMQMLGAYGNTTNNNNAYELSERRYSSLRAPSSSEGWEHQQPATVHGYQMKSYVDNLAKERLEALQSRGEIPTSRSMALGTLSYTQQLALALKQKSQNGLTPGPAPGFENFAGSRSISRQSERSYYGVPSSGNTDTVGAAVANEKKYSSMPDISGLSMSARNMHLPNNKSGYWDPSSGGGGYGASYGRLSNESSLYSNLGSRVGVPSTYDDISQSRGGYRDAYSLPQSATTGTGSLWSRQPFEQFGVAERNGAVGEELRNRSNPINIDNNASSNVDAEAKLLQSFRHCILKLIKLEGSEWLFGQSDGVDEELIDRVAAREKFIYEAEAREINQVGHMGEPLISSVPNCGDGCVWRADLIVSFGVWCIHRVLDLSLMESRPELWGKYTYVLNRLQGVIDPAFSKLRTPMTPCFCLQIPASHQRASPTSANGMLPPAAKPAKGKCTTAVTLLDLIKDVEMAISCRKGRTGTAAGDVAFPKGKENLASVLKRYKRRLSNKPVGMNQDGPGSRKNVTAYGSLG', '1294', '', '', '', 'The rate of development of B. cinerea disease symptoms on primary infected leaves was affected by responses mediated by the genes EIN2, JAR1, EDS4, PAD2, and PAD3, but was largely independent of EDS5, SID2/ICS1, and PAD4. a double ein2 npr1 mutant was significantly more susceptible than ein2 plants, and exogenous application of SA decreased B. cinerea lesion size through an NPR1-dependent mechanism that could be mimicked by the cpr1 mutation. These data indicate that local resistance to B. cinerea requires ethylene-, jasmonate-, and SA-mediated signaling, that the SA affecting this resistance does not require ICS1 and is likely synthesized via PAL, and that camalexin limits lesion development (Ferrari et al. 2003)', 'Camalexin biosynthesis', 'Ferrari et al. 2003'),
	('AT5G04660', 'CYP77A4', 'Cytochrome P450 77A4', 'T1E3.20', '830343', 'NM_120548', 'NP_196086', 'Q9LZ31', 'MFPLISFSPTSLDFTFFAIIISGFVFIITRWNSNSKKRLNLPPGPPGWPVVGNLFQFARSGKPFFEYAEDLKKTYGPIFTLRMGTRTMIILSDATLVHEALIQRGALFASRPAENPTRTIFSCNKFTVNAAKYGPVWRSLRRNMVQNMLSSTRLKEFGKLRQSAMDKLIERIKSEARDNDGLIWVLKNARFAAFCILLEMCFGIEMDEETIEKMDEILKTVLMTVDPRIDDYLPILAPFFSKERKRALEVRREQVDYVVGVIERRRRAIQNPGSDKTASSFSYLDTLFDLKIEGRKTTPSNEELVTLCSEFLNGGTDTTGTAIEWGIAQLIANPEIQSRLYDEIKSTVGDDRRVDEKDVDKMVFLQAFVKELLRKHPPTYFSLTHAVMETTTLAGYDIPAGVNVEVYLPGISEDPRIWNNPKKFDPDRFMLGKEDADITGISGVKMIPFGVGRRICPGLAMATIHVHLMLARMVQEFEWCAHPPGSEIDFAGKLEFTVVMKNPLRAMVKPRI', '512', 'EC 1.14.-.- ', '', '', 'Camalexin originates from tryptophan and its biosynthesis involves the cytochrome P450 enzymes CYP79B2 and CYP71B15 (PAD3). Camalexin induction is a complex process, for which triggering by reactive oxygen species (ROS), salicylic acid signalling, and the glutathione status are important. Targets of the signalling cascade are the tryptophan and camalexin biosynthetic genes, which are strongly transcriptionally upregulated at the sites of pathogen infection (Glawischnig et al. 2004) .', 'Camalexin biosynthesis', 'Glawischnig et al. 2004'),
	('AT5G05260', 'CYP79A2', 'Phenylalanine N-monooxygenase ', 'K18I23.6', '830408', 'NM_120608', 'NP_568153', 'Q9FLC8', 'MLAFIIGLLLLALTMKRKEKKKTMLISPTRNLSLPPGPKSWPLIGNLPEILGRNKPVFRWIHSLMKELNTDIACIRLANTHVIPVTSPRIAREILKKQDSVFATRPLTMGTEYCSRGYLTVAVEPQGEQWKKMRRVVASHVTSKKSFQMMLQKRTEEADNLVRYINNRSVKNRGNAFVVIDLRLAVRQYSGNVARKMMFGIRHFGKGSEDGSGPGLEEIEHVESLFTVLTHLYAFALSDYVPWLRFLDLEGHEKVVSNAMRNVSKYNDPFVDERLMQWRNGKMKEPQDFLDMFIIAKDTDGKPTLSDEEIKAQVTELMLATVDNPSNAAEWGMAEMINEPSIMQKAVEEIDRVVGKDRLVIESDLPNLNYVKACVKEAFRLHPVAPFNLPHMSTTDTVVDGYFIPKGSHVLISRMGIGRNPSVWDKPHKFDPERHLSTNTCVDLNESDLNIISFSAGRRGCMGVDIGSAMTYMLLARLIQGFTWLPVPGKNKIDISESKNDLFMAKPLYAVATPRLAPHVYPT', '529', 'EC 1.14.13.124', 'AraCyc', 'KEGG', 'Arabidopsis expressing CYP79D2 from cassava accumulated aliphatic isopropyl and methylpropyl GSL and showed enhanced resistance against the bacterial soft-rot pathogen Erwinia carotovora whereas Arabidopsis expressing the sorghum CYP79A1 or over-expressing the endogenous CYP79A2 accumulated p-hydroxybenzyl or benzyl GSL respectively and showed increased resistance towards the bacterial pathogen Pseudomonas syringae (Brader et al. 2006)', 'GSL core structure synthesis', 'Brader et al. 2006; Grubb & Abel 2006'),
	('AT5G05730', 'ASA1', 'Anthranilate synthase alpha subunit 1 chloroplastic', 'WEI2', '830457', 'NM_120655', 'NP_196192', 'P32068', 'MSSSMNVATMQALTFSRRLLPSVASRYLSSSSVTVTGYSGRSSAYAPSFRSIKCVSVSPEASIVSDTKKLADASKSTNLIPIYRCIFSDQLTPVLAYRCLVKEDDREAPSFLFESVEPGSQMSSVGRYSVVGAQPAMEIVAKENKVIVMDHNNETMTEEFVEDPMEIPRKISEKWNPDPQLVQDLPDAFCGGWVGFFSYDTVRYVEKRKLPFSKAPEDDRNLPDMHLGLYDDVVVFDHVEKKAYVIHWIRLDGSLPYEKAYSNGMQHLENLVAKLHDIEPPKLAAGNVNLQTRQFGPSLDNSNVTCEEYKEAVVKAKEHILAGDIFQIVLSQRFERRTFADPFEVYRALRVVNPSPYMGYLQARGCILVASSPEILTKVKQNKIVNRPLAGTSKRGKNEVEDKRLEKELLENEKQCAEHIMLVDLGRNDVGKVTKYGSVKVEKLMNIERYSHVMHISSTVTGELQDGLTCWDVLRAALPVGTVSGAPKVKAMELIDELEPTRRGPYSGGFGGVSFTGDMDIALSLRTIVFPTACQYNTMYSYKDANKRREWVAYLQAGAGVVADSDPQDEHCECQNKAAGLARAIDLAESAFVKK', '595', 'EC 4.1.3.27 ', '', '', 'In RNA gel-blot analysis 35S-ATR1 displayed elevated accumulation of ATR1 and Trp gene transcripts including two Trp synthesis genes; ASA1 and TSB1 and three Trp secondary metabolism genes CYP79B2; CYP79B3; and CYP83B1. ASA1 encodes the catalytic alpha-subunit of anthranilate synthase the first committed enzyme of the Trp pathway and TSB1 encodes the Trp synthase beta-subunit activity that converts indole to Trp (Celenza et al. 2005)', 'GSL core structure synthesis / Camalexin biosynthesis', 'Celenza et al. 2005; Schuhegger et al. 2007'),
	('AT5G07690', 'MYB29', 'Transcription factor MYB29 ', 'PMG2', '830662', 'NM_120851', 'NP_196386', 'Q9FLR1', 'MSRKPCCVGEGLKKGAWTAEEDKKLISYIHEHGEGGWRDIPQKAGLKRCGKSCRLRWANYLKPDIKRGEFSYEEEQIIIMLHASRGNKWSVIARHLPKRTDNEIKNYWNTHLKKLLIDKGIDPVTHKPLAYDSNPDEQSQSGSISPKSLPPSSSKNVPEITSSDETPKYDASLSSKKRCFKRSSSTSKLLNKVAARASSMGTILGASIEGTLISSTPLSSCLNDDFSETSQFQMEEFDPFYQSSEHIIDHMKEDISINNSEYDFSQFLEQFSNNEGEEADNTGGGYNQDLLMSDVSSTSVDEDEMMQNITGWSNYLLDHSDFNYDTSQDYDDKNFI', '336', '', '', '', 'A phylogenetic analysis with the R2R3 motif of MYB28 showed that it and two homologues. MYB29 and MYB76 were members of an clade that included three characterized regulators of indole GSLs. Over-expression of the individual MYB genes showed that they all had the capacity to increase the production of aliphatic GSLs in leaves and seeds and induce gene expression of aliphatic biosynthetic genes within leaves. Analysis of leaves and seeds knockout mutants showed that mutants of MYB29 and MYB76 have reductions in only short-chained aliphatic GSLs whereas a mutant in MYB28 has reductions in both short- and long-chained aliphatic GSLs (Sonderby et al. 2007)', 'GSL transcription factor / Camalexin biosynthesis', 'Burow et al. 2015; Sonderby et al. 2010; Sonderby et al. 2007; Stotz et al. 2011'),
	('AT5G07700', 'MYB76', 'Transcription factor MYB76 ', 'HAG2', '830663', 'NM_120852', 'NP_196387', 'Q9SPG5', 'MSKRPYCIGEGLKKGAWTTEEDKKLISYIHDHGEGGWRDIPEKAGLKRCGKSCRLRWTNYLKPDIKRGEFSYEEEQIIIMLHASRGNKWSVIARHLPKRTDNEVKNYWNTHLKKRLIDDGIDPVTHKPLASSNPNPVEPMKFDFQKKSNQDEHSSQSSSTTPASLPLSSNLNSVKSKISSGETQIESGHVSCKKRFGRSSSTSRLLNKVAARASSIGNILSTSIEGTLRSPASSSGLPDSFSQSYEYMIDNKEDLGTSIDLNIPEYDFPQFLEQLINDDDENENIVGPEQDLLMSDFPSTFVDEDDILGDITSWSTYLLDHPNFMYESDQDSDEKNFL', '338', '', '', '', 'A phylogenetic analysis with the R2R3 motif of MYB28 showed that it and two homologues; MYB29 and MYB76 were members of an clade that included three characterized regulators of indole GSLs. Over-expression of the individual MYB genes showed that they all had the capacity to increase the production of aliphatic GSLs in leaves and seeds and induce gene expression of aliphatic biosynthetic genes within leaves. Analysis of leaves and seeds knockout mutants showed that mutants of MYB29 and MYB76 have reductions in only short-chained aliphatic GSLs whereas a mutant in MYB28 has reductions in both short- and long-chained aliphatic GSLs (Sonderby et al. 2007)', 'GSL transcription factor / Camalexin biosynthesis', 'Frerigmann & Gigolashvili 2014; Sonderby et al. 2010; Sonderby et al. 2007; Stotz et al. 2011'),
	('AT5G13220', 'TIFY9', 'Protein TIFY 9', 'JAS1, JAZ10', '831162', 'NM_121325', 'NP_568287', 'Q93ZM9', 'MSKATIELDFLGLEKKQTNNAPKPKFQKFLDRRRSFRDIQGAISKIDPEIIKSLLASTGNNSDSSAKSRSVPSTPREDQPQIPISPVHASLARSSTELVSGTVPMTIFYNGSVSVFQVSRNKAGEIMKVANEAASKKDESSMETDLSVILPTTLRPKLFGQNLEGDLPIARRKSLQRFLEKRKER', '197', '', '', '', 'The effect of low R:FR increasing Arabidopsis susceptibility to B. cinerea was not present in mutants deficient in the biosynthesis of camalexin (pad3) or metabolism of iGS (pen2). In a mutant deficient in the JASMONATE ZIM DOMAIN-10 (JAZ10) protein, which does not respond to low R : FR with increased susceptibility to B. cinerea, supplemental FR failed to down-regulate iGS production. These results indicate that suppression of Arabidopsis immunity against B. cinerea by low R:FR ratios is mediated by reduced levels of Trp-derived defenses, and provide further evidence for a functional role of JAZ10 in the link between phytochrome and jasmonate signaling (Cargnel et al. 2014)', 'Camalexin biosynthesis', 'Cargnel et al. 2014'),
	('AT5G14200', 'IMDH1', '3-isopropylmalate dehydrogenase 3 chloroplastic', 'IMD1', '831270', 'NM_121424', 'NP_196924', 'Q9FMT1', 'MAAFLQTNISLNAIKIVPGKYSSLTDHQFRAPYRIRCAAASPGKKRYNIALLPGDGIGPEVISVAKNVLQKAGSLEGLEFDFKEMPVGGAALDLVGVPLPEETFTAAKLSDAILLGAIGGYKWDKNEKHLRPEMALFYLRRDLKVFANLRPATVLPQLVDASTLKKEVAEGVDMMIVRELTGGIYFGEPRGITINENGEEVGVSTEIYAAHEIDRIARVAFETARKRRGKLCSVDKANVLDASILWRKRVTALASEYPDVELSHMYVDNAAMQLIRDPKQVLTQSLPITFLVIYCLMKLQ', '409', 'EC 1.1.1.85', 'AraCyc', 'KEGG', 'Knocking out either of the candidate genes; AtleuC1 (IIL1) or AtIMD1 (IMD1) would reduced the level of Met-GSLs indicating that both genes are actually involved in Met-GSL biosynthesis (Sawada & Kuwahara et al. 2009)', 'GSL side chain elongation', 'He et al. 2011; He et al. 2009; Sawada & Kuwahara et al. 2009  '),
	('AT5G22300', 'NIT4', 'Bifunctional nitrilase/nitrile hydratase NIT4 ', 'MWD9.8', '832290', 'NM_122135', 'NP_197622', 'P46011', 'MSMQQETSHMTAAPQTNGHQIFPEIDMSAGDSSSIVRATVVQASTVFYDTPATLDKAERLLSEAAENGSQLVVFPEAFIGGYPRGSTFELAIGSRTAKGRDDFRKYHASAIDVPGPEVERLALMAKKYKVYLVMGVIEREGYTLYCTVLFFDSQGLFLGKHRKLMPTALERCIWGFGDGSTIPVFDTPIGKIGAAICWENRMPSLRTAMYAKGIEIYCAPTADSRETWLASMTHIALEGGCFVLSANQFCRRKDYPSPPEYMFSGSEESLTPDSVVCAGGSSIISPLGIVLAGPNYRGEALITADLDLGDIARAKFDFDVVGHYSRPEVFSLNIREHPRKAVSFKTSKVMEDESV', '355', 'EC 3.5.5.1 EC 3.5.5.4 EC 4.2.1.65', '', '', 'Comparison of the amino acid sequences of NIT4 and NIT1 homologs has permitted the identification of typical sequence motifs for NIT4 and NIT1. One of these motifs was mutated in Arabidopsis NIT4 and obtained enzymes that could convert 3-phen-ylpropionitrile three to nearly tenfold faster than the wild-type enzyme (Janowitz et al. 2009)', 'GSL degradation', 'Janowitz et al. 2009; Wittstock & Burow 2010'),
	('AT5G23010', 'MAM1', 'Methylthioalkylmalate synthase 1 chloroplastic', 'IMS3', '832365', 'NM_122207', 'NP_197692', 'Q9FG67', 'MASSLLTSSVMIPTTGSTVVGRSVLPFQSSLHSLRLTHSYKNPALFISCCSSVSKNAATSSTDLKPVVERWPEYIPNKLPDGNYVRVFDTTLRDGEQSPGGSLTPPQKLEIARQLAKLRVDIMEVGFPGSSEEELETIKTIAKTVGNEVDEETGYVPVICAIARCKHRDIEATWEALKYAKRPRILVFTSTSDIHMKYKLKKTQEEVIEMAVSSIRFAKSLGFNDIQFGCEDGGRSDKDFLCKILGEAIKAGVTVVTIGDTVGINMPHEYGELVTYLKANTPGIDDVVVAVHCHNDLGLATANSIAGIRAGARQVEVTINGIGERSGNASLEEVVMALKCRGAYVINGVYTKIDTRQIMATSKMVQEYTGLYVQAHKPIVGANCFVHESGIHQDGILKNRSTYEILSPEDIGIVKSQNSGLVLGKLSGRHAVKDRLKELGYELDDEKLNAVFSLFRDLTKNKKRITDADLKALVTSSDEISLEKLNGANGLKSNGYIPVPQVSSNV', '506', 'EC 2.3.3.- ', 'AraCyc', 'KEGG', 'MAM1 catalyses the condensation step of the first three elongation cycles while MAM3 catalyzes the condensation step of all six elongation cycles in met derived GSL biosynthesis (Redovnikovic et al. 2012)', 'GSL side chain elongation', 'Textor et al. 2007; Zang et al. 2009; Redovnikovic et al. 2012  '),
	('AT5G23020', 'MAM3', 'Methylthioalkylmalate synthase 3 chloroplastic', 'MAM-L', '832366', 'NM_122208', 'NP_197693', 'Q9FN52', 'MASLLLTSSSMITTSCRSMVLRSGLPIGSSFPSLRLTRPYDKATLFVSCCSAESKKVATSATDLKPIMERRPEYIPNKLPHKNYVRVLDTTLRDGEQSPGAALTPPQKLEIARQLAKLRVDIMEVGFPVSSEEEFEAIKTIAKTVGNEVDEETGYVPVICGIARCKKRDIEATWEALKYAKRPRVMLFTSTSEIHMKYKLKKTKEEVIEMAVNSVKYAKSLGFKDIQFGCEDGGRTEKDFICKILGESIKAGATTVGFADTVGINMPQEFGELVAYVIENTPGADDIVFAIHCHNDLGVATANTISGICAGARQVEVTINGIGERSGNAPLEEVVMALKCRGESLMDGVYTKIDSRQIMATSKMVQEHTGMYVQPHKPIVGDNCFVHESGIHQDGILKNRSTYEILSPEDVGIVKSENSGIVLGKLSGRHAVKDRLKELGYEISDEKFNDIFSRYRELTKDKKRITDADLKALVVNGAEISSEKLNSKGINDLMSSPQISAVV', '503', 'EC 2.3.3.-', 'AraCyc', 'KEGG', 'Analysis of MAM3 mutants demonstrated that MAM3 catalyzes the formation of all GSL chain lengths in vivo as well as in vitro making this enzyme the major generator of GSL chain length diversity in the plant. The localization of MAM3 in the chloroplast suggests that this organelle is the site of Met chain elongation (Textor et al. 2007)', 'GSL side chain elongation', 'Textor et al. 2007; Redovnikovic et al. 2012  '),
	('AT5G24960', 'CYP71A14', 'Cytochrome P450 71A14', 'F6A4_170', '832566', 'NM_122405', 'NP_197878', 'P58045', 'MEMIIISLCLATILALLLLKQFLNRTYTAKVNLPPSPWRVPVIGNLHQLSLHPHRSLRSLSHRYGPLMLLHFGRVPVLVVSSSDVAHDLMKTHDLKVANRPQLKVVEKIFNGGREMVFSPYGEYWRQIKSVCIVNLLNKKKVQSFEKVREEEISEMMERVEKASSDSSPLNLSELLLTLTSDVTSRVSLGRKYSKEESMSDFKIQMRKITELVGGFPVGEYIPCLAWIDKLRGVDEKAEEVSKAFGDLMEKVLQEHLDATDKPTLDFVDVLLSLERHERNGVQIRRSDIKFLILDMFLAGTETTYALLEWIMTELIRHPECMKKLQDEIRAKATKLILYISEEDVEDMKYLKAVVKEVLRLHPPLPLLVPRELSEDIKLKGYDIAAGTQVIINAWAIQRDTMTWGIDAEEFRPERHLDSLVDFRGTNFEFIPFGSGRRICPGIGFAMALVEVTLANLVNRFNWRMEVQHSGDEYDLAESTGLDVCRKFPLIVFPSPA', '497', 'EC 1.14.-.- ', 'AraCyc', '', 'Camalexin originates from tryptophan and its biosynthesis involves the cytochrome P450 enzymes CYP79B2 and CYP71B15 (PAD3). Camalexin induction is a complex process, for which triggering by reactive oxygen species (ROS), salicylic acid signalling, and the glutathione status are important. Targets of the signalling cascade are the tryptophan and camalexin biosynthetic genes, which are strongly transcriptionally upregulated at the sites of pathogen infection (Glawischnig et al. 2004) .', 'Camalexin biosynthesis', 'Glawischnig et al. 2004'),
	('AT5G25980', 'TGG2', 'Myrosinase 2 ', 'BGLU37', '832667', 'NM_180745', 'NP_851076', 'Q9C5C2', 'MQHNTYIYILTMKLLGFALAILLVVATCKPEEEITCEENVPFTCSQTDRFNKQDFESDFIFGVASSAYQIEGGRGRGLNVWDGFTHRYPEKGGADLGNGDTTCDSYRTWQKDLDVMEELGVKGYRFSFAWSRILPKGKRSRGINEDGINYYSGLIDGLIARNITPFVTLFHWDLPQSLQDEYEGFLDRTIIDDFKDYADLCFERFGDRVKHWITINQLFTVPTRGYALGTDAPGRCSQWVDKRCYGGDSSTEPYIVAHNQLLAHATVVDLYRTRYKYQGGKIGPVMITRWFLPYDDTLESKQATWRAKEFFLGWFMEPLTKGKYPYIMRKLVGNRLPKFNSTEARLLKGSYDFLGLNYYVTQYAHALDPSPPEKLTAMTDSLANLTSLDANGQPPGPPFSKGSYYHPRGMLNVMEHFKTKYGDPLIYVTENGFSTSGGPIPFTEAFHDYNRIDYLCSHLCFLRKAIKEKRVNVKGYFVWSLGDNYEFCNGYTVRFGLSYVDFNNVTADRDLKASGLWYQSFLRDTTKNQDILRSSLPFKNGDRKSLT', '547', 'EC 3.2.1.147', '', '', 'Glucosinolate breakdown in crushed leaves of tgg1 or tgg2 single mutants was comparable to that of wild-type; indicating redundant enzyme function. In contrast; leaf extracts of tgg1 tgg2 double mutants had undetectable myrosinase activity in vitro and damage-induced breakdown of endogenous GSLs was apparently absent for aliphatic and greatly slowed for indole GSLs (Barth & Jander 2006)', 'GSL degradation', 'Wittstock & Burow 2010'),
	('AT5G26000', 'TGG1', 'Myrosinase 1 ', 'BGLU38', '832669', 'NM_180746', 'NP_851077', 'P37702', 'MKLLMLAFVFLLALATCKGDEFVCEENEPFTCNQTKLFNSGNFEKGFIFGVASSAYQVEGGRGRGLNVWDSFTHRFPEKGGADLGNGDTTCDSYTLWQKDIDVMDELNSTGYRFSIAWSRLLPKGKRSRGVNPGAIKYYNGLIDGLVAKNMTPFVTLFHWDLPQTLQDEYNGFLNKTIVDDFKDYADLCFELFGDRVKNWITINQLYTVPTRGYALGTDAPGRCSPKIDVRCPGGNSSTEPYIVAHNQLLAHAAAVDVYRTKYKDDQKGMIGPVMITRWFLPFDHSQESKDATERAKIFFHGWFMGPLTEGKYPDIMREYVGDRLPEFSETEAALVKGSYDFLGLNYYVTQYAQNNQTIVPSDVHTALMDSRTTLTSKNATGHAPGPPFNAASYYYPKGIYYVMDYFKTTYGDPLIYVTENGFSTPGDEDFEKATADYKRIDYLCSHLCFLSKVIKEKNVNVKGYFAWSLGDNYEFCNGFTVRFGLSYVDFANITGDRDLKASGKWFQKFINVTDEDSTNQDLLRSSVSSKNRDRKSLADA', '541', 'EC 3.2.1.147 EC 3.2.1.21', '', '', 'Glucosinolate breakdown in crushed leaves of tgg1 or tgg2 single mutants was comparable to that of wild-type; indicating redundant enzyme function. In contrast; leaf extracts of tgg1 tgg2 double mutants had undetectable myrosinase activity in vitro and damage-induced breakdown of endogenous GSLs was apparently absent for aliphatic and greatly slowed for indole GSLs (Barth & Jander 2006)', 'GSL degradation', 'Wittstock & Burow 2010'),
	('AT5G27380', 'GSH2', 'Glutathione synthetase chloroplastic', 'GSHB', '832797', 'NM_122620', 'NP_568495', 'P46416', 'MGSGCSSLSYSSSSTCNATVFSISSSPSSSSSLKLNPSSFLFQNPKTLRNQSPLRCGRSFKMESQKPIFDLEKLDDEFVQKLVYDALVWSSLHGLVVGDKSYQKSGNVPGVGLMHAPIALLPTAFPEAYWKQACNVTPLFNELIDRVSLDGKFLQDSLSRTKKVDVFTSRLLDIHSKMLERNKKEDIRLGLHRFDYMLDEETNSLLQIEMNTISCSFPGLSRLVSQLHQSLLRSYGDQIGIDSERVPINTSTIQFADALAKAWLEYSNPRAVVMVIVQPEERNMYDQHLLSSILREKHNIVVIRKTLAEVEKEGSVQEDETLIVGGQAVAVVYFRSGYTPNDHPSESEWNARLLIEESSAVKCPSIAYHLTGSKKIQQELAKPGVLERFLDNKEDIAKLRKCFAGLWSLDDSEIVKQAIEKPGLFVMKPQREGGGNNIYGDDVRENLLRLQKEGEEGNAAYILMQRIFPKVSNMFLVREGVYHKHQAISELGVYGAYLRSKDEVIVNEQSGYLMRTKIASSDEGGVAAGFGVLDSIYLI', '539', 'EC 6.3.2.3', '', '', 'Both gamma glutamyl cysteine ligase (GSH1) and glutathione synthetase (GSH2); which catalyse its synthesis were significantly enriched in bundle sheath (BS) cells that can be related with sulfur and GSL metabolism (Aubry et al. 2014)', 'GSL core structure synthesis', 'Bednarek et al. 2009; Aubry et al. 2014'),
	('AT5G38450', 'CYP735A1', 'Cytokinin hydroxylase', 'MXI10.18', '833833', 'NM_123206', 'NP_198661', 'Q9FF18', 'MLLTILKSLLVIFVTTILRVLYDTISCYWLTPRRIKKIMEQQGVTGPKPRPLTGNILEISAMVSQSASKDCDSIHHDIVGRLLPHYVAWSKQYGKRFIVWNGTDPRLCLTETELIKELLMKHNGVSGRSWLQQQGTKNFIGRGLLMANGQDWHHQRHLAAPAFTGERLKGYARHMVECTSKLVERLRKEVGEGANEVEIGEEMHKLTADIISRTKFGSSFEKGKELFNHLTVLQRRCAQATRHLCFPGSRFLPSKYNREIKSLKKEVERLLIEIIQSRRDCAEMGRSSTHGDDLLGLLLNEMDIDKNNNNNNNNLQLIMDECKTFFFAGHETTALLLTWTTMLLADNPTWQEKVREEVREVFGRNGLPSVDQLSKLTSLSKVINESLRLYPPATLLPRMAFEDLKLGDLTIPKGLSIWIPVLAIHHSEELWGKDANQFNPERFGGRPFASGRHFIPFAAGPRNCIGQQFALMEAKIILATLISKFNFTISKNYRHAPIVVLTIKPKYGVQVILKPLVS', '518', 'EC 1.14.13.-', '', '', 'Camalexin originates from tryptophan and its biosynthesis involves the cytochrome P450 enzymes CYP79B2 and CYP71B15 (PAD3). Camalexin induction is a complex process, for which triggering by reactive oxygen species (ROS), salicylic acid signalling, and the glutathione status are important. Targets of the signalling cascade are the tryptophan and camalexin biosynthetic genes, which are strongly transcriptionally upregulated at the sites of pathogen infection (Glawischnig et al. 2004) .', 'Camalexin biosynthesis', 'Glawischnig et al. 2004'),
	('AT5G40360', 'MYB115', 'Myb domain protein 115 ', 'AtMYB115', '834034', 'NM_123400', 'NP_568581', 'Q1PDP9', 'MYHQNLISSTPNQNSNPHDWDIQNPLFSIHPSAEIPSKYPFMGITSCPNTNVFEEFQYKITNDQNFPTTYNTPFPVISEGISYNMHDVQENTMCGYTAHNQGLIIGCHEPVLVHAVVESQQFNVPQSEDINLVSQSERVTEDKVMFKTDHKKKDIIGKGQWTPTEDELLVRMVKSKGTKNWTSIAKMFQGRVGKQCRERWHNHLRPNIKKNDWSEEEDQILIEVHKIVGNKWTEIAKRLPGRSENIVKNHWNATKRRLHSVRTKRSDAFSPRNNALENYIRSITINNNALMNREVDSITANSEIDSTRCENIVDEVMNLNLHATTSVYVPEQAVLTWGYDFTKCYEPMDDTWMLMNGWN', '359', '', '', '', 'Two conserved TFs; MYB115 and MYB118 were co-expressed with the key enzyme encoding genes in the newly evolved benzoyloxy GSL (GLS) pathway. These TFs interacted with the promoters of the GLS biosynthetic genes and negatively influenced their expression. Similarly the GLS profiles of these two TFs knockouts showed that they influenced the aliphatic GLS accumulation within seed; leaf and flower while they mainly expressed in seeds (Zhang et al. 2015)', 'GSL transcription factor', 'Zhang et al. 2015'),
	('AT5G44070', 'PCS1', 'Glutathione gamma-glutamylcysteinyltransferase 1 ', 'CAD1', '834430', 'NM_123774', 'NP_199220', 'Q9S7Z3', 'MAMASLYRRSLPSPPAIDFSSAEGKLIFNEALQKGTMEGFFRLISYFQTQSEPAYCGLASLSVVLNALSIDPGRKWKGPWRWFDESMLDCCEPLEVVKEKGISFGKVVCLAHCSGAKVEAFRTSQSTIDDFRKFVVKCTSSENCHMISTYHRGVFKQTGTGHFSPIGGYNAERDMALILDVARFKYPPHWVPLKLLWEAMDSIDQSTGKRRGFMLISRPHREPGLLYTLSCKDESWIEIAKYLKEDVPRLVSSQHVDSVEKIISVVFKSLPSNFNQFIRWVAEIRITEDSNQNLSAEEKSRLKLKQLVLKEVHETELFKHINKFLSTVGYEDSLTYAAAKACCQGAEILSGSPSKEFCCRETCVKCIKGPDDSEGTVVTGVVVRDGNEQKVDLLVPSTQTECECGPEATYPAGNDVFTALLLALPPQTWSGIKDQALMHEMKQLISMASLPTLLQEEVLHLRRQLQLLKRCQENKEEDDLAAPAY', '485', 'EC 2.3.2.15', '', '', 'Microarray data of Flg22-inducible expression profiles identified a phytochelatin synthase gene; PCS1 whose corresponding mutants (pcs1-1; pcs1-2 and cad1-3) were all impaired in the callose response to Flg22. The transcriptional and indolic GSL profiles of the pcs1 mutant resemble those of the pen2 mutant; suggesting that it too is involved in the breakdown of 4-methoxy-indol-3-ylmethylGSL (Clay et al. 2009)', 'GSL degradation / Camalexin biosynthesis', 'Clay et al. 2009; Su et al. 2011'),
	('AT5G46760', 'MYC3', 'Transcription factor MYC3', 'AtbHLH5', '834719', 'NM_124046.2', 'NP_199488.1', 'Q9FIP9', 'MNGTTSSINFLTSDDDASAAAMEAFIGTNHHSSLFPPPPQQPPQPQFNEDTLQQRLQALIESAGENWTYAIFWQISHDFDSSTGDNTVILGWGDGYYKGEEDKEKKKNNTNTAEQEHRKRVIRELNSLISGGIGVSDESNDEEVTDTEWFFLVSMTQSFVNGVGLPGESFLNSRVIWLSGSGALTGSGCERAGQGQIYGLKTMVCIATQNGVVELGSSEVISQSSDLMHKVNNLFNFNNGGGNNGVEASSWGFNLNPDQGENDPALWISEPTNTGIESPARVNNGNNSNSNSKSDSHQISKLEKNDISSVENQNRQSSCLVEKDLTFQGGLLKSNETLSFCGNESSKKRTSVSKGSNNDEGMLSFSTVVRSAANDSDHSDLEASVVKEAIVVEPPEKKPRKRGRKPANGREEPLNHVEAERQRREKLNQRFYSLRAVVPNVSKMDKASLLGDAISYINELKSKLQQAESDKEEIQKKLDGMSKEGNNGKGCGSRAKERKSSNQDSTASSIEMEIDVKIIGWDVMIRVQCGKKDHPGARFMEALKELDLEVNHASLSVVNDLMIQQATVKMGSQFFNHDQLKVALMTKVGENY', '592', '', '', '', 'The myc2 myc3 myc4 (myc234) triple mutant was almost completely devoid of GSL and was extremely susceptible to the generalist herbivore Spodoptera littoralis. On the contrary the specialist Pieris brassicae was unaffected by the presence of GSL and preferred to feed on wild-type plants. In addition lack of GSL in myc234 drastically modified S. littoralis feeding behavior. Surprisingly the expression of MYB factors known to regulate GS biosynthesis genes was not altered in myc234; suggesting that MYC2/MYC3/MYC4 are necessary for direct transcriptional activation of GS biosynthesis genes. Yeast two-hybrid and pull-down experiments indicated that MYC2/MYC3/MYC4 interact directly with GS-related MYBs. This specific MYC?MYB interaction plays a crucial role in the regulation of defense secondary metabolite production and underlines the importance of GSL in shaping plant interactions with adapted and nonadapted herbivores (Schweizer et al. 2013)', 'GSL transcription factor', 'Schweizer et al. 2013'),
	('AT5G47230', 'ERF5', 'Ethylene-responsive transcription factor 5', 'ERF-5, ERF102', '834770', 'NM_124094', 'NP_568679', 'O80341', 'MATPNEVSALWFIEKHLLDEASPVATDPWMKHESSSATESSSDSSSIIFGSSSSSFAPIDFSESVCKPEIIDLDTPRSMEFLSIPFEFDSEVSVSDFDFKPSNQNQNQFEPELKSQIRKPPLKISLPAKTEWIQFAAENTKPEVTKPVSEEEKKHYRGVRQRPWGKFAAEIRDPNKRGSRVWLGTFDTAIEAARAYDEAAFRLRGSKAILNFPLEVGKWKPRADEGEKKRKRDDDEKVTVVEKVLKTEQSVDVNGGETFPFVTSNLTELCDWDLTGFLNFPLLSPLSPHPPFGYSQLTVV', '300', '', '', '', 'MKK9, an MKK, is an upstream activator of the MPKs MPK3 and MPK6 both in vitro and in planta. Expression of active MKK9 protein in transgenic plants induces the synthesis of ethylene and camalexin through the activation of the endogenous MPK3 and MPK6 kinases. MKK9-MPK3/MPK6 cascade participates in the regulation of the biosynthesis of ethylene and camalexin and may be an important axis in the stress responses of Arabidopsis (Xu et al. 2008).', 'Camalexin biosynthesis', 'Xu et al. 2008'),
	('AT5G48180', 'NSP5', 'Nitrile-specifier protein 5 ', 'MIF21.7', '834871', 'NM_124193', 'NP_568692', 'Q93XW5', 'MCPVENKWLKVGQKGAGPGARSSHAMTVVGNKVYCFGGELKPTIHIDNDLYVFDLETQEWSIAPATGEAPFPCFGVSMVTIGSTIYVYGGRDDKRRYNGLHSYDTETNEWKLLAPVEEGLPGRSYHSMAGDDRKVYVFGGVTAKGRVNTLHAYDVVDQKWVEYPAAGEACKGRGAPGLVVVEGRIWVLFGFDGNELGDIHCFDLASEQWKAVETTGDVPAARSVFPAVSYGKYIVIYGGEEEPHELMHMGAGKMSGEVYQLDTETLVWERIVCGNEEEKPSQRGWCAFTKAVKDGEEGLLVHGGNSPTNERLDDLVFWGFSHLNVN', '326', '', '', '', 'The seed content of the precursor GSL; 4-methylthiobutylGSL was consistently reduced in nsp3-2; nsp4-1 and nsp5-1 relative to WT (Wittstock et al. 2016)', 'GSL degradation', 'Wittstock & Burow 2010'),
	('AT5G48850', 'SDI1', 'Protein SULFUR DEFICIENCY-INDUCED 1', 'AtSDI1', '834943', 'NM_124262.4. ', 'NP_199696.2', 'Q8GXU5', 'MERSLKKTKNNYNNSIKSNLMKDDELFHVIHKVPCGDTPYVRAKHAQLIEKNPEMAIVWFWKAINTGDRVDSALKDMAVVMKQLDRSEEAIEAIKSFRPRCSKNSQDSLDNVLIDLYKKCGRMEEQVELLKRKLRQIYQGEAFNGKPTKTARSHGKKFQVTVQQEISRLLGNLGWAYMQQAKYLSAEAVYRKAQMVEPDANKSCNLAMCLIKQGRFEEGRLVLDDVLEYRVLGADDCRTRQRAEELLSELESSLPRMRDAEMEDVLGNILDDDFVLGLEEMTSTSFKSKRLPIFEQISSFRNTLVC', '306', '', '', '', 'Sulfur deficiency induced 1 (SD1) and SD2 are ?S marker genes sulfur deficiency that act as major repressors controlling GSL biosynthesis in Arabidopsis under ?S condition. SDI1 and SDI2 expression negatively correlated with GSL biosynthesis in both transcript and metabolite levels. Principal components analysis of transcriptome data indicated that SDI1 regulates aliphatic GSL biosynthesis as part of ?S response. SDI1 was localized to the nucleus and interacted with MYB28 a major transcription factor that promotes aliphatic GSL biosynthesis in both yeast and plant cells (Aarabi et al. 2016)', 'GSL core structure synthesis', 'Aarabi et al. 2016'),
	('AT5G54140', 'ILL3', 'IAA-amino acid hydrolase ILR1-like 3', 'MJP23.12', '835501', 'NM_124794', 'NP_200225', 'O81641', 'MANSSIVALLLLFVIASSVNGGDQEYPNQYLTEALGDKEWLVSVRRQIHENPELLFELHKTSALIRRELDELGVSYSYPVAKTGIVAQIGSGYPPVVALRADMDALPLQELVEWDHKSKIDGKMHACGHDSHTTMLLGAAKLLSKRKRMLNGTVRLLFQPAEEGGAGAFHMIKEGALGDSEAIFGMHVHTGLPTGELATISGPALASTSIFSVRMSGKSPASSETYSCVDPVLAASSTILALQLIISREVDPLLSHVLSVTFMKSGGSEFDVIPAYVEFGGTLRSLTTNGINWLIKRLKEVVEGQAEVQRCKADIDMHEDDHPMYPATVNDHKLHEFTEKVLKLLLGPEKVKPANKVMAGEDFAFYQQKIPGYYIGIGIRNEEIGSVRSVHSPYFFLDENVLPIGSATFAALAEMYLQEHQNQTKSGD', '428', 'EC 3.5.1.-', '', '', 'Camalexin originates from tryptophan and its biosynthesis involves the cytochrome P450 enzymes CYP79B2 and CYP71B15 (PAD3). Camalexin induction is a complex process, for which triggering by reactive oxygen species (ROS), salicylic acid signalling, and the glutathione status are important. Targets of the signalling cascade are the tryptophan and camalexin biosynthetic genes, which are strongly transcriptionally upregulated at the sites of pathogen infection (Glawischnig et al. 2004) .', 'Camalexin biosynthesis', 'Glawischnig et al. 2004'),
	('AT5G54810', 'TSB1', 'Tryptophan synthase beta chain 1 chloroplastic', 'TRPB', '835571', 'NM_124862', 'NP_200292', 'P14671', 'MAASGTSATFRASVSSAPSSSSQLTHLKSPFKAVKYTPLPSSRSKSSSFSVSCTIAKDPPVLMAAGSDPALWQRPDSFGRFGKFGGKYVPETLMHALSELESAFYALATDDDFQRELAGILKDYVGRESPLYFAERLTEHYRRENGEGPLIYLKREDLNHTGAHKINNAVAQALLAKRLGKKRIIAETGAGQHGVATATVCARFGLECIIYMGAQDMERQALNVFRMRLLGAEVRGVHSGTATLKDATSEAIRDWVTNVETTHYILGSVAGPHPYPMMVRDFHAVIGKETRKQALEKWGGKPDVLVACVGGGSNAMGLFHEFVNDTEVRMIGVEAAGFGLDSGKHAATLTKGDVGVLHGAMSYLLQDDDGQIIEPHSISAGLDYPGVGPEHSFFKDMGRAEYYSITDEEALEAFKRVSRLEGIIPALETSHALAYLEKLCPTLSDGTRVVLNFSGRGDKDVQTVAKYLDV', '470', 'EC 4.2.1.20', '', '', 'In RNA-blot analysis; the atr1-2 mutation suppressed elevated expression of Trp genes caused by the cyp83B1 mutation: The ASA1 and TSB1 Trp synthesis genes were suppressed to wild-type levels by atr1-2 (Celenza et al. 2005)', 'GSL core structure synthesis / Camalexin biosynthesis', 'Celenza et al. 2005; Zhao et al. 1998'),
	('AT5G57220', 'CYP81F2', 'Cytochrome P450 81F2 ', 'IGM1', '835828', 'NM_125104', 'NP_200532', 'Q9LVD6', 'MDYVLIVLPLALFLIAYKFLFSSKTQGFNLPPGPTPFPIVGHLHLVKPPVHRLFRRFAEKYGDIFSLRYGSRQVVVISSLPLVRESFTGQNDVILTNRPHFLTAKYVAYDYTTIGTAAYGDHWRNLRRICSLEILSSNRLTGFLSVRKDEIRRLLTKLSREYDGRVVELEPLLADLTFNNIVRMVTGRRYYGDQVHNKEEANLFKKLVTDINDNSGASHPGDYLPILKVFGHGYEKKVKALGEAMDAFLQRLLDECRINGESNTMVSHLLSLQLDQPKYYSDVIIKGLMLSMMLAGTDTAAVTLEWAMANLLKKPEVLKKAKAEIDEKIGEERLVDEPDIANLPYLQNIVSETFRLCPAAPLLVPRSPSEDLKIGGYDIPRGTIVLVNAWAIHRDPRLWDEPEKFMPERFEDQEASKKLMVFGNGRRTCPGATLGQRMVLLALGSLIQCFDWEKVNGEDVDMTENPGMAMRKLVQLRAVCHKRPIMTNLLA', '491', 'EC 1.14.-.- ', 'AraCyc', '', 'All four Arabidopsis CYP81F gene products had the capacity to modify the indole GSL structure. CYP81F1; CYP81F2; and CYP81F3 but not CYP81F4 catalyzed the conversion of indol-3-yl-methyl GSL (I3M) to 4-hydroxy-indol-3-yl-methyl (4OH-I3M) and all four CYP81Fs converted I3M to 1-hydroxy-indol-3-yl-methyl GSL (1OH-I3M) (Pfalz et al. 2011)', 'GSL core structure synthesis', 'Bednarek et al. 2009; Hiruma et al. 2010; Pfalz et al. 2009  '),
	('AT5G60890', 'MYB34', 'Transcription factor MYB34 ', 'ATMYB34', '836210', 'NM_125482', 'NP_200897', 'O64399', 'MVRTPCCKEEGIKKGAWTPEEDQKLIAYLHLHGEGGWRTLPEKAGLKRCGKSCRLRWANYLRPDIKRGEFSPEEDDTIIKLHALKGNKWAAIATSLAGRTDNEIKNYWNTNLKKRLKQKGIDAITHKPINSTGQTGFEPKVNKPVYSSGSARLLNRVASKYAVELNRDLLTGIISGNSTVAEDSQNSGDVDSPTSTLLNKMAATSVLINTTTTYSGFSDNCSFTDEFNEFFNNEEISDIYTTVDNFGFMEELKSILSYGDASAGVIENSPEVNVADAMEFIDSWNEDDNMVGVFV', '295', '', '', '', 'MYB34; MYB51 and MYB122 act together to control the biosynthesis of indole-3-ylmethyl-GSL (I3M) in shoots and roots with MYB34 controlling biosynthesis of indolic GSLs (IGs) mainly in the roots. MYB51 regulating biosynthesis in shoots and MYB122 having an accessory role in the biosynthesis of IGs (Frerigmann & Gigolashvili 2014)', 'GSL transcription factor / Camalexin biosynthesis', 'Celenza et al. 2005; Frerigmann & Gigolashvili 2014 ; Frerigmann et al. 2015'),
	('AT5G61420', 'MYB28', 'Transcription factor MYB28 ', 'PMG1', '836263', 'NM_180910', 'NP_851241', 'Q9SPG2', 'MSRKPCCVGEGLKKGAWTTEEDKKLISYIHDHGEGGWRDIPQKAGLKRCGKSCRLRWTNYLKPEIKRGEFSSEEEQIIIMLHASRGNKWSVIARHLPRRTDNEIKNYWNTHLKKRLMEQGIDPVTHKPLASSSNPTVDENLNSPNASSSDKQYSRSSSMPFLSRPPPSSCNMVSKVSELSSNDGTPIQGSSLSCKKRFKKSSSTSRLLNKVAAKATSIKDILSASMEGSLSATTISHASFFNGFTEQIRNEEDSSNTSLTNTLAEFDPFSPSSLYPEHEINATSDLNMDQDYDFSQFFEKFGGDNHNEENSMNDLLMSDVSQEVSSTSVDDQDNMVGNFEGWSNYLLDHTNFMYDTDSDSLEKHFI', '366', '', '', '', 'In a screen for the transactivation potential of various transcription factors toward GSL biosynthetic genes; MYB28 was identified as a positive regulator of aliphatic methionine-derived GSLs. The content of aliphatic GSLs as well as transcript levels of aliphatic GSL biosynthetic genes were elevated in gain-of-function mutants and decreased in MYB28 RNAi knock-down mutants (Gigolashvili et al. 2007)', 'GSL transcription factor / Camalexin biosynthesis', 'Burow et al. 2015; Gigolashvili et al. 2007; Stotz et al. 2011'),
	('AT5G62680', 'GTR2', 'Protein NRT1/ PTR FAMILY 2.11 ', 'NPF2.11', '836389', 'NM_125663', 'NP_201074', 'Q9LV10', 'MERKPLELESTDNHQNPSSAVYGGSVTAVDSVEEDVQNQKKVVYRGWKVMPFIIGNETFEKLGIIGTLSNLLVYLTAVFNLKSITAATIINAFSGTINFGTFVAAFLCDTYFGRYKTLSVAVIACFLGSFVILLTAAVPQLHPAACGTAADSICNGPSGGQIAFLLMGLGFLVVGAGGIRPCNLAFGADQFNPKSESGKRGIDSFFNWYFFTFTFAQILSLTLVVYVQSNVSWTIGLTIPAVLMFLACLIFFAGDKLYVKIKASGSPLAGIAQVIAVAIKKRGLKPAKQPWLNLYNYYPPKYANSKLKYTDQFRFLDKAAILTPEDKLQPDGKPADPWKLCTMQQVEEVKCIVRVLPIWFASSIYYLTITQQMTYPVFQALQSDRRLGSGGFVIPAATYVVFLMTGMTVFIVVYDRVLVPTMRRITGLDTGITLLQRIGTGIFFATASLVVAGFVEERRRTFALTKPTLGMAPRKGEISSMSAMWLIPQLSLAGVAEAFAAIGQMEFYYKQFPENMRSFAGSIFYVGGGVSSYLGSFLIATVHRTTQNSSGGNWLAEDLNKGRLDLFYFMIAGILAVNFAYFLVMSRWYRYKGSDDEVTTYETNENIIKQQDKNVA', '616', '', '', '', 'Leaf apoplastic fluid analysis and GSL feeding experiments showed two GSL transporters. GTR1 and GTR2 were essential for long-distance transport of GSLs in Arabidopsis and also play key roles in GSL allocation within a mature leaf by effectively importing apoplastically localized GSLs into appropriate cells (Madsen et al. 2014)', 'GSL degradation', 'Nour-Eldin et al. 2012; Madsen et al. 2014'),
	('AT5G65940', 'CHY1', '3-hydroxyisobutyryl-CoA hydrolase 1 ', 'K14B20.11', '836724', 'NM_125991', 'NP_201395', 'Q9LKJ1', 'MAVEMASQSQVLVEEKSSVRILTLNRPKQLNALSFHMISRLLQLFLAFEEDPSVKLVILKGHGRAFCAGGDVAAVVRDINQGNWRLGANYFSSEYMLNYVMATYSKAQVSILNGIVMGGGAGVSVHGRFRIATENTVFAMPETALGLFPDVGASYFLSRLPGFFGEYVGLTGARLDGAEMLACGLATHFVPSTRLTALEADLCRINSNDPTFASTILDAYTQHPRLKQQSAYRRLDVIDRCFSRRTVEEIISALEREATQEADGWISATIQALKKGSPASLKISLRSIREGRLQGVGQCLIREYRMVCHVMKGEISKDFVEGCRAILVDKDKNPKATGGHEG', '378', 'EC 3.1.2.- EC 3.1.2.4', '', '', 'Mutations in the gene At5g65940 previously shown to encode a peroxisomal protein with beta-hydroxyisobutyryl-CoA hydrolase activity and designated as Chy1; lead to a deficiency of benzoic acid-containing GSLs in the seeds (Ibdah and Pichersky 2009)', 'GSL side chain modification', 'Ibdah & Pichersky 2009  ');
/*!40000 ALTER TABLE `genes` ENABLE KEYS */;

-- Dumping structure for table gslbase.genes_references
