Structure of PDB 3e9y Chain A Binding Site BS04
Receptor Information
>3e9y Chain A (length=582) Species:
3702
(Arabidopsis thaliana) [
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FISRFAPDQPRKGADILVEALERQGVETVFAYPGGASMEIHQALTRSSSI
RNVLPRHEQGGVFAAEGYARSSGKPGICIATSGPGATNLVSGLADALLDS
VPLVAITGQVPRRMIGTDAFQETPIVEVTRSITKHNYLVMDVEDIPRIIE
EAFFLATSGRPGPVLVDVPKDIQQQLAIPNWEQAMRLPGYMSRMPKPPED
SHLEQIVRLISESKKPVLYVGGGCLNSSDELGRFVELTGIPVATTLMGLG
SYPCDDELSLHMLGMHGTVYANYAVEHSDLLLAFGVRFDDRVTGKLEAFA
SRAKIVHIDIDSAEIGKNKTPHVSVCGDVKLALQGMNKVLENRAEELKLD
FGVWRNELNVQKQKFPLSFKTFGEAIPPQYAIKVLDELTDGKAIISTGVG
QHQMWAAQFYNYKKPRQWLSSGGLGAMGFGLPAAIGASVANPDAIVVDID
GDGSFIMNVQELATIRVENLPVKVLLLNNQHLGMVMQWEDRFYKANRAHT
FLGDPAQEDEIFPNMLLFAAACGIPAARVTKKADLREAIQTMLDTPGPYL
LDVICPHQEHVLPMIPSGGTFNDVITEGDGRI
Ligand information
Ligand ID
FAB
InChI
InChI=1S/C31H39N9O16P2/c1-12(2)29(47)40-16-6-14(4)13(3)5-15(16)38(27-21(40)28(46)37-31(48)36-27)7-17(41)22(43)18(42)8-53-57(49,50)56-58(51,52)54-9-19-23(44)24(45)30(55-19)39-11-35-20-25(32)33-10-34-26(20)39/h5-6,10-12,17-19,22-24,30,41-45H,7-9H2,1-4H3,(H4-,32,33,34,37,46,48,49,50,51,52)/t17-,18+,19+,22-,23+,24+,30+/m0/s1
InChIKey
VVZGWZAMSAFRNS-UYOVOMPXSA-N
SMILES
Software
SMILES
CACTVS 3.385
CC(C)C(=O)[N+]1=C2C(=O)NC(=O)N=C2N(C[C@H](O)[C@H](O)[C@H](O)CO[P]([O-])(=O)O[P](O)(=O)OC[C@H]3O[C@H]([C@H](O)[C@@H]3O)n4cnc5c(N)ncnc45)c6cc(C)c(C)cc16
OpenEye OEToolkits 1.7.5
Cc1cc2c(cc1C)[N+](=C3C(=O)NC(=O)N=C3N2C[C@@H]([C@@H]([C@@H](COP(=O)([O-])O[P@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)n5cnc6c5ncnc6N)O)O)O)O)O)C(=O)C(C)C
OpenEye OEToolkits 1.7.5
Cc1cc2c(cc1C)[N+](=C3C(=O)NC(=O)N=C3N2CC(C(C(COP(=O)([O-])OP(=O)(O)OCC4C(C(C(O4)n5cnc6c5ncnc6N)O)O)O)O)O)C(=O)C(C)C
CACTVS 3.385
CC(C)C(=O)[N+]1=C2C(=O)NC(=O)N=C2N(C[CH](O)[CH](O)[CH](O)CO[P]([O-])(=O)O[P](O)(=O)OC[CH]3O[CH]([CH](O)[CH]3O)n4cnc5c(N)ncnc45)c6cc(C)c(C)cc16
Formula
C31 H39 N9 O16 P2
Name
FLAVIN-ADENINE DINUCLEOTIDE-N5-ISOBUTYL KETONE
ChEMBL
DrugBank
ZINC
PDB chain
3e9y Chain A Residue 701 [
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Receptor-Ligand Complex Structure
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PDB
3e9y
Crystal structures of two novel sulfonylurea herbicides in complex with Arabidopsis thaliana acetohydroxyacid synthase.
Resolution
3.0 Å
Binding residue
(original residue number in PDB)
R246 G307 G308 G309 T331 L332 M333 L349 G371 R373 D375 R377 D395 I396 G413 D414 V415 M490 G508
Binding residue
(residue number reindexed from 1)
R160 G221 G222 G223 T245 L246 M247 L263 G285 R287 D289 R291 D309 I310 G327 D328 V329 M404 G422
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Y118 G120 G121 A122 S123 E144 T167 F206 Q207 E208 K256 M351 V378 V485 G511 M513 D538 N565 H567 L568 M570 V571 W574 H643
Catalytic site (residue number reindexed from 1)
Y32 G34 G35 A36 S37 E58 T81 F120 Q121 E122 K170 M265 V292 V399 G425 M427 D452 N479 H481 L482 M484 V485 W488 H557
Enzyme Commision number
2.2.1.6
: acetolactate synthase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0003824
catalytic activity
GO:0003984
acetolactate synthase activity
GO:0030976
thiamine pyrophosphate binding
GO:0050660
flavin adenine dinucleotide binding
Biological Process
GO:0009082
branched-chain amino acid biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:3e9y
,
PDBe:3e9y
,
PDBj:3e9y
PDBsum
3e9y
PubMed
19187232
UniProt
P17597
|ILVB_ARATH Acetolactate synthase, chloroplastic (Gene Name=ALS)
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