Structure of PDB 6u9d Chain R Binding Site BS03
Receptor Information
>6u9d Chain R (length=416) Species:
4932
(Saccharomyces cerevisiae) [
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DMDTSFVGLTGGQIFNEMMSRQNVDTVFGYPGGAILPVYDAIHNSDKFNF
VLPKHEQGAGHMAEGYARASGKPGVVLVTSGPGATNVVTPMADAFADGIP
MVVFTGQVPTSAIGTDAFQEADVVGISRSCTKWNVMVKSVEELPLRINEA
FEIATSGRPGPVLVDLPKDVTAAILRNPIPTKTTLPSNALNAQDEFVMQS
INKAADLINLAKKPVLYVGAGILNHADGPRLLKELSDRAQTTTLQGLGQN
ADLIIAVGARFDDRVTGNISKFAPEARRAAGIIHFEVSPKNINKVVQTQI
AVEGDATTNLGKMMSKIFPVKEQTVIKKLSKVANDTLGTMGYGLLVIDID
GDASFNMTLTELSSAVQAGTPVKILILNVTQWQSLFYEHRKQEELDAKLK
EFVPVLLEVEVDKKVP
Ligand information
Ligand ID
FAD
InChI
InChI=1S/C27H33N9O15P2/c1-10-3-12-13(4-11(10)2)35(24-18(32-12)25(42)34-27(43)33-24)5-14(37)19(39)15(38)6-48-52(44,45)51-53(46,47)49-7-16-20(40)21(41)26(50-16)36-9-31-17-22(28)29-8-30-23(17)36/h3-4,8-9,14-16,19-21,26,37-41H,5-7H2,1-2H3,(H,44,45)(H,46,47)(H2,28,29,30)(H,34,42,43)/t14-,15+,16+,19-,20+,21+,26+/m0/s1
InChIKey
VWWQXMAJTJZDQX-UYBVJOGSSA-N
SMILES
Software
SMILES
CACTVS 3.341
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[C@H](O)[C@H](O)[C@H](O)CO[P@](O)(=O)O[P@@](O)(=O)OC[C@H]4O[C@H]([C@H](O)[C@@H]4O)n5cnc6c(N)ncnc56)c2cc1C
OpenEye OEToolkits 1.5.0
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)CC(C(C(COP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)n5cnc6c5ncnc6N)O)O)O)O)O
OpenEye OEToolkits 1.5.0
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)C[C@@H]([C@@H]([C@@H](CO[P@@](=O)(O)O[P@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)n5cnc6c5ncnc6N)O)O)O)O)O
CACTVS 3.341
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[CH](O)[CH](O)[CH](O)CO[P](O)(=O)O[P](O)(=O)OC[CH]4O[CH]([CH](O)[CH]4O)n5cnc6c(N)ncnc56)c2cc1C
ACDLabs 10.04
O=C2C3=Nc1cc(c(cc1N(C3=NC(=O)N2)CC(O)C(O)C(O)COP(=O)(O)OP(=O)(O)OCC6OC(n5cnc4c(ncnc45)N)C(O)C6O)C)C
Formula
C27 H33 N9 O15 P2
Name
FLAVIN-ADENINE DINUCLEOTIDE
ChEMBL
CHEMBL1232653
DrugBank
DB03147
ZINC
ZINC000008215434
PDB chain
6u9d Chain R Residue 701 [
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Receptor-Ligand Complex Structure
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PDB
6u9d
Structures of fungal and plant acetohydroxyacid synthases.
Resolution
3.194 Å
Binding residue
(original residue number in PDB)
R241 G309 N312 T334 L335 Q336 G374 R376 D378 R380 V381 E407 V408 N412
Binding residue
(residue number reindexed from 1)
R158 G221 N224 T243 L244 Q245 G258 R260 D262 R264 V265 E286 V287 N291
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Y113 G115 G116 A117 I118 E139 T162 F201 Q202 E203 K251 V381 G523 M525 D550 V583 W586
Catalytic site (residue number reindexed from 1)
Y30 G32 G33 A34 I35 E56 T79 F118 Q119 E120 K168 V265 G338 M340 D352 V379 W382
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:0016740
transferase activity
GO:0030976
thiamine pyrophosphate binding
GO:0046872
metal ion binding
GO:0050660
flavin adenine dinucleotide binding
Biological Process
GO:0008652
amino acid biosynthetic process
GO:0009082
branched-chain amino acid biosynthetic process
GO:0009097
isoleucine biosynthetic process
GO:0009099
L-valine biosynthetic process
Cellular Component
GO:0005739
mitochondrion
GO:0005948
acetolactate synthase complex
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:6u9d
,
PDBe:6u9d
,
PDBj:6u9d
PDBsum
6u9d
PubMed
32640464
UniProt
P07342
|ILVB_YEAST Acetolactate synthase catalytic subunit, mitochondrial (Gene Name=ILV2)
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