Structure of PDB 2ag1 Chain D Binding Site BS03
Receptor Information
>2ag1 Chain D (length=553) Species:
294
(Pseudomonas fluorescens) [
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MITGGELVVRTLIKAGVEHLFGLHGAHIDTIFQACLDHDVPIIDTRHEAA
AGHAAEGYARAGAKLGVALVTAGGGFTNAVTPIANAWLDRTPVLFLTGSG
ALRDDETNTLQAGIDQVAMAAPITKWAHRVMATEHIPRLVMQAIRAALSA
PRGPVLLDLPWDILMNQIDEDSVIIPDLVLSAHGARPDPADLDQALALLR
KAERPVIVLGSEASRTARKTALSAFVAATGVPVFADYEGLSMLSGLPDAM
RGGLVQNLYSFAKADAAPDLVLMLGARFGLNTGHGSGQLIPHSAQVIQVD
PDACELGRLQGIALGIVADVGGTIEALAQATAQDAAWPDRGDWCAKVTDL
AQERYASIAAKSSSEHALHPFHASQVIAKHVDAGVTVVADGALTYLWLSE
VMSRVKPGGFLCHGYLGSMGVGFGTALGAQVADLEAGRRTILVTGDGSVG
YSIGEFDTLVRKQLPLIVIIMNNQSWGATLHFQQLAVGPNRVTGTRLENG
SYHGVAAAFGADGYHVDSVESFSAALAQALAHNRPACINVAVALDPIPPE
ELI
Ligand information
Ligand ID
TPP
InChI
InChI=1S/C12H18N4O7P2S/c1-8-11(3-4-22-25(20,21)23-24(17,18)19)26-7-16(8)6-10-5-14-9(2)15-12(10)13/h5,7H,3-4,6H2,1-2H3,(H4-,13,14,15,17,18,19,20,21)/p+1
InChIKey
AYEKOFBPNLCAJY-UHFFFAOYSA-O
SMILES
Software
SMILES
CACTVS 3.341
Cc1ncc(C[n+]2csc(CCO[P@@](O)(=O)O[P](O)(O)=O)c2C)c(N)n1
OpenEye OEToolkits 1.5.0
Cc1c(sc[n+]1Cc2cnc(nc2N)C)CCO[P@](=O)(O)OP(=O)(O)O
OpenEye OEToolkits 1.5.0
Cc1c(sc[n+]1Cc2cnc(nc2N)C)CCOP(=O)(O)OP(=O)(O)O
CACTVS 3.341
Cc1ncc(C[n+]2csc(CCO[P](O)(=O)O[P](O)(O)=O)c2C)c(N)n1
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OCCc1sc[n+](c1C)Cc2c(nc(nc2)C)N
Formula
C12 H19 N4 O7 P2 S
Name
THIAMINE DIPHOSPHATE
ChEMBL
CHEMBL1236376
DrugBank
ZINC
ZINC000008215517
PDB chain
2ag1 Chain D Residue 632 [
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Receptor-Ligand Complex Structure
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PDB
2ag1
Structure and mechanism of the ThDP-dependent benzaldehyde lyase from Pseudomonas fluorescens
Resolution
2.58 Å
Binding residue
(original residue number in PDB)
G393 A394 L395 T396 G419 S420 M421 G447 D448 G449 S450 Y453 N475 S477 W478 G479
Binding residue
(residue number reindexed from 1)
G391 A392 L393 T394 G417 S418 M419 G445 D446 G447 S448 Y451 N473 S475 W476 G477
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
L25 G27 A28 H29 I30 E50 T73 L112 Q113 A114 G115 W163 L256 T284 G393 G419 M421 D448 N475 S477 W478 A480 T481 F484 L546
Catalytic site (residue number reindexed from 1)
L23 G25 A26 H27 I28 E48 T71 L110 Q111 A112 G113 W161 L254 T282 G391 G417 M419 D446 N473 S475 W476 A478 T479 F482 L544
Enzyme Commision number
4.1.2.38
: benzoin aldolase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0003824
catalytic activity
GO:0003984
acetolactate synthase activity
GO:0016829
lyase activity
GO:0030976
thiamine pyrophosphate binding
GO:0046872
metal ion binding
GO:0050660
flavin adenine dinucleotide binding
Biological Process
GO:0009097
isoleucine biosynthetic process
GO:0009099
L-valine biosynthetic process
GO:0019752
carboxylic acid metabolic process
Cellular Component
GO:0005948
acetolactate synthase complex
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2ag1
,
PDBe:2ag1
,
PDBj:2ag1
PDBsum
2ag1
PubMed
16302970
UniProt
Q9F4L3
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