Structure of PDB 1bw9 Chain A Binding Site BS02
Receptor Information
>1bw9 Chain A (length=350) Species:
1831
(Rhodococcus sp. (in: high G+C Gram-positive bacteria)) [
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SIDSALNWDGEMTVTRFDSMTGAHFVIRLDSTQLGPAAGGTRAAQYSNLA
DALTDAGKLAGAMTLKMAVSNLPMGGGKSVIALPAPRHSIDPSTWARILR
IHAENIDKLSGNYWTGPDVNTNSADMDTLNDTTEFVFGRSLERGGAGSSA
FTTAVGVFEAMKATVAHRGLGSLDGLTVLVQGLGAVGGSLASLAAEAGAQ
LLVADTDTERVAHAVALGHTAVALEDVLSTPCDVFAPCAMGGVITTEVAR
TLDCSVVAGAANNVIADEAASDILHARGILYAPDFVANAGGAIHLVGREV
LGWSESVVHERAVAIGDTLNQVFEISDNDGVTPDEAARTLAGRRAREAST
Ligand information
Ligand ID
PPY
InChI
InChI=1S/C9H8O3/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5H,6H2,(H,11,12)
InChIKey
BTNMPGBKDVTSJY-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1ccc(cc1)CC(=O)C(=O)O
CACTVS 3.341
OC(=O)C(=O)Cc1ccccc1
ACDLabs 10.04
O=C(C(=O)O)Cc1ccccc1
Formula
C9 H8 O3
Name
3-PHENYLPYRUVIC ACID
ChEMBL
CHEMBL1162488
DrugBank
DB03884
ZINC
ZINC000000901485
PDB chain
1bw9 Chain A Residue 361 [
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Receptor-Ligand Complex Structure
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PDB
1bw9
Phenylalanine dehydrogenase from Rhodococcus sp. M4: high-resolution X-ray analyses of inhibitory ternary complexes reveal key features in the oxidative deamination mechanism.
Resolution
1.5 Å
Binding residue
(original residue number in PDB)
G39 G40 M63 K66 F137 G291 A292 L295
Binding residue
(residue number reindexed from 1)
G39 G40 M63 K66 F137 G291 A292 L295
Annotation score
5
Enzymatic activity
Enzyme Commision number
1.4.1.20
: phenylalanine dehydrogenase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0016491
oxidoreductase activity
GO:0016639
oxidoreductase activity, acting on the CH-NH2 group of donors, NAD or NADP as acceptor
GO:0050175
phenylalanine dehydrogenase activity
Biological Process
GO:0006520
amino acid metabolic process
GO:0006559
L-phenylalanine catabolic process
GO:0009094
L-phenylalanine biosynthetic process
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Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:1bw9
,
PDBe:1bw9
,
PDBj:1bw9
PDBsum
1bw9
PubMed
10029526
UniProt
Q59771
|DHPH_RHOSO Phenylalanine dehydrogenase (Gene Name=pdh)
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