Structure of PDB 3pcg Chain D Binding Site BS01
Receptor Information
>3pcg Chain D (length=200) Species:
303
(Pseudomonas putida) [
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PIELLPETPSQTAGPYVHIGLALEAAGNPTRDQEIWNRLAKPDAPGEHIL
LLGQVYDGNGHLVRDSFLEVWQADANGEYQDAYNLENAFNSFGRTATTFD
AGEWTLHTVKPGVVNNAAGVPMAPHINISLFARGINIHLHTRLYFDDEAQ
ANAKCPVLNLIEQPQRRETLIAKRCEVDGKTAYRFDIRIQGEGETVFFDF
Ligand information
Ligand ID
4HP
InChI
InChI=1S/C8H8O3/c9-7-3-1-6(2-4-7)5-8(10)11/h1-4,9H,5H2,(H,10,11)
InChIKey
XQXPVVBIMDBYFF-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
OC(=O)Cc1ccc(O)cc1
OpenEye OEToolkits 1.5.0
c1cc(ccc1CC(=O)O)O
ACDLabs 10.04
O=C(O)Cc1ccc(O)cc1
Formula
C8 H8 O3
Name
4-HYDROXYPHENYLACETATE
ChEMBL
CHEMBL1772
DrugBank
ZINC
ZINC000000213065
PDB chain
3pcg Chain P Residue 550 [
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Receptor-Ligand Complex Structure
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PDB
3pcg
Structures of competitive inhibitor complexes of protocatechuate 3,4-dioxygenase: multiple exogenous ligand binding orientations within the active site.
Resolution
1.96 Å
Binding residue
(original residue number in PDB)
G14 P15
Binding residue
(residue number reindexed from 1)
G14 P15
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Y79 V114
Catalytic site (residue number reindexed from 1)
Y79 V114
Enzyme Commision number
1.13.11.3
: protocatechuate 3,4-dioxygenase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0005506
iron ion binding
GO:0008199
ferric iron binding
GO:0016702
oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen
GO:0018578
protocatechuate 3,4-dioxygenase activity
GO:0051213
dioxygenase activity
Biological Process
GO:0009056
catabolic process
GO:0042952
beta-ketoadipate pathway
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:3pcg
,
PDBe:3pcg
,
PDBj:3pcg
PDBsum
3pcg
PubMed
9254599
UniProt
P00436
|PCXA_PSEPU Protocatechuate 3,4-dioxygenase alpha chain (Gene Name=pcaG)
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