Structure of PDB 3hhy Chain A Binding Site BS01
Receptor Information
>3hhy Chain A (length=256) Species:
37919
(Rhodococcus opacus) [
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ATADTSPERLAAIAKDALGALNDVILKHGVTYPEYRVFKQWLIDVGEGGE
WPLFLDVFIEHSVEEVLARSRKGTMGSIEGPYYIENSPELPSKCTLPMRE
EDEKITPLVFSGQVTDLDGNGLAGAKVELWHADNDGYYSQFAPHLPEWNL
RGTIIADEEGRYEITTIQPAPYQIPTDGPTGQFIEAQNGHPWRPAHLHLI
VSAPGKESVTTQLYFKGGEWIDSDVASATKPELILDPKTGDDGKNYVTYN
FVLDPA
Ligand information
Ligand ID
FE
InChI
InChI=1S/Fe/q+3
InChIKey
VTLYFUHAOXGGBS-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
CACTVS 3.341
OpenEye OEToolkits 1.5.0
[Fe+3]
Formula
Fe
Name
FE (III) ION
ChEMBL
DrugBank
DB13949
ZINC
PDB chain
3hhy Chain A Residue 281 [
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Receptor-Ligand Complex Structure
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PDB
3hhy
Catechol 1,2-dioxygenase from the Gram-positive Rhodococcus opacus 1CP: Quantitative structure/activity relationship and the crystal structures of native enzyme and catechols adducts.
Resolution
1.55 Å
Binding residue
(original residue number in PDB)
Y162 H220 H222
Binding residue
(residue number reindexed from 1)
Y138 H196 H198
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Y162 Y196 R217 H220 H222
Catalytic site (residue number reindexed from 1)
Y138 Y172 R193 H196 H198
Enzyme Commision number
1.13.11.1
: catechol 1,2-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:0018576
catechol 1,2-dioxygenase activity
GO:0046872
metal ion binding
GO:0051213
dioxygenase activity
Biological Process
GO:0009056
catabolic process
GO:0009712
catechol-containing compound metabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:3hhy
,
PDBe:3hhy
,
PDBj:3hhy
PDBsum
3hhy
PubMed
20040374
UniProt
P95607
|CATA_RHOOP Catechol 1,2-dioxygenase (Fragment) (Gene Name=catA)
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