Structure of PDB 3lxv Chain A Binding Site BS01
Receptor Information
>3lxv Chain A (length=200) Species:
303
(Pseudomonas putida) [
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PIELLPETPSQTAGPYVHIGLALEAAGNPTRDQEIWNRLAKPDAPGEHIL
LLGQVYDGNGHLVRDSFLEVWQADANGEYQDAYNLENAFNSFGRTATTFD
AGEWTLHTVKPGVVNNAAGVPMAPHINISLFARGINIHLHTRLYFDDEAQ
ANAKCPVLNLIEQPQRRETLIAKRCEVDGKTAYRFDIRIQGEGETVFFDF
Ligand information
Ligand ID
CO3
InChI
InChI=1S/CH2O3/c2-1(3)4/h(H2,2,3,4)/p-2
InChIKey
BVKZGUZCCUSVTD-UHFFFAOYSA-L
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C(=O)([O-])[O-]
ACDLabs 10.04
CACTVS 3.341
[O-]C([O-])=O
Formula
C O3
Name
CARBONATE ION
ChEMBL
DrugBank
DB14531
ZINC
PDB chain
3lxv Chain A Residue 206 [
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Receptor-Ligand Complex Structure
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PDB
3lxv
Tyrosine 447 of Protocatechuate 3,4-Dioxygenase Controls Efficient Progress Through Catalysis
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
Y56 R188
Binding residue
(residue number reindexed from 1)
Y56 R188
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Y79 V114 M122 H125 N127
Catalytic site (residue number reindexed from 1)
Y79 V114 M122 H125 N127
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
View graph for
Biological Process
External links
PDB
RCSB:3lxv
,
PDBe:3lxv
,
PDBj:3lxv
PDBsum
3lxv
PubMed
UniProt
P00436
|PCXA_PSEPU Protocatechuate 3,4-dioxygenase alpha chain (Gene Name=pcaG)
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