Structure of PDB 5vxt Chain B Binding Site BS01
Receptor Information
>5vxt Chain B (length=312) Species:
398577
(Burkholderia ambifaria MC40-6) [
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HHHHMSVKVFDTKEVQDLLKAASNAGAGNARTQQIVHRLLGDLFKAIDDL
DITPDEVWAGVNYLNKLGQDGEAALLAAGLGLEKYLDIRMDAEDEAIGLD
GGTPRTIEGPLYVAGAPVRDGVAKIDLDADEGAGPLVIHGTVTGLDGKPV
AGALVECWHANSHGFYSHFDPTGKQSDFNLRGAVKTGADGKYEFRTLMPV
GYGCPPQGATQQLLDRLGRHGNRPAHVHFFVTSDGHRKLTTQFNIEGDPL
IWDDFAYATREELIPPVTAKAGGAALGLKADAYQDIEFNFVLTPRVEGKD
NQIVERLRASAT
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
5vxt Chain B Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
5vxt
Crystal structure of catechol 1,2-dioxygenase from Burkholderia ambifaria
Resolution
1.75 Å
Binding residue
(original residue number in PDB)
Y170 H230 H232
Binding residue
(residue number reindexed from 1)
Y166 H226 H228
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Y170 Y206 R227 H230 H232
Catalytic site (residue number reindexed from 1)
Y166 Y202 R223 H226 H228
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:0009712
catechol-containing compound metabolic process
GO:0019614
catechol-containing compound catabolic process
GO:0042952
beta-ketoadipate pathway
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Molecular Function
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Biological Process
External links
PDB
RCSB:5vxt
,
PDBe:5vxt
,
PDBj:5vxt
PDBsum
5vxt
PubMed
UniProt
B1Z4S0
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