Structure of PDB 8oro Chain AAA Binding Site BS01
Receptor Information
>8oro Chain AAA (length=273) Species:
211146
(Paenarthrobacter nitroguajacolicus) [
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DTYLHETLVFDNKLSYIDNQRDTDGPAILLLPGWCHDHRVYKYLIQELDA
DFRVIVPNWRGHGLSPSEVPDFGYQEQVKDALEILDQLGVETFLPVSHAH
GGWVLVELLEQAGPERAPRGIIMDWLMWAPKPDFAKSLTLLKDPERWREG
THGLFDVWLDGHDEKRVRHHLLEEMADYGYDCWGRSGRVIEDAYGRNGSP
MQMMANLTKTRPIRHIFSQPTEPEYEKINSDFAEQHPWFSYAKLGGPTHF
PAIDVPDRAAVHIREFATAIRQG
Ligand information
Ligand ID
VFH
InChI
InChI=1S/C10H9NO/c1-7-6-10(12)8-4-2-3-5-9(8)11-7/h2-6H,1H3,(H,11,12)
InChIKey
NWINIEGDLHHNLH-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.385
OpenEye OEToolkits 2.0.7
CC1=CC(=O)c2ccccc2N1
Formula
C10 H9 N O
Name
2-methyl-quinolin-4(1H)-one
ChEMBL
CHEMBL1256109
DrugBank
ZINC
ZINC000018284312
PDB chain
8oro Chain AAA Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
8oro
Evolutionary adaptation from hydrolytic to oxygenolytic catalysis at the alpha / beta-hydrolase fold.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
W36 H38 H102 W160 S188 I192 H251
Binding residue
(residue number reindexed from 1)
W34 H36 H100 W158 S186 I190 H249
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.13.11.48
: 3-hydroxy-2-methylquinolin-4-one 2,4-dioxygenase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0016702
oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen
GO:0050586
3-hydroxy-2-methylquinolin-4-one 2,4-dioxygenase activity
GO:0051213
dioxygenase activity
Biological Process
GO:0009056
catabolic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:8oro
,
PDBe:8oro
,
PDBj:8oro
PDBsum
8oro
PubMed
37799987
UniProt
O31266
|HOD_PAENT 1H-3-hydroxy-4-oxoquinaldine 2,4-dioxygenase (Gene Name=hod)
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