Structure of PDB 6g3m Chain A Binding Site BS03
Receptor Information
>6g3m Chain A (length=327) Species:
293
(Brevundimonas diminuta) [
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DRINTVRGPITISEAGFTLTHEHICGSSAGFLRAWPEFFGSRAALVEKAV
RGLRRARAAGVRTIVDVSTFDIGRDVSLLAEVSRAADVHIVAATGLWEDP
PLSMRLRSVEELTQFFLREIQYGIEDTGIRAGIIKVATNGKATPFQELVL
RAAARASLATGVPVTTHTLASQRDGEQQAAIFESEGLSPSRVCIGHSDDT
DDLSYLTALAARGYLIGLDGIPHSAIGLEDNASASALLGNRSWQTRALLI
KALIDQGYMKQILVSNDWLFGFSSYVTNIMDVMDSVNPDGMAFIPLRVIP
FLREKGVSNETLAGITVTNPARFLSPT
Ligand information
Ligand ID
VX
InChI
InChI=1S/C3H9O3P/c1-3-6-7(2,4)5/h3H2,1-2H3,(H,4,5)
InChIKey
UFZOPKFMKMAWLU-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CCO[P@](=O)(C)O
CACTVS 3.341
CCO[P](C)(O)=O
CACTVS 3.341
CCO[P@](C)(O)=O
OpenEye OEToolkits 1.5.0
CCOP(=O)(C)O
ACDLabs 10.04
O=P(O)(OCC)C
Formula
C3 H9 O3 P
Name
O-ETHYLMETHYLPHOSPHONIC ACID ESTER GROUP
ChEMBL
DrugBank
ZINC
ZINC000002557021
PDB chain
6g3m Chain A Residue 404 [
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Receptor-Ligand Complex Structure
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PDB
6g3m
Phosphotriesterase PTE_C23M_4
Resolution
1.665 Å
Binding residue
(original residue number in PDB)
W131 H201 H230 D301
Binding residue
(residue number reindexed from 1)
W97 H167 H196 D267
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
H55 H57 K169 H201 H230 D233 G254 D301
Catalytic site (residue number reindexed from 1)
H21 H23 K135 H167 H196 D199 G220 D267
Enzyme Commision number
3.1.8.1
: aryldialkylphosphatase.
Gene Ontology
Molecular Function
GO:0004063
aryldialkylphosphatase activity
GO:0008270
zinc ion binding
GO:0016787
hydrolase activity
GO:0016788
hydrolase activity, acting on ester bonds
GO:0046872
metal ion binding
Biological Process
GO:0009056
catabolic process
Cellular Component
GO:0005886
plasma membrane
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Biological Process
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Cellular Component
External links
PDB
RCSB:6g3m
,
PDBe:6g3m
,
PDBj:6g3m
PDBsum
6g3m
PubMed
UniProt
P0A434
|OPD_BREDI Parathion hydrolase (Gene Name=opd)
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