Structure of PDB 3urq Chain B Binding Site BS03
Receptor Information
>3urq Chain B (length=322) Species:
293
(Brevundimonas diminuta) [
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DRINTVRGPITISEAGFTLTHEHICGSSAGFLHAWPEFFGSRKALVEKAV
RGLRRARAAGVRTIVDVSTFDCGRDVSLLAEVSRAADVHIVAATGLWIDP
PLSMRLRSVEELTQFFLREIQYGIEDTGIRAGIIKVATTGKATPFQELVL
RAAARASLATGVPVTTHTAASQRDGEQQAAIFESEGLSPSRVCIGHSDDT
DDLSYLTALAARGYLIGLDGIPWSAIASASAILGNRSWQTRALLIKALID
QGYMKQILVSNDWTFGFSSYVTNIMDVLDRVNPDGMAFIPLRVIPFLREK
GVPQETLAGITVTNPARFLSPT
Ligand information
Ligand ID
QMP
InChI
InChI=1S/C7H15O3P/c1-11(8,9)10-7-5-3-2-4-6-7/h7H,2-6H2,1H3,(H,8,9)
InChIKey
SWYGLBJVTQMYSE-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
CP(=O)(O)OC1CCCCC1
ACDLabs 12.01
O=P(O)(OC1CCCCC1)C
CACTVS 3.370
C[P](O)(=O)OC1CCCCC1
Formula
C7 H15 O3 P
Name
cyclohexyl methylphosphonate
ChEMBL
DrugBank
ZINC
ZINC000006068355
PDB chain
3urq Chain B Residue 901 [
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Receptor-Ligand Complex Structure
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PDB
3urq
Enzymes for the homeland defense: optimizing phosphotriesterase for the hydrolysis of organophosphate nerve agents.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
G60 W131 H230 D301 T303 F306
Binding residue
(residue number reindexed from 1)
G26 W97 H196 D262 T264 F267
Annotation score
1
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 D262
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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Cellular Component
External links
PDB
RCSB:3urq
,
PDBe:3urq
,
PDBj:3urq
PDBsum
3urq
PubMed
22809162
UniProt
P0A434
|OPD_BREDI Parathion hydrolase (Gene Name=opd)
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