Structure of PDB 3urq Chain A Binding Site BS01
Receptor Information
>3urq Chain A (length=327) Species:
293
(Brevundimonas diminuta) [
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DRINTVRGPITISEAGFTLTHEHICGSSAGFLHAWPEFFGSRKALVEKAV
RGLRRARAAGVRTIVDVSTFDCGRDVSLLAEVSRAADVHIVAATGLWIDP
PLSMRLRSVEELTQFFLREIQYGIEDTGIRAGIIKVATTGKATPFQELVL
RAAARASLATGVPVTTHTAASQRDGEQQAAIFESEGLSPSRVCIGHSDDT
DDLSYLTALAARGYLIGLDGIPWSAIGLEDNASASAILGNRSWQTRALLI
KALIDQGYMKQILVSNDWTFGFSSYVTNIMDVLDRVNPDGMAFIPLRVIP
FLREKGVPQETLAGITVTNPARFLSPT
Ligand information
Ligand ID
CO
InChI
InChI=1S/Co/q+2
InChIKey
XLJKHNWPARRRJB-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Co+2]
CACTVS 3.341
[Co++]
Formula
Co
Name
COBALT (II) ION
ChEMBL
DrugBank
DB14205
ZINC
PDB chain
3urq Chain A Residue 801 [
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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)
K169 H201 H230
Binding residue
(residue number reindexed from 1)
K135 H167 H196
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 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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Molecular Function
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Biological Process
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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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