Structure of PDB 1p6c Chain B Binding Site BS01
Receptor Information
>1p6c Chain B (length=330) Species:
239
(Flavobacterium sp.) [
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DRINTVRGPITISEAGFTLTHEHICGSSAGFLRAWPEFFGSRKALAEKAV
RGLRRARAAGVRTIVDVSTFDIGRDVSLLAEVSRAADVHIVAATGLWFDP
PLSMRLRSVEELTQFFLREIQYGIEDTGIRAGIIKVATTGKATPFQELVL
KAAARASLATGVPVTTHTAASQRDGEQQAAIFESEGLSPSRVCIGHSDDT
DDLSYLTALAARGYLIGLDGIPWSAIGLEDNASASALLGIRSWQTRALLI
KALIDQGYMKQILVSNDWTFGFSSYVTNIMDVMDRVNPDGMAFIPLRVIP
FLREKGVPQETLAGITVTNPARFLSPTLRA
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
1p6c Chain B Residue 403 [
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Receptor-Ligand Complex Structure
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PDB
1p6c
Enhanced degradation of chemical warfare agents through molecular engineering of the phosphotriesterase active site.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
H55 H57 K169 D301
Binding residue
(residue number reindexed from 1)
H21 H23 K135 D267
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:1p6c
,
PDBe:1p6c
,
PDBj:1p6c
PDBsum
1p6c
PubMed
15369336
UniProt
P0A433
|OPD_SPHSA Parathion hydrolase (Gene Name=opd)
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