Structure of PDB 1p6c Chain B Binding Site BS03
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
EBP
InChI
InChI=1S/C12H19O3P/c1-4-14-16(13,15-5-2)10-12-8-6-11(3)7-9-12/h6-9H,4-5,10H2,1-3H3
InChIKey
QKGBKPZAXXBLJE-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
O=P(OCC)(OCC)Cc1ccc(cc1)C
CACTVS 3.341
CCO[P](=O)(Cc1ccc(C)cc1)OCC
OpenEye OEToolkits 1.5.0
CCOP(=O)(Cc1ccc(cc1)C)OCC
Formula
C12 H19 O3 P
Name
DIETHYL 4-METHYLBENZYLPHOSPHONATE
ChEMBL
DrugBank
DB02138
ZINC
ZINC000002046934
PDB chain
1p6c Chain B Residue 6 [
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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)
Q155 Y156
Binding residue
(residue number reindexed from 1)
Q121 Y122
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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