Structure of PDB 1i0d Chain B Binding Site BS03

Receptor Information
>1i0d Chain B (length=331) Species: 293 (Brevundimonas diminuta) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
GDRINTVRGPITISEAGFTLTHEHICGSSAGFLRAWPEFFGSRKALAEKA
VRGLRRARAAGVRTIVDVSTFDIGRDVSLLAEVSRAADVHIVAATGLWFD
PPLSMRLRSVEELTQFFLREIQYGIEDTGIRAGIIKVATTGKATPFQELV
LKAAARASLATGVPVTTHTAASQRDGEQQAAIFESEGLSPSRVCIGHSDD
TDDLSYLTALAARGYLIGLDHIPHSAIGLEDNASASALLGIRSWQTRALL
IKALIDQGYMKQILVSNDWLFGFSSYVTNIMDVMDRVNPDGMAFIPLRVI
PFLREKGVPQETLAGITVTNPARFLSPTLRA
Ligand information
Ligand IDPEL
InChIInChI=1S/C8H10O/c9-7-6-8-4-2-1-3-5-8/h1-5,9H,6-7H2
InChIKeyWRMNZCZEMHIOCP-UHFFFAOYSA-N
SMILES
SoftwareSMILES
OpenEye OEToolkits 1.5.0c1ccc(cc1)CCO
ACDLabs 10.04
CACTVS 3.341		OCCc1ccccc1
FormulaC8 H10 O
Name2-PHENYL-ETHANOL
ChEMBLCHEMBL448500
DrugBankDB02192
ZINCZINC000000895934
PDB chain1i0d Chain B Residue 414 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB1i0d High resolution X-ray structures of different metal-substituted forms of phosphotriesterase from Pseudomonas diminuta.
Resolution1.3 Å
Binding residue
(original residue number in PDB)		M293 K294 G348 N353
Binding residue
(residue number reindexed from 1)		M260 K261 G315 N320
Annotation score1
Enzymatic activity
Catalytic site (original residue number in PDB) H55 H57 K169 H201 H230 D233 H254 D301
Catalytic site (residue number reindexed from 1) H22 H24 K136 H168 H197 D200 H221 D268
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:1i0d, PDBe:1i0d, PDBj:1i0d
PDBsum1i0d
PubMed11258882
UniProtP0A434|OPD_BREDI Parathion hydrolase (Gene Name=opd)

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