Structure of PDB 1bf6 Chain A Binding Site BS01
Receptor Information
>1bf6 Chain A (length=291) Species:
562
(Escherichia coli) [
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SFDPTGYTLAHEHLHIDLSGFKNNVDCRLDQYAFICQEMNDLMTRGVRNV
IEMTNRYMGRNAQFMLDVMRETGINVVACTGYYQDAFFPEHVATRSVQEL
AQEMVDEIEQGIDGTELKAGIIAEIGTSEGKITPLEEKVFIAAALAHNQT
GRPISTHTSFSTMGLEQLALLQAHGVDLSRVTVGHCDLKDNLDNILKMID
LGAYVQFDTIGKNSYYPDEKRIAMLHALRDRGLLNRVMLSMDITRRSHLK
ANGGYGYDYLLTTFIPQLRQSGFSQADVDVMLRENPSQFFQ
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
1bf6 Chain A Residue 1 [
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Receptor-Ligand Complex Structure
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PDB
1bf6
Biochemical characterization and crystallographic structure of an Escherichia coli protein from the phosphotriesterase gene family.
Resolution
1.7 Å
Binding residue
(original residue number in PDB)
H12 H14 E125 D243
Binding residue
(residue number reindexed from 1)
H11 H13 E124 D242
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
H12 H14 E125 H158 H186 L189 T210 D243
Catalytic site (residue number reindexed from 1)
H11 H13 E124 H157 H185 L188 T209 D242
Enzyme Commision number
3.1.-.-
Gene Ontology
Molecular Function
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
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Molecular Function
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Biological Process
External links
PDB
RCSB:1bf6
,
PDBe:1bf6
,
PDBj:1bf6
PDBsum
1bf6
PubMed
9548740
UniProt
P45548
|PHP_ECOLI Phosphotriesterase homology protein (Gene Name=php)
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