Structure of PDB 3uf9 Chain D Binding Site BS02
Receptor Information
>3uf9 Chain D (length=314) Species:
2287
(Saccharolobus solfataricus) [
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MRIPLVGKDSIESKDIGFTLIHEHLRVFSEAVRQQWPHLYNEDEEFRNAV
NEVKRAMQFGVKTIVDPTVMGLGRDIRFMEKVVKATGINLVAGTGIYIYI
DLPFYFLNRSIDEIADLFIHDIKEGIQGTLNKAGFVKIAADEPGITKDVE
KVIRAAAIANKETKVPIITHSNAHNNTGLEQQRILTEEGVDPGKILIGHL
GDTDNIDYIKKIADKGSFIGLDRYGLDLFLPVDKRNETTLRLIKDGYSDK
IMISHDYCCTIDWGTAKPEYKPKLAPRWSITLIFEDTIPFLKRNGVNEEV
IATIFKENPKKFFS
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
3uf9 Chain D Residue 316 [
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Receptor-Ligand Complex Structure
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PDB
3uf9
Characterisation of the organophosphate hydrolase catalytic activity of SsoPox
Resolution
2.68 Å
Binding residue
(original residue number in PDB)
K137 H170 H199
Binding residue
(residue number reindexed from 1)
K137 H170 H199
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H22 H24 K137 H170 H199 D202 R223 D256
Catalytic site (residue number reindexed from 1)
H22 H24 K137 H170 H199 D202 R223 D256
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
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Molecular Function
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Biological Process
External links
PDB
RCSB:3uf9
,
PDBe:3uf9
,
PDBj:3uf9
PDBsum
3uf9
PubMed
23139857
UniProt
Q97VT7
|PHP_SACS2 Aryldialkylphosphatase (Gene Name=php)
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