Structure of PDB 2vc7 Chain D Binding Site BS03
Receptor Information
>2vc7 Chain D (length=314) Species:
2287
(Saccharolobus solfataricus) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
MRIPLVGKDSIESKDIGFTLIHEHLRVFSEAVRQQWPHLYNEDEEFRNAV
NEVKRAMQFGVKTIVDPTVMGLGRDIRFMEKVVKATGINLVAGTGIYIYI
DLPFYFLNRSIDEIADLFIHDIKEGIQGTLNKAGFVKIAADEPGITKDVE
KVIRAAAIANKETKVPIITHSNAHNNTGLEQQRILTEEGVDPGKILIGHL
GDTDNIDYIKKIADKGSFIGLDRYGLDLFLPVDKRNETTLRLIKDGYSDK
IMISHDYCCTIDWGTAKPEYKPKLAPRWSITLIFEDTIPFLKRNGVNEEV
IATIFKENPKKFFS
Ligand information
Ligand ID
HT5
InChI
InChI=1S/C14H25NO2S/c1-2-3-4-5-6-7-8-9-13(16)15-12-10-11-18-14(12)17/h12H,2-11H2,1H3,(H,15,16)/t12-/m0/s1
InChIKey
PZUMIWRJDZWNPN-LBPRGKRZSA-N
SMILES
Software
SMILES
CACTVS 3.385
CCCCCCCCCC(=O)N[CH]1CCSC1=O
ACDLabs 10.04
O=C(NC1C(O)=[S+]CC1)CCCCCCCCC
CACTVS 3.385
OpenEye OEToolkits 2.0.7
CCCCCCCCCC(=O)N[C@H]1CCSC1=O
OpenEye OEToolkits 2.0.7
CCCCCCCCCC(=O)NC1CCSC1=O
Formula
C14 H25 N O2 S
Name
(4S)-4-(decanoylamino)-5-hydroxy-3,4-dihydro-2H-thiophenium
ChEMBL
CHEMBL4527540
DrugBank
ZINC
PDB chain
2vc7 Chain D Residue 1329 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
2vc7
Structural Basis for Natural Lactonase and Promiscuous Phosphotriesterase Activities.
Resolution
2.05 Å
Binding residue
(original residue number in PDB)
V27 L72 Y97 H170 L226 C258 I261 A266
Binding residue
(residue number reindexed from 1)
V27 L72 Y97 H170 L226 C258 I261 A266
Annotation score
1
Binding affinity
MOAD
: Ki=432.7uM
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
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:2vc7
,
PDBe:2vc7
,
PDBj:2vc7
PDBsum
2vc7
PubMed
18486146
UniProt
Q97VT7
|PHP_SACS2 Aryldialkylphosphatase (Gene Name=php)
[
Back to BioLiP
]