Structure of PDB 3ovx Chain B Binding Site BS01
Receptor Information
>3ovx Chain B (length=217) Species:
9606
(Homo sapiens) [
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LPDSVDWREKGCVTEVKYQGSCGACWAFSAVGALEAQLKLKTGKLVSLSA
QNLVDCSTEKYGNKGCNGGFMTTAFQYIIDNKGIDSDASYPYKAMDQKCQ
YDSKYRAATCSKYTELPYGREDVLKEAVANKGPVSVGVDARHPSFFLYRS
GVYYEPSCTQNVNHGVLVVGYGDLNGKEYWLVKNSWGHNFGEEGYIRMAR
NKGNHCGIASFPSYPEI
Ligand information
Ligand ID
O64
InChI
InChI=1S/C12H11ClF3NO2/c1-2-7(6-18)17-11(19)8-4-3-5-9(10(8)13)12(14,15)16/h3-7H,2H2,1H3,(H,17,19)/t7-/m0/s1
InChIKey
NPWUKONGKBALPD-ZETCQYMHSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.0
CCC(C=O)NC(=O)c1cccc(c1Cl)C(F)(F)F
CACTVS 3.370
CC[C@H](NC(=O)c1cccc(c1Cl)C(F)(F)F)C=O
ACDLabs 12.01
FC(F)(F)c1cccc(C(=O)NC(C=O)CC)c1Cl
CACTVS 3.370
CC[CH](NC(=O)c1cccc(c1Cl)C(F)(F)F)C=O
OpenEye OEToolkits 1.7.0
CC[C@@H](C=O)NC(=O)c1cccc(c1Cl)C(F)(F)F
Formula
C12 H11 Cl F3 N O2
Name
2-chloro-N-[(1S)-1-formylpropyl]-3-(trifluoromethyl)benzamide
ChEMBL
DrugBank
ZINC
ZINC000058639000
PDB chain
3ovx Chain B Residue 218 [
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Receptor-Ligand Complex Structure
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PDB
3ovx
Trifluoromethylphenyl as P2 for ketoamide-based cathepsin S inhibitors.
Resolution
1.49 Å
Binding residue
(original residue number in PDB)
G23 C25 W26 G68 G69 N163 G165
Binding residue
(residue number reindexed from 1)
G23 C25 W26 G68 G69 N163 G165
Annotation score
1
Binding affinity
BindingDB: IC50=31nM
Enzymatic activity
Catalytic site (original residue number in PDB)
Q19 C25 H164 N184
Catalytic site (residue number reindexed from 1)
Q19 C25 H164 N184
Enzyme Commision number
3.4.22.27
: cathepsin S.
Gene Ontology
Molecular Function
GO:0008234
cysteine-type peptidase activity
Biological Process
GO:0006508
proteolysis
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:3ovx
,
PDBe:3ovx
,
PDBj:3ovx
PDBsum
3ovx
PubMed
21030256
UniProt
P25774
|CATS_HUMAN Cathepsin S (Gene Name=CTSS)
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