Structure of PDB 4bz9 Chain C Binding Site BS02
Receptor Information
>4bz9 Chain C (length=413) Species:
6183
(Schistosoma mansoni) [
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SVGIVYGDQYRQLCCSSPKFGDRYALVMDLINAYKLIPELSRVPPLQWDS
PSRMYEAVTAFHSTEYVDALKKLQMLHCEELTADDELLMDSFSLNYDCPG
FPSVFDYSLAAVQGSLAAASALICRHCEVVINWGGGWHHAKRSEASGFCY
LNDIVLAIHRLVSSQTRVLYVDLDLHHGDGVEEAFWYSPRVVTFSVHHAS
PGFFPGTGTWNKLPIFLNGAGRGRFSAFNLPLEEGINDLDWSNAIGPILD
SLNIVIQPSYVVVQCGADCLATDPHRIFRLTNFYPCSLSGYLYAIKKILS
WKVPTLILGGGGYNFPDTARLWTRVTALTIEEVKGKKMTISPEIPEHSYF
SRYGPDFELDIDYFPHTLDSIQKHHRRILEQLRNYADLNKLIYDYDQVYQ
LYNLTGMGSLVPR
Ligand information
Ligand ID
KMY
InChI
InChI=1S/C9H6ClNO2S/c10-7-5-3-1-2-4-6(5)14-8(7)9(12)11-13/h1-4,13H,(H,11,12)
InChIKey
HRXULFWGEYSULN-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 12.01
Clc1c2ccccc2sc1C(=O)NO
OpenEye OEToolkits 1.7.6
c1ccc2c(c1)c(c(s2)C(=O)NO)Cl
CACTVS 3.385
ONC(=O)c1sc2ccccc2c1Cl
Formula
C9 H6 Cl N O2 S
Name
3-chlorobenzothiophene-2-carbohydroxamic acid
ChEMBL
CHEMBL2094337
DrugBank
ZINC
ZINC000000307965
PDB chain
4bz9 Chain C Residue 700 [
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Receptor-Ligand Complex Structure
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PDB
4bz9
Structural Basis for the Inhibition of Histone Deacetylase 8 (Hdac8), a Key Epigenetic Player in the Blood Fluke Schistosoma Mansoni.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
K20 F21 D100 H141 H142 G150 D186 H188 F216 Y341
Binding residue
(residue number reindexed from 1)
K19 F20 D97 H138 H139 G147 D174 H176 F204 Y313
Annotation score
1
Binding affinity
BindingDB: IC50=4365nM
Enzymatic activity
Enzyme Commision number
3.5.1.98
: histone deacetylase.
Gene Ontology
Molecular Function
GO:0004407
histone deacetylase activity
GO:0046872
metal ion binding
Biological Process
GO:0000122
negative regulation of transcription by RNA polymerase II
GO:0006338
chromatin remodeling
Cellular Component
GO:0005634
nucleus
View graph for
Molecular Function
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:4bz9
,
PDBe:4bz9
,
PDBj:4bz9
PDBsum
4bz9
PubMed
24086136
UniProt
A5H660
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