Structure of PDB 4cbt Chain B Binding Site BS03
Receptor Information
>4cbt Chain B (length=352) Species:
9606
(Homo sapiens) [
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KPRFTTGLVYDTLMLKHQCTCGSSSSHPEHAGRIQSIWSRLQETGLRGKC
ECIRGRKATLEELQTVHSEAHTLLYGTNPSDTIWNEVHSAGAARLAVGCV
VELVFKVATGELKNGFAVVRPPGHHAEESTPMGFCYFNSVAVAAKLLQQR
LSVSKILIVDWDVHHGNGTQQAFYSDPSVLYMSLHRYDDGNFFPGSGAPD
EVGTGPGVGFNVNMAFTGGLDPPMGDAEYLAAFRTVVMPIASEFAPDVVL
VSSGFDAVEGHPTPLGGYNLSARCFGYLTKQLMGLAGGRIVLALEGGHDL
TAICDASEACVSALLGNDPLPEKVLQQRPNANAVRSMEKVMEIHSKYWRC
LQ
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
4cbt Chain B Residue 2036 [
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Receptor-Ligand Complex Structure
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PDB
4cbt
Design, synthesis, and biological evaluation of potent and selective class IIa histone deacetylase (HDAC) inhibitors as a potential therapy for Huntington's disease.
Resolution
3.03 Å
Binding residue
(original residue number in PDB)
C667 C669 H675
Binding residue
(residue number reindexed from 1)
C19 C21 H27
Annotation score
1
Enzymatic activity
Enzyme Commision number
3.5.1.98
: histone deacetylase.
External links
PDB
RCSB:4cbt
,
PDBe:4cbt
,
PDBj:4cbt
PDBsum
4cbt
PubMed
24261862
UniProt
P56524
|HDAC4_HUMAN Histone deacetylase 4 (Gene Name=HDAC4)
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