Structure of PDB 2hjh Chain A Binding Site BS03
Receptor Information
>2hjh Chain A (length=325) Species:
4932
(Saccharomyces cerevisiae) [
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DPLAKKQTVRLIKDLQVLCTRLRLSNFFTIDHFIQKLHTARKILVLTGAG
VSTSLGIPDFRSSEGFYSKIKHLGLDDPQDVFNYNIFMHDPSVFYNIANM
VLPPEKIYSPLHSFIKMLQMKGKLLRNYTQNIDNLESYAGISTDKLVQCH
GSFATATCVTCHWNLPGERIFNKIRNLELPLCPYCYKKRREYFPERPPYI
LNSYGVLKPDITFFGEALPNKFHKSIREDILECDLLICIGTSLKVAPVSE
IVNMVPSHVPQVLINRDPVKHAEFDLSLLGYCDDIAAMVAQKCGWTIPHK
KWNDLKNKNFKCQEKDKGVYVVTSD
Ligand information
Ligand ID
NCA
InChI
InChI=1S/C6H6N2O/c7-6(9)5-2-1-3-8-4-5/h1-4H,(H2,7,9)
InChIKey
DFPAKSUCGFBDDF-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1cc(cnc1)C(=O)N
CACTVS 3.341
NC(=O)c1cccnc1
ACDLabs 10.04
O=C(N)c1cccnc1
Formula
C6 H6 N2 O
Name
NICOTINAMIDE
ChEMBL
CHEMBL1140
DrugBank
DB02701
ZINC
ZINC000000005878
PDB chain
2hjh Chain A Residue 900 [
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Receptor-Ligand Complex Structure
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PDB
2hjh
Autoregulation of the yeast Sir2 deacetylase by reaction and trapping of a pseudosubstrate motif in the active site
Resolution
1.85 Å
Binding residue
(original residue number in PDB)
I271 P272 F274
Binding residue
(residue number reindexed from 1)
I57 P58 F60
Annotation score
5
Binding affinity
BindingDB: IC50=<50000nM
Enzymatic activity
Catalytic site (original residue number in PDB)
P272 D273 F274 R275 N345 D347 H364
Catalytic site (residue number reindexed from 1)
P58 D59 F60 R61 N131 D133 H150
Enzyme Commision number
2.3.1.286
: protein acetyllysine N-acetyltransferase.
Gene Ontology
Molecular Function
GO:0070403
NAD+ binding
View graph for
Molecular Function
External links
PDB
RCSB:2hjh
,
PDBe:2hjh
,
PDBj:2hjh
PDBsum
2hjh
PubMed
UniProt
P06700
|SIR2_YEAST NAD-dependent histone deacetylase SIR2 (Gene Name=SIR2)
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