Structure of PDB 2h2h Chain A Binding Site BS02
Receptor Information
>2h2h Chain A (length=234) Species:
2336
(Thermotoga maritima) [
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MKMKEFLDLLNESRLTVTLTGAGISTPSGIPDFNVFDIDFFYSHPEEFYR
FAKEGIFPMLQAKPNLAHVLLAKLEEKGLIEAVITQNIDRLHQRAGSKKV
IELHGNVEEYYCVRCEKKYTVEDVIKKLESSDVPLCDDCNSLIRPNIVFF
GENLPQDALREAIGLSSRASLMIVLGSSLVVYPAAELPLITVRSGGKLVI
VNLGETPFDDIATLKYNMDVVEFARRVMEEGGIS
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
2h2h Chain A Residue 1001 [
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Receptor-Ligand Complex Structure
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PDB
2h2h
The structural basis of sirtuin substrate affinity
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
C124 C148
Binding residue
(residue number reindexed from 1)
C112 C136
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
P31 D32 F33 N99 D101 H116
Catalytic site (residue number reindexed from 1)
P31 D32 F33 N87 D89 H104
Enzyme Commision number
2.3.1.286
: protein acetyllysine N-acetyltransferase.
Gene Ontology
Molecular Function
GO:0008270
zinc ion binding
GO:0016740
transferase activity
GO:0017136
NAD-dependent histone deacetylase activity
GO:0034979
NAD-dependent protein lysine deacetylase activity
GO:0046872
metal ion binding
GO:0051287
NAD binding
GO:0070403
NAD+ binding
Biological Process
GO:0006338
chromatin remodeling
GO:0006476
protein deacetylation
Cellular Component
GO:0005737
cytoplasm
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2h2h
,
PDBe:2h2h
,
PDBj:2h2h
PDBsum
2h2h
PubMed
16768447
UniProt
Q9WYW0
|NPD_THEMA NAD-dependent protein deacetylase (Gene Name=cobB)
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