Structure of PDB 2h2f Chain A Binding Site BS02
Receptor Information
>2h2f Chain A (length=234) Species:
2336
(Thermotoga maritima) [
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MKMKEFLDLLNESRLTVTLTGAGISTPSGIPDQNVFDIDFFYSHPEEFYR
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
2h2f Chain A Residue 1001 [
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Receptor-Ligand Complex Structure
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PDB
2h2f
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 N99 D101 H116
Catalytic site (residue number reindexed from 1)
P31 D32 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:2h2f
,
PDBe:2h2f
,
PDBj:2h2f
PDBsum
2h2f
PubMed
16768447
UniProt
Q9WYW0
|NPD_THEMA NAD-dependent protein deacetylase (Gene Name=cobB)
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