Structure of PDB 1s7g Chain D Binding Site BS02
Receptor Information
>1s7g Chain D (length=240) Species:
2234
(Archaeoglobus fulgidus) [
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EDEIRKAAEILAKSKHAVVFTGAGISAGLWRKYDPEEVASISGFKRNPRA
FWEFSMEMKDKLFAEPNPAHYAIAELERMGIVKAVITQNIDMLHQRAGSR
RVLELHGSMDKLDCLDCHETYDWSEFVEDFNKGEIPRCRKCGSYYVKPRV
VLFGEPLPQRTLFEAIEEAKHCDAFMVVGSSLVVYPAAELPYIAKKAGAK
MIIVNAEPTMADPIFDVKIIGKAGEVLPKIVEEVKRLRSE
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
1s7g Chain D Residue 608 [
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Receptor-Ligand Complex Structure
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PDB
1s7g
Structural basis for the mechanism and regulation of sir2 enzymes
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
H17 E180 H183
Binding residue
(residue number reindexed from 1)
H16 E168 H171
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
N101 D103 H118
Catalytic site (residue number reindexed from 1)
N89 D91 H106
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:0036054
protein-malonyllysine demalonylase activity
GO:0036055
protein-succinyllysine desuccinylase activity
GO:0046872
metal ion binding
GO:0051287
NAD binding
GO:0070403
NAD+ binding
Biological Process
GO:0006338
chromatin remodeling
GO:0006476
protein deacetylation
GO:0036049
peptidyl-lysine desuccinylation
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:1s7g
,
PDBe:1s7g
,
PDBj:1s7g
PDBsum
1s7g
PubMed
15023335
UniProt
O30124
|NPD2_ARCFU NAD-dependent protein deacylase 2 (Gene Name=cobB2)
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