Structure of PDB 1m2n Chain B Binding Site BS01
Receptor Information
>1m2n Chain B (length=249) Species:
2234
(Archaeoglobus fulgidus) [
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MDEKLLKTIAESKYLVALTGAGVSAESGIPTFRGKDGLWNRYRPEELANP
QAFAKDPEKVWKWYAWRMEKVFNAQPNKAHQAFAELERLGVLKCLITQNV
DGLHERAGSRNVIHLHGSLRVVRCTSCNNSFEVESAPKIPPLPKCDKCGS
LLRPGVVWAGEMLPPDVLDAAMREVERADVIIVAGTSAVVQPAASLPLIV
KQRGGAIIEINPDETPLTPIADYSLRGKAGEVMDELVRHVRKALSLKLN
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
1m2n Chain B Residue 999 [
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Receptor-Ligand Complex Structure
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PDB
1m2n
Structural basis for the NAD-dependent deacetylase mechanism of Sir2
Resolution
2.6 Å
Binding residue
(original residue number in PDB)
C124 C127 C145
Binding residue
(residue number reindexed from 1)
C124 C127 C145
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
P30 T31 F32 R33 N99 D101 H116
Catalytic site (residue number reindexed from 1)
P30 T31 F32 R33 N99 D101 H116
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:0070403
NAD+ binding
Biological Process
GO:0006338
chromatin remodeling
GO:0006476
protein deacetylation
GO:0036048
protein desuccinylation
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:1m2n
,
PDBe:1m2n
,
PDBj:1m2n
PDBsum
1m2n
PubMed
12091395
UniProt
O28597
|NPD1_ARCFU NAD-dependent protein deacylase 1 (Gene Name=cobB1)
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