Structure of PDB 5cnp Chain F Binding Site BS01
Receptor Information
>5cnp Chain F (length=169) Species:
243277
(Vibrio cholerae O1 biovar El Tor str. N16961) [
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NSQLTLRALERGDLRFIHNLNNNRNIMSYWFEEPYESFDELEELYNKHIH
DNAERRFVVEDAQKNLIGLVELIEINYIHRSAEFQIIIAPEHQGKGFART
LINRALDYSFTILNLHKIYLHVAVENPKAVHLYEECGFVEEGHLVEEFFI
NGRYQDVKRMYILQSKYLN
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
5cnp Chain F Residue 201 [
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Receptor-Ligand Complex Structure
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PDB
5cnp
Substrate-Induced Allosteric Change in the Quaternary Structure of the Spermidine N-Acetyltransferase SpeG.
Resolution
2.38 Å
Binding residue
(original residue number in PDB)
E33 E75
Binding residue
(residue number reindexed from 1)
E32 E74
Annotation score
1
Enzymatic activity
Enzyme Commision number
2.3.1.57
: diamine N-acetyltransferase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0004145
diamine N-acetyltransferase activity
GO:0016746
acyltransferase activity
GO:0016747
acyltransferase activity, transferring groups other than amino-acyl groups
GO:0046872
metal ion binding
Biological Process
GO:0006598
polyamine catabolic process
GO:0046203
spermidine catabolic process
GO:0046208
spermine catabolic process
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:5cnp
,
PDBe:5cnp
,
PDBj:5cnp
PDBsum
5cnp
PubMed
26410587
UniProt
Q9KL03
|ATDA_VIBCH Spermidine N(1)-acetyltransferase (Gene Name=speG)
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