Structure of PDB 1j7u Chain A Binding Site BS01
Receptor Information
>1j7u Chain A (length=263) Species:
1351
(Enterococcus faecalis) [
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AKMRISPELKKLIEKYRCVKDTEGMSPAKVYKLVGENENLYLKMTDSRYK
GTTYDVEREKDMMLWLEGKLPVPKVLHFERHDGWSNLLMSEADGVLCSEE
YEDEQSPEKIIELYAECIRLFHSIDISDCPYTNSLDSRLAELDYLLNNDL
ADVDCENWEEDTPFKDPRELYDFLKTEKPEEELVFSHGDLGDSNIFVKDG
KVSGFIDLGRSGRADKWYDIAFCVRSIREDIGEEQYVELFFDLLGIKPDW
EKIKYYILLDELF
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
1j7u Chain A Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
1j7u
Structural analyses of nucleotide binding to an aminoglycoside phosphotransferase.
Resolution
2.4 Å
Binding residue
(original residue number in PDB)
N195 D208
Binding residue
(residue number reindexed from 1)
N194 D207
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
K44 D190 N195 D208
Catalytic site (residue number reindexed from 1)
K43 D189 N194 D207
Enzyme Commision number
2.7.1.95
: kanamycin kinase.
Gene Ontology
Molecular Function
GO:0005524
ATP binding
GO:0008910
kanamycin kinase activity
GO:0016301
kinase activity
GO:0016773
phosphotransferase activity, alcohol group as acceptor
Biological Process
GO:0016310
phosphorylation
GO:0046677
response to antibiotic
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:1j7u
,
PDBe:1j7u
,
PDBj:1j7u
PDBsum
1j7u
PubMed
11467935
UniProt
P0A3Y5
|KKA3_ENTFL Aminoglycoside 3'-phosphotransferase (Gene Name=aphA)
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