Structure of an enzyme required for aminoglycoside antibiotic resistance reveals homology to eukaryotic protein kinases
Hon, W. C. ; McKay, G. A. ; Thompson, Paul R ; Sweet, R. M. ; Yang, D. S. ; Wright, G. D. ; Berghuis, A. M.
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Keywords
*Anti-Bacterial Agents
Binding Sites
Crystallography
*Drug Resistance, Microbial
Enterococcus
Eukaryotic Cells
Kanamycin Kinase
Molecular Sequence Data
Phosphotransferases (Alcohol Group Acceptor)
Protein Kinases
Protein Structure, Secondary
Protein Structure, Tertiary
Sequence Homology, Amino Acid
Signal Transduction
Staphylococcus
Biochemistry
Enzymes and Coenzymes
Medicinal-Pharmaceutical Chemistry
Therapeutics
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Abstract
Bacterial resistance to aminoglycoside antibiotics is almost exclusively accomplished through either phosphorylation, adenylylation, or acetylation of the antibacterial agent. The aminoglycoside kinase, APH(3')-IIIa, catalyzes the phosphorylation of a broad spectrum of aminoglycoside antibiotics. The crystal structure of this enzyme complexed with ADP was determined at 2.2 A. resolution. The three-dimensional fold of APH(3')-IIIa reveals a striking similarity to eukaryotic protein kinases despite a virtually complete lack of sequence homology. Nearly half of the APH(3')-IIIa sequence adopts a conformation identical to that seen in these kinases. Substantial differences are found in the location and conformation of residues presumably responsible for second-substrate specificity. These results indicate that APH(3') enzymes and eukaryotic-type protein kinases share a common ancestor.
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Cell. 1997 Jun 13;89(6):887-95. doi:10.1016/S0092-8674(00)80274-3
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At the time of publication, Paul Thompson was not yet affiliated with UMass Medical School.