Journal article
The molecular basis of the expansive substrate specificity of the antibiotic resistance enzyme aminoglycoside acetyltransferase-6'-aminoglycoside phosphotransferase-2". The role of ASP-99 as an active site base important for acetyl transfer
Abstract
The most frequent determinant of aminoglycoside antibiotic resistance in Gram-positive bacterial pathogens is a bifunctional enzyme, aminoglycoside acetyltransferase-6'-aminoglycoside phosphotransferase-2" (AAC(6')- aminoglycoside phosphotransferase-2", capable of modifying a wide selection of clinically relevant antibiotics through its acetyltransferase and kinase activities. The aminoglycoside acetyltransferase domain of the enzyme, …
Authors
Boehr DD; Jenkins SI; Wright GD
Journal
The Journal of Biological Chemistry, Vol. 278, No. 15, pp. 12873–12880
Publication Date
April 11, 2003
DOI
10.1074/jbc.M211680200
ISSN
0021-9258
Fields of Research (FoR)
Medical Subject Headings (MeSH)
AcetyltransferasesAmino Acid SequenceAmino Acid SubstitutionAspartic AcidBinding SitesDNA PrimersHydrogen-Ion ConcentrationKineticsMolecular Sequence DataMutagenesis, Site-DirectedPhosphotransferases (Alcohol Group Acceptor)Protein ConformationRecombinant ProteinsSequence AlignmentSequence Homology, Amino AcidSubstrate Specificity