Journal article
Active site labeling of the gentamicin resistance enzyme AAC(6')-APH(2") by the lipid kinase inhibitor wortmannin
Abstract
BACKGROUND: Aminoglycoside antibiotic resistance is largely the result of the production of enzymes that covalently modify the drugs including kinases (APHs) with structural and functional similarity to protein and lipid kinases. One of the most important aminoglycoside resistance enzymes is AAC(6')-APH(2"), a bifunctional enzyme with both aminoglycoside acetyltransferase and kinase activities. Knowledge of enzyme active site structure is …
Authors
Boehr DD; Lane WS; Wright GD
Journal
Chemistry & Biology, Vol. 8, No. 8, pp. 791–800
Publication Date
8 2001
ISSN
1074-5521
Fields of Research (FoR)
Medical Subject Headings (MeSH)
AcetyltransferasesAdenosine TriphosphateAmino Acid SequenceAndrostadienesBinding SitesDose-Response Relationship, DrugDrug DesignDrug Resistance, BacterialEnzyme InhibitorsEscherichia coliGentamicinsKanamycin KinaseKineticsLysineMolecular Sequence DataMutagenesis, Site-DirectedPhosphoinositide-3 Kinase InhibitorsPhosphotransferases (Alcohol Group Acceptor)Protein Structure, TertiaryRecombinant Fusion ProteinsSequence Homology, Amino AcidWortmannin