Abstract
The sequence of the gyrase B subunit gene from Staphylococcus aureus strains resistant to the gyrase B subunit inhibitors cyclothialidine, coumermycin, and novobiocin has been determined. The residues altered in the resistant gyrase B subunits map to the ATP-binding region, suggesting that the drugs inhibit ATP binding and hydrolysis. The pattern of cross- resistances indicates that the detailed binding mode of the compounds differs.
Cite
CITATION STYLE
Stieger, M., Angehen, P., Wohlgensinger, B., & Gmünder, H. (1996). GyrB mutations in Staphylococcus aureus strains resistant to cyclothialidine, coumermycin, and novobiocin. Antimicrobial Agents and Chemotherapy. American Society for Microbiology. https://doi.org/10.1128/aac.40.4.1060
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.