Mutations in Three Distinct Loci Cause Resistance to Peptide Deformylase Inhibitors in Bacillus subtilis
Author:
Affiliation:
1. Protein Maturation, Cell Fate and Therapeutics, ISV, UPR2355, Centre National de la Recherche Scientifique, Bât. 23A, 1 avenue de la Terrasse, F-91198 Gif-sur-Yvette Cedex, France
Abstract
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Link
https://journals.asm.org/doi/pdf/10.1128/AAC.01340-08
Reference33 articles.
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2. Allaire, M., Y. Li, R. E. MacKenzie, and M. Cygler. 1998. The 3-D structure of a folate-dependent dehydrogenase/cyclohydrolase bifunctional enzyme at 1.5 Å resolution. Structure6:173-182.
3. Angelaccio, S., S. Pascarella, E. Fattori, F. Bossa, W. Strong, and V. Schirch. 1992. Serine hydroxymethyltransferase: origin of substrate specificity. Biochemistry31:155-162.
4. Peptide Deformylase as an Antibacterial Drug Target: Target Validation and Resistance Development
5. Arnold, H. H. 1977. Initiation of protein synthesis in bacillus subtilis in the presence of trimethoprim or aminopterin. Biochim. Biophys. Acta476:76-87.
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