Abstract
Background: D-Ala:D-Lac and D-Ala:D-Ser ligases are key enzymes in vancomycin resistance. Results: The VanG D-Ala:D-Ser ligase structure provided insight into its molecular specificity and allowed the selection of a specific peptide inhibitor. Conclusion: D-Ala:D-Lac and D-Ala:D-Ser ligases share specific determinants. Significance: This study sheds light on the molecular specificity and evolution of D-Ala:D-X ligases and could help in designing inhibitors to overcome vancomycin resistance. © 2012 by The American Society for Biochemistry and Molecular Biology, Inc.
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CITATION STYLE
Meziane-Cherif, D., Saul, F. A., Haouz, A., & Courvalin, P. (2012). Structural and functional characterization of VanG D-Ala:D-Ser ligase associated with vancomycin resistance in Enterococcus faecalis. Journal of Biological Chemistry, 287(45), 37583–37592. https://doi.org/10.1074/jbc.M112.405522
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