Antibiotics and Antibiotic Resistance—Mur Ligases as an Antibacterial Target

Author:

Hervin Vincent1,Roy Vincent1ORCID,Agrofoglio Luigi A.1ORCID

Affiliation:

1. ICOA UMR CNRS 7311, Université d’Orléans et CNRS, Rue de Chartres, 45067 Orléans, France

Abstract

The emergence of Multidrug Resistance (MDR) strains of bacteria has accelerated the search for new antibacterials. The specific bacterial peptidoglycan biosynthetic pathway represents opportunities for the development of novel antibacterial agents. Among the enzymes involved, Mur ligases, described herein, and especially the amide ligases MurC-F are key targets for the discovery of multi-inhibitors, as they share common active sites and structural features.

Funder

EUROFERI program

CHemBio

Techsab

RTR Motivhealth

Labex programs SYNOR

IRON

Publisher

MDPI AG

Subject

Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science

Reference171 articles.

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4. Casimir Davaine (1812–1882) and the therapeutics of anthrax and livestock septicemia;Jean;Rev. D’histoire Pharm.,1973

5. Koch, R. (2023, November 08). Berliner Klinische Wochen-Schrift. Available online: https://babel.hathitrust.org/cgi/pt?id=mdp.39015020075001&seq=7.

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