Inhibition of D-Ala:D-Ala ligase through a phosphorylated form of the antibiotic D-cycloserine
journal contributionposted on 15.07.2020 by Sarah Batson, Cesira de Chiara, Vita Majce, Adrian J Lloyd, Stanislav Gobec, Dean Rea, Vilmos Fülöp, Christopher W Thoroughgood, Katie J Simmons, Christopher G Dowson, Colin WG Fishwick, Luiz Pedro S de Carvalho, David I Roper
Any type of content formally published in an academic journal, usually following a peer-review process.
D-cycloserine is an antibiotic which targets sequential bacterial cell wall peptidoglycan biosynthesis enzymes: alanine racemase and D-alanine:D-alanine ligase. By a combination of structural, chemical and mechanistic studies here we show that the inhibition of D-alanine:D-alanine ligase by the antibiotic D-cycloserine proceeds via a distinct phosphorylated form of the drug. This mechanistic insight reveals a bimodal mechanism of action for a single antibiotic on different enzyme targets and has significance for the design of future inhibitor molecules based on this chemical structure.