The Francis Crick Institute
s41467-017-02118-7.pdf (922.48 kB)

Inhibition of D-Ala:D-Ala ligase through a phosphorylated form of the antibiotic D-cycloserine

Download (922.48 kB)
journal contribution
posted on 2020-07-15, 11:00 authored 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
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.