Chemistry Research Laboratory, Department of Chemistry, University of Oxford, Oxford, OX1 3TA, UK.
Chem Commun (Camb). 2019 Aug 22;55(69):10214-10217. doi: 10.1039/c9cc04145a.
The l,d-transpeptidases (Ldts) are promising antibiotic targets for treating tuberculosis. We report screening of cysteine-reactive inhibitors against LdtMt2 from Mycobacterium tuberculosis. Structural studies on LdtMt2 with potent inhibitor ebselen reveal opening of the benzisoselenazolone ring by a nucleophilic cysteine, forming a complex involving extensive hydrophobic interactions with a substrate-binding loop.
l,d-转肽酶(Ldts)是治疗结核病有前景的抗生素靶标。我们报告了针对结核分枝杆菌 LdtMt2 的半胱氨酸反应性抑制剂的筛选。与强效抑制剂依布硒啉在结构上对 LdtMt2 的研究表明,亲核半胱氨酸使苯并硒唑啉环打开,形成一个涉及与底物结合环广泛疏水相互作用的复合物。