Centro de Biologia Molecular Estrutural (CEBIME), Departamento de Bioquímica, Universidade Federal de Santa Catarina, Campus Trindade, 88040-900 Florianópolis, SC, Brazil.
Eur J Med Chem. 2013 Jun;64:35-41. doi: 10.1016/j.ejmech.2013.04.018. Epub 2013 Apr 16.
YopH plays a relevant role in three pathogenic species of Yersinia. Due to its importance in the prevention of the inflammatory response of the host, this enzyme has become a valid target for the identification and development of new inhibitors. In this work, an in-house library of 283 synthetic compounds was assayed against recombinant YopH from Yersinia enterocolitica. From these, four chalcone derivatives and one sulfonamide were identified for the first time as competitive inhibitors of YopH with binding affinity in the low micromolar range. Molecular modeling investigations indicated that the new inhibitors showed similar binding modes, establishing polar and hydrophobic contacts with key residues of the YopH binding site.
YopH 在三种致病性耶尔森氏菌中发挥着重要作用。由于其在宿主炎症反应预防中的重要性,这种酶已成为鉴定和开发新抑制剂的有效靶点。在这项工作中,对来自小肠结肠炎耶尔森氏菌的重组 YopH 对 283 种合成化合物的库进行了测定。其中,四种查尔酮衍生物和一种磺胺首次被鉴定为 YopH 的竞争性抑制剂,其结合亲和力在低微摩尔范围内。分子建模研究表明,新抑制剂表现出相似的结合模式,与 YopH 结合位点的关键残基建立了极性和疏水接触。