排序酶A
分拣酶
金黄色葡萄球菌
化学
脂质Ⅱ
毒力
微生物学
细菌
体内
细菌蛋白
生物化学
生物
酶
生物合成
生物技术
基因
遗传学
作者
Stella Cascioferro,Demetrio Raffa,Benedetta Maggio,Maria Valeria Raimondi,Domenico Schillaci,Giuseppe Daidone
标识
DOI:10.1021/acs.jmedchem.5b00779
摘要
Here, we describe the most promising small synthetic organic compounds that act as potent Sortase A inhibitors and cater the potential to be developed as antivirulence drugs. Sortase A is a polypeptide of 206 amino acids, which catalyzes two sequential reactions: (i) thioesterification and (ii) transpeptidation. Sortase A is involved in the process of bacterial adhesion by anchoring LPXTG-containing proteins to lipid II. Sortase A inhibitors do not affect bacterial growth, but they restrain the virulence of pathogenic bacterial strains, thereby preventing infections caused by Staphylococcus aureus or other Gram-positive bacteria. The efficacy of the most promising inhibitors needs to be comprehensively evaluated in in vivo models of infection, in order to select compounds eligible for the treatment of bacterial infections in humans.
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