白喉棒状杆菌
毒力
谷氨酸棒杆菌
结核分枝杆菌
聚酮合酶
聚酮
棒状杆菌
微生物学
生物合成
生物
生物化学
化学
计算生物学
肺结核
酶
细菌
白喉
基因
遗传学
病毒学
医学
接种疫苗
病理
作者
Rong Chen,Jingting C. Yuan,Xiaoqian Shi,Wen-Jian Tang,Xiang Liu
标识
DOI:10.1016/j.bbrc.2021.12.083
摘要
Mycolic acids (MAs) are unique components of cell envelope of Mycobacterium or Corynebacterium and are key factors of their virulence to human. In order to develop new anti-Tuberculosis (TB) drugs, many efforts have paid on investigation of structures and functions of proteins involved in the biosynthesis pathway of MAs. FadD32 and polyketide synthase 13 (pks13) catalyze the last step of MAs synthesis. Here we present the crystal structures of FadD32 with substrates and holo-form of ACP-domain from Corynebacterium diphtheriae. The crystal structures and in vitro biochemical assays provide new insights into the assembly of FadD32 and pks13.
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