蛋白酶
生物合成
天然产物
生物化学
产品(数学)
生物
自然(考古学)
细胞生物学
化学
计算生物学
酶
古生物学
几何学
数学
作者
Fumihiro Ishikawa,Chiharu Uchida,Genzoh Tanabe
标识
DOI:10.1021/acschembio.4c00304
摘要
Protein degradation is a tightly regulated biological process that maintains bacterial proteostasis. ClpPs are a highly conserved family of serine proteases that associate with the AAA + ATPase (an ATPase associated with diverse cellular activities) to degrade protein substrates. Identification and biochemical characterization of protein substrates for the AAA + ATPase-dependent ClpP degradation systems are considered essential for gaining an understanding of the molecular operation of the complex ClpP degradation machinery. Consequently, expanding the repertoire of protein substrates that can be degraded in vitro and within bacterial cells is necessary. Here, we report that AAA + ATPase-ClpP proteolytic complexes promote degradation of the secondary metabolite surfactin synthetases SrfAA, SrfAB, and SrfAC in
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