支架蛋白
细胞生物学
死孢子体1
生物
功能(生物学)
信号转导衔接蛋白
信号转导
泛素
脚手架
机制(生物学)
计算生物学
生物化学
自噬
基因
医学
认识论
生物医学工程
哲学
细胞凋亡
作者
Jorge Moscat,María T. Diaz‐Meco,Marie W. Wooten
标识
DOI:10.1016/j.tibs.2006.12.002
摘要
Signal specificity of multifunctional enzymes is achieved through protein-protein interactions involving specific domains on scaffold proteins. p62 (also known as sequestosome 1) is such a scaffold protein that possesses PB1 and UBA domains, and the TRAF6 binding sequence. Proteins recruited to these domains enable p62 to integrate kinase-activated and ubiquitin-mediated signaling pathways. The biological function of p62 has been studied in diverse systems and processes such as osteoclastogenesis, inflammation, differentiation, neurotrophin biology and obesity. The availability of mice in which p62 has been genetically inactivated is providing new insight into the mechanism and function of p62 at a whole-organism level.
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