共 41 条
Signal integration and diversification through the p62 scaffold protein
被引:271
作者:

Moscat, Jorge
论文数: 0 引用数: 0
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机构: Univ Cincinnati, Dept Genome Sci, Genome Res Inst, Cincinnati, OH 45237 USA

Diaz-Meco, Maria T.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Cincinnati, Dept Genome Sci, Genome Res Inst, Cincinnati, OH 45237 USA

Wooten, Marie W.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Cincinnati, Dept Genome Sci, Genome Res Inst, Cincinnati, OH 45237 USA
机构:
[1] Univ Cincinnati, Dept Genome Sci, Genome Res Inst, Cincinnati, OH 45237 USA
[2] Auburn Univ, Dept Biol Sci, Program Cell & Mol Biosci, Auburn, AL 36849 USA
关键词:
D O I:
10.1016/j.tibs.2006.12.002
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
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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页码:95 / 100
页数:6
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