Kile Benjamin T, Schulman Brenda A, Alexander Warren S, Nicola Nicos A, Martin Helene M E, Hilton Douglas J
The Walter and Eliza Hall Institute of Medical Research and The Cooperative Research Centre for Cellular Growth Factors, Parkville, Victoria, Australia.
Trends Biochem Sci. 2002 May;27(5):235-41. doi: 10.1016/s0968-0004(02)02085-6.
Although initially identified in the suppressor of cytokine signaling (SOCS) family of proteins, the C-terminal SOCS box has now been identified in more than 40 proteins in nine different families. Growing evidence suggests that the SOCS box, similar to the F-box, acts as a bridge between specific substrate-binding domains and the more generic proteins that comprise a large family of E3 ubiquitin protein ligases. In this way, SOCS proteins regulate protein turnover by targeting proteins for polyubiquitination and, therefore, for proteasome-mediated degradation.
尽管最初是在细胞因子信号转导抑制因子(SOCS)蛋白家族中发现的,但现在已在九个不同家族的40多种蛋白质中鉴定出C末端SOCS框。越来越多的证据表明,SOCS框与F-box类似,充当特定底物结合域与构成E3泛素蛋白连接酶大家族的更通用蛋白质之间的桥梁。通过这种方式,SOCS蛋白通过将蛋白质靶向多聚泛素化,从而调节蛋白质周转,进而介导蛋白酶体介导的降解。