接合作用
蛋白酶体
Skp1型
NEDD8公司
F盒蛋白
泛素
泛素连接酶
细胞生物学
卡林
磷酸化
细胞分裂控制蛋白4
蛋白质降解
泛素蛋白连接酶类
化学
泛素结合酶
生物化学
生物
基因
出处
期刊:Science's STKE
[American Association for the Advancement of Science (AAAS)]
日期:2001-08-28
卷期号:2001 (97)
被引量:25
标识
DOI:10.1126/stke.2001.97.pe2
摘要
Regulated degradation of proteins is essential for viability and is involved in the control of many signal transduction pathways. von Arnim discusses a new model for how substrates destined for degradation by the 26S proteasome may be presented to the proteasome through a physical interaction between the proteasome and a complex consisting of the substrate and a ubiquitin-ligase. The new model suggests that the SCF (Skp1/cullin/F-box) protein complex may physically associate with the proteasome and that this interaction may be regulated by posttranslational modifications, such as phosphorylation or the covalent attachment of the Nedd8 protein, called neddylation. Additionally, other proteins may compete with the SCF complexes for binding to the proteasome and thus present another layer of regulation for controlling substrate targeting for ubiquitin-mediated degradation.
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