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The intricacies of p21 phosphorylation - Protein/protein interactions, subcellular localization and stability

期刊

CELL CYCLE
卷 5, 期 12, 页码 1313-1319

出版社

TAYLOR & FRANCIS INC
DOI: 10.4161/cc.5.12.2863

关键词

Akt/PKB; p21 Cip1 Waf1 Sdi1; cyclin; cdk; cell cycle; phosphorylation; degradation; protein/protein interaction; PKC; p27 Kip1

资金

  1. Biotechnology and Biological Sciences Research Council [BB/C508134/1] Funding Source: researchfish
  2. Biotechnology and Biological Sciences Research Council [BB/C508134/1] Funding Source: Medline

向作者/读者索取更多资源

p21 was originally described as functioning as a cell cycle regulator via inhibition of both cyclin-dependent kinases and processive DNA replication. Nowadays it is recognized to play other fundamental roles including transcriptional regulation and the modulation of apoptosis. Each of these functions of p21 is achieved through direct p21/protein interactions and the subcellular localization of p21 plays an important part in dictating the binding partners to which p21 is exposed. Over recent years, a number of phosphorylation sites in p21 have been identified, these being targeted by several important intracellular signalling protein kinases. Here we review the state of our knowledge of p21 phosphorylation with respect to the kinases involved and the molecular biological effects of each phosphorylation event.

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