4.5 Review

What controls TOR?

期刊

IUBMB LIFE
卷 60, 期 8, 页码 483-496

出版社

WILEY
DOI: 10.1002/iub.56

关键词

enzyme mechanisms; eukaryotic gene expression; molecular genetics; phosphoinositides; protein function; protein synthesis; signal transduction

资金

  1. NIGMS NIH HHS [R01 GM079176-03, R01 GM079176] Funding Source: Medline

向作者/读者索取更多资源

The target of rapamycin (TOR) is a protein kinase with numerous functions in cell growth control. Some of these functions can be potently inhibited by rapamycin, an immunosuppressive and potential anticancer drug. TOR exists as part of two functionally distinct protein complexes. The functions of TOR complex 1 (TORC1) are effectively inhibited by rapamycin, but the mechanism for this inhibition remains elusive. The identification of TORC2 and recent reports that rapamycin can inhibit TORC2 functions, in some cases, challenge current models of TOR regulation. This review discusses the latest findings in yeast and mammals on the possible mechanisms that control TOR activity leading to its many cellular functions. (c) 2008 IUBMB.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据