4.4 Review

The secret life of kinases: insights into non-catalytic signalling functions from pseudokinases

期刊

BIOCHEMICAL SOCIETY TRANSACTIONS
卷 45, 期 -, 页码 665-681

出版社

PORTLAND PRESS LTD
DOI: 10.1042/BST20160331

关键词

-

资金

  1. Australian Government Research Training Program Scholarship
  2. National Health and Medical Research Council of Australia (NHMRC) fellowship [1105754]
  3. NHMRC Project grants [1057905, 1067289, 1124735, 1124737]
  4. NHMRC IRIISS [9000220]
  5. Victorian Government Operational Infrastructure
  6. National Health and Medical Research Council of Australia [1067289, 1057905, 1124735, 1124737] Funding Source: NHMRC

向作者/读者索取更多资源

Over the past decade, our understanding of the mechanisms by which pseudokinases, which comprise similar to 10% of the human and mouse kinomes, mediate signal transduction has advanced rapidly with increasing structural, biochemical, cellular and genetic studies. Pseudokinases are the catalytically defective counterparts of conventional, active protein kinases and have been attributed functions as protein interaction domains acting variously as allosteric modulators of conventional protein kinases and other enzymes, as regulators of protein trafficking or localisation, as hubs to nucleate assembly of signalling complexes, and as transmembrane effectors of such functions. Here, by categorising mammalian pseudokinases based on their known functions, we illustrate the mechanistic diversity among these proteins, which can be viewed as a window into understanding the non-catalytic functions that can be exerted by conventional protein kinases.

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

4.4
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