4.6 Review

RAFTK/Pyk2-mediated cellular signalling

期刊

CELLULAR SIGNALLING
卷 12, 期 3, 页码 123-133

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/S0898-6568(99)00076-5

关键词

tyrosine kinases; RAFTK/Pyk2; FAK; signalling

资金

  1. NCI NIH HHS [CA76226] Funding Source: Medline
  2. NHLBI NIH HHS [HL55445, HL51456] Funding Source: Medline

向作者/读者索取更多资源

Intracellular signal transduction following extracellular ligation by a wide variety of surface molecules involves the activation and tyrosine phosphorylation of protein tyrosine kinases (PTKs). Tyrosine phosphorylation, controlled by the coordinated actions of protein tyrosine phosphatases (PTPs) and tyrosine kinases, is a critical regulatory mechanism for various physiological processes, including cell growth, differentiation, metabolism, cell cycle regulation and cytoskeleton function. The focal adhesion PTK family consists of the focal adhesion kinase (FAK) and the RAFTK/Pyk2 kinase (also known as CAK-beta and CADTK). RAFTK/Pyk2 can be activated by a variety of extracellular signals that elevate intracellular calcium concentration, and by stress signals. RAFTK/Pyk2 is expressed mainly in the central nervous system and in cells derived from hematopoietic lineages, while FAK is widely expressed in various tissues and links transmembrane integrin receptors to intracellular pathways. This review describes the role of RAFTK/Pyk2 in Various signalling cascades and details the differential signalling by FAK and RAFTK/Pyk2. (C) 2000 Elsevier Science Inc. All rights reserved.

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

4.6
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