4.2 Review

Rap-Interacting Proteins are Key Players in the Rap Symphony Orchestra

期刊

CELLULAR PHYSIOLOGY AND BIOCHEMISTRY
卷 39, 期 1, 页码 137-156

出版社

KARGER
DOI: 10.1159/000445612

关键词

Small G-proteins; Cancer; Cell adhesion; Cell migration

资金

  1. NSFC [U1302225, 81473342, 81460417, 81460253, 81560455]
  2. High-End Talent Grant of Yunnan Province, China [2012HA008]

向作者/读者索取更多资源

Rap, a member of the Ras-like small G-protein family, is a key node among G-protein coupled receptors (GPCR), receptor tyrosine kinases (RTKs), ion channels and many other downstream pathways. Rap plays a unique role in cell morphogenesis, adhesion, migration, exocytosis, proliferation, apoptosis and carcinogenesis. The complexity and diversity of Rap functions are tightly regulated by Rap-interacting proteins such as GEFs, GAPs, Rap effectors and scaffold proteins. These interacting proteins decide the subcellular localization of Rap, the interaction modes with downstream Rap effectors and tune Rap as an atypical molecular conductor, coupling extra-and intracellular signals to various pathways. In this review, we summarize four groups of Rap-interacting proteins, highlight their distinctions in Rap-binding properties and interactive modes and discuss their contribution to the spatiotemporal regulation of Rap as well as the implications of targeting Rap-interacting proteins in human cancer therapy. (C) 2016 The Author(s) Published by S. Karger AG, Basel

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

4.2
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