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SH2结构域蛋白的人类和小鼠补体——确定磷酸酪氨酸信号传导的边界。

The human and mouse complement of SH2 domain proteins-establishing the boundaries of phosphotyrosine signaling.

作者信息

Liu Bernard A, Jablonowski Karl, Raina Monica, Arcé Michael, Pawson Tony, Nash Piers D

机构信息

Ben May Institute for Cancer Research and the Committee on Cancer Biology, The University of Chicago, Chicago, Illinois 60637.

Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto M5G 1X5, Canada.

出版信息

Mol Cell. 2006 Jun 23;22(6):851-868. doi: 10.1016/j.molcel.2006.06.001.

Abstract

SH2 domains are interaction modules uniquely dedicated to the recognition of phosphotyrosine sites and are embedded in proteins that couple protein-tyrosine kinases to intracellular signaling pathways. Here, we report a comprehensive bioinformatics, structural, and functional view of the human and mouse complement of SH2 domain proteins. This information delimits the set of SH2-containing effectors available for PTK signaling and will facilitate the systems-level analysis of pTyr-dependent protein-protein interactions and PTK-mediated signal transduction. The domain-based architecture of SH2-containing proteins is of more general relevance for understanding the large family of protein interaction domains and the modular organization of the majority of human proteins.

摘要

SH2结构域是专门用于识别磷酸酪氨酸位点的相互作用模块,嵌入在将蛋白酪氨酸激酶与细胞内信号通路偶联的蛋白质中。在此,我们报告了人源和小鼠源SH2结构域蛋白的全面生物信息学、结构及功能视图。这些信息界定了可用于PTK信号传导的含SH2效应器集合,并将促进对酪氨酸磷酸化依赖性蛋白质-蛋白质相互作用和PTK介导的信号转导进行系统水平的分析。含SH2蛋白基于结构域的架构对于理解蛋白质相互作用结构域大家族以及大多数人类蛋白质的模块化组织具有更广泛的相关性。

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