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BRCT结构域:磷酸肽结合与信号传导模块。

BRCT domains: phosphopeptide binding and signaling modules.

作者信息

Rodriguez Maria C, Songyang Zhou

机构信息

1Verna and Marrs McLean Department of Biochemistry and Molecular Biology, Baylor College of Medicine, One Baylor Plaza, Houston, Texas 77030, USA.

出版信息

Front Biosci. 2008 May 1;13:5905-15. doi: 10.2741/3125.

Abstract

The BRCA1 C-terminus (BRCT) domains are essential for the tumor suppressor function of BRCA1, and have been found in a variety of proteins from bacteria to men. Recent studies demonstrate that the BRCT domain constitutes a novel phosphopeptide binding region. In this review we seek to discuss the recent biochemical and structural data that have helped elucidate the molecular basis of BRCT domain function and BRCT-mediated interactions, with special emphasis on the role of phospho-specific interactions in key networks that regulate DNA repair. Finally we offer predictions on additional phospho-interacting BRCT domains and potential in vivo binding sites for several BRCT domains.

摘要

BRCA1的C末端(BRCT)结构域对于BRCA1的肿瘤抑制功能至关重要,并且在从细菌到人类的多种蛋白质中都有发现。最近的研究表明,BRCT结构域构成了一个新的磷酸肽结合区域。在这篇综述中,我们试图讨论最近的生化和结构数据,这些数据有助于阐明BRCT结构域功能和BRCT介导的相互作用的分子基础,特别强调磷酸特异性相互作用在调节DNA修复的关键网络中的作用。最后,我们对其他磷酸相互作用的BRCT结构域以及几个BRCT结构域潜在的体内结合位点进行了预测。

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