Institute of Biochemistry and Molecular Biology II, Medical Faculty and University Hospital Düsseldorf, Heinrich Heine University Düsseldorf, 40225 Düsseldorf, Germany.
Center for Interdisciplinary Biosciences, P. J. Šafárik University, 040 01 Košice, Slovakia.
Cells. 2023 Aug 12;12(16):2054. doi: 10.3390/cells12162054.
SRC homology 3 (SH3) domains are fundamental modules that enable the assembly of protein complexes through physical interactions with a pool of proline-rich/noncanonical motifs from partner proteins. They are widely studied modular building blocks across all five kingdoms of life and viruses, mediating various biological processes. The SH3 domains are also implicated in the development of human diseases, such as cancer, leukemia, osteoporosis, Alzheimer's disease, and various infections. A database search of the human proteome reveals the existence of 298 SH3 domains in 221 SH3 domain-containing proteins (SH3DCPs), ranging from 13 to 720 kilodaltons. A phylogenetic analysis of human SH3DCPs based on their multi-domain architecture seems to be the most practical way to classify them functionally, with regard to various physiological pathways. This review further summarizes the achievements made in the classification of SH3 domain functions, their binding specificity, and their significance for various diseases when exploiting SH3 protein modular interactions as drug targets.
SRC 同源结构域 3(SH3)是基本模块,能够通过与伴侣蛋白中富含脯氨酸/非经典基序的库进行物理相互作用,组装蛋白质复合物。它们是在所有五个生命王国和病毒中广泛研究的模块化构建块,介导各种生物过程。SH3 结构域还与人类疾病的发展有关,如癌症、白血病、骨质疏松症、阿尔茨海默病和各种感染。对人类蛋白质组的数据库搜索揭示了 221 种 SH3 结构域包含蛋白(SH3DCP)中存在 298 个 SH3 结构域,分子量范围为 13 至 720 千道尔顿。基于其多结构域结构的人类 SH3DCP 的系统发育分析似乎是对其进行功能分类的最实用方法,涉及各种生理途径。当利用 SH3 蛋白模块化相互作用作为药物靶点时,这篇综述进一步总结了 SH3 结构域功能分类、结合特异性及其对各种疾病的意义方面的成就。