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鉴定一个富含脯氨酸的十氨基酸SH3结合位点。

Identification of a ten-amino acid proline-rich SH3 binding site.

作者信息

Ren R, Mayer B J, Cicchetti P, Baltimore D

机构信息

Rockefeller University, New York, NY 10021.

出版信息

Science. 1993 Feb 19;259(5098):1157-61. doi: 10.1126/science.8438166.

Abstract

The Src homology 3 (SH3) region is a small protein domain present in a very large group of proteins, including cytoskeletal elements and signaling proteins. It is believed that SH3 domains serve as modules that mediate protein-protein associations and, along with Src homology 2 (SH2) domains, regulate cytoplasmic signaling. The SH3 binding sites of two SH3 binding proteins were localized to a nine- or ten-amino acid stretch very rich in proline residues. Similar SH3 binding motifs exist in the formins, proteins that function in pattern formation in embryonic limbs of the mouse, and one subtype of the muscarinic acetylcholine receptor. Identification of the SH3 binding site provides a basis for understanding the interaction between the SH3 domains and their targets.

摘要

Src同源3(SH3)区域是一个小的蛋白质结构域,存在于非常多的蛋白质中,包括细胞骨架成分和信号蛋白。人们认为SH3结构域作为介导蛋白质-蛋白质相互作用的模块,与Src同源2(SH2)结构域一起调节细胞质信号传导。两种SH3结合蛋白的SH3结合位点定位于富含脯氨酸残基的九或十个氨基酸片段。在小鼠胚胎肢体模式形成中起作用的formin蛋白和毒蕈碱型乙酰胆碱受体的一个亚型中也存在类似的SH3结合基序。SH3结合位点的鉴定为理解SH3结构域与其靶标之间的相互作用提供了基础。

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