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第三类亲密接触:无序结构域与蛋白质相互作用

Close encounters of the third kind: disordered domains and the interactions of proteins.

作者信息

Tompa Peter, Fuxreiter Monika, Oldfield Christopher J, Simon Istvan, Dunker A Keith, Uversky Vladimir N

机构信息

Institute of Enzymology, Biological Research Center, Hungarian Academy of Sciences, Budapest, Hungary.

出版信息

Bioessays. 2009 Mar;31(3):328-35. doi: 10.1002/bies.200800151.

Abstract

Protein-protein interactions are thought to be mediated by domains, which are autonomous folding units of proteins. Recently, a second type of interaction has been suggested, mediated by short segments termed linear motifs, which are related to recognition elements of intrinsically disordered regions. Here, we propose a third kind of protein-protein recognition mechanism, mediated by disordered regions longer than 20-30 residues. Bioinformatics predictions and well-characterized examples, such as the kinase-inhibitory domain of Cdk inhibitors and the Wiskott-Aldrich syndrome protein (WASP)-homology domain 2 of actin-binding proteins, show that these disordered regions conform to the definition of domains rather than motifs, i.e., they represent functional, evolutionary, and structural units. Their functions are distinct from those of short motifs and ordered domains, and establish a third kind of interaction principle. With these points, we argue that these long disordered regions should be recognized as a distinct class of biologically functional protein domains.

摘要

蛋白质-蛋白质相互作用被认为是由结构域介导的,结构域是蛋白质的自主折叠单元。最近,有人提出了第二种相互作用类型,由称为线性基序的短片段介导,这些短片段与内在无序区域的识别元件有关。在这里,我们提出了第三种蛋白质-蛋白质识别机制,由长度超过20 - 30个残基的无序区域介导。生物信息学预测以及特征明确的实例,如细胞周期蛋白依赖性激酶抑制剂的激酶抑制结构域和肌动蛋白结合蛋白的威斯科特-奥尔德里奇综合征蛋白(WASP)同源结构域2,表明这些无序区域符合结构域而非基序的定义,即它们代表功能、进化和结构单元。它们的功能不同于短基序和有序结构域的功能,并建立了第三种相互作用原则。基于这些观点,我们认为这些长无序区域应被视为一类独特的具有生物学功能的蛋白质结构域。

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