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短线性基序的属性。

Attributes of short linear motifs.

作者信息

Davey Norman E, Van Roey Kim, Weatheritt Robert J, Toedt Grischa, Uyar Bora, Altenberg Brigitte, Budd Aidan, Diella Francesca, Dinkel Holger, Gibson Toby J

机构信息

Structural and Computational Biology Unit, European Molecular Biology Laboratory, Heidelberg, Germany.

出版信息

Mol Biosyst. 2012 Jan;8(1):268-81. doi: 10.1039/c1mb05231d. Epub 2011 Sep 12.

Abstract

Traditionally, protein-protein interactions were thought to be mediated by large, structured domains. However, it has become clear that the interactome comprises a wide range of binding interfaces with varying degrees of flexibility, ranging from rigid globular domains to disordered regions that natively lack structure. Enrichment for disorder in highly connected hub proteins and its correlation with organism complexity hint at the functional importance of disordered regions. Nevertheless, they have not yet been extensively characterised. Shifting the attention from globular domains to disordered regions of the proteome might bring us closer to elucidating the dense and complex connectivity of the interactome. An important class of disordered interfaces are the compact mono-partite, short linear motifs (SLiMs, or eukaryotic linear motifs (ELMs)). They are evolutionarily plastic and interact with relatively low affinity due to the limited number of residues that make direct contact with the binding partner. These features confer to SLiMs the ability to evolve convergently and mediate transient interactions, which is imperative to network evolution and to maintain robust cell signalling, respectively. The ability to discriminate biologically relevant SLiMs by means of different attributes will improve our understanding of the complexity of the interactome and aid development of bioinformatics tools for motif discovery. In this paper, the curated instances currently available in the Eukaryotic Linear Motif (ELM) database are analysed to provide a clear overview of the defining attributes of SLiMs. These analyses suggest that functional SLiMs have higher levels of conservation than their surrounding residues, frequently evolve convergently, preferentially occur in disordered regions and often form a secondary structure when bound to their interaction partner. These results advocate searching for small groupings of residues in disordered regions with higher relative conservation and a propensity to form the secondary structure. Finally, the most interesting conclusions are examined in regard to their functional consequences.

摘要

传统上,人们认为蛋白质-蛋白质相互作用是由大的结构化结构域介导的。然而,现在已经清楚的是,蛋白质相互作用组包含各种具有不同程度灵活性的结合界面,从刚性的球状结构域到天然缺乏结构的无序区域。高度连接的枢纽蛋白中无序区域的富集及其与生物体复杂性的相关性暗示了无序区域的功能重要性。然而,它们尚未得到广泛的表征。将注意力从球状结构域转移到蛋白质组的无序区域可能会使我们更接近阐明蛋白质相互作用组的密集和复杂连接性。一类重要的无序界面是紧凑的单部分短线性基序(SLiMs,或真核线性基序(ELMs))。它们在进化上具有可塑性,并且由于与结合伴侣直接接触的残基数量有限,相互作用亲和力相对较低。这些特征赋予SLiMs趋同进化和介导瞬时相互作用的能力,这分别对于网络进化和维持稳健的细胞信号传导至关重要。通过不同属性区分生物学上相关的SLiMs的能力将提高我们对蛋白质相互作用组复杂性的理解,并有助于开发用于基序发现的生物信息学工具。在本文中,对真核线性基序(ELM)数据库中当前可用的经过整理的实例进行了分析,以清晰概述SLiMs的定义属性。这些分析表明,功能性SLiMs比其周围残基具有更高水平的保守性,经常趋同进化,优先出现在无序区域,并且在与相互作用伴侣结合时通常形成二级结构。这些结果主张在无序区域中寻找具有较高相对保守性和形成二级结构倾向的小残基分组。最后,研究了最有趣的结论及其功能后果。

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