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模式真核生物基因组中编码的杂合激酶和流氓激酶。

Hybrid and rogue kinases encoded in the genomes of model eukaryotes.

作者信息

Rakshambikai Ramaswamy, Gnanavel Mutharasu, Srinivasan Narayanaswamy

机构信息

Molecular Biophysics Unit, Indian Institute of Science, Bangalore, India.

出版信息

PLoS One. 2014 Sep 25;9(9):e107956. doi: 10.1371/journal.pone.0107956. eCollection 2014.

Abstract

The highly modular nature of protein kinases generates diverse functional roles mediated by evolutionary events such as domain recombination, insertion and deletion of domains. Usually domain architecture of a kinase is related to the subfamily to which the kinase catalytic domain belongs. However outlier kinases with unusual domain architectures serve in the expansion of the functional space of the protein kinase family. For example, Src kinases are made-up of SH2 and SH3 domains in addition to the kinase catalytic domain. A kinase which lacks these two domains but retains sequence characteristics within the kinase catalytic domain is an outlier that is likely to have modes of regulation different from classical src kinases. This study defines two types of outlier kinases: hybrids and rogues depending on the nature of domain recombination. Hybrid kinases are those where the catalytic kinase domain belongs to a kinase subfamily but the domain architecture is typical of another kinase subfamily. Rogue kinases are those with kinase catalytic domain characteristic of a kinase subfamily but the domain architecture is typical of neither that subfamily nor any other kinase subfamily. This report provides a consolidated set of such hybrid and rogue kinases gleaned from six eukaryotic genomes-S.cerevisiae, D. melanogaster, C.elegans, M.musculus, T.rubripes and H.sapiens-and discusses their functions. The presence of such kinases necessitates a revisiting of the classification scheme of the protein kinase family using full length sequences apart from classical classification using solely the sequences of kinase catalytic domains. The study of these kinases provides a good insight in engineering signalling pathways for a desired output. Lastly, identification of hybrids and rogues in pathogenic protozoa such as P.falciparum sheds light on possible strategies in host-pathogen interactions.

摘要

蛋白激酶高度模块化的特性产生了由结构域重组、结构域插入和缺失等进化事件介导的多种功能作用。通常,激酶的结构域架构与其激酶催化结构域所属的亚家族相关。然而,具有异常结构域架构的异常激酶在蛋白激酶家族功能空间的扩展中发挥作用。例如,Src激酶除了激酶催化结构域外,还由SH2和SH3结构域组成。一种缺乏这两个结构域但在激酶催化结构域内保留序列特征的激酶是一种异常激酶,其调控模式可能不同于经典的Src激酶。本研究根据结构域重组的性质定义了两种类型的异常激酶:杂种激酶和无赖激酶。杂种激酶是指催化激酶结构域属于一个激酶亚家族,但结构域架构是另一个激酶亚家族典型的激酶。无赖激酶是指具有一个激酶亚家族典型的激酶催化结构域,但结构域架构既不是该亚家族也不是任何其他激酶亚家族典型的激酶。本报告提供了一组从酿酒酵母、黑腹果蝇、秀丽隐杆线虫、小家鼠、红鳍东方鲀和智人这六个真核生物基因组中收集的此类杂种激酶和无赖激酶,并讨论了它们的功能。这些激酶的存在使得有必要重新审视蛋白激酶家族的分类方案,除了仅使用激酶催化结构域序列的经典分类外,还应使用全长序列。对这些激酶的研究为设计期望输出的信号通路提供了很好的见解。最后,在恶性疟原虫等致病原生动物中鉴定杂种激酶和无赖激酶,有助于揭示宿主 - 病原体相互作用中的可能策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/260b/4177888/dd69c1a7dd6b/pone.0107956.g001.jpg

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