Kinch Lisa N, Grishin Nick V
Howard Hughes Medical Institute and Department of Biochemistry, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Biochim Biophys Acta. 2013 Dec;1828(12):2937-43. doi: 10.1016/j.bbamem.2013.06.031. Epub 2013 Jul 8.
Endopeptidase classification based on catalytic mechanism and evolutionary history has proven to be invaluable to the study of proteolytic enzymes. Such general mechanistic- and evolutionary- based groupings have launched experimental investigations, because knowledge gained for one family member tends to apply to the other closely related enzymes. The serine endopeptidases represent one of the most abundant and diverse groups, with their apparently successful proteolytic mechanism having arisen independently many times throughout evolution, giving rise to the well-studied soluble chemotrypsins and subtilisins, among many others. A large and diverse family of polytopic transmembrane proteins known as rhomboids has also evolved the serine protease mechanism. While the spatial structure, mechanism, and biochemical function of this family as intramembrane proteases has been established, the cellular roles of these enzymes as well as their natural substrates remain largely undetermined. While the evolutionary history of rhomboid proteases has been debated, sorting out the relationships among current day representatives should provide a solid basis for narrowing the knowledge gap between their biochemical and cellular functions. Indeed, some functional characteristics of rhomboid proteases can be gleaned from their evolutionary relationships. Finally, a specific case where phylogenetic profile analysis has identified proteins that contain a C-terminal processing motif (GlyGly-Cterm) as co-occurring with a set of bacterial rhomboid proteases provides an example of potential target identification through bioinformatics. This article is part of a Special Issue entitled: Intramembrane Proteases.
基于催化机制和进化史的内肽酶分类已被证明对蛋白水解酶的研究具有极高价值。这种基于一般机制和进化的分组引发了实验研究,因为从一个家族成员获得的知识往往适用于其他密切相关的酶。丝氨酸内肽酶是最丰富多样的酶类之一,其明显成功的蛋白水解机制在整个进化过程中多次独立出现,产生了许多经过充分研究的可溶性胰蛋白酶和枯草杆菌蛋白酶等。一个被称为类菱形蛋白酶的大型多样的多跨膜蛋白家族也进化出了丝氨酸蛋白酶机制。虽然这个家族作为膜内蛋白酶的空间结构、机制和生化功能已经确定,但这些酶在细胞中的作用以及它们的天然底物在很大程度上仍未明确。虽然类菱形蛋白酶的进化史一直存在争议,但梳理当今代表之间的关系应该为缩小其生化功能和细胞功能之间的知识差距提供坚实基础。事实上,类菱形蛋白酶的一些功能特征可以从它们的进化关系中推断出来。最后,系统发育谱分析确定含有C末端加工基序(甘氨酸-甘氨酸- C末端)的蛋白质与一组细菌类菱形蛋白酶同时出现的一个具体案例,提供了一个通过生物信息学识别潜在靶点的例子。本文是名为:膜内蛋白酶的特刊的一部分。