Suppr超能文献

ATP 结合盒蛋白的进化史。

Evolutionary history of ATP-binding cassette proteins.

机构信息

Department of Biology, Massachusetts Institute of Technology.

出版信息

FEBS Lett. 2020 Dec;594(23):3882-3897. doi: 10.1002/1873-3468.13985. Epub 2020 Nov 21.

Abstract

ATP-binding cassette (ABC) proteins are found in every sequenced genome and evolved deep in the phylogenetic tree of life. ABC proteins form one of the largest homologous protein families, with most being involved in substrate transport across biological membranes, and a few cytoplasmic members regulating in essential processes like translation. The predominant ABC protein classification scheme is derived from human members, but the increasing number of fully sequenced genomes permits to reevaluate this paradigm in the light of the evolutionary history the ABC-protein superfamily. As we study the diversity of substrates, mechanisms, and physiological roles of ABC proteins, knowledge of the evolutionary relationships highlights similarities and differences that can be attributed to specific branches in protein divergence. While alignments and trees built on natural sequence variation account for the evolutionary divergence of ABC proteins, high-throughput experiments and next-generation sequencing creating experimental sequence variation are instrumental in identifying functional constraints. The combination of natural and experimentally produced sequence variation allows a broader and more rational study of the function and physiological roles of ABC proteins.

摘要

三磷酸腺苷结合盒(ABC)蛋白存在于每个已测序的基因组中,并在生命之树的系统发育中进化得非常深。ABC 蛋白形成了最大的同源蛋白家族之一,大多数参与跨生物膜的底物运输,少数细胞质成员参与翻译等基本过程的调节。主要的 ABC 蛋白分类方案源自人类成员,但随着越来越多的全基因组测序,人们可以根据 ABC 蛋白超家族的进化历史重新评估这一范例。当我们研究 ABC 蛋白的底物、机制和生理作用的多样性时,对进化关系的了解突出了可以归因于蛋白质分歧特定分支的相似性和差异性。虽然基于自然序列变异构建的比对和树可以解释 ABC 蛋白的进化分歧,但高通量实验和下一代测序产生的实验序列变异对于识别功能约束至关重要。自然和实验产生的序列变异的结合允许更广泛和更合理地研究 ABC 蛋白的功能和生理作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验