Protein domains of low sequence complexity—dark matter of the proteome

IF 7.5 1区 生物学 Q1 CELL BIOLOGY Genes & development Pub Date : 2024-03-19 DOI:10.1101/gad.351465.123
Steven L. McKnight
{"title":"Protein domains of low sequence complexity—dark matter of the proteome","authors":"Steven L. McKnight","doi":"10.1101/gad.351465.123","DOIUrl":null,"url":null,"abstract":"This perspective begins with a speculative consideration of the properties of the earliest proteins to appear during evolution. What did these primitive proteins look like, and how were they of benefit to early forms of life? I proceed to hypothesize that primitive proteins have been preserved through evolution and now serve diverse functions important to the dynamics of cell morphology and biological regulation. The primitive nature of these modern proteins is easy to spot. They are composed of a limited subset of the 20 amino acids used by traditionally evolved proteins and thus are of low sequence complexity. This chemical simplicity limits protein domains of low sequence complexity to forming only a crude and labile type of protein structure currently hidden from the computational powers of machine learning. I conclude by hypothesizing that this structural weakness represents the underlying virtue of proteins that, at least for the moment, constitute the dark matter of the proteome.","PeriodicalId":12591,"journal":{"name":"Genes & development","volume":"34 1","pages":""},"PeriodicalIF":7.5000,"publicationDate":"2024-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Genes & development","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1101/gad.351465.123","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

This perspective begins with a speculative consideration of the properties of the earliest proteins to appear during evolution. What did these primitive proteins look like, and how were they of benefit to early forms of life? I proceed to hypothesize that primitive proteins have been preserved through evolution and now serve diverse functions important to the dynamics of cell morphology and biological regulation. The primitive nature of these modern proteins is easy to spot. They are composed of a limited subset of the 20 amino acids used by traditionally evolved proteins and thus are of low sequence complexity. This chemical simplicity limits protein domains of low sequence complexity to forming only a crude and labile type of protein structure currently hidden from the computational powers of machine learning. I conclude by hypothesizing that this structural weakness represents the underlying virtue of proteins that, at least for the moment, constitute the dark matter of the proteome.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
序列复杂度低的蛋白质结构域--蛋白质组中的暗物质
这一视角首先对进化过程中最早出现的蛋白质的特性进行了推测性思考。这些原始蛋白质是什么样的,它们是如何造福于早期生命形式的?我进而假设,原始蛋白质在进化过程中被保留了下来,现在发挥着对细胞形态动态和生物调控非常重要的各种功能。这些现代蛋白质的原始性质很容易发现。它们由传统进化蛋白质所使用的 20 个氨基酸的有限子集组成,因此序列复杂度较低。这种化学上的简单性限制了低序列复杂性的蛋白质结构域,使其只能形成一种粗糙、易变的蛋白质结构类型,目前还无法利用机器学习的计算能力。最后,我假设这种结构上的弱点代表了蛋白质的潜在优点,至少在目前构成了蛋白质组的暗物质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Genes & development
Genes & development 生物-发育生物学
CiteScore
17.50
自引率
1.90%
发文量
71
审稿时长
3-6 weeks
期刊介绍: Genes & Development is a research journal published in association with The Genetics Society. It publishes high-quality research papers in the areas of molecular biology, molecular genetics, and related fields. The journal features various research formats including Research papers, short Research Communications, and Resource/Methodology papers. Genes & Development has gained recognition and is considered as one of the Top Five Research Journals in the field of Molecular Biology and Genetics. It has an impressive Impact Factor of 12.89. The journal is ranked #2 among Developmental Biology research journals, #5 in Genetics and Heredity, and is among the Top 20 in Cell Biology (according to ISI Journal Citation Reports®, 2021).
期刊最新文献
mTORC1, the maestro of cell metabolism and growth PROSER1 modulates DNA demethylation through dual mechanisms to prevent syndromic developmental malformations Evidence for dual roles of histone H3 lysine 4 in antagonizing Polycomb group function and promoting target gene expression Proteomic insights into circadian transcription regulation: novel E-box interactors revealed by proximity labeling BRCA1 and BRCA2: from cancer susceptibility to synthetic lethality
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1