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Evolution, folding, and design of TIM barrels and related proteins
Proteins are chief actors in life that perform a myriad of exquisite functions. This diversity has been enabled through the evolution and diversification of protein folds. Analysis of sequences and structures strongly suggest that numerous protein pieces have been reused as building blocks and propa...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8250049/ https://www.ncbi.nlm.nih.gov/pubmed/33453500 http://dx.doi.org/10.1016/j.sbi.2020.12.007 |
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author | Romero-Romero, Sergio Kordes, Sina Michel, Florian Höcker, Birte |
author_facet | Romero-Romero, Sergio Kordes, Sina Michel, Florian Höcker, Birte |
author_sort | Romero-Romero, Sergio |
collection | PubMed |
description | Proteins are chief actors in life that perform a myriad of exquisite functions. This diversity has been enabled through the evolution and diversification of protein folds. Analysis of sequences and structures strongly suggest that numerous protein pieces have been reused as building blocks and propagated to many modern folds. This information can be traced to understand how the protein world has diversified. In this review, we discuss the latest advances in the analysis of protein evolutionary units, and we use as a model system one of the most abundant and versatile topologies, the TIM-barrel fold, to highlight the existing common principles that interconnect protein evolution, structure, folding, function, and design. |
format | Online Article Text |
id | pubmed-8250049 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-82500492021-07-12 Evolution, folding, and design of TIM barrels and related proteins Romero-Romero, Sergio Kordes, Sina Michel, Florian Höcker, Birte Curr Opin Struct Biol Article Proteins are chief actors in life that perform a myriad of exquisite functions. This diversity has been enabled through the evolution and diversification of protein folds. Analysis of sequences and structures strongly suggest that numerous protein pieces have been reused as building blocks and propagated to many modern folds. This information can be traced to understand how the protein world has diversified. In this review, we discuss the latest advances in the analysis of protein evolutionary units, and we use as a model system one of the most abundant and versatile topologies, the TIM-barrel fold, to highlight the existing common principles that interconnect protein evolution, structure, folding, function, and design. Elsevier Science 2021-06 /pmc/articles/PMC8250049/ /pubmed/33453500 http://dx.doi.org/10.1016/j.sbi.2020.12.007 Text en © 2020 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Romero-Romero, Sergio Kordes, Sina Michel, Florian Höcker, Birte Evolution, folding, and design of TIM barrels and related proteins |
title | Evolution, folding, and design of TIM barrels and related proteins |
title_full | Evolution, folding, and design of TIM barrels and related proteins |
title_fullStr | Evolution, folding, and design of TIM barrels and related proteins |
title_full_unstemmed | Evolution, folding, and design of TIM barrels and related proteins |
title_short | Evolution, folding, and design of TIM barrels and related proteins |
title_sort | evolution, folding, and design of tim barrels and related proteins |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8250049/ https://www.ncbi.nlm.nih.gov/pubmed/33453500 http://dx.doi.org/10.1016/j.sbi.2020.12.007 |
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