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Dynamic New World: Refining Our View of Protein Structure, Function and Evolution

Proteins are crucial to the functioning of all lifeforms. Traditional understanding posits that a single protein occupies a single structure (“fold”), which performs a single function. This view is radically challenged with the recognition that high structural dynamism—the capacity to be extra “flop...

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Autor principal: Mannige, Ranjan V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5302727/
https://www.ncbi.nlm.nih.gov/pubmed/28250374
http://dx.doi.org/10.3390/proteomes2010128
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author Mannige, Ranjan V.
author_facet Mannige, Ranjan V.
author_sort Mannige, Ranjan V.
collection PubMed
description Proteins are crucial to the functioning of all lifeforms. Traditional understanding posits that a single protein occupies a single structure (“fold”), which performs a single function. This view is radically challenged with the recognition that high structural dynamism—the capacity to be extra “floppy”—is more prevalent in functional proteins than previously assumed. As reviewed here, this dynamic take on proteins affects our understanding of protein “structure”, function, and evolution, and even gives us a glimpse into protein origination. Specifically, this review will discuss historical developments concerning protein structure, and important new relationships between dynamism and aspects of protein sequence, structure, binding modes, binding promiscuity, evolvability, and origination. Along the way, suggestions will be provided for how key parts of textbook definitions—that so far have excluded membership to intrinsically disordered proteins (IDPs)—could be modified to accommodate our more dynamic understanding of proteins.
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spelling pubmed-53027272017-02-27 Dynamic New World: Refining Our View of Protein Structure, Function and Evolution Mannige, Ranjan V. Proteomes Review Proteins are crucial to the functioning of all lifeforms. Traditional understanding posits that a single protein occupies a single structure (“fold”), which performs a single function. This view is radically challenged with the recognition that high structural dynamism—the capacity to be extra “floppy”—is more prevalent in functional proteins than previously assumed. As reviewed here, this dynamic take on proteins affects our understanding of protein “structure”, function, and evolution, and even gives us a glimpse into protein origination. Specifically, this review will discuss historical developments concerning protein structure, and important new relationships between dynamism and aspects of protein sequence, structure, binding modes, binding promiscuity, evolvability, and origination. Along the way, suggestions will be provided for how key parts of textbook definitions—that so far have excluded membership to intrinsically disordered proteins (IDPs)—could be modified to accommodate our more dynamic understanding of proteins. MDPI 2014-03-07 /pmc/articles/PMC5302727/ /pubmed/28250374 http://dx.doi.org/10.3390/proteomes2010128 Text en © 2014 by the author; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Mannige, Ranjan V.
Dynamic New World: Refining Our View of Protein Structure, Function and Evolution
title Dynamic New World: Refining Our View of Protein Structure, Function and Evolution
title_full Dynamic New World: Refining Our View of Protein Structure, Function and Evolution
title_fullStr Dynamic New World: Refining Our View of Protein Structure, Function and Evolution
title_full_unstemmed Dynamic New World: Refining Our View of Protein Structure, Function and Evolution
title_short Dynamic New World: Refining Our View of Protein Structure, Function and Evolution
title_sort dynamic new world: refining our view of protein structure, function and evolution
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5302727/
https://www.ncbi.nlm.nih.gov/pubmed/28250374
http://dx.doi.org/10.3390/proteomes2010128
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