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Using Pseudoenzymes to Probe Evolutionary Design Principles of Enzymes

Enzymes are governed by unique evolutionary design principles as their catalytic sites were shown to induce long-range evolutionary conservation gradients. We have recently used a comparative bioinformatics approach to disentangle structural determinants from other possible determinants of the evolu...

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Detalles Bibliográficos
Autores principales: Sharir-Ivry, Avital, Xia, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6572901/
https://www.ncbi.nlm.nih.gov/pubmed/31236007
http://dx.doi.org/10.1177/1176934319855937
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author Sharir-Ivry, Avital
Xia, Yu
author_facet Sharir-Ivry, Avital
Xia, Yu
author_sort Sharir-Ivry, Avital
collection PubMed
description Enzymes are governed by unique evolutionary design principles as their catalytic sites were shown to induce long-range evolutionary conservation gradients. We have recently used a comparative bioinformatics approach to disentangle structural determinants from other possible determinants of the evolutionary conservation gradients. The approach is based on comparing the evolutionary patterns of enzymes to those of pseudoenzymes with the same tertiary structure where the catalytic functionality is turned off. This approach provides a way to evaluate several hypotheses regarding the origin of the observed evolutionary conservation gradient in enzymes. The conclusions from such comparative analyses are important for a better understanding of the unique evolutionary design principles of enzymes, which can in turn potentially guide the design of new and improved enzymes.
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spelling pubmed-65729012019-06-24 Using Pseudoenzymes to Probe Evolutionary Design Principles of Enzymes Sharir-Ivry, Avital Xia, Yu Evol Bioinform Online Commentary Enzymes are governed by unique evolutionary design principles as their catalytic sites were shown to induce long-range evolutionary conservation gradients. We have recently used a comparative bioinformatics approach to disentangle structural determinants from other possible determinants of the evolutionary conservation gradients. The approach is based on comparing the evolutionary patterns of enzymes to those of pseudoenzymes with the same tertiary structure where the catalytic functionality is turned off. This approach provides a way to evaluate several hypotheses regarding the origin of the observed evolutionary conservation gradient in enzymes. The conclusions from such comparative analyses are important for a better understanding of the unique evolutionary design principles of enzymes, which can in turn potentially guide the design of new and improved enzymes. SAGE Publications 2019-06-13 /pmc/articles/PMC6572901/ /pubmed/31236007 http://dx.doi.org/10.1177/1176934319855937 Text en © The Author(s) 2019 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Commentary
Sharir-Ivry, Avital
Xia, Yu
Using Pseudoenzymes to Probe Evolutionary Design Principles of Enzymes
title Using Pseudoenzymes to Probe Evolutionary Design Principles of Enzymes
title_full Using Pseudoenzymes to Probe Evolutionary Design Principles of Enzymes
title_fullStr Using Pseudoenzymes to Probe Evolutionary Design Principles of Enzymes
title_full_unstemmed Using Pseudoenzymes to Probe Evolutionary Design Principles of Enzymes
title_short Using Pseudoenzymes to Probe Evolutionary Design Principles of Enzymes
title_sort using pseudoenzymes to probe evolutionary design principles of enzymes
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6572901/
https://www.ncbi.nlm.nih.gov/pubmed/31236007
http://dx.doi.org/10.1177/1176934319855937
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