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Using mechanism similarity to understand enzyme evolution
Enzyme reactions take place in the active site through a series of catalytic steps, which are collectively termed the enzyme mechanism. The catalytic step is thereby the individual unit to consider for the purposes of building new enzyme mechanisms — i.e. through the mix and match of individual cata...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842563/ https://www.ncbi.nlm.nih.gov/pubmed/36659981 http://dx.doi.org/10.1007/s12551-022-01022-9 |
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author | Ribeiro, António J. M. Riziotis, Ioannis G. Tyzack, Jonathan D. Borkakoti, Neera Thornton, Janet M. |
author_facet | Ribeiro, António J. M. Riziotis, Ioannis G. Tyzack, Jonathan D. Borkakoti, Neera Thornton, Janet M. |
author_sort | Ribeiro, António J. M. |
collection | PubMed |
description | Enzyme reactions take place in the active site through a series of catalytic steps, which are collectively termed the enzyme mechanism. The catalytic step is thereby the individual unit to consider for the purposes of building new enzyme mechanisms — i.e. through the mix and match of individual catalytic steps, new enzyme mechanisms and reactions can be conceived. In the case of natural evolution, it has been shown that new enzyme functions have emerged through the tweaking of existing mechanisms by the addition, removal, or modification of some catalytic steps, while maintaining other steps of the mechanism intact. Recently, we have extracted and codified the information on the catalytic steps of hundreds of enzymes in a machine-readable way, with the aim of automating this kind of evolutionary analysis. In this paper, we illustrate how these data, which we called the “rules of enzyme catalysis”, can be used to identify similar catalytic steps across enzymes that differ in their overall function and/or structural folds. A discussion on a set of three enzymes that share part of their mechanism is used as an exemplar to illustrate how this approach can reveal divergent and convergent evolution of enzymes at the mechanistic level. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12551-022-01022-9. |
format | Online Article Text |
id | pubmed-9842563 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-98425632023-01-18 Using mechanism similarity to understand enzyme evolution Ribeiro, António J. M. Riziotis, Ioannis G. Tyzack, Jonathan D. Borkakoti, Neera Thornton, Janet M. Biophys Rev Review Enzyme reactions take place in the active site through a series of catalytic steps, which are collectively termed the enzyme mechanism. The catalytic step is thereby the individual unit to consider for the purposes of building new enzyme mechanisms — i.e. through the mix and match of individual catalytic steps, new enzyme mechanisms and reactions can be conceived. In the case of natural evolution, it has been shown that new enzyme functions have emerged through the tweaking of existing mechanisms by the addition, removal, or modification of some catalytic steps, while maintaining other steps of the mechanism intact. Recently, we have extracted and codified the information on the catalytic steps of hundreds of enzymes in a machine-readable way, with the aim of automating this kind of evolutionary analysis. In this paper, we illustrate how these data, which we called the “rules of enzyme catalysis”, can be used to identify similar catalytic steps across enzymes that differ in their overall function and/or structural folds. A discussion on a set of three enzymes that share part of their mechanism is used as an exemplar to illustrate how this approach can reveal divergent and convergent evolution of enzymes at the mechanistic level. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12551-022-01022-9. Springer Berlin Heidelberg 2022-12-03 /pmc/articles/PMC9842563/ /pubmed/36659981 http://dx.doi.org/10.1007/s12551-022-01022-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Ribeiro, António J. M. Riziotis, Ioannis G. Tyzack, Jonathan D. Borkakoti, Neera Thornton, Janet M. Using mechanism similarity to understand enzyme evolution |
title | Using mechanism similarity to understand enzyme evolution |
title_full | Using mechanism similarity to understand enzyme evolution |
title_fullStr | Using mechanism similarity to understand enzyme evolution |
title_full_unstemmed | Using mechanism similarity to understand enzyme evolution |
title_short | Using mechanism similarity to understand enzyme evolution |
title_sort | using mechanism similarity to understand enzyme evolution |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842563/ https://www.ncbi.nlm.nih.gov/pubmed/36659981 http://dx.doi.org/10.1007/s12551-022-01022-9 |
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