Paradigms of convergent evolution in enzymes

There are many occurrences of enzymes catalysing the same reaction but having significantly different structures. Leveraging the comprehensive information on enzymes stored in the Mechanism and Catalytic Site Atlas (M-CSA), we present a collection of 34 cases for which there is sufficient evidence of functional convergence without an evolutionary link. For each case, we compare enzymes which have identical Enzyme Commission numbers (i.e. catalyse the same reaction), but different identifiers in the CATH data resource (i.e. different folds). We focus on similarities between their sequences, structures, active site geometries, cofactors and catalytic mechanisms. These features are then assessed to evaluate whether all the evidence for these structurally diverse proteins supports their independent evolution to catalyse the same chemical reaction. Our approach combines published literature information with knowledge-based computational resources from, amongst others, M-CSA, PDBe and PDBsum, supported by tailor-made software to explore active site structures and assess similarities in mechanism. We find that there are multiple types of convergent functional evolution observed to date, and it is necessary to investigate sequence, structure, active site geometry and enzyme mechanisms to describe such convergence accurately.

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Publication Details

Journal
FEBS Journal
Published
2024-11-22
DOI
https://doi.org/10.1111/febs.17332
Citations
8
Primary Topic
Enzyme Catalysis and Immobilization
Type
article
Field-Weighted Citation Impact
1.87

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article

Paradigms of convergent evolution in enzymes

Ioannis G. Riziotis, António J. M. Ribeiro, Janet M. Thornton, Neera Borkakoti et al.
8 citations
FEBS Journal
Enzyme Catalysis and Immobilization
1.87
article

Paradigms of convergent evolution in enzymes

Ioannis G. Riziotis, António J. M. Ribeiro, Janet M. Thornton, Neera Borkakoti, Jenny C. Kafas, Gabriel Ong
article en
8 citations

Abstract

There are many occurrences of enzymes catalysing the same reaction but having significantly different structures. Leveraging the comprehensive information on enzymes stored in the Mechanism and Catalytic Site Atlas (M-CSA), we present a collection of 34 cases for which there is sufficient evidence of functional convergence without an evolutionary link. For each case, we compare enzymes which have identical Enzyme Commission numbers (i.e. catalyse the same reaction), but different identifiers in the CATH data resource (i.e. different folds). We focus on similarities between their sequences, structures, active site geometries, cofactors and catalytic mechanisms. These features are then assessed to evaluate whether all the evidence for these structurally diverse proteins supports their independent evolution to catalyse the same chemical reaction. Our approach combines published literature information with knowledge-based computational resources from, amongst others, M-CSA, PDBe and PDBsum, supported by tailor-made software to explore active site structures and assess similarities in mechanism. We find that there are multiple types of convergent functional evolution observed to date, and it is necessary to investigate sequence, structure, active site geometry and enzyme mechanisms to describe such convergence accurately.

FEBS JournalVol. 292(3)
European Bioinformatics Institute (GB)
European Molecular Biology Laboratory, Biotechnology and Biological Sciences Research Council
Openalex Percentile: Top 14%
Enzyme Catalysis and Immobilization
1.87
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Paradigms of convergent evolution in enzymes — Ioannis G. Riziotis, António J. M. Ribeiro, et al. · FEBS Journal (2024) | TGRS Research Map | TGRS