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Capturing the geometry, function, and evolution of enzymes with 3D templates

Structural templates are 3D signatures representing protein functional sites, such as ligand binding cavities, metal coordination motifs, or catalytic sites. Here we explore methods to generate template libraries and algorithms to query structures for conserved 3D motifs. Applications of templates a...

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Detalles Bibliográficos
Autores principales: Riziotis, Ioannis G., Thornton, Janet M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9207746/
https://www.ncbi.nlm.nih.gov/pubmed/35762726
http://dx.doi.org/10.1002/pro.4363
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author Riziotis, Ioannis G.
Thornton, Janet M.
author_facet Riziotis, Ioannis G.
Thornton, Janet M.
author_sort Riziotis, Ioannis G.
collection PubMed
description Structural templates are 3D signatures representing protein functional sites, such as ligand binding cavities, metal coordination motifs, or catalytic sites. Here we explore methods to generate template libraries and algorithms to query structures for conserved 3D motifs. Applications of templates are discussed, as well as some exemplar cases for examining evolutionary links in enzymes. We also introduce the concept of using more than one template per structure to represent flexible sites, as an approach to better understand catalysis through snapshots captured in enzyme structures. Functional annotation from structure is an important topic that has recently resurfaced due to the new more accurate methods of protein structure prediction. Therefore, we anticipate that template‐based functional site detection will be a powerful tool in the task of characterizing a vast number of new protein models.
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spelling pubmed-92077462022-06-27 Capturing the geometry, function, and evolution of enzymes with 3D templates Riziotis, Ioannis G. Thornton, Janet M. Protein Sci Reviews Structural templates are 3D signatures representing protein functional sites, such as ligand binding cavities, metal coordination motifs, or catalytic sites. Here we explore methods to generate template libraries and algorithms to query structures for conserved 3D motifs. Applications of templates are discussed, as well as some exemplar cases for examining evolutionary links in enzymes. We also introduce the concept of using more than one template per structure to represent flexible sites, as an approach to better understand catalysis through snapshots captured in enzyme structures. Functional annotation from structure is an important topic that has recently resurfaced due to the new more accurate methods of protein structure prediction. Therefore, we anticipate that template‐based functional site detection will be a powerful tool in the task of characterizing a vast number of new protein models. John Wiley & Sons, Inc. 2022-06-20 2022-07 /pmc/articles/PMC9207746/ /pubmed/35762726 http://dx.doi.org/10.1002/pro.4363 Text en © 2022 The Authors. Protein Science published by Wiley Periodicals LLC on behalf of The Protein Society. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Riziotis, Ioannis G.
Thornton, Janet M.
Capturing the geometry, function, and evolution of enzymes with 3D templates
title Capturing the geometry, function, and evolution of enzymes with 3D templates
title_full Capturing the geometry, function, and evolution of enzymes with 3D templates
title_fullStr Capturing the geometry, function, and evolution of enzymes with 3D templates
title_full_unstemmed Capturing the geometry, function, and evolution of enzymes with 3D templates
title_short Capturing the geometry, function, and evolution of enzymes with 3D templates
title_sort capturing the geometry, function, and evolution of enzymes with 3d templates
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9207746/
https://www.ncbi.nlm.nih.gov/pubmed/35762726
http://dx.doi.org/10.1002/pro.4363
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