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Evolution of Methods for the Study of Cobalamin-Dependent Radical SAM Enzymes

[Image: see text] While bioinformatic evidence of cobalamin-dependent radical S-adenosylmethionine (SAM) enzymes has existed since the naming of the radical SAM superfamily in 2001, none were biochemically characterized until 2011. In the past decade, the field has flourished as methodological advan...

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Autores principales: Sinner, Erica K., Marous, Daniel R., Townsend, Craig A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8950095/
https://www.ncbi.nlm.nih.gov/pubmed/35341020
http://dx.doi.org/10.1021/acsbiomedchemau.1c00032
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author Sinner, Erica K.
Marous, Daniel R.
Townsend, Craig A.
author_facet Sinner, Erica K.
Marous, Daniel R.
Townsend, Craig A.
author_sort Sinner, Erica K.
collection PubMed
description [Image: see text] While bioinformatic evidence of cobalamin-dependent radical S-adenosylmethionine (SAM) enzymes has existed since the naming of the radical SAM superfamily in 2001, none were biochemically characterized until 2011. In the past decade, the field has flourished as methodological advances have facilitated study of the subfamily. Because of the ingenuity and perseverance of researchers in this field, we now have functional, mechanistic, and structural insight into how this class of enzymes harnesses the power of both the cobalamin and radical SAM cofactors to achieve catalysis. All of the early characterized enzymes in this subfamily were methylases, but the activity of these enzymes has recently been expanded beyond methylation. We anticipate that the characterized functions of these enzymes will become both better understood and increasingly diverse with continued study.
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spelling pubmed-89500952022-03-25 Evolution of Methods for the Study of Cobalamin-Dependent Radical SAM Enzymes Sinner, Erica K. Marous, Daniel R. Townsend, Craig A. ACS Bio Med Chem Au [Image: see text] While bioinformatic evidence of cobalamin-dependent radical S-adenosylmethionine (SAM) enzymes has existed since the naming of the radical SAM superfamily in 2001, none were biochemically characterized until 2011. In the past decade, the field has flourished as methodological advances have facilitated study of the subfamily. Because of the ingenuity and perseverance of researchers in this field, we now have functional, mechanistic, and structural insight into how this class of enzymes harnesses the power of both the cobalamin and radical SAM cofactors to achieve catalysis. All of the early characterized enzymes in this subfamily were methylases, but the activity of these enzymes has recently been expanded beyond methylation. We anticipate that the characterized functions of these enzymes will become both better understood and increasingly diverse with continued study. American Chemical Society 2021-10-13 /pmc/articles/PMC8950095/ /pubmed/35341020 http://dx.doi.org/10.1021/acsbiomedchemau.1c00032 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Sinner, Erica K.
Marous, Daniel R.
Townsend, Craig A.
Evolution of Methods for the Study of Cobalamin-Dependent Radical SAM Enzymes
title Evolution of Methods for the Study of Cobalamin-Dependent Radical SAM Enzymes
title_full Evolution of Methods for the Study of Cobalamin-Dependent Radical SAM Enzymes
title_fullStr Evolution of Methods for the Study of Cobalamin-Dependent Radical SAM Enzymes
title_full_unstemmed Evolution of Methods for the Study of Cobalamin-Dependent Radical SAM Enzymes
title_short Evolution of Methods for the Study of Cobalamin-Dependent Radical SAM Enzymes
title_sort evolution of methods for the study of cobalamin-dependent radical sam enzymes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8950095/
https://www.ncbi.nlm.nih.gov/pubmed/35341020
http://dx.doi.org/10.1021/acsbiomedchemau.1c00032
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