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Radical SAM Enzymes and Metallocofactor Assembly: A Structural Point of View
[Image: see text] This Review focuses on the structure–function relationship of radical S-adenosyl-l-methionine (SAM) enzymes involved in the assembly of metallocofactors corresponding to the active sites of [FeFe]-hydrogenase and nitrogenase [MoFe]-protein. It does not claim to correspond to an ext...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10114646/ https://www.ncbi.nlm.nih.gov/pubmed/37102176 http://dx.doi.org/10.1021/acsbiomedchemau.1c00044 |
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author | Nicolet, Yvain Cherrier, Mickael V. Amara, Patricia |
author_facet | Nicolet, Yvain Cherrier, Mickael V. Amara, Patricia |
author_sort | Nicolet, Yvain |
collection | PubMed |
description | [Image: see text] This Review focuses on the structure–function relationship of radical S-adenosyl-l-methionine (SAM) enzymes involved in the assembly of metallocofactors corresponding to the active sites of [FeFe]-hydrogenase and nitrogenase [MoFe]-protein. It does not claim to correspond to an extensive review on the assembly machineries of these enzyme active sites, for which many good reviews are already available, but instead deals with the contribution of structural data to the understanding of their chemical mechanism (Buren et al. Chem. Rev.2020, 142 ( (25), ) 11006−11012; Britt et al. Chem. Sci.2020, 11 ( (38), ), 10313–1032334123177). Hence, we will present the history and current knowledge about the radical SAM maturases HydE, HydG, and NifB as well as what, in our opinion, should be done in the near future to overcome the existing barriers in our understanding of this fascinating chemistry that intertwine organic radicals and organometallic complexes. |
format | Online Article Text |
id | pubmed-10114646 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-101146462023-04-25 Radical SAM Enzymes and Metallocofactor Assembly: A Structural Point of View Nicolet, Yvain Cherrier, Mickael V. Amara, Patricia ACS Bio Med Chem Au [Image: see text] This Review focuses on the structure–function relationship of radical S-adenosyl-l-methionine (SAM) enzymes involved in the assembly of metallocofactors corresponding to the active sites of [FeFe]-hydrogenase and nitrogenase [MoFe]-protein. It does not claim to correspond to an extensive review on the assembly machineries of these enzyme active sites, for which many good reviews are already available, but instead deals with the contribution of structural data to the understanding of their chemical mechanism (Buren et al. Chem. Rev.2020, 142 ( (25), ) 11006−11012; Britt et al. Chem. Sci.2020, 11 ( (38), ), 10313–1032334123177). Hence, we will present the history and current knowledge about the radical SAM maturases HydE, HydG, and NifB as well as what, in our opinion, should be done in the near future to overcome the existing barriers in our understanding of this fascinating chemistry that intertwine organic radicals and organometallic complexes. American Chemical Society 2021-11-20 /pmc/articles/PMC10114646/ /pubmed/37102176 http://dx.doi.org/10.1021/acsbiomedchemau.1c00044 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 | Nicolet, Yvain Cherrier, Mickael V. Amara, Patricia Radical SAM Enzymes and Metallocofactor Assembly: A Structural Point of View |
title | Radical SAM Enzymes and Metallocofactor Assembly:
A Structural Point of View |
title_full | Radical SAM Enzymes and Metallocofactor Assembly:
A Structural Point of View |
title_fullStr | Radical SAM Enzymes and Metallocofactor Assembly:
A Structural Point of View |
title_full_unstemmed | Radical SAM Enzymes and Metallocofactor Assembly:
A Structural Point of View |
title_short | Radical SAM Enzymes and Metallocofactor Assembly:
A Structural Point of View |
title_sort | radical sam enzymes and metallocofactor assembly:
a structural point of view |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10114646/ https://www.ncbi.nlm.nih.gov/pubmed/37102176 http://dx.doi.org/10.1021/acsbiomedchemau.1c00044 |
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