Cargando…

Iron-sulfur flavoenzymes: the added value of making the most ancient redox cofactors and the versatile flavins work together

Iron-sulfur (Fe-S) flavoproteins form a broad and growing class of complex, multi-domain and often multi-subunit proteins coupling the most ancient cofactors (the Fe-S clusters) and the most versatile coenzymes (the flavin coenzymes, FMN and FAD). These enzymes catalyse oxidoreduction reactions usua...

Descripción completa

Detalles Bibliográficos
Autor principal: Vanoni, Maria Antonietta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8097209/
https://www.ncbi.nlm.nih.gov/pubmed/33947244
http://dx.doi.org/10.1098/rsob.210010
_version_ 1783688309982101504
author Vanoni, Maria Antonietta
author_facet Vanoni, Maria Antonietta
author_sort Vanoni, Maria Antonietta
collection PubMed
description Iron-sulfur (Fe-S) flavoproteins form a broad and growing class of complex, multi-domain and often multi-subunit proteins coupling the most ancient cofactors (the Fe-S clusters) and the most versatile coenzymes (the flavin coenzymes, FMN and FAD). These enzymes catalyse oxidoreduction reactions usually acting as switches between donors of electron pairs and acceptors of single electrons, and vice versa. Through selected examples, the enzymes' structure−function relationships with respect to rate and directionality of the electron transfer steps, the role of the apoprotein and its dynamics in modulating the electron transfer process will be discussed.
format Online
Article
Text
id pubmed-8097209
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher The Royal Society
record_format MEDLINE/PubMed
spelling pubmed-80972092021-05-24 Iron-sulfur flavoenzymes: the added value of making the most ancient redox cofactors and the versatile flavins work together Vanoni, Maria Antonietta Open Biol Review Iron-sulfur (Fe-S) flavoproteins form a broad and growing class of complex, multi-domain and often multi-subunit proteins coupling the most ancient cofactors (the Fe-S clusters) and the most versatile coenzymes (the flavin coenzymes, FMN and FAD). These enzymes catalyse oxidoreduction reactions usually acting as switches between donors of electron pairs and acceptors of single electrons, and vice versa. Through selected examples, the enzymes' structure−function relationships with respect to rate and directionality of the electron transfer steps, the role of the apoprotein and its dynamics in modulating the electron transfer process will be discussed. The Royal Society 2021-05-05 /pmc/articles/PMC8097209/ /pubmed/33947244 http://dx.doi.org/10.1098/rsob.210010 Text en © 2021 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Review
Vanoni, Maria Antonietta
Iron-sulfur flavoenzymes: the added value of making the most ancient redox cofactors and the versatile flavins work together
title Iron-sulfur flavoenzymes: the added value of making the most ancient redox cofactors and the versatile flavins work together
title_full Iron-sulfur flavoenzymes: the added value of making the most ancient redox cofactors and the versatile flavins work together
title_fullStr Iron-sulfur flavoenzymes: the added value of making the most ancient redox cofactors and the versatile flavins work together
title_full_unstemmed Iron-sulfur flavoenzymes: the added value of making the most ancient redox cofactors and the versatile flavins work together
title_short Iron-sulfur flavoenzymes: the added value of making the most ancient redox cofactors and the versatile flavins work together
title_sort iron-sulfur flavoenzymes: the added value of making the most ancient redox cofactors and the versatile flavins work together
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8097209/
https://www.ncbi.nlm.nih.gov/pubmed/33947244
http://dx.doi.org/10.1098/rsob.210010
work_keys_str_mv AT vanonimariaantonietta ironsulfurflavoenzymestheaddedvalueofmakingthemostancientredoxcofactorsandtheversatileflavinsworktogether