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Class C Radical SAM Methyltransferases Involved in Anaerobic Heme Degradation

[Image: see text] Class C radical SAM methyltransferases catalyze a diverse array of difficult chemical transformations in the biosynthesis of a range of compounds of biomedical importance. Phylogenetic analysis suggests that all of these enzymes are related to “CpdH” (formerly “HemN”) and “HemW”, p...

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Autores principales: Mathew, Liju G., Brimberry, Marley, Lanzilotta, William N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10114669/
https://www.ncbi.nlm.nih.gov/pubmed/37101744
http://dx.doi.org/10.1021/acsbiomedchemau.1c00047
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author Mathew, Liju G.
Brimberry, Marley
Lanzilotta, William N.
author_facet Mathew, Liju G.
Brimberry, Marley
Lanzilotta, William N.
author_sort Mathew, Liju G.
collection PubMed
description [Image: see text] Class C radical SAM methyltransferases catalyze a diverse array of difficult chemical transformations in the biosynthesis of a range of compounds of biomedical importance. Phylogenetic analysis suggests that all of these enzymes are related to “CpdH” (formerly “HemN”) and “HemW”, proteins with essential roles in anaerobic heme biosynthesis and heme transport, respectively. These functions are essential to anaerobic metabolism in Escherichia coli. Interestingly, evolution has come full circle, and the divergence of this protein sequence/fold has resulted in the class C radical SAM methyltransferases. Several pathogenic organisms have further adapted this fold to catalyze the anaerobic degradation of heme. In this review, we summarize what is known about the mechanism of anaerobic heme degradation and the evolutionary implications.
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spelling pubmed-101146692023-04-25 Class C Radical SAM Methyltransferases Involved in Anaerobic Heme Degradation Mathew, Liju G. Brimberry, Marley Lanzilotta, William N. ACS Bio Med Chem Au [Image: see text] Class C radical SAM methyltransferases catalyze a diverse array of difficult chemical transformations in the biosynthesis of a range of compounds of biomedical importance. Phylogenetic analysis suggests that all of these enzymes are related to “CpdH” (formerly “HemN”) and “HemW”, proteins with essential roles in anaerobic heme biosynthesis and heme transport, respectively. These functions are essential to anaerobic metabolism in Escherichia coli. Interestingly, evolution has come full circle, and the divergence of this protein sequence/fold has resulted in the class C radical SAM methyltransferases. Several pathogenic organisms have further adapted this fold to catalyze the anaerobic degradation of heme. In this review, we summarize what is known about the mechanism of anaerobic heme degradation and the evolutionary implications. American Chemical Society 2021-12-27 /pmc/articles/PMC10114669/ /pubmed/37101744 http://dx.doi.org/10.1021/acsbiomedchemau.1c00047 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 Mathew, Liju G.
Brimberry, Marley
Lanzilotta, William N.
Class C Radical SAM Methyltransferases Involved in Anaerobic Heme Degradation
title Class C Radical SAM Methyltransferases Involved in Anaerobic Heme Degradation
title_full Class C Radical SAM Methyltransferases Involved in Anaerobic Heme Degradation
title_fullStr Class C Radical SAM Methyltransferases Involved in Anaerobic Heme Degradation
title_full_unstemmed Class C Radical SAM Methyltransferases Involved in Anaerobic Heme Degradation
title_short Class C Radical SAM Methyltransferases Involved in Anaerobic Heme Degradation
title_sort class c radical sam methyltransferases involved in anaerobic heme degradation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10114669/
https://www.ncbi.nlm.nih.gov/pubmed/37101744
http://dx.doi.org/10.1021/acsbiomedchemau.1c00047
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