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Environment and coordination of FeMo–co in the nitrogenase metallochaperone NafY
In nitrogenase biosynthesis, the iron-molybdenum cofactor (FeMo–co) is externally assembled at scaffold proteins and delivered to the NifDK nitrogenase component by the NafY metallochaperone. Here we have used nuclear magnetic resonance, molecular dynamics, and functional analysis to elucidate the e...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
RSC
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8496260/ https://www.ncbi.nlm.nih.gov/pubmed/34704049 http://dx.doi.org/10.1039/d1cb00086a |
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author | Phillips, Aaron H. Hernandez, Jose A. Payá-Tormo, Lucía Burén, Stefan Cuevas-Zuviría, Bruno Pacios, Luis F. Pelton, Jeffrey G. Wemmer, David E. Rubio, Luis M. |
author_facet | Phillips, Aaron H. Hernandez, Jose A. Payá-Tormo, Lucía Burén, Stefan Cuevas-Zuviría, Bruno Pacios, Luis F. Pelton, Jeffrey G. Wemmer, David E. Rubio, Luis M. |
author_sort | Phillips, Aaron H. |
collection | PubMed |
description | In nitrogenase biosynthesis, the iron-molybdenum cofactor (FeMo–co) is externally assembled at scaffold proteins and delivered to the NifDK nitrogenase component by the NafY metallochaperone. Here we have used nuclear magnetic resonance, molecular dynamics, and functional analysis to elucidate the environment and coordination of FeMo–co in NafY. H(121) stands as the key FeMo–co ligand. Regions near FeMo–co diverge from H(121) and include the η1, α1, α2 helical lobe and a narrow path between H(121) and C(196). |
format | Online Article Text |
id | pubmed-8496260 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | RSC |
record_format | MEDLINE/PubMed |
spelling | pubmed-84962602021-10-25 Environment and coordination of FeMo–co in the nitrogenase metallochaperone NafY Phillips, Aaron H. Hernandez, Jose A. Payá-Tormo, Lucía Burén, Stefan Cuevas-Zuviría, Bruno Pacios, Luis F. Pelton, Jeffrey G. Wemmer, David E. Rubio, Luis M. RSC Chem Biol Chemistry In nitrogenase biosynthesis, the iron-molybdenum cofactor (FeMo–co) is externally assembled at scaffold proteins and delivered to the NifDK nitrogenase component by the NafY metallochaperone. Here we have used nuclear magnetic resonance, molecular dynamics, and functional analysis to elucidate the environment and coordination of FeMo–co in NafY. H(121) stands as the key FeMo–co ligand. Regions near FeMo–co diverge from H(121) and include the η1, α1, α2 helical lobe and a narrow path between H(121) and C(196). RSC 2021-07-28 /pmc/articles/PMC8496260/ /pubmed/34704049 http://dx.doi.org/10.1039/d1cb00086a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Phillips, Aaron H. Hernandez, Jose A. Payá-Tormo, Lucía Burén, Stefan Cuevas-Zuviría, Bruno Pacios, Luis F. Pelton, Jeffrey G. Wemmer, David E. Rubio, Luis M. Environment and coordination of FeMo–co in the nitrogenase metallochaperone NafY |
title | Environment and coordination of FeMo–co in the nitrogenase metallochaperone NafY |
title_full | Environment and coordination of FeMo–co in the nitrogenase metallochaperone NafY |
title_fullStr | Environment and coordination of FeMo–co in the nitrogenase metallochaperone NafY |
title_full_unstemmed | Environment and coordination of FeMo–co in the nitrogenase metallochaperone NafY |
title_short | Environment and coordination of FeMo–co in the nitrogenase metallochaperone NafY |
title_sort | environment and coordination of femo–co in the nitrogenase metallochaperone nafy |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8496260/ https://www.ncbi.nlm.nih.gov/pubmed/34704049 http://dx.doi.org/10.1039/d1cb00086a |
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