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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: RSC 2021
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).
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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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