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Metal Preferences and Metallation

The metal binding preferences of most metalloproteins do not match their metal requirements. Thus, metallation of an estimated 30% of metalloenzymes is aided by metal delivery systems, with ∼25% acquiring preassembled metal cofactors. The remaining ∼70% are presumed to compete for metals from buffer...

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Detalles Bibliográficos
Autores principales: Foster, Andrew W., Osman, Deenah, Robinson, Nigel J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4192464/
https://www.ncbi.nlm.nih.gov/pubmed/25160626
http://dx.doi.org/10.1074/jbc.R114.588145
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author Foster, Andrew W.
Osman, Deenah
Robinson, Nigel J.
author_facet Foster, Andrew W.
Osman, Deenah
Robinson, Nigel J.
author_sort Foster, Andrew W.
collection PubMed
description The metal binding preferences of most metalloproteins do not match their metal requirements. Thus, metallation of an estimated 30% of metalloenzymes is aided by metal delivery systems, with ∼25% acquiring preassembled metal cofactors. The remaining ∼70% are presumed to compete for metals from buffered metal pools. Metallation is further aided by maintaining the relative concentrations of these pools as an inverse function of the stabilities of the respective metal complexes. For example, magnesium enzymes always prefer to bind zinc, and these metals dominate the metalloenzymes without metal delivery systems. Therefore, the buffered concentration of zinc is held at least a million-fold below magnesium inside most cells.
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spelling pubmed-41924642014-10-10 Metal Preferences and Metallation Foster, Andrew W. Osman, Deenah Robinson, Nigel J. J Biol Chem Minireviews The metal binding preferences of most metalloproteins do not match their metal requirements. Thus, metallation of an estimated 30% of metalloenzymes is aided by metal delivery systems, with ∼25% acquiring preassembled metal cofactors. The remaining ∼70% are presumed to compete for metals from buffered metal pools. Metallation is further aided by maintaining the relative concentrations of these pools as an inverse function of the stabilities of the respective metal complexes. For example, magnesium enzymes always prefer to bind zinc, and these metals dominate the metalloenzymes without metal delivery systems. Therefore, the buffered concentration of zinc is held at least a million-fold below magnesium inside most cells. American Society for Biochemistry and Molecular Biology 2014-10-10 2014-08-26 /pmc/articles/PMC4192464/ /pubmed/25160626 http://dx.doi.org/10.1074/jbc.R114.588145 Text en © 2014 by The American Society for Biochemistry and Molecular Biology, Inc. Author's Choice—Final version full access. Creative Commons Attribution Unported License (http://creativecommons.org/licenses/by/3.0/) applies to Author Choice Articles
spellingShingle Minireviews
Foster, Andrew W.
Osman, Deenah
Robinson, Nigel J.
Metal Preferences and Metallation
title Metal Preferences and Metallation
title_full Metal Preferences and Metallation
title_fullStr Metal Preferences and Metallation
title_full_unstemmed Metal Preferences and Metallation
title_short Metal Preferences and Metallation
title_sort metal preferences and metallation
topic Minireviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4192464/
https://www.ncbi.nlm.nih.gov/pubmed/25160626
http://dx.doi.org/10.1074/jbc.R114.588145
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