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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Biochemistry and Molecular Biology
2014
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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. |
format | Online Article Text |
id | pubmed-4192464 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
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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