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• W1561944490 abstract "Publisher Summary The chapter focuses on the copper ferroxidases and discusses the role of copper in iron metabolism. The physiologic linkage between copper and iron is now well understood at the molecular level, in terms of the gene products that metabolically link these two essential metal nutrients. The central component in this linkage is a multicopper ferroxidase: ceruloplasmin, Fet3p, in mammals. However, each of these copper proteins relies on a copper ATPase found in the membrane of a specific vesicular compartment for the copper necessary for each protein's activation. The copper pumping that any one of these ATPases does may be, critical to copper homeostasis as well for copper excretion, for example. These pumps in turn rely on a protein, a copper chaperone that ferries the copper from the plasma membrane copper permease through the cytosol to this vesicular compartment. The permease relies on a plasma membrane cuprireductase to supply it with the Cu(I) as substrate for uptake. Nonetheless, irrespective of whether or how a defect in any one of these enzymes, transporters, chaperones, or pumps may contribute to a dysfunction in copper handling, there most certainly will be a direct impact on the copper incorporation into one or more of these ferroxidases leading to a secondary effect on iron homeostasis. The copper ferroxidases are central to this secondary nutritional, metabolic, essentially epistatic relationship between copper and iron in eukaryotes." @default.
• W1561944490 created "2016-06-24" @default.
• W1561944490 creator A5023724784 @default.
• W1561944490 date "2002-01-01" @default.
• W1561944490 modified "2023-10-03" @default.
• W1561944490 title "FET3P, ceruloplasmin, and the role of copper in iron metabolism" @default.
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• W1561944490 doi "https://doi.org/10.1016/s0065-3233(02)60055-5" @default.
• W1561944490 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/12418179" @default.
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