Copper-induced trafficking of the cU-ATPases: a key mechanism for copper homeostasis.
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Abstract
References (35)
The Wilson disease gene is a putative copper transporting P–type ATPase similar to the Menkes gene
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Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper–transporting ATPase
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The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene
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Copper-induced apical trafficking of ATP7B in polarized hepatoma cells provides a mechanism for biliary copper excretion
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Sequence, mapping and disruption of CCC2, a gene that cross‐complements the Ca2+‐sensitive phenotype of csg1 mutants and encodes a P‐type ATPase belonging to the Cu2+‐ATPase subfamily
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Effect of the toxic milk mutation (tx) on the function and intracellular localization of Wnd, the murine homologue of the Wilson copper ATPase
2001 • 96 citations
Functional analysis and intracellular localization of the human menkes protein (MNK) stably expressed from a cDNA construct in Chinese hamster ovary cells (CHO-K1)
1998 • 89 citations
Characterization of the Menkes Protein Copper-Binding Domains and Their Role in Copper-Induced Protein Relocalization
1999 • 77 citations
Defective Copper-Induced Trafficking and Localization of the Menkes Protein in Patients With Mild and Copper-Treated Classical Menkes Disease
1999 • 68 citations
Intracellular localization and loss of copper responsiveness of Mnk, the murine homologue of the Menkes protein, in cells from blotchy (Mo blo) and brindled (Mo br) mouse mutants
1999 • 60 citations
Structure of the P-type ATPases
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On the Mechanism of ATP‐Driven Ca2+ Transport by the Calcium ATPase of Sarcoplasmic Reticulum
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