Copper-regulated Trafficking of the Menkes Disease Copper ATPase Is Associated with Formation of a Phosphorylated Catalytic Intermediate
Open Access
- 1 November 2002
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 277 (48), 46736-46742
- https://doi.org/10.1074/jbc.m208864200
Abstract
No abstract availableKeywords
This publication has 36 references indexed in Scilit:
- The Menkes copper transporter is required for the activation of tyrosinaseHuman Molecular Genetics, 2000
- Correction of the Copper Transport Defect of Menkes Patient Fibroblasts by Expression of the Menkes and Wilson ATPasesJournal of Biological Chemistry, 1998
- Functional expression of the Wilson disease protein reveals mislocalization and impaired copper-dependent trafficking of the common H1069Q mutationProceedings of the National Academy of Sciences, 1998
- Restoration of Holoceruloplasmin Synthesis in LEC Rat after Infusion of Recombinant Adenovirus Bearing WND cDNAJournal of Biological Chemistry, 1998
- Evolution of Substrate Specificities in the P-Type ATPase SuperfamilyJournal of Molecular Evolution, 1998
- Biochemical Characterization of the Wilson Disease Protein and Functional Expression in the Yeast Saccharomyces cerevisiaeJournal of Biological Chemistry, 1997
- Biochemical characterization and intracellular localization of the Menkes disease proteinProceedings of the National Academy of Sciences, 1996
- Menkes disease mutations and response to early copper histidine treatmentNature Genetics, 1996
- Organization of P-type ATPases: significance of structural diversityBiochemistry, 1995
- Expression of the Menkes gene homologue in mouse tissues lack of effect of copper on the mRNA levelsFEBS Letters, 1994