N-terminal Domains of Human Copper-transporting Adenosine Triphosphatases (the Wilson's and Menkes Disease Proteins) Bind Copper Selectively in Vivo and in Vitro with Stoichiometry of One Copper Per Metal-binding Repeat
Open Access
- 1 July 1997
- journal article
- Published by Elsevier
- Vol. 272 (30) , 18939-18944
- https://doi.org/10.1074/jbc.272.30.18939
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Organization of P-type ATPases: significance of structural diversityBiochemistry, 1995
- Cellular Copper TransportAnnual Review of Nutrition, 1995
- The Wilson disease gene: spectrum of mutations and their consequencesNature Genetics, 1995
- Occipital horn syndrome and a mild Menkes phenotype associated with splice site mutations at the MNK locusNature Genetics, 1994
- Characterization of the Wilson disease gene encoding a P-type copper transporting ATPase: genomic organization, alternative splicing, and structure/function predictionsHuman Molecular Genetics, 1994
- The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease geneNature Genetics, 1993
- The Wilson disease gene is a putative copper transporting P–type ATPase similar to the Menkes geneNature Genetics, 1993
- Isolation and Characterization of a Human Liver cDNA as a Candidate Gene for Wilson DiseaseBiochemical and Biophysical Research Communications, 1993
- Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper–transporting ATPaseNature Genetics, 1993
- Cadmium resistance from Staphylococcus aureus plasmid pI258 cadA gene results from a cadmium-efflux ATPase.Proceedings of the National Academy of Sciences, 1989