The Role of GMXCXXC Metal Binding Sites in the Copper-induced Redistribution of the Menkes Protein
Open Access
- 1 April 1999
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 274 (16) , 11170-11177
- https://doi.org/10.1074/jbc.274.16.11170
Abstract
No abstract availableKeywords
This publication has 30 references indexed in Scilit:
- Caenorhabditis elegans cDNA for a Menkes/Wilson Disease Gene Homologue and Its Function in a Yeast CCC2 Gene Deletion MutantThe Journal of Biochemistry, 1997
- BACTERIAL HEAVY METAL RESISTANCE: New SurprisesAnnual Review of Microbiology, 1996
- Cellular Copper TransportAnnual Review of Nutrition, 1995
- 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 subfamilyYeast, 1995
- 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 of a candidate gene for Menkes disease and evidence that it encodes a copper–transporting ATPaseNature Genetics, 1993
- Isolation of a partial candidate gene for Menkes disease by positional cloningNature Genetics, 1993
- Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding proteinNature Genetics, 1993
- Ion motive ATPases. I. Ubiquity, properties, and significance to cell functionTrends in Biochemical Sciences, 1987