Copper specifically regulates intracellular phosphorylation of the Wilson's disease protein, a human copper-transporting ATPase (Q42507758)

1 November 2017

title

Copper specifically regulates intracellular phosphorylation of the Wilson's disease protein, a human copper-transporting ATPase (English)

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1 November 2017

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S M Vanderwerf

1

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1 November 2017

M J Cooper

series ordinal

2

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1 November 2017

I V Stetsenko

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3

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S Lutsenko

series ordinal

4

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1 November 2017

language of work or name

English

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publication date

26 July 2001

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Journal of Biological Chemistry

1 November 2017

number of pages

6

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based on heuristic

inferred from page(s)

published in

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1 November 2017

volume

276

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1 November 2017

issue

39

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1 November 2017

page(s)

36289-36294

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Cellular copper transport

1 November 2017

cites work

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https://api.crossref.org/works/10.1074%2FJBC.M102055200

Molecular mechanisms of copper homeostasis

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M102055200

Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPase

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M102055200

The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M102055200

The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M102055200

ATP-dependent copper transport by the Menkes protein in membrane vesicles isolated from cultured Chinese hamster ovary cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M102055200

Correction of the copper transport defect of Menkes patient fibroblasts by expression of the Menkes and Wilson ATPases.

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M102055200

Functional expression of the Wilson disease protein reveals mislocalization and impaired copper-dependent trafficking of the common H1069Q mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M102055200

Identification of the copper regulon in Saccharomyces cerevisiae by DNA microarrays

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M102055200

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M102055200

The copines, a novel class of C2 domain-containing, calcium-dependent, phospholipid-binding proteins conserved from Paramecium to humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M102055200

Biochemical Characterization of the Wilson Disease Protein and Functional Expression in the Yeast Saccharomyces cerevisiae

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M102055200

Copper-induced apical trafficking of ATP7B in polarized hepatoma cells provides a mechanism for biliary copper excretion

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M102055200

Interaction of the copper chaperone HAH1 with the Wilson disease protein is essential for copper homeostasis

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M102055200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M102055200

The Lys1010-Lys1325 fragment of the Wilson's disease protein binds nucleotides and interacts with the N-terminal domain of this protein in a copper-dependent manner

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M102055200

Expression, Purification, and Metal Binding Properties of the N-terminal Domain from the Wilson Disease Putative Copper-transporting ATPase (ATP7B)

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M102055200

21 January 2018

Identifiers

DOI

10.1074/JBC.M102055200

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1 November 2017

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