The SLC31 (Ctr) copper transporter family (Q28182277)

Copper-dependent degradation of the Saccharomyces cerevisiae plasma membrane copper transporter Ctr1p in the apparent absence of endocytosis.

Europe PubMed Central

title

The SLC31 (Ctr) copper transporter family (English)

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Michael J Petris

1

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language of work or name

English

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publication date

February 2004

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published in

Pfluegers Archiv

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volume

447

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issue

5

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page(s)

752-5

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cites work

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Cellular copper transport and metabolism

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Isolation of a murine copper transporter gene, tissue specific expression and functional complementation of a yeast copper transport mutant.

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Ctr6, a vacuolar membrane copper transporter in Schizosaccharomyces pombe

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Biochemical and genetic analyses of yeast and human high affinity copper transporters suggest a conserved mechanism for copper uptake

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Microcytic anaemia mice have a mutation in Nramp2, a candidate iron transporter gene

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Copper-stimulated endocytosis and degradation of the human copper transporter, hCtr1

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High affinity copper transport protein in the lizard Podarcis sicula: molecular cloning, functional characterization and expression in somatic tissues, follicular oocytes and eggs.

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A widespread transposable element masks expression of a yeast copper transport gene.

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A delicate balance: homeostatic control of copper uptake and distribution

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Molecular characterization of hCTR1, the human copper uptake protein

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Molecular mechanisms of copper uptake and distribution

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Essential role for mammalian copper transporter Ctr1 in copper homeostasis and embryonic development

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Molecular characterization of a putative Arabidopsis thaliana copper transporter and its yeast homologue

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Function, structure, and mechanism of intracellular copper trafficking proteins

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Micropinocytosis of transferrin by developing red cells: an electron-microscopic study utilizing ferritin-conjugated transferrin and ferritin-conjugated antibodies to transferrin

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The Saccharomyces cerevisiae copper transport protein (Ctr1p). Biochemical characterization, regulation by copper, and physiologic role in copper uptake.

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Nramp2 is mutated in the anemic Belgrade (b) rat: evidence of a role for Nramp2 in endosomal iron transport.

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Biochemical characterization of the human copper transporter Ctr1

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Characterization of mouse embryonic cells deficient in the ctr1 high affinity copper transporter. Identification of a Ctr1-independent copper transport system

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The N-terminus of the human copper transporter 1 (hCTR1) is localized extracellularly, and interacts with itself

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Characterization of the Saccharomyces cerevisiae high affinity copper transporter Ctr3.

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Biochemical characterization and subcellular localization of human copper transporter 1 (hCTR1)

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The copper transporter CTR1 provides an essential function in mammalian embryonic development

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Metal transporters that contribute copper to metallochaperones in Saccharomyces cerevisiae

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hCTR1: a human gene for copper uptake identified by complementation in yeast

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Cloning and characterization of a mammalian proton-coupled metal-ion transporter

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