Functional expression in yeast of the human secretory pathway Ca(2+), Mn(2+)-ATPase defective in Hailey-Hailey disease (Q24291997)

Journal of Biological Chemistry

GOA release 2020-03-11

Hailey-Hailey disease

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Van-Khue Ton

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Debjani Mandal

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Cordelia Vahadji

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Rajini Rao

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language of work or name

English

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publication date

22 February 2002

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published in

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volume

277

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issue

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page(s)

6422-7

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cites work

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Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease

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Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca(2+) pump

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Inactivation of the KIPMR1 gene of Kluyveromyces lactis results in defective cell-wall morphogenesis.

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Magnesium and manganese ions modulate Ca2+ uptake and its energetic coupling in sarcoplasmic reticulum

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Elevated cytosolic free Ca2+ concentrations and massive Ca2+ accumulation within vacuoles, in yeast mutant lacking PMR1, a homolog of Ca2+ -ATPase

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Adenosine 5'-triphosphate dependent fluxes of manganese and and hydrogen ions in sarcoplasmic reticulum vesicles

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Phenotypic screening of mutations in Pmr1, the yeast secretory pathway Ca2+/Mn2+-ATPase, reveals residues critical for ion selectivity and transport

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7 January 2021

Disruption of PMR1, encoding a Ca2+-ATPase homolog in Yarrowia lipolytica, affects secretion and processing of homologous and heterologous proteins

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Ca2+-ATPases and their expression in the mammary gland of pregnant and lactating rats

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7 January 2021