Copper-transporting ATPases
"Copper-transporting ATPases" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
P-type ATPases which transport copper ions across membranes in prokaryotic and eukaryotic cells. They possess a conserved CYSTEINE-HISTIDINE-SERINE (CPx) amino acid motif within their transmembrane helices that functions in cation translocation and catalytic activation, and an N-terminal copper-binding CxxC motif that regulates enzyme activity. They play essential roles in intracellular copper homeostasis through regulating the uptake, efflux and storage of copper ions, and in cuproprotein biosynthesis.
Descriptor ID |
D000073840
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MeSH Number(s) |
D08.811.277.040.025.314.500 D12.776.157.530.450.250.656 D12.776.157.530.813.500 D12.776.543.585.450.250.656 D12.776.543.585.813.500
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Concept/Terms |
Copper-transporting ATPases- Copper-transporting ATPases
- ATPases, Copper-transporting
- Copper transporting ATPases
- Cu(+)-transporting ATPases
- Copper-transporting Adenosine Triphosphatases
- Adenosine Triphosphatases, Copper-transporting
- Copper transporting Adenosine Triphosphatases
- Triphosphatases, Copper-transporting Adenosine
- Copper-transporting ATPase
- ATPase, Copper-transporting
- Copper transporting ATPase
- Cu-transporting ATPases
- ATPases, Cu-transporting
- Cu transporting ATPases
Wilson Disease Protein- Wilson Disease Protein
- ATP7B Cu-binding P type ATPase
- ATP7B Cu binding P type ATPase
- Copper-transporting ATPase 2
- Copper transporting ATPase 2
- ATPase, Cu++ transporting, beta Polypeptide (Wilson Disease)
- Wilson Disease Cu-binding P Type ATPase
- Wilson Disease Cu binding P Type ATPase
Copper-transporting ATPase 1- Copper-transporting ATPase 1
- ATPase 1, Copper-transporting
- Copper transporting ATPase 1
- Copper Pump 1
- Menkes Disease-associated Protein
- Menkes Disease associated Protein
- ATP7A Protein
- ATPase Copper Transporting alpha
Pineal Night-specific ATPase- Pineal Night-specific ATPase
- ATPase, Pineal Night-specific
- Night-specific ATPase, Pineal
- Pineal Night specific ATPase
- PINA Enzyme
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Below are MeSH descriptors whose meaning is more general than "Copper-transporting ATPases".
Below are MeSH descriptors whose meaning is more specific than "Copper-transporting ATPases".
This graph shows the total number of publications written about "Copper-transporting ATPases" by people in this website by year, and whether "Copper-transporting ATPases" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2010 | 0 | 1 | 1 |
2011 | 0 | 1 | 1 |
2017 | 0 | 1 | 1 |
2018 | 1 | 0 | 1 |
2019 | 2 | 1 | 3 |
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Below are the most recent publications written about "Copper-transporting ATPases" by people in Profiles.
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Melatonin: A hypothesis regarding its use to treat Wilson disease. Med Hypotheses. 2019 Dec; 133:109408.
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Wilson's disease: A new perspective review on its genetics, diagnosis and treatment. Front Biosci (Elite Ed). 2019 06 01; 11(1):166-185.
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Plasma transfusion combined with chelating therapy alleviates fulminant Wilson's disease with a single Arg778Leu heterozygote mutation. Ann Hepatol. 2019 Mar - Apr; 18(2):393-396.
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Metallothionein is elevated in liver and duodenum of Atp7b(-/-) mice. Biometals. 2018 08; 31(4):617-625.
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Pili torti, pale and elastic skin, and severe neurological impairment. J Dtsch Dermatol Ges. 2018 Mar; 16(3):360-363.
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Severe dysfunction of respiratory chain and cholesterol metabolism in Atp7b(-/-) mice as a model for Wilson disease. Biochim Biophys Acta. 2011 Dec; 1812(12):1607-15.
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Genetic analysis of BIRC4/XIAP as a putative modifier gene of Wilson disease. J Inherit Metab Dis. 2010 Dec; 33 Suppl 3:S233-40.