"Coatomer Protein" 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.
A 700-kDa cytosolic protein complex consisting of seven equimolar subunits (alpha, beta, beta', gamma, delta, epsilon and zeta). COATOMER PROTEIN and ADP-RIBOSYLATION FACTOR 1 are principle components of COAT PROTEIN COMPLEX I and are involved in vesicle transport between the ENDOPLASMIC RETICULUM and the GOLGI APPARATUS.
| Descriptor ID |
D020756
|
| MeSH Number(s) |
D12.776.543.990.300.300
|
| Concept/Terms |
Coatomer epsilon Subunit- Coatomer epsilon Subunit
- epsilon-COP
- Coatomer Subunit epsilon-COP
- Coatomer Subunit epsilon COP
- epsilon-COP, Coatomer Subunit
|
Below are MeSH descriptors whose meaning is more general than "Coatomer Protein".
Below are MeSH descriptors whose meaning is more specific than "Coatomer Protein".
This graph shows the total number of publications written about "Coatomer Protein" by people in this website by year, and whether "Coatomer Protein" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2009 | 1 | 0 | 1 |
| 2013 | 0 | 1 | 1 |
| 2015 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2019 | 0 | 1 | 1 |
| 2021 | 1 | 1 | 2 |
| 2022 | 1 | 0 | 1 |
| 2023 | 0 | 1 | 1 |
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Below are the most recent publications written about "Coatomer Protein" by people in Profiles.
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Imaging findings of COPA Syndrome. Pediatr Radiol. 2023 05; 53(5):844-853.
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A Zebra at the Rodeo: Dyspnea, Hematuria, and a Family History of Arthritis. Arthritis Care Res (Hoboken). 2022 02; 74(2):165-170.
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COPB2 loss of function causes a coatopathy with osteoporosis and developmental delay. Am J Hum Genet. 2021 09 02; 108(9):1710-1724.
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Combined immunodeficiency due to a mutation in the ?1 subunit of the coat protein I complex. J Clin Invest. 2021 02 01; 131(3).
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H2O2 induces nuclear transport of the receptor tyrosine kinase c-MET in breast cancer cells via a membrane-bound retrograde trafficking mechanism. J Biol Chem. 2019 05 24; 294(21):8516-8528.
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Copa Syndrome: a Novel Autosomal Dominant Immune Dysregulatory Disease. J Clin Immunol. 2016 05; 36(4):377-387.
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COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritis. Nat Genet. 2015 Jun; 47(6):654-60.
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Systematic identification of molecular subtype-selective vulnerabilities in non-small-cell lung cancer. Cell. 2013 Oct 24; 155(3):552-66.
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Coatomer-dependent protein delivery to lipid droplets. J Cell Sci. 2009 Jun 01; 122(Pt 11):1834-41.
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A role for the host coatomer and KDEL receptor in early vaccinia biogenesis. Proc Natl Acad Sci U S A. 2009 Jan 06; 106(1):163-8.