 Calnexin
"Calnexin" 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 lectin found in ENDOPLASMIC RETICULUM membranes that binds to specific N-linked OLIGOSACCHARIDES found on newly synthesized proteins. It may play role in PROTEIN FOLDING or retention and degradation of misfolded proteins in the endoplasmic reticulum.
| Descriptor ID |
D037281
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| MeSH Number(s) |
D12.644.360.372.311 D12.776.157.125.412.311 D12.776.476.387.311 D12.776.503.295 D12.776.543.162
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| Concept/Terms |
Calnexin- Calnexin
- Phosphoprotein pp90
- pp90, Phosphoprotein
- IP90 Protein
- Integral Membrane Protein IP90
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Below are MeSH descriptors whose meaning is more general than "Calnexin".
Below are MeSH descriptors whose meaning is more specific than "Calnexin".
This graph shows the total number of publications written about "Calnexin" by people in this website by year, and whether "Calnexin" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2004 | 0 | 2 | 2 | | 2005 | 0 | 1 | 1 |
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Below are the most recent publications written about "Calnexin" by people in Profiles.
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Goebel SM, Alvestad RM, Coultrap SJ, Browning MD. Tyrosine phosphorylation of the N-methyl-D-aspartate receptor is enhanced in synaptic membrane fractions of the adult rat hippocampus. Brain Res Mol Brain Res. 2005 Dec 07; 142(1):65-79.
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Wang Q, Downey GP, Herrera-Abreu MT, Kapus A, McCulloch CA. SHP-2 modulates interleukin-1-induced Ca2+ flux and ERK activation via phosphorylation of phospholipase Cgamma1. J Biol Chem. 2005 Mar 04; 280(9):8397-406.
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Coughlan CM, Walker JL, Cochran JC, Wittrup KD, Brodsky JL. Degradation of mutated bovine pancreatic trypsin inhibitor in the yeast vacuole suggests post-endoplasmic reticulum protein quality control. J Biol Chem. 2004 Apr 09; 279(15):15289-97.
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Toyofuku K, Wada I, Spritz RA, Hearing VJ. The molecular basis of oculocutaneous albinism type 1 (OCA1): sorting failure and degradation of mutant tyrosinases results in a lack of pigmentation. Biochem J. 2001 Apr 15; 355(Pt 2):259-69.
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