Shaker Superfamily of Potassium Channels
"Shaker Superfamily of Potassium Channels" 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.
Voltage-gated potassium channels whose primary subunits contain six transmembrane segments and form tetramers to create a pore with a voltage sensor. They are related to their founding member, shaker protein, Drosophila.
| Descriptor ID |
D051637
|
| MeSH Number(s) |
D12.776.157.530.400.600.900.500 D12.776.543.550.450.750.900.500 D12.776.543.585.400.750.900.624
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Shaker Superfamily of Potassium Channels".
Below are MeSH descriptors whose meaning is more specific than "Shaker Superfamily of Potassium Channels".
This graph shows the total number of publications written about "Shaker Superfamily of Potassium Channels" by people in this website by year, and whether "Shaker Superfamily of Potassium Channels" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1996 | 0 | 1 | 1 |
| 1998 | 0 | 1 | 1 |
| 1999 | 0 | 2 | 2 |
| 2000 | 0 | 1 | 1 |
| 2001 | 0 | 1 | 1 |
| 2003 | 0 | 1 | 1 |
| 2006 | 1 | 0 | 1 |
| 2008 | 5 | 0 | 5 |
| 2009 | 1 | 0 | 1 |
| 2010 | 0 | 1 | 1 |
| 2011 | 0 | 1 | 1 |
| 2012 | 1 | 0 | 1 |
| 2013 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
| 2025 | 1 | 0 | 1 |
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Below are the most recent publications written about "Shaker Superfamily of Potassium Channels" by people in Profiles.
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Potentiation of the Kv1 family K(+) channel by cortisone analogues. ACS Chem Biol. 2012 10 19; 7(10):1641-6.
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Analogs of the sea anemone potassium channel blocker ShK for the treatment of autoimmune diseases. Inflamm Allergy Drug Targets. 2011 Oct; 10(5):313-21.
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Cortisone dissociates the Shaker family K+ channels from their beta subunits. Nat Chem Biol. 2008 Nov; 4(11):708-14.
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Functional coupling between the Kv1.1 channel and aldoketoreductase Kvbeta1. J Biol Chem. 2008 Mar 28; 283(13):8634-42.
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Potassium channel receptor site for the inactivation gate and quaternary amine inhibitors. Nature. 2001 Jun 07; 411(6838):657-61.
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k-Opioid receptor activation of a dendrotoxin-sensitive potassium channel mediates presynaptic inhibition of mossy fiber neurotransmitter release. Mol Pharmacol. 1996 Jul; 50(1):80-5.