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Entity

Name
alpha-7-containing nAChR
Namespace
HBP
Namespace Version
20181221
Namespace URL
https://raw.githubusercontent.com/pharmacome/terminology/bd0996a28201cad363557315043c6392e31abf58/export/hbp-names.belns

Appears in Networks 2

albuquerque2009 v1.0.0

This file encodes the article Mammalian Nicotinic Acetylcholine Receptors: From Structure to Function by Albuquerque et al, 2009

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Out-Edges 2

p(HBP:"alpha-7-containing nAChR") increases bp(GO:"calcium ion transport into cytosol") View Subject | View Object

Receptors composed of alpha7 subunits are known to desensitize rapidly and to have a high Ca2+:Na+ permeability ratio that exceeds that of the glutamate NMDA receptor, and the 3-4:1 ratio of most other nAChRs (8, 68, 78, 387). As a result, quite distinctly from other nAChRs and even other ligand-activated ion channels, the opening of alpha7 nAChR channels can impact on several Ca2+-dependent mechanisms, including activation of second messenger pathways (328, 456). PubMed:19126755

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p(HBP:"alpha-7-containing nAChR") increases act(p(HGNC:CHRNA7)) View Subject | View Object

For example, those that contain the α 7 subunit ( α 7 * ) as a homomeric or heteromeric receptor most commonly also have accompany- ing characteristics. They bind α -bungarotoxin, have relatively low affinity for nicotine and have relatively fast kinetics. PubMed:26472524

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If you find BEL Commons useful in your work, please consider citing: Hoyt, C. T., Domingo-Fernández, D., & Hofmann-Apitius, M. (2018). BEL Commons: an environment for exploration and analysis of networks encoded in Biological Expression Language. Database, 2018(3), 1–11.