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In-Edges 1

a(MESH:Bungarotoxins) decreases act(a(CHEBI:decamethonium)) View Subject | View Object

alpha􏰂-BGT blocked the electroplaque’s electrical response in vivo and the microsac’s ion flux response to nicotinic agonists in vitro; alpha􏰂-BGT also blocked the binding of radioactive decamethonium to the detergent extract PubMed:23038257

Out-Edges 1

a(CHEBI:decamethonium) decreases act(a(MESH:"Receptors, Nicotinic")) View Subject | View Object

It was now possible to follow reversible binding to these purified membranes using the nicotinic agonist decamethonium as the radioactive ligand (by the method of equilibrium dialysis that Gilbert and Müller-Hill (9) used to identify the lac repressor) PubMed:23038257

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BEL Commons is developed and maintained in an academic capacity by Charles Tapley Hoyt and Daniel Domingo-Fernández at the Fraunhofer SCAI Department of Bioinformatics with support from the IMI project, AETIONOMY. It is built on top of PyBEL, an open source project. Please feel free to contact us here to give us feedback or report any issues. Also, see our Publishing Notes and Data Protection information.

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.