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Appears in Networks 3

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Out-Edges 4

p(FPLX:SRC) increases act(a(CHEBI:nicotine)) View Subject | View Object

The neuroprotective effects of nicotine are blocked by inhibitors of either PI3K or SRC family kinases, and nicotine evokes an increase in levels of phosphorylated AKT, B-cell chronic lymphocytic leukemia/lymphoma (BCL2), and BCL-2-like protein (Shimohama and Kihara, 2001), which are further downstream in the PI3K/AKT pathway (Fig. 3). PubMed:19293145

act(p(FPLX:SRC), ma(kin)) increases p(HGNC:CHRNA7, pmod(Ph)) View Subject | View Object

Furthermore, Src-family kinases (SFKs) directly phosphorylate the cytoplasmic loop of α7 nAChRs in the plasma membrane. PubMed:17009926

act(p(FPLX:SRC), ma(kin)) increases p(FPLX:CHRN, pmod(Ph, Tyr)) View Subject | View Object

Although the mechanisms that regulate phosphorylation of AChRs are still essen- tially unknown, protein tyrosine phosphorylation by the SFKs has been shown to affect peripheral AChRs in various ways, depending on the tis- sue, subunit type and functional role of the receptors involved. PubMed:22040696

act(p(FPLX:SRC), ma(kin)) increases p(FPLX:CHRN, pmod(Ph, Tyr)) View Subject | View Object

In Torpedo electric organ, phosphorylation of AChRs by SFKs causes subtle changes in desensitization kinetics but not in I max , the maximal current flowing through the receptor channel [141–143]. PubMed:22040696

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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.