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Appears in Networks 1

In-Edges 2

Out-Edges 2

p(HGNC:PRKN, var("p.Lys161Asn")) association path(MESH:"Parkinsonian Disorders") View Subject | View Object

An interesting point is that the mutated Parkin species K161N, which is associated with AR-JP, could still ubiquitinate p38, suggesting that it is not loss of function that underlies the human disease (see above). PubMed:14556719

p(HGNC:PRKN, var("p.Lys161Asn")) increases p(HGNC:AIMP2, pmod(Ub)) View Subject | View Object

An interesting point is that the mutated Parkin species K161N, which is associated with AR-JP, could still ubiquitinate p38, suggesting that it is not loss of function that underlies the human disease (see above). PubMed:14556719

About

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.