p(HGNC:MAPK9) increases p(HGNC:MAPT, pmod(Ph))

View Subject View Object

PubMed:12428809

Among the specific “proline-dependent” kinases that can phosphorylate protein tau at dif- ferent sites in vitro, special attention is dedicated to glycogen-synthase kinase-3β (GSK-3β) (Michel et al., 1998), mitogen-activated protein kinase (MAPK) (Drewes et al., 1992), stress-activated protein kinases (SAPKs) (Goedert et al., 1997) and cyclin-dependent kinases (CDKs) including cdc2 and cdk5 (Baumann et al., 1993; Patrick et al., 1999).

Related Edges 4

• p(FPLX:ERK) increases p(HGNC:MAPT, pmod(Ph))
• p(HGNC:CDK1) increases p(HGNC:MAPT, pmod(Ph))
• p(HGNC:CDK5) increases p(HGNC:MAPT, pmod(Ph))
• p(HGNC:GSK3B) increases p(HGNC:MAPT, pmod(Ph))

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.

---