p(FPLX:AMPK) increases a(CHEBI:"NAD(+)")

View Subject View Object

PubMed:30116051

SIRT1 is activated by AMPK- mediated increases in nicotinamide, and it drives the ALN by inhibiting mTORC1, inducing FOXO1 and FOXO3 and activating key regulatory proteins such as ATG5, ATG7 and LC3.

Related Edges 7

• a(CHEBI:"NAD(+)") increases act(p(HGNC:SIRT1))
• act(p(HGNC:SIRT1)) decreases act(p(FPLX:mTORC1))
• act(p(HGNC:SIRT1)) increases act(p(HGNC:FOXO1))
• act(p(HGNC:SIRT1)) increases act(p(HGNC:FOXO3))
• act(p(HGNC:SIRT1)) increases act(p(HGNC:ATG5))
• act(p(HGNC:SIRT1)) increases act(p(HGNC:ATG7))
• act(p(HGNC:SIRT1)) increases act(p(HGNC:MAP1LC3A))

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.

---