Gene interactions and pathways from curated databases and text-mining

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MAPK7 — MEF2D

Pathways - manually collected, often from reviews:

  • OpenBEL Selventa BEL large corpus: MEF2D → MAPK7 (directlyIncreases, MAPK7 Activity, MEF2D Activity) Kato et al., J Biol Chem 2000*
    Evidence: Here, we demonstrate that, in addition to MEF2C, BMK1 phosphorylates and activates MEF2A and MEF2D but not MEF2B. The blocking of BMK1 signaling inhibits the epidermal growth factor-dependent activation of these three MEF2 transcription factors. The sites phosphorylated by activated BMK1 were mapped to Ser-355, Thr-312, and Thr-319 of MEF2A and Ser-179 of MEF2D both in vitro and in vivo.
  • BioCarta control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk): ERK5 (MAPK7) → MEF2/MYOD complex (MYOD1-MEF2C_MEF2B_MEF2D_MEF2A) (transcription, activates)

Protein-Protein interactions - manually collected from original source literature:

Studies that report less than 10 interactions are marked with *

Text-mined interactions from Literome

Kato et al., J Biol Chem 2000 : Here, we demonstrate that, in addition to MEF2C, BMK1 phosphorylates and activates MEF2A and MEF2D but not MEF2B
Zhao et al., Arch Biochem Biophys 2002 (Arteriosclerosis) : The exclusive activation of MEF2D by BMK1 appears required for this cooperative upregulation of c-jun in VSMC, and coactivation of p38 and BMK1 also has additive effects on the activation of a reporter gene linked to the c-jun promoter in our experimental system
Aziz et al., Epigenetics 2010 (MAP Kinase Signaling System) : Modulation of the interaction between Ash2L/MLL2 and Mef2d by the p38a MAPK signaling pathway in turns provides fine tuning of the muscle-specific gene expression program