Forskolin and IBMX elevate intracellular cAMP levels, which in turn activate PKA, a kinase with the capacity to phosphorylate numerous proteins. This phosphorylation can lead to modifications in protein activity, potentially affecting proteins akin to C9orf40. Other molecules, such as PMA, act as activators of protein kinase C (PKC), ushering in the phosphorylation of a variety of substrates. In parallel, ionophores like Ionomycin and A23187 disrupt calcium homeostasis, triggering calcium-dependent signaling mechanisms that could intersect with the regulatory domains of proteins similar to C9orf40. LY294002, U0126, and SB203580 are representatives that target the core of signaling cascades such as PI3K/AKT and MAPK/ERK. These inhibitors modulate the phosphorylation status and activity of kinases within these pathways, which can have a bearing on the activity of proteins governed by these cascades.
Furthermore, epigenetic modifiers like Trichostatin A and 5-Azacytidine induce alterations in gene expression patterns through their inhibition of histone deacetylases and DNA methyltransferases, respectively. These changes in the chromatin landscape can consequently affect the expression and function of a wide array of proteins. The Aurora kinase inhibitor ZM-447439 adds to this arsenal by influencing cell cycle progression and potentially affecting proteins involved in this fundamental cellular process.
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