Chemical activators of THUMPD2 can engage various intracellular signaling pathways to lead to its activation. Phorbol 12-myristate 13-acetate (PMA) activates protein kinase C (PKC), which may phosphorylate THUMPD2, enabling its functional activity. Forskolin, by elevating intracellular cAMP levels, activates protein kinase A (PKA), which can also target THUMPD2 for phosphorylation. Activation of PKA is a common mechanism for many of the chemicals listed, including 8-Bromoadenosine 3',5'-cyclic monophosphate (8-Br-cAMP) and Dibutyryl-cAMP, which both serve as analogs of cAMP and can penetrate cell membranes to act directly on this kinase, leading to the activation of THUMPD2 through phosphorylation. Similarly, Sphingosine, once inside the cell, is metabolized to sphingosine-1-phosphate (S1P), which can activate kinases that may target THUMPD2 for activation via phosphorylation.
The inhibition of protein phosphatases by Calyculin A and Okadaic Acid can also result in the activation of THUMPD2, as the prevention of dephosphorylation keeps proteins, including THUMPD2, in a phosphorylated, active state. Ionomycin, by increasing intracellular calcium, can activate calcium-dependent kinases that have the potential to phosphorylate and activate THUMPD2. Thapsigargin acts similarly by inhibiting the sarcoplasmic/endoplasmic reticulum Ca2+ ATPase (SERCA), leading to increased cytosolic calcium levels that can activate kinases that phosphorylate THUMPD2. Anisomycin triggers the activation of JNK and p38 MAP kinase pathways, which include kinases capable of phosphorylating THUMPD2. Lastly, Bryostatin 1 modulates PKC, which can have downstream effects on the phosphorylation state of proteins such as THUMPD2, whereas Bisindolylmaleimide I, through its inhibitory action on PKC, can result in the compensatory activation of PKA, which subsequently can phosphorylate and activate THUMPD2.
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