Date published: 2025-9-19

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1700110M21Rik Activators

Chemical activators of proline rich 30 utilize various cellular pathways to modulate the protein's activity. Bisindolylmaleimide I operates by inhibiting protein kinase C (PKC), a negative regulator of proline rich 30. When PKC activity is reduced, the suppression it exerts on proline rich 30 is lifted, resulting in the protein's activation. Similarly, PMA directly stimulates PKC, which can then phosphorylate and activate proline rich 30. Forskolin, by elevating intracellular cAMP levels, leads to the activation of protein kinase A (PKA). Activated PKA can phosphorylate proline rich 30, thus enhancing its activity. Dibutyryl cAMP, a cAMP analog, also activates PKA, achieving the same effect. Ionomycin raises intracellular calcium levels, which activate calcium-dependent protein kinases that can phosphorylate and trigger proline rich 30.

Furthermore, the compound okadaic acid, by inhibiting phosphatases like PP1 and PP2A, prevents the dephosphorylation of proteins, thereby maintaining proline rich 30 in a phosphorylated and active state. Anisomycin activates stress-activated protein kinases such as JNK, which are known to phosphorylate certain proteins, possibly including proline rich 30. Calyculin A, another phosphatase inhibitor, similarly promotes the phosphorylation state of proteins, including proline rich 30. Thapsigargin's mechanism involves the inhibition of the SERCA pump, leading to increased cytosolic calcium levels which can initiate signaling cascades that activate proline rich 30. Staurosporine, although a PKC inhibitor, can at low concentrations activate other kinases that may target and activate proline rich 30. Epigallocatechin Gallate, by inhibiting certain protein kinases, can lead to the activation of alternate kinases which may then phosphorylate proline rich 30. Lastly, sphingosine, by inhibiting PKC, can remove inhibitory phosphorylations on proline rich 30, resulting in its activation. Each chemical, through its unique interaction with cellular signaling pathways, can contribute to the regulatory control of proline rich 30's activity state.

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