Date published: 2025-9-14

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PUS7L Activators

Chemical activators of PUS7L can engage in various biochemical interactions to enhance its enzymatic activity. Zinc Chloride, for instance, may bind to the active site of PUS7L, leading to a conformational change that optimizes its catalytic function. Magnesium Sulfate plays a crucial role as a cofactor for many enzymes, and its addition can be essential for the activation of PUS7L, ensuring the proper configuration for enzymatic activity. Similarly, Sodium Orthovanadate, acting as a phosphatase inhibitor, can preserve the phosphorylation state of proteins, which may include PUS7L, thus maintaining the protein in an active conformation. Forskolin, known to elevate cAMP levels, indirectly activates protein kinase A (PKA), which can then phosphorylate PUS7L, resulting in its activation.

Ionomycin, by increasing intracellular calcium levels, may activate calcium/calmodulin-dependent kinases that are capable of phosphorylating PUS7L, thereby activating it. Activation of protein kinase C (PKC) by Phorbol 12-myristate 13-acetate (PMA) could also lead to the phosphorylation and consequent activation of PUS7L. Epidermal Growth Factor (EGF) engages its receptor to trigger the MAPK/ERK pathway, which can culminate in the phosphorylation and activation of PUS7L. Insulin, through its receptor interaction, activates the PI3K/AKT pathway and can target PUS7L for subsequent phosphorylation and activation. Anisomycin, despite its role as a protein synthesis inhibitor, can activate JNK signaling, which might lead to the phosphorylation and activation of PUS7L. Reactive oxygen species such as Hydrogen Peroxide can activate oxidative stress-related signaling pathways, which may phosphorylate and thus activate PUS7L. Lithium Chloride, by inhibiting GSK-3β, can activate the Wnt signaling pathway, potentially leading to the phosphorylation and activation of PUS7L. Lastly, compounds like Sodium Selenite can engage in the activation of signaling pathways that affect protein functions, including the activation state of PUS7L.

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