Date published: 2025-11-3

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OTTMUSG00000015050 Activators

PHDS58, representing the cell receptor alpha chain V region, is a crucial component in the intricate network of cellular signaling. As a receptor, PHDS58's primary function is to transduce external signals into the cell, initiating a cascade of intracellular events that dictate cellular responses. This process is finely regulated and involves multiple steps, including ligand binding, receptor conformational changes, and subsequent activation of downstream signaling pathways. The activation of PHDS58 is, therefore, a pivotal event in cellular communication, modulating crucial processes like cell differentiation, activation, and proliferation. The mechanism of activation of PHDS58 revolves around the modification of its structural and functional properties, primarily through phosphorylation. Phosphorylation acts as a molecular switch, altering the conformational state of PHDS58, thereby modulating its affinity for ligands and its ability to interact with co-receptors and intracellular signaling molecules. The chemicals listed in the table above are hypothesized to activate PHDS58 indirectly by influencing the phosphorylation landscape within the cell. By either inhibiting phosphatases or activating kinases, these chemicals increase the phosphorylation levels of key proteins in the signaling pathways associated with PHDS58. This modification enhances the functional capability of PHDS58, enabling it to efficiently transduce signals upon ligand binding.

Understanding the activation mechanisms of PHDS58 is crucial for deciphering the complex signaling networks in which it operates. The indirect activators identified offer insights into the broader regulatory framework governing PHDS58 activity. By manipulating kinase and phosphatase activities, these activators shed light on the intricate interplay of phosphorylation events that underlie the functional modulation of PHDS58. This knowledge is pivotal in unraveling the molecular basis of signal transduction processes involving PHDS58 and can provide a foundation for further exploration into its role in cellular physiology and pathology.

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