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Receptor-type tyrosine-protein phosphatase delta (PTPRD) is a transmembrane protein and enzyme belonging to the protein tyrosine phosphatase (PTP) family, which regulates signal transduction, cell growth, differentiation, mitotic cycle, and neuronal development[1][3]. Its extracellular region contains immunoglobulin-like and fibronectin type III-like domains, contributing to cell adhesion and synaptic specificity[2][3]. PTPRD is expressed highly in the brain, especially in the cerebellum and specific peripheral tissues. It acts as the receptor for the hormone asprosin in the nervous system, influencing appetite and metabolism[1]. PTPRD has been implicated as a tumor suppressor gene and is associated with multiple human diseases, including neuropsychiatric disorders, cancer, neuropathic pain, and addiction, and is the molecular target of experimental therapeutics being studied for addiction and pain management[2][4].
Inhibition of phosphatase activity, affecting neuronal signaling and neuroinflammation. Modulation of STING-IFN-I pathway in neuropathic pain[2]
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