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MICAL-like protein 1 (MICALL1) is a cytoplasmic scaffold protein involved in regulating tubular recycling endosome identity, membrane tubulation, and receptor/lipid recycling[1][2][3][4]. It binds phosphatidic acid and various small GTPases, notably Rab8a and Rab35, and recruits EHD1 and other proteins critical for assembling and regulating protein–lipid complexes on endosomal membranes[1][2][4]. MICALL1 is essential for the formation of tubular endosomes, endocytic recycling, and the trafficking of cell surface receptors, as well as for processes such as ciliogenesis, cytokinesis, and cell migration[1][2][3][4]. Diseases associated with MICALL1 include macular degeneration and Bardet-Bidl syndrome[3]. Currently, there are no known drugs that directly target MICALL1, nor is it classified as a conventional therapeutic target such as a receptor or enzyme[3].
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