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TBCC domain-containing protein 1 (TBCCD1) is a centrosomal protein related to tubulin cofactor C. It localizes primarily at the centrosome, spindle midzone, and basal bodies of primary and motile cilia. TBCCD1 depletion causes centrosome and Golgi disorganization, slows cell migration, and impairs primary cilia assembly, indicating its central role in internal cell organization and the dynamics of the cytoskeleton. TBCCD1 has homologs conserved across eukaryotes and contains both a TBCC domain, important for microtubule function, and a CARP domain, suggesting possible links between microtubule and actin cytoskeletons. Unlike TBCC or RP2, TBCCD1 does not share GTPase-activating protein (GAP) activity towards tubulin, but its full molecular functions are not yet entirely defined[1].
None known. There are no described pharmacological mechanisms of action for drugs targeting TBCCD1[1].
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