31hp
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Crystal structure of tau tubulin kinase 2 (TTBK2) in complex with compound 62
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Structural highlights
DiseaseTTBK2_HUMAN Spinocerebellar ataxia type 11. The disease is caused by mutations affecting the gene represented in this entry. FunctionTTBK2_HUMAN Serine/threonine kinase that acts as a key regulator of ciliogenesis: controls the initiation of ciliogenesis by binding to the distal end of the basal body and promoting the removal of CCP110, which caps the mother centriole, leading to the recruitment of IFT proteins, which build the ciliary axoneme. Has some substrate preference for proteins that are already phosphorylated on a Tyr residue at the +2 position relative to the phosphorylation site. Able to phosphorylate tau on serines in vitro.[1] [2] References
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This page was last modified 19:57, 29 July 2026.