9m1k
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Cryo-EM structure of the TBC-DE-Arl2-beta-tubulin complex with GTP
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Structural highlights
DiseaseTBCE_HUMAN Sanjad-Sakati syndrome;Autosomal recessive Kenny-Caffey syndrome. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. FunctionTBCE_HUMAN Tubulin-folding protein; involved in the second step of the tubulin folding pathway. Seems to be implicated in the maintenance of the neuronal microtubule network. Involved in regulation of tubulin heterodimer dissociation.[1] References
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This page was last modified 09:18, 22 October 2025.