22aj | pdb_000022aj
From Proteopedia
GDP human alpha1A/beta3 S239C microtubule
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Structural highlights
DiseaseTBA1A_HUMAN Lissencephaly due to TUBA1A mutation. The disease is caused by mutations affecting the gene represented in this entry. FunctionTBA1A_HUMAN Tubulin is the major constituent of microtubules. It binds two moles of GTP, one at an exchangeable site on the beta chain and one at a non-exchangeable site on the alpha chain. Contents | ||||||||||||||||||||
This page was last modified 15:46, 1 April 2026.