9hkr
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NMR structure of the C-terminal domain of the human SPAG1 protein
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Structural highlights
DiseaseSPAG1_HUMAN Primary ciliary dyskinesia. The disease is caused by mutations affecting the gene represented in this entry. FunctionSPAG1_HUMAN May play a role in the cytoplasmic assembly of the ciliary dynein arms (By similarity). May play a role in fertilization. Binds GTP and has GTPase activity.[1] [2] References
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This page was last modified 14:08, 1 July 2026.