9cxh
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Structure of PDE6C in complex with the rod inhibitory p gamma subunit in the presence of cGMP
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Structural highlights
DiseasePDE6C_HUMAN Progressive cone dystrophy;Achromatopsia. The disease is caused by mutations affecting the gene represented in this entry. FunctionContents | ||||||||||||||||||||
This page was last modified 06:30, 18 December 2024.