6zc3
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Small-molecule inhibitors of the PDZ domain of Dishevelled proteins interrupt Wnt signalling
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Structural highlights
DiseaseDVL3_HUMAN Autosomal dominant Robinow syndrome. The disease is caused by variants affecting the gene represented in this entry. FunctionDVL3_HUMAN Involved in the signal transduction pathway mediated by multiple Wnt genes.[UniProtKB:Q61062] Contents | ||||||||||||||||||||
This page was last modified 13:46, 24 January 2024.