8s6a
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X-ray structure of Dishevelled 3 PDZ domain in a complex with a class III peptide ligand
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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 10:17, 12 March 2025.