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The crystal structure of a collagen galactosylhydroxylysyl glucosyltransferase from human
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Structural highlights
DiseasePLOD3_HUMAN Connective tissue disorder due to lysyl hydroxylase-3 deficiency. The disease is caused by mutations affecting the gene represented in this entry. FunctionPLOD3_HUMAN Forms hydroxylysine residues in -Xaa-Lys-Gly- sequences in collagens. These hydroxylysines serve as sites of attachment for carbohydrate units and are essential for the stability of the intermolecular collagen cross-links.[UniProtKB:P24802] Contents | ||||||||||||||||||||
This page was last modified 10:19, 22 May 2024.