6wfv | pdb_00006wfv

The crystal structure of a collagen galactosylhydroxylysyl glucosyltransferase from human

spinqualitylabelsall models 6wfv, resolution 1.70Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 6wfv is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Method: X-ray diffraction, Resolution 1.7Å Ligands: MG, MN, TRS, UDP Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Disease PLOD3_HUMAN Connective tissue disorder due to lysyl hydroxylase-3 deficiency. The disease is caused by mutations affecting the gene represented in this entry. Function PLOD3_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]

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