8cvx | pdb_00008cvx

Human glycogenin-1 and glycogen synthase-1 complex in the presence of glucose-6-phosphate

spinqualitylabelsall models 8cvx, resolution 3.50Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 8cvx is a 8 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Ligands: G6P Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Disease [GYS1_HUMAN] Glycogen storage disease due to muscle and heart glycogen synthase deficiency. The disease is caused by variants affecting the gene represented in this entry. Function [GYS1_HUMAN] Transfers the glycosyl residue from UDP-Glc to the non-reducing end of alpha-1,4-glucan.[UniProtKB:P13834]

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