9yg5 | pdb_00009yg5

VPS13A/Ct-XKR1

spinqualitylabelsall models 9yg5, resolution 3.41Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 9yg5 is a 2 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: Electron Microscopy, Resolution 3.41Å Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Disease XK_HUMAN McLeod neuroacanthocytosis syndrome. The disease is caused by variants affecting the gene represented in this entry. Function XK_HUMAN Recruits the lipid transfer protein VPS13A from lipid droplets to the endoplasmic reticulum (ER) membrane.

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