8vlx | pdb_00008vlx

HTT in complex with HAP40 and a small molecule.

spinqualitylabelsall models 8vlx, resolution 2.60Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 8vlx 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 2.6Å Ligands: A1ACS Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Disease HD_HUMAN Juvenile Huntington disease;Huntington disease. The disease is caused by mutations affecting the gene represented in this entry. Function HD_HUMAN May play a role in microtubule-mediated transport or vesicle function.

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