8s7a

HSPB8acd-C99S/F155T/A156S

spinqualitylabelsall models 8s7a, resolution 1.95Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 8s7a 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 1.951Å Ligands: GOL, SO4 Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Disease HSPB8_HUMAN Autosomal dominant distal axonal motor neuropathy-myofibrillar myopathy syndrome;Autosomal dominant Charcot-Marie-Tooth disease type 2L;Distal hereditary motor neuropathy type 2. The disease is caused by variants affecting the gene represented in this entry. The disease is caused by variants affecting the gene represented in this entry. Function HSPB8_HUMAN Displays temperature-dependent chaperone activity.

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