8yad | pdb_00008yad

structure of SPG11-SPG15 complex

spinqualitylabelsall models 8yad, resolution 4.02Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 8yad 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 4.02Å Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Disease SPTCS_HUMAN Autosomal recessive Charcot-Marie-Tooth disease type 2X;Juvenile amyotrophic lateral sclerosis;Autosomal recessive spastic paraplegia type 11. 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. The disease is caused by variants affecting the gene represented in this entry. Function SPTCS_HUMAN May play a role in neurite plasticity by maintaining cytoskeleton stability and regulating synaptic vesicle transport.

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