9b6c

Human asparagine synthetase Arg-142 to Ile-142 (R142I) variant

spinqualitylabelsall models 9b6c, resolution 3.35Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 9b6c 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 3.35Å Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Disease ASNS_HUMAN Congenital microcephaly-severe encephalopathy-progressive cerebral atrophy syndrome. The disease is caused by mutations affecting the gene represented in this entry. Function ASNS_HUMAN

Proteopedia Page Contributors and Editors (what is this?)

OCA