Fig. 1From: Cellular and molecular mechanisms of aspartoacylase and its role in Canavan diseaseThe ASPA protein structure. The structure of the human ASPA homodimer (PDB: 2O53) [44] is shown with the two subunits in blue and yellow. The N-terminal region covering residues 1–212 (upper panel) and C-terminal region spanning residues 212–313 (lower panel) are highlightedBack to article page