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. 2015 Apr 17;1(1):e4. doi: 10.1212/01.NXG.0000464295.65736.da

Figure 1. DNM1 mutations and structure.

Figure 1

(A) Structure-based domain architecture of human DNM1. The A177P and K206N mutations occur in the G domain and the G359A mutation occurs in the middle domain. The location of the mouse Dnm1Ftfl (A408T) mutation is indicated above the middle domain. (B) Positions of the amino acid substitutions in the DNM1 crystal structure, shown as a ribbon-type representation.