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. Author manuscript; available in PMC: 2018 Sep 21.
Published in final edited form as: Cell Chem Biol. 2017 Sep 21;24(9):1161–1180. doi: 10.1016/j.chembiol.2017.08.028

Figure 4. Mutant IDH.

Figure 4

(A) The reaction catalyzed by wild-type IDH is the decarboxylation of isocitrate to α-ketoglutarate. (B) The reaction catalyzed by mutant IDH1 and IDH2 is the reduction of α-ketoglutarate to D-2-hydroxyglutarate. (C) Structures of AG-120 (ivosidenib) and AG-221 (enasidenib), which inhibit mutant IDH1 and IDH2 respectively.