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. Author manuscript; available in PMC: 2020 Sep 1.
Published in final edited form as: Trends Biochem Sci. 2019 May 9;44(9):765–781. doi: 10.1016/j.tibs.2019.04.006

Figure I. Base Excision by DNA Glycosylases.

Figure I.

(A) Putative mechanism of glycosidic bond cleavage. Addition of a water molecule or an amine group to the oxocarbenium intermediate would produce an AP site or an iminium crosslink, respectively. (B) Key catalytic residues required for base excision. Carboxylate (aspartate/glutamate) and carboxamide (asparagine/glutamine) functional groups are depicted both as lowest-energy resonance forms (left) and as resonance hybrids (right).