Summary information and primary citation

PDB-id
4b9s; DSSR-derived features in text and JSON formats
Class
transferase-DNA
Method
X-ray (1.73 Å)
Summary
Structure of the high fidelity DNA polymerase i with an oxidative formamidopyrimidine-dg DNA lesion outside of the pre-insertion site.
Reference
Gehrke TH, Lischke U, Gasteiger KL, Schneider S, Arnold S, Muller HC, Stephenson DS, Zipse H, Carell T (2013): "Unexpected Non-Hoogsteen-Based Mutagenicity Mechanism of Fapy-DNA Lesions." Nat.Chem.Biol., 9, 455. doi: 10.1038/NCHEMBIO.1254.
Abstract
8-Oxopurines (8-oxodG and 8-oxodA) and formamidopyrimidines (FaPydG and FaPydA) are major oxidative DNA lesions involved in cancer development and aging. Their mutagenicity is believed to result from a conformational shift of the N9-C1' glycosidic bonds from anti to syn, which allows the lesions to form noncanonical Hoogsteen-type base pairs with incoming triphosphates during DNA replication. Here we present biochemical data and what are to our knowledge the first crystal structures of carbocyclic FaPydA and FaPydG containing DNA in complex with a high-fidelity polymerase. Crystallographic snapshots show that the cFaPy lesions keep the anti geometry of the glycosidic bond during error-free and error-prone replication. The observed dG·dC→dT·dA transversion mutations are the result of base shifting and tautomerization.

Cartoon-block schematics in six views (download the tarball)

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