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4B9S

Structure of the high fidelity DNA polymerase I with an oxidative formamidopyrimidine-dG DNA lesion outside of the pre-insertion site.

Summary for 4B9S
Entry DOI10.2210/pdb4b9s/pdb
Related2XO7 2XY5 2XY6 2XY7 2Y1I 2Y1J 4B9L 4B9M 4B9N 4B9T 4B9U 4B9V
Related PRD IDPRD_900003
DescriptorDNA POLYMERASE, 5'-D(*AP*CP*CP*TP*GP*AP*CP*TP*CP*TP)-3', 5'-D(*CP*AP*TP*FOXP*AP*GP*AP*GP*TP*CP*AP*GP*GP*TP*TP)-3', ... (7 entities in total)
Functional Keywordstransferase-dna complex, oxidative dna lesion, dna damage, translesion dna synthesis, replication, transferase/dna
Biological sourceGEOBACILLUS STEAROTHERMOPHILUS
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Total number of polymer chains3
Total formula weight78938.55
Authors
Gehrke, T.H.,Lischke, U.,Arnold, S.,Schneider, S.,Carell, T. (deposition date: 2012-09-06, release date: 2013-04-17, Last modification date: 2023-12-20)
Primary citationGehrke, T.H.,Lischke, U.,Gasteiger, K.L.,Schneider, S.,Arnold, S.,Muller, H.C.,Stephenson, D.S.,Zipse, H.,Carell, T.
Unexpected Non-Hoogsteen-Based Mutagenicity Mechanism of Fapy-DNA Lesions.
Nat.Chem.Biol., 9:455-, 2013
Cited by
PubMed 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.
PubMed: 23685671
DOI: 10.1038/NCHEMBIO.1254
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.73 Å)
Structure validation

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