1U48
Extension of a cytosine-8-oxoguanine base pair
Summary for 1U48
| Entry DOI | 10.2210/pdb1u48/pdb |
| Related | 1U45 1U47 1U49 1U4B |
| Related PRD ID | PRD_900003 |
| Descriptor | DNA primer strand, DNA template strand with 8-oxoguanine, DNA polymerase I, ... (7 entities in total) |
| Functional Keywords | dna polymerase i; dna replication; klenow fragment; protein-dna complex; 8oxoguanine; dna lesion; translation replication, transferase-dna complex, transferase/dna |
| Biological source | Geobacillus stearothermophilus |
| Total number of polymer chains | 3 |
| Total formula weight | 75018.90 |
| Authors | Hsu, G.W.,Ober, M.,Carell, T.,Beese, L.S. (deposition date: 2004-07-23, release date: 2004-09-14, Last modification date: 2023-08-23) |
| Primary citation | Hsu, G.W.,Ober, M.,Carell, T.,Beese, L.S. Error-prone replication of oxidatively damaged DNA by a high-fidelity DNA polymerase. Nature, 431:217-221, 2004 Cited by PubMed Abstract: Aerobic respiration generates reactive oxygen species that can damage guanine residues and lead to the production of 8-oxoguanine (8oxoG), the major mutagenic oxidative lesion in the genome. Oxidative damage is implicated in ageing and cancer, and its prevalence presents a constant challenge to DNA polymerases that ensure accurate transmission of genomic information. When these polymerases encounter 8oxoG, they frequently catalyse misincorporation of adenine in preference to accurate incorporation of cytosine. This results in the propagation of G to T transversions, which are commonly observed somatic mutations associated with human cancers. Here, we present sequential snapshots of a high-fidelity DNA polymerase during both accurate and mutagenic replication of 8oxoG. Comparison of these crystal structures reveals that 8oxoG induces an inversion of the mismatch recognition mechanisms that normally proofread DNA, such that the 8oxoG.adenine mismatch mimics a cognate base pair whereas the 8oxoG.cytosine base pair behaves as a mismatch. These studies reveal a fundamental mechanism of error-prone replication and show how 8oxoG, and DNA lesions in general, can form mismatches that evade polymerase error-detection mechanisms, potentially leading to the stable incorporation of lethal mutations. PubMed: 15322558DOI: 10.1038/nature02908 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (2.1 Å) |
Structure validation
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