5IZP
Solution Structure of DNA Dodecamer with 8-oxoguanine at 10th Position
Summary for 5IZP
Entry DOI | 10.2210/pdb5izp/pdb |
Related | 5IV1 |
NMR Information | BMRB: 30044 |
Descriptor | DNA (5'-D(*CP*GP*CP*GP*AP*AP*TP*TP*CP*(8OG)P*CP*G)-3') (1 entity in total) |
Functional Keywords | drew-dickerson, dna, dodecamer, non-canonical, modified dna, oxidized dna, dna damage, dna adduct, lesion |
Biological source | synthetic construct |
Total number of polymer chains | 2 |
Total formula weight | 7358.78 |
Authors | Gruber, D.R.,Hoppins, J.J.,Miears, H.L.,Kiryutin, A.S.,Kasymov, R.D.,Yurkovskaya, A.V.,Zharkov, D.O.,Smirnov, S.L. (deposition date: 2016-03-25, release date: 2016-08-03, Last modification date: 2024-05-01) |
Primary citation | Hoppins, J.J.,Gruber, D.R.,Miears, H.L.,Kiryutin, A.S.,Kasymov, R.D.,Petrova, D.V.,Endutkin, A.V.,Popov, A.V.,Yurkovskaya, A.V.,Fedechkin, S.O.,Brockerman, J.A.,Zharkov, D.O.,Smirnov, S.L. 8-Oxoguanine Affects DNA Backbone Conformation in the EcoRI Recognition Site and Inhibits Its Cleavage by the Enzyme. Plos One, 11:e0164424-e0164424, 2016 Cited by PubMed Abstract: 8-oxoguanine is one of the most abundant and impactful oxidative DNA lesions. However, the reasons underlying its effects, especially those not directly explained by the altered base pairing ability, are poorly understood. We report the effect of the lesion on the action of EcoRI, a widely used restriction endonuclease. Introduction of 8-oxoguanine inside, or adjacent to, the GAATTC recognition site embedded within the Drew-Dickerson dodecamer sequence notably reduced the EcoRI activity. Solution NMR revealed that 8-oxoguanine in the DNA duplex causes substantial alterations in the sugar-phosphate backbone conformation, inducing a BI→BII transition. Moreover, molecular dynamics of the complex suggested that 8-oxoguanine, although does not disrupt the sequence-specific contacts formed by the enzyme with DNA, shifts the distribution of BI/BII backbone conformers. Based on our data, we propose that the disruption of enzymatic cleavage can be linked with the altered backbone conformation and dynamics in the free oxidized DNA substrate and, possibly, at the protein-DNA interface. PubMed: 27749894DOI: 10.1371/journal.pone.0164424 PDB entries with the same primary citation |
Experimental method | SOLUTION NMR |
Structure validation
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