5IV1

Solution Structure of DNA Dodecamer with 8-oxoguanine at 4th Position

「2N0L」から置き換えられました

5IV1 の概要

• エントリーDOI: 10.2210/pdb5iv1/pdb
• 関連するPDBエントリー: 5IZP
• NMR情報: BMRB: 25528,30038
• 分子名称: DNA (5'-D(*CP*GP*CP*(8OG)P*AP*AP*TP*TP*CP*GP*CP*G)-3') (1 entity in total)
• 機能のキーワード: drew-dickerson, dna, dodecamer, non-canonical, modified dna, oxidized dna, dna damage, dna adduct, lesion
• 由来する生物種: synthetic construct
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 7358.78

構造登録者

Miears, H.L.,Gruber, D.R.,Hoppins, J.J.,Kiryutin, A.S.,Kasymov, R.D.,Yurkovskaya, A.V.,Zharkov, D.O.,Smirnov, S.L. (登録日: 2016-03-18, 公開日: 2016-07-27, 最終更新日: 2024-05-01)

主引用文献

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

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: 27749894
DOI: 10.1371/journal.pone.0164424

実験手法

SOLUTION NMR