6G3X
Native Structure of the mouse 8-oxoguanine DNA Glycosylase mOGG1
6G3X の概要
エントリーDOI | 10.2210/pdb6g3x/pdb |
分子名称 | N-glycosylase/DNA lyase, NICKEL (II) ION (3 entities in total) |
機能のキーワード | n-glycosylase, dna lyase, dna binding protein |
由来する生物種 | Mus musculus (Mouse) |
タンパク質・核酸の鎖数 | 3 |
化学式量合計 | 107508.65 |
構造登録者 | |
主引用文献 | Visnes, T.,Cazares-Korner, A.,Hao, W.,Wallner, O.,Masuyer, G.,Loseva, O.,Mortusewicz, O.,Wiita, E.,Sarno, A.,Manoilov, A.,Astorga-Wells, J.,Jemth, A.S.,Pan, L.,Sanjiv, K.,Karsten, S.,Gokturk, C.,Grube, M.,Homan, E.J.,Hanna, B.M.F.,Paulin, C.B.J.,Pham, T.,Rasti, A.,Berglund, U.W.,von Nicolai, C.,Benitez-Buelga, C.,Koolmeister, T.,Ivanic, D.,Iliev, P.,Scobie, M.,Krokan, H.E.,Baranczewski, P.,Artursson, P.,Altun, M.,Jensen, A.J.,Kalderen, C.,Ba, X.,Zubarev, R.A.,Stenmark, P.,Boldogh, I.,Helleday, T. Small-molecule inhibitor of OGG1 suppresses proinflammatory gene expression and inflammation. Science, 362:834-839, 2018 Cited by PubMed Abstract: The onset of inflammation is associated with reactive oxygen species and oxidative damage to macromolecules like 7,8-dihydro-8-oxoguanine (8-oxoG) in DNA. Because 8-oxoguanine DNA glycosylase 1 (OGG1) binds 8-oxoG and because -deficient mice are resistant to acute and systemic inflammation, we hypothesized that OGG1 inhibition may represent a strategy for the prevention and treatment of inflammation. We developed TH5487, a selective active-site inhibitor of OGG1, which hampers OGG1 binding to and repair of 8-oxoG and which is well tolerated by mice. TH5487 prevents tumor necrosis factor-α-induced OGG1-DNA interactions at guanine-rich promoters of proinflammatory genes. This, in turn, decreases DNA occupancy of nuclear factor κB and proinflammatory gene expression, resulting in decreased immune cell recruitment to mouse lungs. Thus, we present a proof of concept that targeting oxidative DNA repair can alleviate inflammatory conditions in vivo. PubMed: 30442810DOI: 10.1126/science.aar8048 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.1 Å) |
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