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3O1V

Iron-Catalyzed Oxidation Intermediates Captured in A DNA Repair Dioxygenase

3O1V の概要
エントリーDOI10.2210/pdb3o1v/pdb
関連するPDBエントリー3O1M 3O1O 3O1P 3O1R 3O1S 3O1T 3O1U
分子名称Alpha-ketoglutarate-dependent dioxygenase AlkB, DNA (5'-D(*AP*GP*GP*TP*AP*AP*(MDJ)P*AP*CP*CP*GP*T)-3'), DNA (5'-D(*AP*AP*CP*GP*GP*TP*AP*TP*TP*AP*CP*CP*T)-3'), ... (6 entities in total)
機能のキーワードdemethylase, oxidoreductase
由来する生物種Escherichia coli
詳細
タンパク質・核酸の鎖数3
化学式量合計30846.41
構造登録者
Yi, C.,Jia, G.,Hou, G.,Dai, Q.,Zhang, W.,Zheng, G.,Jian, X.,Yang, C.-G.,Cui, Q.,He, C. (登録日: 2010-07-22, 公開日: 2010-11-17, 最終更新日: 2024-10-30)
主引用文献Yi, C.,Jia, G.,Hou, G.,Dai, Q.,Zhang, W.,Zheng, G.,Jian, X.,Yang, C.G.,Cui, Q.,He, C.
Iron-catalysed oxidation intermediates captured in a DNA repair dioxygenase.
Nature, 468:330-333, 2010
Cited by
PubMed Abstract: Mononuclear iron-containing oxygenases conduct a diverse variety of oxidation functions in biology, including the oxidative demethylation of methylated nucleic acids and histones. Escherichia coli AlkB is the first such enzyme that was discovered to repair methylated nucleic acids, which are otherwise cytotoxic and/or mutagenic. AlkB human homologues are known to play pivotal roles in various processes. Here we present structural characterization of oxidation intermediates for these demethylases. Using a chemical cross-linking strategy, complexes of AlkB-double stranded DNA (dsDNA) containing 1,N(6)-etheno adenine (εA), N(3)-methyl thymine (3-meT) and N(3)-methyl cytosine (3-meC) are stabilized and crystallized, respectively. Exposing these crystals, grown under anaerobic conditions containing iron(II) and α-ketoglutarate (αKG), to dioxygen initiates oxidation in crystallo. Glycol (from εA) and hemiaminal (from 3-meT) intermediates are captured; a zwitterionic intermediate (from 3-meC) is also proposed, based on crystallographic observations and computational analysis. The observation of these unprecedented intermediates provides direct support for the oxidative demethylation mechanism for these demethylases. This study also depicts a general mechanistic view of how a methyl group is oxidatively removed from different biological substrates.
PubMed: 21068844
DOI: 10.1038/nature09497
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.9 Å)
構造検証レポート
Validation report summary of 3o1v
検証レポート(詳細版)ダウンロードをダウンロード

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件を2025-06-18に公開中

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