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2MS6

Human Telomeric G-quadruplex DNA sequence (TTAGGGT)4 complexed with Flavonoid Quercetin

2MS6 の概要
エントリーDOI10.2210/pdb2ms6/pdb
関連するPDBエントリー2MS5
NMR情報BMRB: 25107
分子名称DNA_(5'-D(*TP*TP*AP*GP*GP*GP*T)-3'), 3,5,7,3',4'-PENTAHYDROXYFLAVONE (2 entities in total)
機能のキーワードdna g-quadruplex, quercetin, telomeric sequence, dna
由来する生物種synthetic construct
タンパク質・核酸の鎖数4
化学式量合計9278.25
構造登録者
Kumar, A.,Tawani, A. (登録日: 2014-07-24, 公開日: 2015-01-28, 最終更新日: 2024-05-01)
主引用文献Tawani, A.,Kumar, A.
Structural Insight into the interaction of Flavonoids with Human Telomeric Sequence
Sci Rep, 5:17574-17574, 2015
Cited by
PubMed Abstract: Flavonoids are a group of naturally available compounds that are an attractive source for drug discovery. Their potential to act as anti-tumourigenic and anti-proliferative agents has been reported previously but is not yet fully understood. Targeting human telomeric G-quadruplex DNA could be one of the mechanisms by which these flavonoids exert anticancer activity. We have performed detailed biophysical studies for the interaction of four representative flavonoids, Luteolin, Quercetin, Rutin and Genistein, with the human telomeric G-quadruplex sequence tetramolecular d-(T2AG3T) (Tel7). In addition, we used NMR spectroscopy to derive the first model for the complex formed between Quercetin and G-quadruplex sequence. The model showed that Quercetin stabilises the G-quadruplex structure and does not open the G-tetrad. It interacts with the telomeric sequence through π-stacking at two sites: between T1pT2 and between G6pT7. Based on our findings, we suggest that Quercetin could be a potent candidate for targeting the telomere and thus, act as a potent anti-cancer agent.
PubMed: 26627543
DOI: 10.1038/srep17574
主引用文献が同じPDBエントリー
実験手法
SOLUTION NMR
構造検証レポート
Validation report summary of 2ms6
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2026-01-28に公開中

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