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6CCW

Hybrid-2 form Human Telomeric G Quadruplex in Complex with Epiberberine

6CCW の概要
エントリーDOI10.2210/pdb6ccw/pdb
NMR情報BMRB: 30402
分子名称DNA (26-MER), Epiberberine (2 entities in total)
機能のキーワードg-quadruplex, complex, telomere, dna
由来する生物種Homo sapiens (Human)
タンパク質・核酸の鎖数1
化学式量合計8536.63
構造登録者
Lin, C.,Yang, D.Z. (登録日: 2018-02-07, 公開日: 2018-06-20, 最終更新日: 2024-05-15)
主引用文献Lin, C.,Wu, G.,Wang, K.,Onel, B.,Sakai, S.,Shao, Y.,Yang, D.
Molecular Recognition of the Hybrid-2 Human Telomeric G-Quadruplex by Epiberberine: Insights into Conversion of Telomeric G-Quadruplex Structures.
Angew. Chem. Int. Ed. Engl., 57:10888-10893, 2018
Cited by
PubMed Abstract: Human telomeres can form DNA G-quadruplex (G4), an attractive target for anticancer drugs. Human telomeric G4s bear inherent structure polymorphism, challenging for understanding specific recognition by ligands or proteins. Protoberberines are medicinal natural-products known to stabilize telomeric G4s and inhibit telomerase. Here we report epiberberine (EPI) specifically recognizes the hybrid-2 telomeric G4 predominant in physiologically relevant K solution and converts other telomeric G4 forms to hybrid-2, the first such example reported. Our NMR structure in K solution shows EPI binding induces extensive rearrangement of the previously disordered 5'-flanking and loop segments to form an unprecedented four-layer binding pocket specific to the hybrid-2 telomeric G4; EPI recruits the (-1) adenine to form a "quasi-triad" intercalated between the external tetrad and a T:T:A triad, capped by a T:T base pair. Our study provides structural basis for small-molecule drug design targeting the human telomeric G4.
PubMed: 29888501
DOI: 10.1002/anie.201804667
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 6ccw
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2026-04-22に公開中

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