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6VAR

61 nt human Hepatitis B virus epsilon pre-genomic RNA

6VAR の概要
エントリーDOI10.2210/pdb6var/pdb
NMR情報BMRB: 30701
分子名称RNA (61-MER) (1 entity in total)
機能のキーワードnon-coding rna, viral rna, rna
由来する生物種Hepatitis B virus
タンパク質・核酸の鎖数1
化学式量合計19541.49
構造登録者
主引用文献LeBlanc, R.M.,Kasprzak, W.K.,Longhini, A.P.,Olenginski, L.T.,Abulwerdi, F.,Ginocchio, S.,Shields, B.,Nyman, J.,Svirydava, M.,Del Vecchio, C.,Ivanic, J.,Schneekloth Jr., J.S.,Shapiro, B.A.,Dayie, T.K.,Le Grice, S.F.J.
Structural insights of the conserved "priming loop" of hepatitis B virus pre-genomic RNA.
J.Biomol.Struct.Dyn., :1-13, 2021
Cited by
PubMed Abstract: Initiation of protein-primed (-) strand DNA synthesis in hepatitis B virus (HBV) requires interaction of the viral polymerase with a -acting regulatory signal, designated epsilon (ε), located at the 5'-end of its pre-genomic RNA (pgRNA). Binding of polymerase to ε is also necessary for pgRNA encapsidation. While the mechanistic basis of this interaction remains elusive, mutagenesis studies suggest its internal 6-nt "priming loop" provides an important structural contribution. ε might therefore be considered a promising target for small molecule interventions to complement current nucleoside-analog based anti-HBV therapies. An ideal prerequisite to any RNA-directed small molecule strategy would be a detailed structural description of this important element. Herein, we present a solution NMR structure for HBV ε which, in combination with molecular dynamics and docking simulations, reports on a flexible ligand "pocket", reminiscent of those observed in proteins. We also demonstrate the binding of the selective estrogen receptor modulators (SERMs) Raloxifene, Bazedoxifene, and a derivative to the priming loop.Communicated by Ramaswamy H. Sarma.
PubMed: 34155954
DOI: 10.1080/07391102.2021.1934544
主引用文献が同じPDBエントリー
実験手法
SOLUTION NMR
SOLUTION SCATTERING
構造検証レポート
Validation report summary of 6var
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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