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5NPG

Solution structure of Drosophila melanogaster Loquacious dsRBD1

5NPG の概要
エントリーDOI10.2210/pdb5npg/pdb
NMR情報BMRB: 34124
分子名称Loquacious, isoform F (1 entity in total)
機能のキーワードdsrbd, rna interference, sirna, rna binding protein
由来する生物種Drosophila melanogaster (Fruit fly)
タンパク質・核酸の鎖数1
化学式量合計9105.57
構造登録者
主引用文献Tants, J.N.,Fesser, S.,Kern, T.,Stehle, R.,Geerlof, A.,Wunderlich, C.,Juen, M.,Hartlmuller, C.,Bottcher, R.,Kunzelmann, S.,Lange, O.,Kreutz, C.,Forstemann, K.,Sattler, M.
Molecular basis for asymmetry sensing of siRNAs by the Drosophila Loqs-PD/Dcr-2 complex in RNA interference.
Nucleic Acids Res., 45:12536-12550, 2017
Cited by
PubMed Abstract: RNA interference defends against RNA viruses and retro-elements within an organism's genome. It is triggered by duplex siRNAs, of which one strand is selected to confer sequence-specificity to the RNA induced silencing complex (RISC). In Drosophila, Dicer-2 (Dcr-2) and the double-stranded RNA binding domain (dsRBD) protein R2D2 form the RISC loading complex (RLC) and select one strand of exogenous siRNAs according to the relative thermodynamic stability of base-pairing at either end. Through genome editing we demonstrate that Loqs-PD, the Drosophila homolog of human TAR RNA binding protein (TRBP) and a paralog of R2D2, forms an alternative RLC with Dcr-2 that is required for strand choice of endogenous siRNAs in S2 cells. Two canonical dsRBDs in Loqs-PD bind to siRNAs with enhanced affinity compared to miRNA/miRNA* duplexes. Structural analysis, NMR and biophysical experiments indicate that the Loqs-PD dsRBDs can slide along the RNA duplex to the ends of the siRNA. A moderate but notable binding preference for the thermodynamically more stable siRNA end by Loqs-PD alone is greatly amplified in complex with Dcr-2 to initiate strand discrimination by asymmetry sensing in the RLC.
PubMed: 29040648
DOI: 10.1093/nar/gkx886
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 5npg
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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