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8J6M

SIDT1 protein

8J6M の概要
エントリーDOI10.2210/pdb8j6m/pdb
EMDBエントリー36008
分子名称Green fluorescent protein,SID1 transmembrane family member 1, CHOLESTEROL, ZINC ION, ... (6 entities in total)
機能のキーワードtransport t1, transcription
由来する生物種Aequorea victoria
詳細
タンパク質・核酸の鎖数2
化学式量合計251901.31
構造登録者
Zhang, J.T.,Jiang, D.H. (登録日: 2023-04-26, 公開日: 2024-05-01, 最終更新日: 2025-07-02)
主引用文献Zhang, J.,Zhan, C.,Fan, J.,Wu, D.,Zhang, R.,Wu, D.,Chen, X.,Lu, Y.,Li, M.,Lin, M.,Gong, J.,Jiang, D.
Structural insights into double-stranded RNA recognition and transport by SID-1.
Nat.Struct.Mol.Biol., 31:1095-1104, 2024
Cited by
PubMed Abstract: RNA uptake by cells is critical for RNA-mediated gene interference (RNAi) and RNA-based therapeutics. In Caenorhabditis elegans, RNAi is systemic as a result of SID-1-mediated double-stranded RNA (dsRNA) across cells. Despite the functional importance, the underlying mechanisms of dsRNA internalization by SID-1 remain elusive. Here we describe cryogenic electron microscopy structures of SID-1, SID-1-dsRNA complex and human SID-1 homologs SIDT1 and SIDT2, elucidating the structural basis of dsRNA recognition and import by SID-1. The homodimeric SID-1 homologs share conserved architecture, but only SID-1 possesses the molecular determinants within its extracellular domains for distinguishing dsRNA from single-stranded RNA and DNA. We show that the removal of the long intracellular loop between transmembrane helix 1 and 2 attenuates dsRNA uptake and systemic RNAi in vivo, suggesting a possible endocytic mechanism of SID-1-mediated dsRNA internalization. Our study provides mechanistic insights into dsRNA internalization by SID-1, which may facilitate the development of dsRNA applications based on SID-1.
PubMed: 38664565
DOI: 10.1038/s41594-024-01276-9
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (2.77 Å)
構造検証レポート
Validation report summary of 8j6m
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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