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6ES4

A cryptic RNA-binding domain mediates Syncrip recognition and exosomal partitioning of miRNA targets

6ES4 の概要
エントリーDOI10.2210/pdb6es4/pdb
分子名称Syncrip, isoform K, SULFATE ION, 1,2-ETHANEDIOL, ... (4 entities in total)
機能のキーワードmirna, exosome, syncrip, rna-binding, rna
由来する生物種Drosophila melanogaster (Fruit fly)
タンパク質・核酸の鎖数2
化学式量合計50675.56
構造登録者
主引用文献Hobor, F.,Dallmann, A.,Ball, N.J.,Cicchini, C.,Battistelli, C.,Ogrodowicz, R.W.,Christodoulou, E.,Martin, S.R.,Castello, A.,Tripodi, M.,Taylor, I.A.,Ramos, A.
A cryptic RNA-binding domain mediates Syncrip recognition and exosomal partitioning of miRNA targets.
Nat Commun, 9:831-831, 2018
Cited by
PubMed Abstract: Exosomal miRNA transfer is a mechanism for cell-cell communication that is important in the immune response, in the functioning of the nervous system and in cancer. Syncrip/hnRNPQ is a highly conserved RNA-binding protein that mediates the exosomal partition of a set of miRNAs. Here, we report that Syncrip's amino-terminal domain, which was previously thought to mediate protein-protein interactions, is a cryptic, conserved and sequence-specific RNA-binding domain, designated NURR (N-terminal unit for RNA recognition). The NURR domain mediates the specific recognition of a short hEXO sequence defining Syncrip exosomal miRNA targets, and is coupled by a non-canonical structural element to Syncrip's RRM domains to achieve high-affinity miRNA binding. As a consequence, Syncrip-mediated selection of the target miRNAs implies both recognition of the hEXO sequence by the NURR domain and binding of the RRM domains 5' to this sequence. This structural arrangement enables Syncrip-mediated selection of miRNAs with different seed sequences.
PubMed: 29483512
DOI: 10.1038/s41467-018-03182-3
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.2 Å)
構造検証レポート
Validation report summary of 6es4
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2026-02-04に公開中

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