6ES4
A cryptic RNA-binding domain mediates Syncrip recognition and exosomal partitioning of miRNA targets
6ES4 の概要
| エントリーDOI | 10.2210/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 | 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. (登録日: 2017-10-19, 公開日: 2018-03-07, 最終更新日: 2024-10-23) |
| 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: 29483512DOI: 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
検証レポート(詳細版)
をダウンロード






