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9GEK

Structure of the FAST1-FAST2-RAP module from human FASTKD4 by carrier-driven crystallisation with maltose binding protein from E. coli.

9GEK の概要
エントリーDOI10.2210/pdb9gek/pdb
分子名称Maltose/maltodextrin-binding periplasmic protein,FAST kinase domain-containing protein 4,FAST kinase domain-containing protein 4, 3,6,9,12,15,18-HEXAOXAICOSANE-1,20-DIOL, PHOSPHATE ION, ... (6 entities in total)
機能のキーワードmitochondrial rna splicing, rna stability, rna binding, mitochondrial disease, rna binding protein
由来する生物種Homo sapiens (human)
詳細
タンパク質・核酸の鎖数1
化学式量合計81252.29
構造登録者
Hothorn, M.,Lau, K.,Yang, X. (登録日: 2024-08-07, 公開日: 2025-01-15, 最終更新日: 2025-03-19)
主引用文献Yang, X.,Stentenbach, M.,Hughes, L.A.,Siira, S.J.,Lau, K.,Hothorn, M.,Martinou, J.C.,Rackham, O.,Filipovska, A.
The Vsr-like protein FASTKD4 regulates the stability and polyadenylation of the MT-ND3 mRNA.
Nucleic Acids Res., 53:-, 2025
Cited by
PubMed Abstract: Expression of the compact mitochondrial genome is regulated by nuclear encoded, mitochondrially localized RNA-binding proteins (RBPs). RBPs regulate the lifecycles of mitochondrial RNAs from transcription to degradation by mediating RNA processing, maturation, stability and translation. The Fas-activated serine/threonine kinase (FASTK) family of RBPs has been shown to regulate and fine-tune discrete aspects of mitochondrial gene expression. Although the roles of specific targets of FASTK proteins have been elucidated, the molecular mechanisms of FASTK proteins in mitochondrial RNA metabolism remain unclear. Therefore, we resolved the structure of FASTKD4 at atomic level that includes the RAP domain and the two FAST motifs, creating a positively charged cavity resembling that of the very short patch repair endonuclease. Our biochemical studies show that FASTKD4 binds the canonical poly(A) tail of MT-ND3 enabling its maturation and translation. The in vitro role of FASTKD4 is consistent with its loss in cells that results in decreased MT-ND3 polyadenylation, which destabilizes this messenger RNA in mitochondria.
PubMed: 39727163
DOI: 10.1093/nar/gkae1261
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.15 Å)
構造検証レポート
Validation report summary of 9gek
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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