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6J80

Human mitochondrial Oligoribonuclease in complex with poly-dT DNA

6J80 の概要
エントリーDOI10.2210/pdb6j80/pdb
分子名称Oligoribonuclease, mitochondrial, DNA (5'-D(P*TP*TP*TP*TP*TP*TP*T)-3'), CITRIC ACID, ... (5 entities in total)
機能のキーワードexoribonuclease, mitochonrial oligoribonuclease, hydrolase, hydrolase-dna complex, hydrolase/dna
由来する生物種Homo sapiens (Human)
詳細
タンパク質・核酸の鎖数3
化学式量合計44229.24
構造登録者
Chu, L.Y.,Agrawal, S.,Yuan, H.S. (登録日: 2019-01-18, 公開日: 2019-08-28, 最終更新日: 2023-11-22)
主引用文献Chu, L.Y.,Agrawal, S.,Chen, Y.P.,Yang, W.Z.,Yuan, H.S.
Structural insights into nanoRNA degradation by human Rexo2.
Rna, 25:737-746, 2019
Cited by
PubMed Abstract: Human RNA exoribonuclease 2 (Rexo2) is an evolutionarily conserved 3'-to-5' DEDDh-family exonuclease located primarily in mitochondria. Rexo2 degrades small RNA oligonucleotides of <5 nucleotides (nanoRNA) in a way similar to Oligoribonuclease (ORN), suggesting that it plays a role in RNA turnover in mitochondria. However, how Rexo2 preferentially binds and degrades nanoRNA remains elusive. Here, we show that Rexo2 binds small RNA and DNA oligonucleotides with the highest affinity, and it is most robust in degrading small nanoRNA into mononucleotides in the presence of magnesium ions. We further determined three crystal structures of Rexo2 in complex with single-stranded RNA or DNA at resolutions of 1.8-2.2 Å. Rexo2 forms a homodimer and interacts mainly with the last two 3'-end nucleobases of substrates by hydrophobic and π-π stacking interactions via Leu53, Trp96, and Tyr164, signifying its preference in binding and degrading short oligonucleotides without sequence specificity. Crystal structure of Rexo2 is highly similar to that of the RNA-degrading enzyme ORN, revealing a two-magnesium-ion-dependent hydrolysis mechanism. This study thus provides the molecular basis for human Rexo2, showing how it binds and degrades nanoRNA into nucleoside monophosphates and plays a crucial role in RNA salvage pathways in mammalian mitochondria.
PubMed: 30926754
DOI: 10.1261/rna.070557.119
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.812 Å)
構造検証レポート
Validation report summary of 6j80
検証レポート(詳細版)ダウンロードをダウンロード

246905

件を2025-12-31に公開中

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