7NZ8

Crystal structure of mouse ADAT2/ADAT3 tRNA deamination complex 2

7NZ8 の概要

• エントリーDOI: 10.2210/pdb7nz8/pdb
• 分子名称: tRNA-specific adenosine deaminase 2, Probable inactive tRNA-specific adenosine deaminase-like protein 3, ZINC ION, ... (4 entities in total)
• 機能のキーワード: trna modification, wobble adenine, inosine, adat, intellectual disability, neurological disorders, hydrolase
• 由来する生物種: Mus musculus (Mouse); 詳細
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 55688.21

構造登録者

Ramos Morales, E.,Romier, C. (登録日: 2021-03-23, 公開日: 2021-05-05, 最終更新日: 2024-01-31)

主引用文献

Ramos-Morales, E.,Bayam, E.,Del-Pozo-Rodriguez, J.,Salinas-Giege, T.,Marek, M.,Tilly, P.,Wolff, P.,Troesch, E.,Ennifar, E.,Drouard, L.,Godin, J.D.,Romier, C.
The structure of the mouse ADAT2/ADAT3 complex reveals the molecular basis for mammalian tRNA wobble adenosine-to-inosine deamination.
Nucleic Acids Res., 49:6529-6548, 2021

PubMed Abstract: Post-transcriptional modification of tRNA wobble adenosine into inosine is crucial for decoding multiple mRNA codons by a single tRNA. The eukaryotic wobble adenosine-to-inosine modification is catalysed by the ADAT (ADAT2/ADAT3) complex that modifies up to eight tRNAs, requiring a full tRNA for activity. Yet, ADAT catalytic mechanism and its implication in neurodevelopmental disorders remain poorly understood. Here, we have characterized mouse ADAT and provide the molecular basis for tRNAs deamination by ADAT2 as well as ADAT3 inactivation by loss of catalytic and tRNA-binding determinants. We show that tRNA binding and deamination can vary depending on the cognate tRNA but absolutely rely on the eukaryote-specific ADAT3 N-terminal domain. This domain can rotate with respect to the ADAT catalytic domain to present and position the tRNA anticodon-stem-loop correctly in ADAT2 active site. A founder mutation in the ADAT3 N-terminal domain, which causes intellectual disability, does not affect tRNA binding despite the structural changes it induces but most likely hinders optimal presentation of the tRNA anticodon-stem-loop to ADAT2.

PubMed: 34057470
DOI: 10.1093/nar/gkab436

実験手法

X-RAY DIFFRACTION (2.12 Å)