2MS1
Solution NMR structure of tRNApro:MLV Nucleocapsid Protein (1:1) Complex
2MS1 の概要
エントリーDOI | 10.2210/pdb2ms1/pdb |
関連するPDBエントリー | 2MQT 2MQV 2MS0 |
NMR情報 | BMRB: 25101 |
分子名称 | Nucleocapsid protein p10, tRNApro, ZINC ION (3 entities in total) |
機能のキーワード | rna/protein, viral protein-rna complex, retroviral primer annealing, nucleocapsid chaperone, viral protein/rna |
由来する生物種 | Murine leukemia virus 詳細 |
細胞内の位置 | Gag-Pol polyprotein: Host cell membrane ; Lipid-anchor . Matrix protein p15: Virion . Capsid protein p30: Virion . Nucleocapsid protein p10: Virion : P03355 |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 29387.22 |
構造登録者 | |
主引用文献 | Miller, S.B.,Yildiz, F.Z.,Lo, J.A.,Wang, B.,D'Souza, V.M. A structure-based mechanism for tRNA and retroviral RNA remodelling during primer annealing. Nature, 515:591-595, 2014 Cited by PubMed Abstract: To prime reverse transcription, retroviruses require annealing of a transfer RNA molecule to the U5 primer binding site (U5-PBS) region of the viral genome. The residues essential for primer annealing are initially locked in intramolecular interactions; hence, annealing requires the chaperone activity of the retroviral nucleocapsid (NC) protein to facilitate structural rearrangements. Here we show that, unlike classical chaperones, the Moloney murine leukaemia virus NC uses a unique mechanism for remodelling: it specifically targets multiple structured regions in both the U5-PBS and tRNA(Pro) primer that otherwise sequester residues necessary for annealing. This high-specificity and high-affinity binding by NC consequently liberates these sequestered residues--which are exactly complementary--for intermolecular interactions. Furthermore, NC utilizes a step-wise, entropy-driven mechanism to trigger both residue-specific destabilization and residue-specific release. Our structures of NC bound to U5-PBS and tRNA(Pro) reveal the structure-based mechanism for retroviral primer annealing and provide insights as to how ATP-independent chaperones can target specific RNAs amidst the cellular milieu of non-target RNAs. PubMed: 25209668DOI: 10.1038/nature13709 主引用文献が同じPDBエントリー |
実験手法 | SOLUTION NMR |
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