1SYZ
Solution structure of the S. Cerevisiae U6 intramolecular stem loop (ISL) RNA at pH 5.7
1SYZ の概要
エントリーDOI | 10.2210/pdb1syz/pdb |
関連するPDBエントリー | 1LC6 1NC0 1NZ1 1sy4 1sy5 |
分子名称 | U6 INTRAMOLECULAR STEM-LOOP RNA (1 entity in total) |
機能のキーワード | rna, stem-loop, gnra-like tetratloop, a-c wobble pair, internal loop |
タンパク質・核酸の鎖数 | 1 |
化学式量合計 | 7668.61 |
構造登録者 | Reiter, N.J.,Blad, H.,Abildgaard, F.,Butcher, S.E. (登録日: 2004-04-02, 公開日: 2004-11-09, 最終更新日: 2024-05-22) |
主引用文献 | Reiter, N.J.,Blad, H.,Abildgaard, F.,Butcher, S.E. Dynamics in the U6 RNA Intramolecular Stem-Loop: A Base Flipping Conformational Change. Biochemistry, 43:13739-13747, 2004 Cited by PubMed Abstract: The U6 RNA intramolecular stem-loop (ISL) structure is an essential component of the spliceosome and binds a metal ion required for pre-messenger RNA splicing. The metal binding internal loop region of the stem contains a partially protonated C67-(+)A79 base pair (pK(a) = 6.5) and an unpaired U80 nucleotide that is stacked within the helix at pH 7.0. Here, we determine that protonation occurs with an exchange lifetime of approximately 20 micros and report the solution structures of the U6 ISL at pH 5.7. The differences between pH 5.7 and 7.0 structures reveal that the pH change significantly alters the RNA conformation. At lower pH, U80 is flipped out into the major groove. Base flipping involves a purine stacking interaction of flanking nucleotides, inversion of the sugar pucker 5' to the flipped base, and phosphodiester backbone rearrangement. Analysis of residual dipolar couplings as a function of pH indicates that base flipping is not restricted to a local conformational change. Rather, base flipping alters the alignment of the upper and lower helices. The alternative conformations of the U6 ISL reveal striking structural similarities with both the NMR and crystal structures of domain 5 of self-splicing group II introns. These structures suggest that base flipping at an essential metal binding site is a conserved feature of the splicing machinery for both the spliceosome and group II self-splicing introns. PubMed: 15504036DOI: 10.1021/bi048815y 主引用文献が同じPDBエントリー |
実験手法 | SOLUTION NMR |
構造検証レポート
検証レポート(詳細版)をダウンロード