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4MEG

In vitro evolved glmS ribozyme triple mutant, magnesium ion complex

4MEG の概要
エントリーDOI10.2210/pdb4meg/pdb
関連するPDBエントリー4MEH
分子名称glmS triple mutant ribozyme, (121-MER) ribozyme, MAGNESIUM ION, ... (4 entities in total)
機能のキーワードglms ribozyme fold, rna, self-cleavage, transesterification, metalloribozyme
タンパク質・核酸の鎖数2
化学式量合計49933.46
構造登録者
Lau, M.W.L.,Ferre-D'Amare, A.R. (登録日: 2013-08-26, 公開日: 2013-10-16, 最終更新日: 2023-09-20)
主引用文献Lau, M.W.,Ferre-D'Amare, A.R.
An in vitro evolved glmS ribozyme has the wild-type fold but loses coenzyme dependence.
Nat.Chem.Biol., 9:805-810, 2013
Cited by
PubMed Abstract: Uniquely among known ribozymes, the glmS ribozyme-riboswitch requires a small-molecule coenzyme, glucosamine-6-phosphate (GlcN6P). Although consistent with its gene-regulatory function, the use of GlcN6P is unexpected because all of the other characterized self-cleaving ribozymes use RNA functional groups or divalent cations for catalysis. To determine what active site features make this ribozyme reliant on GlcN6P and to evaluate whether it might have evolved from a coenzyme-independent ancestor, we isolated a GlcN6P-independent variant through in vitro selection. Three active site mutations suffice to generate a highly reactive RNA that adopts the wild-type fold but uses divalent cations for catalysis and is insensitive to GlcN6P. Biochemical and crystallographic comparisons of wild-type and mutant ribozymes show that a handful of functional groups fine-tune the RNA to be either coenzyme or cation dependent. These results indicate that a few mutations can confer new biochemical activities on structured RNAs. Thus, families of structurally related ribozymes with divergent function may exist.
PubMed: 24096303
DOI: 10.1038/nchembio.1360
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (3.1 Å)
構造検証レポート
Validation report summary of 4meg
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2026-02-04に公開中

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