Minimum secondary structure requirements for catalytic activity of a self-splicing group I intron
Author:
Publisher
American Chemical Society (ACS)
Subject
Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/bi00479a027
Reference34 articles.
1. Deletion of nonconserved helices near the 3' end of the rRNA intron of Tetrahymena thermophila alters self-splicing but not core catalytic activity.
2. One binding site determines sequence specificity of Tetrahymena pre-rRNA self-splicing, trans-splicing, and RNA enzyme activity
3. Molecular genetics of group I introns: RNA structures and protein factors required for splicing — a review
4. Structural conventions for group I introns
5. Bacteriophage SP6-specific RNA polymerase. I. Isolation and characterization of the enzyme.
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1. Cryo-EM structures of full-length Tetrahymena ribozyme at 3.1 Å resolution;Nature;2021-08-11
2. Optimization of a novel biophysical model using large scale in vivo antisense hybridization data displays improved prediction capabilities of structurally accessible RNA regions;Nucleic Acids Research;2017-02-21
3. Recycling of Informational Units Leads to Selection of Replicators in a Prebiotic Soup;Chemistry & Biology;2013-02
4. A Two-Piece Derivative of a Group I Intron RNA as a Platform for Designing Self-Assembling RNA Templates to Promote Peptide Ligation;Journal of Nucleic Acids;2012
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