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The dawn of dominance by the mature domain in tRNA splicing
- Source :
- Proceedings of the National Academy of Sciences of the United States of America 104 (2007): 12300–12305. doi:10.1073/pnas.0705537104, info:cnr-pdr/source/autori:Tocchini-Valentini G.D.; Fruscoloni P.; Tocchini-Valentini G.P./titolo:The dawn of dominance by the mature domain in tRNA splicing/doi:10.1073%2Fpnas.0705537104/rivista:Proceedings of the National Academy of Sciences of the United States of America/anno:2007/pagina_da:12300/pagina_a:12305/intervallo_pagine:12300–12305/volume:104
- Publication Year :
- 2007
- Publisher :
- Proceedings of the National Academy of Sciences, 2007.
-
Abstract
- The relationship between enzyme architecture and substrate specificity among archaeal pre-tRNA splicing endonucleases has been investigated more deeply, by using biochemical assays and model building. The enzyme from Archeoglobus fulgidus (AF) is particularly interesting: it cleaves the bulge–helix–bulge target without requiring the mature tRNA domain, but, when the target is a bulge–helix–loop, the mature domain is required. A model of AF based on its electrostatic potential shows three polar patches interacting with the pre-tRNA substrate. A simple deletion mutant of the AF endonuclease lacking two of the three polar patches no longer cleaves the bulge–helix–loop substrate with or without the mature domain. This single deletion shows a possible path for the evolution of eukaryal splicing endonucleases from the archaeal enzyme.
- Subjects :
- Models, Molecular
Archaeal Proteins
RNA Splicing
Molecular Sequence Data
Static Electricity
Plasma protein binding
Substrate Specificity
Endonuclease
RNA, Transfer
Humans
Amino Acid Sequence
Binding site
Peptide sequence
chemistry.chemical_classification
Binding Sites
Multidisciplinary
Base Sequence
biology
Archaeoglobus fulgidus
Biological Sciences
Protein Structure, Tertiary
Enzyme
Biochemistry
chemistry
Structural Homology, Protein
RNA splicing
Transfer RNA
biology.protein
Nucleic Acid Conformation
Protein Binding
Subjects
Details
- ISSN :
- 10916490 and 00278424
- Volume :
- 104
- Database :
- OpenAIRE
- Journal :
- Proceedings of the National Academy of Sciences
- Accession number :
- edsair.doi.dedup.....df44bf9b898554aafcac83ab8ab3bc65
- Full Text :
- https://doi.org/10.1073/pnas.0705537104