Abstract
2/3-O-[Bz(NO2)-Orn(Boc)]-5-O-Piv-Ado (1) and its deoxy analog: 3-O-[Bz(NO2)-Orn(Boc)]-5-O-Piv-2- dAdo (2) were designed and synthesized as substrates for the model ribosome reaction we used to demonstrate the crucial role of A76 2-OH of peptidyl-tRNA in the rate acceleration of peptide bond formation during protein biosynthesis.
Keywords: Design, peptide synthesis, nucleoside synthesis, ribosome catalysis
Protein & Peptide Letters
Title: Design and Synthesis of Substrates for Model Ribosomal Reactions
Volume: 16 Issue: 4
Author(s): Stanislav G. Bayryamov, Nikolay G. Vassilev, Miroslav A. Rangelov, Aneta P. Mladjova and Dimiter D. Petkov
Affiliation:
Keywords: Design, peptide synthesis, nucleoside synthesis, ribosome catalysis
Abstract: 2/3-O-[Bz(NO2)-Orn(Boc)]-5-O-Piv-Ado (1) and its deoxy analog: 3-O-[Bz(NO2)-Orn(Boc)]-5-O-Piv-2- dAdo (2) were designed and synthesized as substrates for the model ribosome reaction we used to demonstrate the crucial role of A76 2-OH of peptidyl-tRNA in the rate acceleration of peptide bond formation during protein biosynthesis.
Export Options
About this article
Cite this article as:
Bayryamov G. Stanislav, Vassilev G. Nikolay, Rangelov A. Miroslav, Mladjova P. Aneta and Petkov D. Dimiter, Design and Synthesis of Substrates for Model Ribosomal Reactions, Protein & Peptide Letters 2009; 16 (4) . https://dx.doi.org/10.2174/092986609787848009
DOI https://dx.doi.org/10.2174/092986609787848009 |
Print ISSN 0929-8665 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5305 |
- Author Guidelines
- Graphical Abstracts
- Fabricating and Stating False Information
- Research Misconduct
- Post Publication Discussions and Corrections
- Publishing Ethics and Rectitude
- Increase Visibility of Your Article
- Archiving Policies
- Peer Review Workflow
- Order Your Article Before Print
- Promote Your Article
- Manuscript Transfer Facility
- Editorial Policies
- Allegations from Whistleblowers