3′(2′)‐O‐Aminoacylnucleotides as polypeptide acceptors at the ribosomal peptidyltransferase center
- 2 April 1970
- journal article
- Published by Wiley in FEBS Letters
- Vol. 7 (2) , 112-113
- https://doi.org/10.1016/0014-5793(70)80133-8
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Substrate specificity of ribosomal peptidyl transferase: 2′(3′)-O-aminoacyl nucleosides as acceptors of the peptide chain on the amino acid siteJournal of Molecular Biology, 1969
- Structural requirements for inhibition of polyphenylalanine synthesis by aminoacyl and nucleotidyl analogues of puromycinBiochimica et Biophysica Acta (BBA) - Nucleic Acids and Protein Synthesis, 1969
- Ribosome-catalysed peptidyl transfer: the polyphenylalanine systemJournal of Molecular Biology, 1968
- Release of peptide chains from the polylysyl-tRNA-ribosome complex by cytidylyl-(3′→5′)-2′(3′)-O-glycyladenosineBiochimica et Biophysica Acta (BBA) - Nucleic Acids and Protein Synthesis, 1967
- Inhibition of protein synthesis by aminoacyl 3′(2′)-adenosineBiochimica et Biophysica Acta (BBA) - Nucleic Acids and Protein Synthesis, 1966
- Structural Requirements for Puromycin Inhibition of Protein SynthesisNature, 1963