Sulfoxide configuration in sparsomycin determines time-dependent and competitive inhibition of peptidyl transferase
- 8 December 1984
- journal article
- research article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 125 (2), 784-789
- https://doi.org/10.1016/0006-291x(84)90607-7
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- Importance of the hydrophobic sulfoxide substituent on nontoxic analogs of sparsomycinAntimicrobial Agents and Chemotherapy, 1984
- Structure-activity relationships of sparsomycin and its analogs: octylsparsomycin: The first analog more active than sparsomycinJournal of Medicinal Chemistry, 1984
- Necessity of the sulfoxide moiety for the biochemical and biological properties of an analog of sparsomycinBiochemical and Biophysical Research Communications, 1983
- The chemical modification of Escherichia coli ribosomes with methyl p-nitrobenzenesulfonate. Evidence for the involvement of a histidine residue in the functioning of the ribosomal peptidyl transferaseCanadian Journal of Biochemistry, 1980
- Inhibitors of protein synthesis V Irreversible interaction of antibiotics with an initiation complexNucleic Acids Research, 1975
- New synthesis of .alpha.-amino acids from nitrilesJournal of the American Chemical Society, 1974
- [45] Peptidyl-puromycin synthesis on polyribosomes from Escherichia coliMethods in Enzymology, 1974
- A versatile reagent for aldehyde synthesis. Methyl methylthiomethyl sulfoxide.Tetrahedron Letters, 1971
- The mechanism of the reaction of phenyl methyl sulfoxide with acetic anhydrideTetrahedron Letters, 1968
- Lysis of Escherichia coli with a neutral detergentBiochimica et Biophysica Acta (BBA) - Nucleic Acids and Protein Synthesis, 1967