Lincomycin
Author:
Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-642-46403-4_8.pdf
Reference23 articles.
1. Barber, M., Waterworth, P.M.: Antibacterial activity of lincomycin and pristinamycin: A comparison with erythromycin. Br. Med. J. 1964 II, 603–606
2. Celma, M.L., Monro, R.E., Vazquez, D.: Substrate and Antibiotic Binding Sites at the Peptidyl Transferase Centre of E. coli Ribosomes. FEBS Lett. 6, 273–277 (1970)
3. Celma, M.L., Monro, R.E., Vazquez, D.: Substrate and antibiotic binding sites at the peptidyl transferase centre of E. coli ribosomes: binding of UACCA-Leu to 50S subunits. FEBS Lett. 13, 247–251 (1971)
4. Cerna, J., Rychlik, I., Zemlicka, J., Chladek, S.: Substrate specificity of ribosomal peptidyl transferase. II. 2′ (3′)-O-aminoacyl nucleosides as acceptors of the peptidyl chain in the fragment reaction. Biochim. Biophys. Acta 204, 203–209 (1970)
5. Chang, F.N.: Studies on antibiotic inhibitors of the 50S subunits of bacterial ribosomes. Ph.D. thesis. Univ. of Wisconsin (1968)
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1. Conformations in solution and bound to bacterial ribosomes of ketolides, HMR 3647 (telithromycin) and RU 72366: A new class of highly potent antibacterials;Bioorganic & Medicinal Chemistry;2000-07
2. Lincomycin and clindamycin conformations. A fragment shared by macrolides, ketolides and lincosamides determined from TRNOE ribosome-bound conformations;Bioorganic & Medicinal Chemistry;2000-06
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