| Autor: |
Stanley RE; Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut, USA., Blaha G, Grodzicki RL, Strickler MD, Steitz TA |
| Jazyk: |
angličtina |
| Zdroj: |
Nature structural & molecular biology [Nat Struct Mol Biol] 2010 Mar; Vol. 17 (3), pp. 289-93. Date of Electronic Publication: 2010 Feb 14. |
| DOI: |
10.1038/nsmb.1755 |
| Abstrakt: |
Viomycin and capreomycin belong to the tuberactinomycin family of antibiotics, which are among the most effective antibiotics against multidrug-resistant tuberculosis. Here we present two crystal structures of the 70S ribosome in complex with three tRNAs and bound to either viomycin or capreomycin at 3.3- and 3.5-A resolution, respectively. Both antibiotics bind to the same site on the ribosome, which lies at the interface between helix 44 of the small ribosomal subunit and helix 69 of the large ribosomal subunit. The structures of these complexes suggest that the tuberactinomycins inhibit translocation by stabilizing the tRNA in the A site in the pretranslocation state. In addition, these structures show that the tuberactinomycins bind adjacent to the binding sites for the paromomycin and hygromycin B antibiotics, which may enable the development of new derivatives of tuberactinomycins that are effective against drug-resistant strains. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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