| Literature DB >> 11389850 |
C M Spahn1, G Blaha, R K Agrawal, P Penczek, R A Grassucci, C A Trieber, S R Connell, D E Taylor, K H Nierhaus, J Frank.
Abstract
Tet(O) belongs to a class of ribosomal protection proteins that mediate tetracycline resistance. It is a G protein that shows significant sequence similarity to elongation factor EF-G. Here we present a cryo-electron microscopic reconstruction, at 16 A resolution, of its complex with the E. coli 70S ribosome. Tet(O) was bound in the presence of a noncleavable GTP analog to programmed ribosomal complexes carrying fMet-tRNA in the P site. Tet(O) is directly visible as a mass close to the A-site region, similar in shape and binding position to EF-G. However, there are important differences. One of them is the different location of the tip of domain IV, which in the Tet(O) case, does not overlap with the ribosomal A site but is directly adjacent to the primary tetracycline binding site. Our findings give insights into the mechanism of tetracycline resistance.Entities:
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Year: 2001 PMID: 11389850 DOI: 10.1016/s1097-2765(01)00238-6
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970