Literature DB >> 21875584

The structure of helix 89 of 23S rRNA is important for peptidyl transferase function of Escherichia coli ribosome.

Dmitry E Burakovsky1, Petr V Sergiev, Maria A Steblyanko, Andrey L Konevega, Alexey A Bogdanov, Olga A Dontsova.   

Abstract

Helix 89 of the 23S rRNA connects ribosomal peptidyltransferase center and elongation factor binding site. Secondary structure of helix 89 determined by X-ray structural analysis involves less base pairs then could be drawn for the helix of the same primary structure. It can be that alternative secondary structure might be realized at some stage of translation. Here by means of site-directed mutagenesis we stabilized either the "X-ray" structure or the structure with largest number of paired nucleotides. Mutation UU2492-3C which aimed to provide maximal pairing of the helix 89 of the 23S rRNA was lethal. Mutant ribosomes were unable to catalyze peptide transfer independently either with aminoacyl-tRNA or puromycin.
Copyright © 2011. Published by Elsevier B.V.

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Year:  2011        PMID: 21875584     DOI: 10.1016/j.febslet.2011.08.030

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  11 in total

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5.  Structure of BipA in GTP form bound to the ratcheted ribosome.

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Review 6.  Computational studies of molecular machines: the ribosome.

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10.  Chemical footprinting reveals conformational changes of 18S and 28S rRNAs at different steps of translation termination on the human ribosome.

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Journal:  RNA       Date:  2015-12-11       Impact factor: 4.942

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