Literature DB >> 14654696

A conserved chloramphenicol binding site at the entrance to the ribosomal peptide exit tunnel.

Katherine S Long1, Bo T Porse.   

Abstract

The antibiotic chloramphenicol produces modifications in 23S rRNA when bound to ribosomes from the bacterium Escherichia coli and the archaeon Halobacterium halobium and irradiated with 365 nm light. The modifications map to nucleotides m(5)U747 and C2611/C2612, in domains II and V, respectively, of E.coli 23S rRNA and G2084 (2058 in E.coli numbering) in domain V of H.halobium 23S rRNA. The modification sites overlap with a portion of the macrolide binding site and cluster at the entrance to the peptide exit tunnel. The data correlate with the recently reported chloramphenicol binding site on an archaeal ribosome and suggest that a similar binding site is present on the E.coli ribosome.

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Year:  2003        PMID: 14654696      PMCID: PMC291879          DOI: 10.1093/nar/gkg945

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  38 in total

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Authors:  P S Lovett
Journal:  Gene       Date:  1996-11-07       Impact factor: 3.688

5.  Different nucleotide changes in the large rRNA gene of the mitochondrial DNA confer chloramphenicol resistance on two human cell lines.

Authors:  H Blanc; C W Adams; D C Wallace
Journal:  Nucleic Acids Res       Date:  1981-11-11       Impact factor: 16.971

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Journal:  J Bacteriol       Date:  1998-01       Impact factor: 3.490

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Journal:  Antimicrob Agents Chemother       Date:  1982-05       Impact factor: 5.191

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  9 in total

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4.  Effect of codon adaptation on codon-level and gene-level translation efficiency in vivo.

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Authors:  George P Dinos; Constantinos M Athanassopoulos; Dionissia A Missiri; Panagiota C Giannopoulou; Ioannis A Vlachogiannis; Georgios E Papadopoulos; Dionissios Papaioannou; Dimitrios L Kalpaxis
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7.  Synthesis and evaluation of chloramphenicol homodimers: molecular target, antimicrobial activity, and toxicity against human cells.

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Review 8.  Antibiotic drugs targeting bacterial RNAs.

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9.  The ribosome can prevent aggregation of partially folded protein intermediates: studies using the Escherichia coli ribosome.

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