Evidence map›Paper›PMID 40175819›Full record

ArticleBiomolecular NMR assignments2025

NMR characterisation of the antibiotic resistance-mediating 32mer RNA from the 23S ribosomal RNA.

Christina Muhs, Lena Kemper, Christian Richter, Francesca Lavore, Markus Weingarth, Anna Wacker, Harald Schwalbe

Abstract read
In one paragraph

Article in Biomolecular NMR assignments, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Christina MuhsCenter for Biomolecular Magnetic Resonance (BMRZ), Institute for Organic Chemistry and Chemical Biology, Frankfurt am Main, Goethe University, Max-von-Laue-Straße 7, 60438, Frankfurt am Main, Germany.
Lena KemperCenter for Biomolecular Magnetic Resonance (BMRZ), Institute for Organic Chemistry and Chemical Biology, Frankfurt am Main, Goethe University, Max-von-Laue-Straße 7, 60438, Frankfurt am Main, Germany.
Christian RichterCenter for Biomolecular Magnetic Resonance (BMRZ), Institute for Organic Chemistry and Chemical Biology, Frankfurt am Main, Goethe University, Max-von-Laue-Straße 7, 60438, Frankfurt am Main, Germany.
Francesca LavoreBijvoet Centre for Biomolecular Research, Department of Chemistry, NMR Spectroscopy, Utrecht University, Padualaan 8, Utrecht, 3584 CH, The Netherlands.
Markus WeingarthBijvoet Centre for Biomolecular Research, Department of Chemistry, NMR Spectroscopy, Utrecht University, Padualaan 8, Utrecht, 3584 CH, The Netherlands.
Anna WackerCenter for Biomolecular Magnetic Resonance (BMRZ), Institute for Organic Chemistry and Chemical Biology, Frankfurt am Main, Goethe University, Max-von-Laue-Straße 7, 60438, Frankfurt am Main, Germany.
Harald SchwalbeCenter for Biomolecular Magnetic Resonance (BMRZ), Institute for Organic Chemistry and Chemical Biology, Frankfurt am Main, Goethe University, Max-von-Laue-Straße 7, 60438, Frankfurt am Main, Germany. schwalbe@nmr.uni-frankfurt.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The increasing prevalence of antibiotic resistance represents a significant public health concern, underscoring the urgent need for the development of novel therapeutic strategies. The antibiotic effects of macrolides, the second most widely used class of antibiotics, are counteracted by Erm proteins through the methylation of adenosine 2058 of the 23S ribosomal RNA (rRNA) (~ 2900 nucleotides), yielding either monomethylated or dimethylated A2058. This methylation is the molecular basis for preventing macrolides from binding and leads to the development of resistance of bacteria including Staphylococcus, Streptococcus and Enterococcus. While the function of Erm proteins have been thoroughly investigated, the role of the ribosomal RNA in acquiring antibiotic resistance is frequently underestimated, given that the ribosomal RNA is the actual target for methylation. Here, we present the comprehensive

Indexed as

Drug Resistance, MicrobialNuclear Magnetic Resonance, BiomolecularRNA, Ribosomal, 23SMethylationRNA, Ribosomal, 23S23S ribosomal RNAAntibiotic resistanceDMAErythromycin methyl transferasem6ASolution NMR-spectroscopy

Identifiers

PMID40175819
PMCPMC12116650

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.