Evidence map›Paper›PMID 32342856›Full record

ArticleEcoSal Plus2020

Inhibition of RNA Polymerase by Rifampicin and Rifamycin-Like Molecules.

Hamed Mosaei, Nikolay Zenkin

Open access · greenAbstract readHistorical Article
In one paragraph

Article in EcoSal Plus, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
0.5field-weighted citation impact, top 23% of its field
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

33 citing papers in PubMed, 48 citations in OpenAlex.

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  14. HflX mediates rifampicin resistance inFrontiers in microbiology · 2026
    Article
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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

2 authors at 1 institution in 1 country.

Hamed MosaeiCentre for Bacterial Cell Biology, Biosciences Institute, Newcastle University, Newcastle Upon Tyne, NE2 4AX, UK.
Nikolay ZenkinCentre for Bacterial Cell Biology, Biosciences Institute, Newcastle University, Newcastle Upon Tyne, NE2 4AX, UK.
Newcastle University · GB

Funding

Medical Research Council 217189/Z/19/ZMedical Research Council MR/T000740/1Wellcome TrustWellcome Trust 102851/Z/13/Z
6 · The paper itself

Abstract

RNA polymerases (RNAPs) accomplish the first step of gene expression in all living organisms. However, the sequence divergence between bacterial and human RNAPs makes the bacterial RNAP a promising target for antibiotic development. The most clinically important and extensively studied class of antibiotics known to inhibit bacterial RNAP are the rifamycins. For example, rifamycins are a vital element of the current combination therapy for treatment of tuberculosis. Here, we provide an overview of the history of the discovery of rifamycins, their mechanisms of action, the mechanisms of bacterial resistance against them, and progress in their further development.

Indexed as

Anti-Bacterial AgentsBacteriaDNA-Directed RNA PolymerasesDrug Resistance, BacterialEscherichia coliHistory, 20th CenturyMicrobial Sensitivity TestsMolecular StructureMycobacterium tuberculosisRifampinAnti-Bacterial AgentsDNA-Directed RNA PolymerasesRifampin

Identifiers

PMID32342856
PMCPMC11168578
OpenAlexW3017762452

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.