Evidence map›Paper›PMID 29438582›Full record

ArticleChemMedChem2018

Insights into the Target Interaction of Naturally Occurring Muraymycin Nucleoside Antibiotics.

Stefan Koppermann, Zheng Cui, Patrick D Fischer, Xiachang Wang, Jannine Ludwig, Jon S Thorson, Steven G Van Lanen, Christian Ducho

Abstract read
In one paragraph

Article in ChemMedChem, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

17 citing papers in PubMed, 32 citations in OpenAlex.

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  6. A Sub-Micromolar MraYMolecules (Basel, Switzerland) · 2022
    Article
  7. Enzymatic CJournal of the American Chemical Society · 2021
    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

8 authors at 3 institutions in 3 countries.

Stefan KoppermannDepartment of Pharmacy, Pharmaceutical and Medicinal Chemistry, Saarland University, Campus C2 3, 66123, Saarbrücken, Germany.ORCID 0000-0003-3905-4295
Zheng CuiDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, 789 S. Limestone Street, Lexington, KY, 40536, USA.
Patrick D FischerDepartment of Pharmacy, Pharmaceutical and Medicinal Chemistry, Saarland University, Campus C2 3, 66123, Saarbrücken, Germany.
Xiachang WangJiangsu Key Laboratory for Functional Substance of Chinese Medicine, School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, 210023, P.R. China.ORCID 0000-0002-1106-1904
Jannine LudwigDepartment of Pharmacy, Pharmaceutical and Medicinal Chemistry, Saarland University, Campus C2 3, 66123, Saarbrücken, Germany.
Jon S ThorsonDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, 789 S. Limestone Street, Lexington, KY, 40536, USA.ORCID 0000-0002-7148-0721
Steven G Van LanenDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, 789 S. Limestone Street, Lexington, KY, 40536, USA.
Christian DuchoDepartment of Pharmacy, Pharmaceutical and Medicinal Chemistry, Saarland University, Campus C2 3, 66123, Saarbrücken, Germany.ORCID 0000-0002-0629-9993
Saarland University · DEUniversity of Kentucky · USNanjing University of Chinese Medicine · CN

Funding

Kentucky Center for Clinical and Translational ScienceUL1TR001998 · NCATS · UNIVERSITY OF KENTUCKY · PI HARTMANN, KATHERINE E, KERN, PHILIP A · 2016 to 2025
$34.2M
Biosynthesis of nucleoside antibiotics targeting bacterial translocase IR01AI087849 · NIAID · UNIVERSITY OF KENTUCKY · PI VAN LANEN, STEVEN GARY · 2011 to 2020
$3.3M
NCATS NIH HHS UL1 TR001998NIAID NIH HHS R01 AI087849
6 · The paper itself

Abstract

Muraymycins are a subclass of antimicrobially active uridine-derived natural products. Biological data on several muraymycin analogues have been reported, including some inhibitory in vitro activities toward their target protein, the bacterial membrane enzyme MraY. However, a structure-activity relationship (SAR) study on naturally occurring muraymycins based on such in vitro data has been missing so far. In this work, we report a detailed SAR investigation on representatives of the four muraymycin subgroups A-D using a fluorescence-based in vitro MraY assay. For some muraymycins, inhibition of MraY with IC

Indexed as

Anti-Bacterial AgentsBacterial ProteinsCrystallography, X-RayEscherichia coliEscherichia coli InfectionsHumansMolecular Docking SimulationNucleosidesNucleotidesPeptidesStaphylococcal InfectionsStaphylococcus aureusStructure-Activity RelationshipTransferasesTransferases (Other Substituted Phosphate Groups)UreaAnti-Bacterial AgentsBacterial ProteinsmraY protein, Bacteriamuraymycin A1muraymycin C1muraymycin D1NucleosidesNucleotidesPeptidesTransferasesTransferases (Other Substituted Phosphate Groups)Ureaactivity assaysantibioticsnatural productsnucleosidesstructure-activity relationships

Identifiers

PMID29438582
PMCPMC6019934
OpenAlexW2790058880

What OpenQuestion holds

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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.