Evidence map›Paper›PMID 38668630›Full record

ArticleACS chemical biology2024

Divergence of Classical and C-Ring-Cleaved Angucyclines: Elucidation of Early Tailoring Steps in Lugdunomycin and Thioangucycline Biosynthesis.

Aleksi Nuutila, Xiansha Xiao, Helga U van der Heul, Gilles P van Wezel, Pedro Dinis, Somayah S Elsayed, Mikko Metsä-Ketelä

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in ACS chemical biology, 2024. 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. The Diels-Alder Reaction as a Key Step in Natural Product Synthesis.Progress in the chemistry of organic natural products · 2026
    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.

Aleksi NuutilaDepartment of Life Technologies, University of Turku, FIN20014 Turku, Finland.ORCID 0009-0001-6993-2119
Xiansha XiaoMolecular Biotechnology, Leiden University, PO Box 9505, 2300RA Leiden, The Netherlands.
Helga U van der HeulMolecular Biotechnology, Leiden University, PO Box 9505, 2300RA Leiden, The Netherlands.
Gilles P van WezelMolecular Biotechnology, Leiden University, PO Box 9505, 2300RA Leiden, The Netherlands.ORCID 0000-0003-0341-1561
Pedro DinisDepartment of Life Technologies, University of Turku, FIN20014 Turku, Finland.
Somayah S ElsayedMolecular Biotechnology, Leiden University, PO Box 9505, 2300RA Leiden, The Netherlands.ORCID 0000-0003-3837-6137
Mikko Metsä-KeteläDepartment of Life Technologies, University of Turku, FIN20014 Turku, Finland.ORCID 0000-0003-3176-2908

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Angucyclines are an important group of microbial natural products that display tremendous chemical diversity. Classical angucyclines are composed of a tetracyclic benz[

Indexed as

StreptomycesAngucyclines and AngucyclinonesAnthraquinonesBiological ProductsHydroxylationAngucyclines and AngucyclinonesAnthraquinonesBiological Products

Identifiers

PMID38668630
PMCPMC11106748

What OpenQuestion holds

Textmetadata
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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.