Evidence map›Paper›PMID 34123072›Full record

ArticleChemical science2020

Chemoenzymatic elaboration of the Raper-Mason pathway unravels the structural diversity within eumelanin pigments.

Qing Zhe Ni, Brianna N Sierra, James J La Clair, Michael D Burkart

Abstract read
In one paragraph

Article in Chemical science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Fungi as a source of eumelanin: current understanding and prospects.Journal of industrial microbiology & biotechnology · 2023
    Article
  6. Article
  7. Article
  8. Article
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

4 authors.

Qing Zhe NiDepartment of Chemistry and Biochemistry, University of California San Diego, 9500 Gilman Drive La Jolla CA 92093-0358 USA mburkart@ucsd.edu.ORCID https://orcid.org/0000-0001-6205-1119
Brianna N SierraDepartment of Chemistry and Biochemistry, University of California San Diego, 9500 Gilman Drive La Jolla CA 92093-0358 USA mburkart@ucsd.edu.ORCID https://orcid.org/0000-0001-8207-3569
James J La ClairDepartment of Chemistry and Biochemistry, University of California San Diego, 9500 Gilman Drive La Jolla CA 92093-0358 USA mburkart@ucsd.edu.ORCID https://orcid.org/0000-0001-6500-4107
Michael D BurkartDepartment of Chemistry and Biochemistry, University of California San Diego, 9500 Gilman Drive La Jolla CA 92093-0358 USA mburkart@ucsd.edu.ORCID https://orcid.org/0000-0002-4472-2254

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Melanin is a central polymer in living organisms, yet our understanding of its molecular structure remains unresolved. Here, we apply a biosynthetic approach to explore the composite structures accessible in one type of melanin, eumelanin. Using a combination of solid-state NMR, dynamic nuclear polarization, and electron microscopy, we reveal how a variety of monomers are enzymatically polymerized into their corresponding eumelanin pigments. We demonstrate how this approach can be used to unite structure with an understanding of enzymatic activity, substrate scope, and the regulation of nanostructural features. Overall, this data reveals how intermediate metabolites of the Raper-Mason metabolic pathway contribute to polymerization, allowing us to revisit the original proposal of how eumelanin is biosynthesized.

Identifiers

PMID34123072
PMCPMC8163323

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Registered trials

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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.