Evidence map›Paper›PMID 26959241›Full record

ArticleOrganic letters2016

Combinatorial Generation of Chemical Diversity by Redox Enzymes in Chaetoviridin Biosynthesis.

Michio Sato, Jaclyn M Winter, Shinji Kishimoto, Hiroshi Noguchi, Yi Tang, Kenji Watanabe

Abstract read
In one paragraph

Article in Organic letters, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
4.9field-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

21 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Naturally Occurring Organohalogen Compounds-A Comprehensive Review.Progress in the chemistry of organic natural products · 2023
    Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Chemoenzymatic Total Synthesis of Natural Products.Accounts of chemical research · 2021
    Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. RadH: A Versatile Halogenase for Integration into Synthetic Pathways.Angewandte Chemie (International ed. in English) · 2017
    Article
  19. Article
  20. 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

6 authors at 2 institutions in 2 countries.

Michio SatoDepartment of Pharmaceutical Sciences, University of Shizuoka , Shizuoka 422-8526, Japan.
Jaclyn M WinterDepartment of Chemical and Biomolecular Engineering, University of California , Los Angeles, California 90095, United States.
Shinji KishimotoDepartment of Pharmaceutical Sciences, University of Shizuoka , Shizuoka 422-8526, Japan.
Hiroshi NoguchiDepartment of Pharmaceutical Sciences, University of Shizuoka , Shizuoka 422-8526, Japan.
Yi TangDepartment of Chemical and Biomolecular Engineering, University of California , Los Angeles, California 90095, United States.
Kenji WatanabeDepartment of Pharmaceutical Sciences, University of Shizuoka , Shizuoka 422-8526, Japan.
University of Shizuoka · JPUniversity of California, Los Angeles · US

Funding

Rediscovering Natural Chemical Diversity -1DP1GM106413DP1GM106413 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TANG, YI · 2012 to 2016
$3.9M
Characterization and Engineering of Fungal Megasynthases in Escherichia coliR01GM085128 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TANG, YI · 2008 to 2016
$2.1M
NCCDPHP CDC HHS 1DP1GM106413NIGMS NIH HHS DP1 GM106413NIGMS NIH HHS R01 GM085128
6 · The paper itself

Abstract

Chaetoviridins constitute a large family of structurally related secondary metabolites isolated from Chaetomium fungi. To elucidate the biosynthesis pathway and understand how the chemical diversity of chaetoviridins is generated, gene deletion and in vitro characterization of the four post-PKS modifications enzymes were undertaken. CazL and CazP were identified to have substrate promiscuity that facilitates the formation of nonchlorinated analogues. In addition, enzymatic oxidation and reduction combined with spontaneous dehydration and lactonization of the intermediates further expand the chemical diversity.

Indexed as

Biosynthetic PathwaysChaetomiumFuransGene DeletionMolecular StructureOxidation-ReductionPolyketide SynthasesPyroneschaetoviridin AFuransPolyketide SynthasesPyrones

Identifiers

PMID26959241
PMCPMC4903021
OpenAlexW2293810321

What OpenQuestion holds

Textmetadata
LicenceTDM
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.