Evidence map›Paper›PMID 30018376›Full record

ArticleNature communications2018

A radical S-adenosyl-L-methionine enzyme and a methyltransferase catalyze cyclopropane formation in natural product biosynthesis.

Wen-Bing Jin, Sheng Wu, Xiao-Hong Jian, Hua Yuan, Gong-Li Tang

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

24 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
  2. Article
  3. Mechanistic insight into radicalNatural product reports · 2026
    Review
  4. Structural and Spectroscopic Basis for Catalysis by a Class C RadicalJournal of the American Chemical Society · 2026
    Article
  5. Article
  6. Article
  7. Structural and Spectroscopic Basis for Catalysis by a Class C RadicalbioRxiv : the preprint server for biology · 2026
    Article
  8. Article
  9. Article
  10. Natural product reports · 2023
    Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Functional Diversity of HemN-like Proteins.ACS bio & med chem Au · 2022
    Review
  16. Review
  17. Article
  18. Review
  19. Review
  20. 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

5 authors at 1 institution in 1 country.

Wen-Bing JinState Key Laboratory of Bio-organic and Natural Products Chemistry, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Road, Shanghai, 200032, China.ORCID http://orcid.org/0000-0002-3528-7297
Sheng WuState Key Laboratory of Bio-organic and Natural Products Chemistry, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Road, Shanghai, 200032, China.
Xiao-Hong JianState Key Laboratory of Bio-organic and Natural Products Chemistry, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Road, Shanghai, 200032, China.
Hua YuanState Key Laboratory of Bio-organic and Natural Products Chemistry, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Road, Shanghai, 200032, China. huayuan@sioc.ac.cn.ORCID http://orcid.org/0000-0002-5938-7751
Gong-Li TangState Key Laboratory of Bio-organic and Natural Products Chemistry, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Road, Shanghai, 200032, China. gltang@sioc.ac.cn.ORCID http://orcid.org/0000-0003-3149-4683
Shanghai Institute of Organic Chemistry · CN

Funding

Chinese Academy of Sciences (CAS) XDB20000000, QYZDJ-SSW-SLH037National Natural Science Foundation of China (National Science Foundation of China) 21632007, 21502217 and 21621002
6 · The paper itself

Abstract

Cyclopropanation of unactivated olefinic bonds via addition of a reactive one-carbon species is well developed in synthetic chemistry, whereas natural cyclopropane biosynthesis employing this strategy is very limited. Here, we identify a two-component cyclopropanase system, composed of a HemN-like radical S-adenosyl-L-methionine (SAM) enzyme C10P and a methyltransferase C10Q, catalyzes chemically challenging cyclopropanation in the antitumor antibiotic CC-1065 biosynthesis. C10P uses its [4Fe-4S] cluster for reductive cleavage of the first SAM to yield a highly reactive 5'-deoxyadenosyl radical, which abstracts a hydrogen from the second SAM to produce a SAM methylene radical that adds to an sp

Indexed as

Antibiotics, AntineoplasticBacterial ProteinsBiocatalysisCloning, MolecularCyclopropanesDuocarmycinsEscherichia coliGene ExpressionGenetic VectorsIndolesIronIron-Sulfur ProteinsMethyltransferasesRecombinant ProteinsS-AdenosylhomocysteineS-AdenosylmethionineAntibiotics, AntineoplasticBacterial ProteinsCC 1065CyclopropanesDuocarmycinsIndolesIronIron-Sulfur ProteinsMethyltransferasesRecombinant ProteinsS-AdenosylhomocysteineS-AdenosylmethionineSulfur

Identifiers

PMID30018376
PMCPMC6050322
OpenAlexW2828551540

What OpenQuestion holds

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LicenceCC BY
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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.