Evidence map›Paper›PMID 35851739›Full record

ArticleAngewandte Chemie (International ed. in English)2022

Cytochrome P450

Yongwei Zhao, Edward Marschall, Maxine Treisman, Alasdair McKay, Leo Padva, Max Crüsemann, David R Nelson, David L Steer, Ralf B Schittenhelm, Julien Tailhades and 1 more

Erratum issuedAbstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Article
  2. Article
  3. Myxarylin: TotalJournal of the American Chemical Society · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Biosynthesis of Macrocyclic Peptides by Formation and Crosslinking ofbioRxiv : the preprint server for biology · 2025
    Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Yongwei ZhaoDepartment of Biochemistry and Molecular Biology, The Monash Biomedicine Discovery Institute, Monash University, Clayton, VIC 3800, Australia.
Edward MarschallDepartment of Biochemistry and Molecular Biology, The Monash Biomedicine Discovery Institute, Monash University, Clayton, VIC 3800, Australia.ORCID 0000-0001-5218-2844
Maxine TreismanDepartment of Biochemistry and Molecular Biology, The Monash Biomedicine Discovery Institute, Monash University, Clayton, VIC 3800, Australia.
Alasdair McKayDepartment of Chemistry, Monash University, Clayton, VIC 3800, Australia.
Leo PadvaInstitute of Pharmaceutical Biology, University of Bonn, 53115, Bonn, Germany.
Max CrüsemannInstitute of Pharmaceutical Biology, University of Bonn, 53115, Bonn, Germany.
David R NelsonDepartment of Microbiology, Immunology and Biochemistry, University of Tennessee, Memphis, TN 38163, USA.
David L SteerMonash Proteomics and Metabolomics Facility, Monash University, Clayton, VIC 3800, Australia.
Ralf B SchittenhelmMonash Proteomics and Metabolomics Facility, Monash University, Clayton, VIC 3800, Australia.
Julien TailhadesDepartment of Biochemistry and Molecular Biology, The Monash Biomedicine Discovery Institute, Monash University, Clayton, VIC 3800, Australia.
Max J CryleDepartment of Biochemistry and Molecular Biology, The Monash Biomedicine Discovery Institute, Monash University, Clayton, VIC 3800, Australia.ORCID 0000-0002-9739-6157

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report our investigation of the utility of peptide crosslinking cytochrome P450 enzymes from biarylitide biosynthesis to generate a range of cyclic tripeptides from simple synthons. The crosslinked tripeptides produced by this P450 include both tyrosine-histidine (A-N-B) and tyrosine-tryptophan (A-O-B) crosslinked tripeptides, the latter a rare example of a phenolic crosslink to an indole moiety. Tripeptides are easily isolated following proteolytic removal of the leader peptide and can incorporate a wide range of amino acids in the residue inside the crosslinked tripeptide. Given the utility of peptide crosslinks in important natural products and the synthetic challenge that these can represent, P450 enzymes have the potential to play roles as important tools in the generation of high-value cyclic tripeptides for incorporation in synthesis, which can be yet further diversified using selective chemical techniques through specific handles contained within these tripeptides.

Indexed as

HistidineTyrosineCytochrome P-450 Enzyme SystemPeptide BiosynthesisPeptidesCytochrome P-450 Enzyme SystemHistidinePeptidesTyrosineAmino AcidsBiocatalysisCytochrome P450MetalloenzymesPeptide CrosslinkingPeptide CyclisationPeptides

Identifiers

PMID35851739
PMCPMC9542247

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.