Evidence map›Paper›PMID 39856061›Full record

ArticleNature communications2025

Broad substrate scope C-C oxidation in cyclodipeptides catalysed by a flavin-dependent filament.

Emmajay Sutherland, Christopher J Harding, Tancrède du Monceau de Bergendal, Gordon J Florence, Katrin Ackermann, Bela E Bode, Silvia Synowsky, Ramasubramanian Sundaramoorthy, Clarissa Melo Czekster

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Emmajay SutherlandUniversity of St Andrews, School of Biology, North Haugh, Biomolecular Sciences Building, St Andrews, UK.ORCID http://orcid.org/0000-0001-5150-4346
Christopher J HardingUniversity of St Andrews, School of Biology, North Haugh, Biomolecular Sciences Building, St Andrews, UK.ORCID http://orcid.org/0000-0003-0388-6460
Tancrède du Monceau de BergendalUniversity of St Andrews, School of Biology, North Haugh, Biomolecular Sciences Building, St Andrews, UK.ORCID http://orcid.org/0009-0008-4661-6405
Gordon J FlorenceUniversity of St Andrews, EaStCHEM School of Chemistry, North Haugh, Purdie Building, St Andrews, UK.
Katrin AckermannUniversity of St Andrews, EaStCHEM School of Chemistry, North Haugh, Purdie Building, St Andrews, UK.
Bela E BodeUniversity of St Andrews, EaStCHEM School of Chemistry, North Haugh, Purdie Building, St Andrews, UK.ORCID http://orcid.org/0000-0002-3384-271X
Silvia SynowskyUniversity of St Andrews, BSRC Mass Spectrometry and Proteomics Facility, North Haugh, Biomolecular Sciences Building, St Andrews, UK.
Ramasubramanian SundaramoorthyLaboratory of Chromatin Structure and Function, MCDB, School of Life Sciences, University of Dundee, Dundee, UK. R.Z.Sundaramoorthy@dundee.ac.uk.
Clarissa Melo CzeksterUniversity of St Andrews, School of Biology, North Haugh, Biomolecular Sciences Building, St Andrews, UK. cmc27@st-andrews.ac.uk.ORCID http://orcid.org/0000-0002-7163-4057

Funding

RCUK | Biotechnology and Biological Sciences Research Council (BBSRC) BB/R013780/1Wellcome TrustWellcome Trust (Wellcome) 223816/Z/21/Z
6 · The paper itself

Abstract

Cyclic dipeptides are produced by organisms across all domains of life, with many exhibiting anticancer and antimicrobial properties. Oxidations are often key to their biological activities, particularly C-C bond oxidation catalysed by tailoring enzymes including cyclodipeptide oxidases. These flavin-dependent enzymes are underexplored due to their intricate three-dimensional arrangement involving multiple copies of two distinct small subunits, and mechanistic details underlying substrate selection and catalysis are lacking. Here, we determined the structure and mechanism of the cyclodipeptide oxidase from the halophile Nocardiopsis dassonvillei (NdasCDO), a component of the biosynthetic pathway for nocazine natural products. We demonstrated that NdasCDO forms filaments in solution, with a covalently bound flavin mononucleotide (FMN) cofactor at the interface between three distinct subunits. The enzyme exhibits promiscuity, processing various cyclic dipeptides as substrates in a distributive manner. The reaction is optimal at high pH and involves the formation of a radical intermediate. Pre-steady-state kinetics, a significant solvent kinetic isotope effect, and the absence of viscosity effects suggested that a step linked to FMN regeneration controlled the reaction rate. Our work elucidates the complex mechanistic and structural characteristics of this dehydrogenation reaction, positioning NdasCDO as a promising biocatalyst and expanding the FMN-dependent oxidase family to include enzyme filaments.

Indexed as

Bacterial ProteinsDipeptidesFlavinsOxidoreductasesPeptides, CyclicActinobacteriaBiocatalysisCatalysisFlavin MononucleotideHydrogen-Ion ConcentrationKineticsModels, MolecularOxidation-ReductionSubstrate SpecificityBacterial ProteinsDipeptidesFlavin MononucleotideFlavinsOxidoreductasesPeptides, Cyclic

Identifiers

PMID39856061
PMCPMC11760959

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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.