Evidence map›Paper›PMID 28581482›Full record

ArticleNature chemical biology2017

Parallel evolution of non-homologous isofunctional enzymes in methionine biosynthesis.

Karine Bastard, Alain Perret, Aline Mariage, Thomas Bessonnet, Agnès Pinet-Turpault, Jean-Louis Petit, Ekaterina Darii, Pascal Bazire, Carine Vergne-Vaxelaire, Clémence Brewee and 11 more

Erratum issuedAbstract read
PubMed Publisher
In one paragraph

Article in Nature chemical biology, 2017. 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 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.7field-weighted citation impact, top 16% 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, 47 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Engineering of methionine-auxotrophMetabolic engineering communications · 2024
    Article
  7. pH-dependent regulation of an acidophilicApplied and environmental microbiology · 2024
    Article
  8. Article
  9. Review
  10. Article
  11. The coralScience advances · 2022
    Article
  12. Article
  13. Frontiers in cellular and infection microbiology · 2021
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 3 institutions in 1 country.

Karine BastardCEA, DRF, Genoscope, Evry, France.
Alain PerretCEA, DRF, Genoscope, Evry, France.
Aline MariageCEA, DRF, Genoscope, Evry, France.
Thomas BessonnetCEA, DRF, Genoscope, Evry, France.
Agnès Pinet-TurpaultCEA, DRF, Genoscope, Evry, France.
Jean-Louis PetitCEA, DRF, Genoscope, Evry, France.
Ekaterina DariiCEA, DRF, Genoscope, Evry, France.
Pascal BazireCEA, DRF, Genoscope, Evry, France.
Carine Vergne-VaxelaireCEA, DRF, Genoscope, Evry, France.
Clémence BreweeCEA, DRF, Genoscope, Evry, France.
Adrien DebardCEA, DRF, Genoscope, Evry, France.
Virginie PellouinCEA, DRF, Genoscope, Evry, France.
Marielle Besnard-GonnetCEA, DRF, Genoscope, Evry, France.
François ArtiguenaveCEA, DRF, Centre National de Génotypage, Evry, France.
Claudine MédigueCEA, DRF, Genoscope, Evry, France.
David VallenetCEA, DRF, Genoscope, Evry, France.
Antoine DanchinInstitute of Cardiometabolism and Nutrition (ICAN), Hôpital de la Pitié-Salpêtrière, Paris, France.ORCID http://orcid.org/0000-0002-6350-5001
Anne ZaparuchaCEA, DRF, Genoscope, Evry, France.
Jean WeissenbachCEA, DRF, Genoscope, Evry, France.
Marcel SalanoubatCEA, DRF, Genoscope, Evry, France.
Véronique de BerardinisCEA, DRF, Genoscope, Evry, France.
Centre National de la Recherche Scientifique · FRCommissariat à l'Énergie Atomique et aux Énergies Alternatives · FRSorbonne Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Experimental validation of enzyme function is crucial for genome interpretation, but it remains challenging because it cannot be scaled up to accommodate the constant accumulation of genome sequences. We tackled this issue for the MetA and MetX enzyme families, phylogenetically unrelated families of acyl-L-homoserine transferases involved in L-methionine biosynthesis. Members of these families are prone to incorrect annotation because MetX and MetA enzymes are assumed to always use acetyl-CoA and succinyl-CoA, respectively. We determined the enzymatic activities of 100 enzymes from diverse species, and interpreted the results by structural classification of active sites based on protein structure modeling. We predict that >60% of the 10,000 sequences from these families currently present in databases are incorrectly annotated, and suggest that acetyl-CoA was originally the sole substrate of these isofunctional enzymes, which evolved to use exclusively succinyl-CoA in the most recent bacteria. We also uncovered a divergent subgroup of MetX enzymes in fungi that participate only in L-cysteine biosynthesis as O-succinyl-L-serine transferases.

Indexed as

Evolution, MolecularAcetyltransferasesAcinetobacterEscherichia coliMethionineAcetyltransferasesMethionine

Identifiers

PMID28581482
OpenAlexW2624237745

What OpenQuestion holds

Textmetadata
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.