Evidence map›Paper›PMID 25460274›Full record

ReviewCurrent opinion in structural biology2014

The structural biology of patellamide biosynthesis.

Jesko Koehnke, Andrew F Bent, Wael E Houssen, Greg Mann, Marcel Jaspars, James H Naismith

Abstract readReview
In one paragraph

Review in Current opinion in structural biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. 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. Design, synthesis,RSC advances · 2026
    Article
  2. Review
  3. Article
  4. Review
  5. Biochemical characterization of a cyanobactin arginine-Chemical communications (Cambridge, England) · 2022
    Article
  6. Article
  7. Review
  8. A roadmap for metagenomic enzyme discovery.Natural product reports · 2021
    Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Review
  17. Bypassing the proline/thiazoline requirement of the macrocyclase PatG.Chemical communications (Cambridge, England) · 2017
    Article
  18. Review
  19. Article
  20. Molecular basis for the broad substrate selectivity of a peptide prenyltransferase.Proceedings of the National Academy of Sciences of the United States of America · 2016
    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.

Jesko Koehnke *BSRC, North Haugh, The University, St Andrews, KY16 9ST.
Andrew F Bent *BSRC, North Haugh, The University, St Andrews, KY16 9ST.
Wael E Houssen *Marine Biodiscovery Centre, Department of Chemistry, University of Aberdeen, Meston Walk, Aberdeen, AB24 3UE.
Greg Mann *BSRC, North Haugh, The University, St Andrews, KY16 9ST.
Marcel Jaspars *Marine Biodiscovery Centre, Department of Chemistry, University of Aberdeen, Meston Walk, Aberdeen, AB24 3UE.
James H Naismith *BSRC, North Haugh, The University, St Andrews, KY16 9ST.

Funding

Biotechnology and Biological Sciences Research Council BB/K015508/1European Research Council 339367
6 · The paper itself

Abstract

The biosynthetic pathways for patellamide and related natural products have recently been studied by structural biology. These pathways produce molecules that have a complex framework and exhibit a diverse array of activity due to the variability of the amino acids that are found in them. As these molecules are difficult to synthesize chemically, exploitation of their properties has been modest. The patellamide pathway involves amino acid heterocyclization, peptide cleavage, peptide macrocyclization, heterocycle oxidation and epimerization; closely related products are also prenylated. Enzyme activities have been identified for all these transformations except epimerization, which may be spontaneous. This review highlights the recent structural and mechanistic work on amino acid heterocyclization, peptide cleavage and peptide macrocyclization. This work should help in using the enzymes to produce novel analogs of the natural products enabling an exploitation of their properties.

Indexed as

Biosynthetic PathwaysAmino AcidsAmino Acid SequenceBacteriaDimethylallyltranstransferaseHeterocyclic CompoundsMolecular Sequence DataPeptides, CyclicProtein ConformationAmino AcidsDimethylallyltranstransferaseHeterocyclic CompoundsPeptides, Cyclic

Identifiers

PMID25460274
PMCPMC4268494

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.