Evidence map›Paper›PMID 26104711›Full record

ReviewMicrobiology spectrum2015

The λ Integrase Site-specific Recombination Pathway.

Arthur Landy

Open access · greenAbstract readReview
In one paragraph

Review in Microbiology spectrum, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 8% 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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 67 citations in OpenAlex.

  1. Pooled it
  2. Staphylococcal Cassette ChromosomeAntibiotics (Basel, Switzerland) · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Characterization of a New TemperatePathogens (Basel, Switzerland) · 2022
    Article
  13. Article
  14. Article
  15. The integrase of genomic island GIFrontiers in microbiology · 2022
    Article
  16. Review
  17. Archaeal tyrosine recombinases.FEMS microbiology reviews · 2021
    Review
  18. Article
  19. Article
  20. DNA binding induces aProceedings of the National Academy of Sciences of the United States of America · 2020
    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

1 author at 1 institution in 1 country.

Arthur LandyDivision of Biology and Medicine, Brown University, Providence, RI.
Brown University · US

Funding

MECHANISMS OF SITE SPECIFIC RECOMBINATIONR01GM062723 · NIGMS · BROWN UNIVERSITY · PI LANDY, ARTHUR · 2000 to 2012
$6.4M
RECOMBINATION INTERMEDIATES-- PROPERTIES &PROCESSINGR01GM033928 · NIGMS · BROWN UNIVERSITY · PI LANDY, ARTHUR · 1985 to 2011
$6.2M
NIGMS NIH HHS GM033928NIGMS NIH HHS GM062723NIGMS NIH HHS R01 GM033928NIGMS NIH HHS R01 GM062723
6 · The paper itself

Abstract

The site-specific recombinase encoded by bacteriophage λ (Int) is responsible for integrating and excising the viral chromosome into and out of the chromosome of its Escherichia coli host. Int carries out a reaction that is highly directional, tightly regulated, and depends upon an ensemble of accessory DNA bending proteins acting on 240 bp of DNA encoding 16 protein binding sites. This additional complexity enables two pathways, integrative and excisive recombination, whose opposite, and effectively irreversible, directions are dictated by different physiological and environmental signals. Int recombinase is a heterobivalent DNA binding protein and each of the four Int protomers, within a multiprotein 400 kDa recombinogenic complex, is thought to bind and, with the aid of DNA bending proteins, bridge one arm- and one core-type DNA site. In the 12 years since the publication of the last review focused solely on the λ site-specific recombination pathway in Mobile DNA II, there has been a great deal of progress in elucidating the molecular details of this pathway. The most dramatic advances in our understanding of the reaction have been in the area of X-ray crystallography where protein-DNA structures have now been determined for of all of the DNA-protein interfaces driving the Int pathway. Building on this foundation of structures, it has been possible to derive models for the assembly of components that determine the regulatory apparatus in the P-arm, and for the overall architectures that define excisive and integrative recombinogenic complexes. The most fundamental additional mechanistic insights derive from the application of hexapeptide inhibitors and single molecule kinetics.

Indexed as

Recombination, GeneticBacteriophage lambdaCrystallography, X-RayDNAEscherichia coliIntegrasesModels, BiologicalModels, MolecularNucleic Acid ConformationProtein BindingProtein ConformationDNAIntegrases

Identifiers

PMID26104711
PMCPMC5710010
OpenAlexW880029171

What OpenQuestion holds

Textmetadata
LicenceTDM
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.