Evidence map›Paper›PMID 30340458›Full record

ArticleBMC genomics2018

Context-specific interactions in literature-curated protein interaction databases.

R Greg Stacey, Michael A Skinnider, Jenny H L Chik, Leonard J Foster

Abstract read
In one paragraph

Article in BMC genomics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
–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

19 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Modulation of TvRAD51 Recombinase inPathogens (Basel, Switzerland) · 2025
    Article
  6. Psychiatric Genomics 2025: State of the Art and the Path Forward.The Psychiatric clinics of North America · 2025
    Review
  7. Article
  8. Software and Databases for Protein-Protein Docking.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  9. Article
  10. Review
  11. Article
  12. Contextualized Protein-Protein Interactions.Patterns (New York, N.Y.) · 2021
    Article
  13. Article
  14. Mapping, Structure and Modulation of PPI.Frontiers in chemistry · 2021
    Review
  15. Article
  16. Article
  17. Review
  18. Profiling theeLife · 2019
    Article
  19. Review
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

4 authors.

R Greg StaceyMichael Smith Laboratories, University of British Columbia, Vancouver, V6T 1Z4, Canada. richard.greg.stacey@msl.ubc.ca.ORCID http://orcid.org/0000-0002-4496-8131
Michael A SkinniderMichael Smith Laboratories, University of British Columbia, Vancouver, V6T 1Z4, Canada.
Jenny H L ChikCurrent Address: International Collaboration On Repair Discoveries (ICORD), Vancouver Coastal Health Research Institute and Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada.
Leonard J FosterMichael Smith Laboratories, University of British Columbia, Vancouver, V6T 1Z4, Canada. foster@msl.ubc.ca.

Funding

Canadian Institutes of Health Research MOP77688Genome British Columbia 214PROGenome Canada 214PRO
6 · The paper itself

Abstract

backgroundDatabases of literature-curated protein-protein interactions (PPIs) are often used to interpret high-throughput interactome mapping studies and estimate error rates. These databases combine interactions across thousands of published studies and experimental techniques. Because the tendency for two proteins to interact depends on the local conditions, this heterogeneity of conditions means that only a subset of database PPIs are interacting during any given experiment. A typical use of these databases as gold standards in interactome mapping projects, however, assumes that PPIs included in the database are indeed interacting under the experimental conditions of the study.

resultsUsing raw data from 20 co-fractionation experiments and six published interactomes, we demonstrate that this assumption is often false, with up to 55% of purported gold standard interactions showing no evidence of interaction, on average. We identify a subset of CORUM database complexes that do show consistent evidence of interaction in co-fractionation studies, and we use this subset as gold standards to dramatically improve interactome mapping as judged by the number of predicted interactions at a given error rate.

conclusionsWe recommend using this CORUM subset as the gold standard set in future co-fractionation studies. More generally, we recommend using the subset of literature-curated PPIs that are specific to the experimental context whenever possible.

Indexed as

Databases, ProteinComputational BiologyProtein Interaction MappingInteractomeLiterature curated databaseProtein-protein interactionProteomics

Identifiers

PMID30340458
PMCPMC6194712

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.