Evidence map›Paper›PMID 25938916›Full record

ArticlePLoS computational biology2015

Predicting peptide-mediated interactions on a genome-wide scale.

T Scott Chen, Donald Petrey, Jose Ignacio Garzon, Barry Honig

Abstract read
In one paragraph

Article in PLoS computational biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Proteome-wide prediction of interactions between structured domains and peptide motifs reveals functionally coherent subnetworks.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. 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

4 authors.

T Scott ChenHoward Hughes Medical Institute, Columbia University, New York, New York, United States of America; Department of Systems Biology, Columbia University, New York, New York, United States of America; Department of Biochemistry and Molecular Biophysics, Columbia University, New York, New York, United States of America; Center for Computational Biology and Bioinformatics, Columbia University, New York, New York, United States of America.
Donald PetreyHoward Hughes Medical Institute, Columbia University, New York, New York, United States of America; Department of Systems Biology, Columbia University, New York, New York, United States of America; Department of Biochemistry and Molecular Biophysics, Columbia University, New York, New York, United States of America; Center for Computational Biology and Bioinformatics, Columbia University, New York, New York, United States of America.
Jose Ignacio GarzonHoward Hughes Medical Institute, Columbia University, New York, New York, United States of America; Department of Systems Biology, Columbia University, New York, New York, United States of America; Department of Biochemistry and Molecular Biophysics, Columbia University, New York, New York, United States of America; Center for Computational Biology and Bioinformatics, Columbia University, New York, New York, United States of America.
Barry HonigHoward Hughes Medical Institute, Columbia University, New York, New York, United States of America; Department of Systems Biology, Columbia University, New York, New York, United States of America; Department of Biochemistry and Molecular Biophysics, Columbia University, New York, New York, United States of America; Center for Computational Biology and Bioinformatics, Columbia University, New York, New York, United States of America.

Funding

COMPUTER STUDIES OF PROTEIN STRUCTURE AND FUNCTIONR01GM030518 · NIGMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI HONIG, BARRY H · 1985 to 2020
$4.5M
High-performance compute cluster for biomedical computingS10OD012351 · OD · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CALIFANO, ANDREA · 2012 to 2012
$2.0M
Howard Hughes Medical InstituteNIGMS NIH HHS R01 GM030518NIGMS NIH HHS R01-GM030518
6 · The paper itself

Abstract

We describe a method to predict protein-protein interactions (PPIs) formed between structured domains and short peptide motifs. We take an integrative approach based on consensus patterns of known motifs in databases, structures of domain-motif complexes from the PDB and various sources of non-structural evidence. We combine this set of clues using a Bayesian classifier that reports the likelihood of an interaction and obtain significantly improved prediction performance when compared to individual sources of evidence and to previously reported algorithms. Our Bayesian approach was integrated into PrePPI, a structure-based PPI prediction method that, so far, has been limited to interactions formed between two structured domains. Around 80,000 new domain-motif mediated interactions were predicted, thus enhancing PrePPI's coverage of the human protein interactome.

Indexed as

AlgorithmsBayes TheoremComputational BiologyDatabases, ProteinGenome, HumanHumansLikelihood FunctionsModels, BiologicalProtein Interaction Domains and MotifsProtein Interaction MappingProteomicsSupport Vector Machine

Identifiers

PMID25938916
PMCPMC4418708

What Socratic 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 Socratic graph.