Evidence map›Paper›PMID 22710164›Full record

ReviewFEBS letters2012

The application of modular protein domains in proteomics.

Joshua A Jadwin, Mari Ogiue-Ikeda, Kazuya Machida

Abstract readReview
In one paragraph

Review in FEBS letters, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Human Vitamin K Epoxide Reductase as a Target of Its Redox Protein.International journal of molecular sciences · 2022
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Src homology 2 domains enhance tyrosine phosphorylationThe Journal of biological chemistry · 2018
    Article
  13. Article
  14. Review
  15. Selection of recombinant anti-SH3 domain antibodies by high-throughput phage display.Protein science : a publication of the Protein Society · 2015
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

3 authors.

Joshua A JadwinDepartment of Genetics and Developmental Biology, Raymond and Beverly Sackler Laboratory of Genetics and Molecular Medicine, University of Connecticut Health Center, 400 Farmington Avenue, Farmington, CT 06030, USA.
Mari Ogiue-Ikeda
Kazuya Machida

Funding

Dynamics and Topology of Phosphotyrosine-SH2 Interaction NetworksU01CA154966 · NCI · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI MAYER, BRUCE J., WHITE, FOREST M · 2011 to 2015
$2.4M
A novel molecular diagnostic approach to classify lung cancers and predict responRC1CA146843 · NCI · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI HAURA, ERIC B., MAYER, BRUCE J. · 2009 to 2010
$983k
NCI NIH HHS R01 CA146846NCI NIH HHS RC1 CA146843NCI NIH HHS U01 CA154966
6 · The paper itself

Abstract

The ability of modular protein domains to independently fold and bind short peptide ligands both in vivo and in vitro has allowed a significant number of protein-protein interaction studies to take advantage of them as affinity and detection reagents. Here, we refer to modular domain based proteomics as "domainomics" to draw attention to the potential of using domains and their motifs as tools in proteomics. In this review we describe core concepts of domainomics, established and emerging technologies, and recent studies by functional category. Accumulation of domain-motif binding data should ultimately provide the foundation for domain-specific interactomes, which will likely reveal the underlying substructure of protein networks as well as the selectivity and plasticity of signal transduction.

Indexed as

Amino Acid MotifsAnimalsBinding SitesComputational BiologyCross-Linking ReagentsGenomeHumansLigandsPeptide LibraryProlineProtein Interaction MappingProtein Structure, TertiaryProteomicsSignal TransductionCross-Linking ReagentsLigandsPeptide LibraryProline

Identifiers

PMID22710164
PMCPMC3413744

What Socratic 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 Socratic graph.