Evidence map›Paper›PMID 17316440›Full record

ArticleGenome biology2007

Clustering of phosphorylation site recognition motifs can be exploited to predict the targets of cyclin-dependent kinase.

Alan M Moses, Jean-Karim Hériché, Richard Durbin

Abstract read
In one paragraph

Article in Genome biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing 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

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

  1. Pooled it
  2. Mapping the proteome landscape inPlant signaling & behavior · 2026
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  8. Accelerated Multiphosphorylated Peptide Synthesis.Organic process research & development · 2022
    Review
  9. Review
  10. Article
  11. CRL4Genes · 2022
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Regulatory mechanisms in postsynaptic phosphorylation networks.Current opinion in structural biology · 2019
    Review
  18. Synthetic-Evolution Reveals Narrow Paths to Regulation of theInternational journal of biological sciences · 2019
    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.

Alan M MosesWellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1HH, UK. am8@sanger.ac.uk
Jean-Karim Hériché
Richard Durbin

Funding

Wellcome Trust
6 · The paper itself

Abstract

Protein kinases are critical to cellular signalling and post-translational gene regulation, but their biological substrates are difficult to identify. We show that cyclin-dependent kinase (CDK) consensus motifs are frequently clustered in CDK substrate proteins. Based on this, we introduce a new computational strategy to predict the targets of CDKs and use it to identify new biologically interesting candidates. Our data suggest that regulatory modules may exist in protein sequence as clusters of short sequence motifs.

Indexed as

Models, GeneticAmino Acid MotifsComputational BiologyCyclin-Dependent KinasesHumansPhosphorylationProteinsProteomicsYeastsCyclin-Dependent KinasesProteins

Identifiers

PMID17316440
PMCPMC1852407

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.