Evidence map›Paper›PMID 32553169›Full record

ArticleCell reports2020

Proline-Rich Motifs Control G2-CDK Target Phosphorylation and Priming an Anchoring Protein for Polo Kinase Localization.

Mihkel Örd, Kait Kaarel Puss, Rait Kivi, Kaidi Möll, Tuuliki Ojala, Irina Borovko, Ilona Faustova, Rainis Venta, Ervin Valk, Mardo Kõivomägi and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2020. 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
1.9field-weighted citation impact, top 16% 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

21 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Decoding Cdk1 control: from mitotic thresholds to meiotic specificity.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2026
    Review
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  16. Bipartite binding of the N terminus of Skp2 to cyclin A.Structure (London, England : 1993) · 2021
    Article
  17. Docking to a Basic Helix Promotes Specific Phosphorylation by G1-Cdk1.International journal of molecular sciences · 2021
    Article
  18. Budding yeast relies on GScience advances · 2021
    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

11 authors at 2 institutions in 2 countries.

Mihkel ÖrdInstitute of Technology, University of Tartu, Tartu 50411, Estonia.
Kait Kaarel PussInstitute of Technology, University of Tartu, Tartu 50411, Estonia.
Rait KiviInstitute of Technology, University of Tartu, Tartu 50411, Estonia.
Kaidi MöllInstitute of Technology, University of Tartu, Tartu 50411, Estonia.
Tuuliki OjalaInstitute of Technology, University of Tartu, Tartu 50411, Estonia.
Irina BorovkoInstitute of Technology, University of Tartu, Tartu 50411, Estonia.
Ilona FaustovaInstitute of Technology, University of Tartu, Tartu 50411, Estonia.
Rainis VentaInstitute of Technology, University of Tartu, Tartu 50411, Estonia.
Ervin ValkInstitute of Technology, University of Tartu, Tartu 50411, Estonia.
Mardo KõivomägiDepartment of Biology, Stanford University, Stanford, CA 94305, USA.
Mart LoogInstitute of Technology, University of Tartu, Tartu 50411, Estonia. Electronic address: mart.loog@ut.ee.
University of Tartu · EEStanford University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The hydrophobic patch (hp), a docking pocket on cyclins of CDKs (cyclin-dependent kinases), has been thought to accommodate a single short linear motif (SLiM), the "RxL or Cy" docking motif. Here we show that hp can bind different motifs with high specificity. We identify a PxxPxF motif that is necessary for G2-cyclin Clb3 function in S. cerevisiae, and that mediates Clb3-Cdk1 phosphorylation of Ypr174c (proposed name: Cdc5 SPB anchor-Csa1) to regulate the localization of Polo kinase Cdc5. Similar motifs exist in other Clb3-Cdk1 targets. Our work completes the set of docking specificities for the four major cyclins: LP, RxL, PxxPxF, and LxF motifs for G1-, S-, G2-, and M-phase cyclins, respectively. Further, we show that variations in motifs can change their specificity for human cyclins. This diversity could provide complexity for the encoding of CDK thresholds to achieve ordered cell-cycle phosphorylation.

Indexed as

Cell CycleCell Cycle CheckpointsCell Cycle ProteinsCyclin-Dependent KinasesHumansPhosphorylationProlineSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSubstrate SpecificityCell Cycle ProteinsCyclin-Dependent KinasesProlineSaccharomyces cerevisiae Proteinscell cyclecyclin-dependent kinaseintrinsically disordered regionskinase specificityPolo kinaseshort linear motifSLiM

Identifiers

PMID32553169
PMCPMC7301157
OpenAlexW3034777788

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.