Evidence map›Paper›PMID 16342414›Full record

ArticleMolecular and cellular biochemistry2005

A global view of CK2 function and regulation.

Allison Poole, Tim Poore, Sricharan Bandhakavi, Richard O McCann, David E Hanna, Claiborne V C Glover

Abstract read
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In one paragraph

Article in Molecular and cellular biochemistry, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Casein Kinase 2 Signaling in White Matter Stroke.Frontiers in molecular biosciences · 2022
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Frontiers in cellular and infection microbiology · 2019
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Casein kinase II promotes target silencing by miRISC through direct phosphorylation of the DEAD-box RNA helicase CGH-1.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  17. Article
  18. Article
  19. Mitochondrial protein import under kinase surveillance.Microbial cell (Graz, Austria) · 2014
    Review
  20. Does casein kinase II phosphorylation of Maf1 trigger RNA polymerase III activation?Proceedings of the National Academy of Sciences of the United States of America · 2011
    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

6 authors.

Allison PooleDepartment of Biochemistry and Molecular Biology, Life Sciences Building, The University of Georgia, Athens, GA, USA.
Tim Poore
Sricharan Bandhakavi
Richard O McCann
David E Hanna
Claiborne V C Glover

Funding

STRUCTURE AND FUNCTION OF AN RNA POL II CTD PHOSPHATASER01GM060298 · NIGMS · UNIVERSITY OF GEORGIA (UGA) · PI GLOVER, CLAIBORNE V · 2000 to 2004
$1.1M
NIGMS NIH HHS R01-GM60298
6 · The paper itself

Abstract

The wealth of biochemical, molecular, genetic, genomic, and bioinformatic resources available in S. cerevisiae make it an excellent system to explore the global role of CK2 in a model organism. Traditional biochemical and genetic studies have revealed that CK2 is required for cell viability, cell cycle progression, cell polarity, ion homeostasis, and other functions, and have identified a number of potential physiological substrates of the enzyme. Data mining of available bioinformatic resources indicates that (1) there are likely to be hundreds of CK2 targets in this organism, (2) the majority of predicted CK2 substrates are involved in various aspects of global gene expression, (3) CK2 is present in several nuclear protein complexes predicted to have a role in chromatin structure and remodeling, transcription, or RNA metabolism, and (4) CK2 is localized predominantly in the nucleus. These bioinformatic results suggest that the observed phenotypic consequences of CK2 depletion may lie downstream of primary defects in chromatin organization and/or global gene expression. Further progress in defining the physiological role of CK2 will almost certainly require a better understanding of the mechanism of regulation of the enzyme. Beginning with the crystal structure of the human CK2 holoenzyme, we present a molecular model of filamentous CK2 that is consistent with earlier proposals that filamentous CK2 represents an inactive form of the enzyme. The potential role of filamentous CK2 in regulation in vivo is discussed.

Indexed as

Casein Kinase IICell NucleusComputational BiologyGene Expression Regulation, EnzymologicHoloenzymesHumansModels, MolecularNuclear MatrixPhosphorylationSaccharomyces cerevisiaeSignal TransductionSubstrate SpecificityCasein Kinase IIHoloenzymes

Identifiers

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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.