Evidence map›Paper›PMID 15928075›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2005

Building a human kinase gene repository: bioinformatics, molecular cloning, and functional validation.

Jaehong Park, Yanhui Hu, T V S Murthy, Fredrik Vannberg, Binghua Shen, Andreas Rolfs, Jessica E Hutti, Lewis C Cantley, Joshua Labaer, Ed Harlow and 1 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

25 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Controllability analysis of the directed human protein interaction network identifies disease genes and drug targets.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  3. Article
  4. Article
  5. Oncogenic Signaling Adaptor Proteins.Journal of genetics and genomics = Yi chuan xue bao · 2015
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. High-throughput ectopic expression screen for tamoxifen resistance identifies an atypical kinase that blocks autophagy.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
  14. Article
  15. Article
  16. High-throughput screens in diploid cells identify factors that contribute to the acquisition of chromosomal instability.Proceedings of the National Academy of Sciences of the United States of America · 2010
    Article
  17. Article
  18. Article
  19. Production and sequence validation of a complete full length ORF collection for the pathogenic bacterium Vibrio cholerae.Proceedings of the National Academy of Sciences of the United States of America · 2008
    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 1 institution in 1 country.

Jaehong ParkHarvard Institute of Proteomics, Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, 320 Charles Street, Cambridge, MA 02141, USA.
Yanhui Hu
T V S Murthy
Fredrik Vannberg
Binghua Shen
Andreas Rolfs
Jessica E Hutti
Lewis C Cantley
Joshua Labaer
Ed Harlow
Leonardo Brizuela
Harvard University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Kinases catalyze the phosphorylation of proteins, lipids, sugars, nucleosides, and other important cellular metabolites and play key regulatory roles in all aspects of eukaryotic cell physiology. Here, we describe the mining of public databases to collect the sequence information of all identified human kinase genes and the cloning of the corresponding ORFs. We identified 663 genes, 511 encoding protein kinases, and 152 encoding nonprotein kinases. We describe the successful cloning and sequence verification of 270 of these genes. Subcloning of this gene set in mammalian expression vectors and their use in high-throughput cell-based screens allowed the validation of the clones at the level of expression and the identification of previously uncharacterized modulators of the survivin promoter. Moreover, expressions of the kinase genes in bacteria, followed by autophosphorylation assays, identified 21 protein kinases that showed autocatalytic activity. The work described here will facilitate the functional assaying of this important gene family in phenotypic screens and their use in biochemical and structural studies.

Indexed as

Cloning, MolecularComputational BiologyDatabases, GeneticAnimalsBiological AssayCatalysisCell LineCellsGene Expression RegulationGenetic VectorsHumansMolecular Sequence DataPhenotypePhosphorylationPlasmidsPromoter Regions, GeneticProtein KinasesRecombinant Proteins

Identifiers

PMID15928075
PMCPMC1149441
OpenAlexW2043052104

What OpenQuestion holds

Textmetadata
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.