Evidence map›Paper›PMID 1333843›Full record

ArticleMolecular biology of the cell1992

Identification of the domains in cyclin A required for binding to, and activation of, p34cdc2 and p32cdk2 protein kinase subunits.

H Kobayashi, E Stewart, R Poon, J P Adamczewski, J Gannon, T Hunt

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 1992. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

60 citing papers in PubMed, 193 citations in OpenAlex.

  1. Article
  2. Atypical cyclins: the extended family portrait.Cellular and molecular life sciences : CMLS · 2020
    Review
  3. Article
  4. Mechanisms of Mitotic Kinase Regulation: A Structural Perspective.Frontiers in cell and developmental biology · 2018
    Review
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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 at 1 institution in 1 country.

H KobayashiICRF Clare Hall Laboratories, South Mimms, Herts, England.
E Stewart
R Poon
J P Adamczewski
J Gannon
T Hunt
RF Laboratories (United States) · US

Funding

Wellcome Trust
6 · The paper itself

Abstract

The binding of cyclin A to p34cdc2 and p32cdk2 and the protein kinase activity of the complexes has been measured by cell-free translation of the corresponding mRNA in extracts of frog eggs, followed by immunoprecipitation. A variety of mutant cyclin A molecules have been constructed and tested in this assay. Small deletions and point mutations of highly conserved residues in the 100-residue "cyclin box" abolish binding and activation of both p34cdc2 and p32cdk2. By contrast, large deletions at the N-terminus have no effect on kinase binding and activation, until they remove residues beyond 161, where the first conserved amino acids are found in all known examples of cyclin A. At the C-terminus, removal of 14 or more amino acids abolishes activity. We also demonstrate that deletion of, or point mutations, in the cyclin A homologue of the 10-residue "destruction box," previously described in cyclin B (Glotzer et al., 1991) abolish cyclin proteolysis at the transition from M-phase to interphase.

Indexed as

CDC2-CDC28 KinasesCyclin-Dependent KinasesProtein Serine-Threonine KinasesAmino Acid SequenceAnimalsBase SequenceBinding SitesCDC2 Protein KinaseCells, CulturedCyclin-Dependent Kinase 2CyclinsElectrophoresis, Polyacrylamide GelMolecular Sequence DataMutationOocytesPoint MutationCDC2-CDC28 KinasesCDC2 Protein KinaseCdk2 protein, XenopusCyclin-Dependent Kinase 2Cyclin-Dependent KinasesCyclinsProtamine KinaseProtein KinasesProtein Serine-Threonine KinasesRNA, MessengerXenopus Proteins

Identifiers

PMID1333843
PMCPMC275694
OpenAlexW2131717330

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.