Evidence map›Paper›PMID 30401537›Full record

ReviewBiochimica et biophysica acta. Molecular cell research2019

Serine-threonine protein phosphatases: Lost in translation.

Victoria Kolupaeva

Abstract readReview
In one paragraph

Review in Biochimica et biophysica acta. Molecular cell research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

8 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. A Highly Selective MNK Inhibitor Rescues Deficits Associated with Fragile X Syndrome in Mice.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2021
    Article
  6. Article
  7. Review
  8. 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

1 author at 1 institution in 1 country.

Victoria KolupaevaNYU College of Dentistry, Department of Basic Science and Craniofacial Biology, 345 E 24th St, New York, NY 10010, United States of America. Electronic address: kolupv01@nyu.edu.
New York University · US

Funding

Translational Control in Cartilage Biology. - Resubmission - 1R01AR063128 · NIAMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI KOLUPAEVA, VICTORIA · 2013 to 2017
$1.8M
NIAMS NIH HHS R01 AR063128
6 · The paper itself

Abstract

Protein synthesis is one of the most complex and energy-consuming processes in eukaryotic cells and therefore is tightly regulated. One of the main mechanisms of translational control is post-translational modifications of the components of translational apparatus. Phosphorylation status of translation factors depends on the balanced action of kinases and phosphatases. While many kinase-dependent events are well defined, phosphatases that counteract phosphorylation are rarely determined. This mini-review focuses on the regulation of activity of translational initiation factors by serine/threonine phosphatases.

Indexed as

Eukaryotic Initiation Factor-2Eukaryotic Initiation Factor-4EEukaryotic Initiation FactorsPeptide Initiation FactorsPhosphoprotein PhosphatasesPhosphoproteinsPhosphorylationProtein BiosynthesisProtein KinasesProtein Phosphatase 1Protein Phosphatase 2Protein Processing, Post-TranslationalRibosomal Protein S6 KinasesEukaryotic Initiation Factor-2Eukaryotic Initiation Factor-4EEukaryotic Initiation FactorsPeptide Initiation FactorsPhosphoprotein PhosphatasesPhosphoproteinsProtein KinasesProtein Phosphatase 1Protein Phosphatase 2Ribosomal Protein S6 Kinases4E-BPPP1PP2ATranslation

Identifiers

PMID30401537
PMCPMC6430236
OpenAlexW2888404180

What OpenQuestion holds

Textmetadata
LicenceTDM
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.