Evidence map›Paper›PMID 25890336›Full record

ArticleBMC systems biology2015

Identification of AMP-activated protein kinase targets by a consensus sequence search of the proteome.

Traci L Marin, Brendan Gongol, Marcy Martin, Stephanie J King, Lemar Smith, David A Johnson, Shankar Subramaniam, Shu Chien, John Y-J Shyy

Open access · diamondAbstract read
In one paragraph

Article in BMC systems biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Roles of KLF4 and AMPK in the inhibition of glycolysis by pulsatile shear stress in endothelial cells.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  8. Role ofPhysiological reviews · 2021
    Review
  9. Epigenetic Regulation of Autophagy Beyond the Cytoplasm: A Review.Frontiers in cell and developmental biology · 2021
    Review
  10. Endothelial mechanobiology.APL bioengineering · 2020
    Article
  11. Article
  12. Shear stress regulation of miR-93 and miR-484 maturation through nucleolin.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  13. Article
  14. AMPK: An Epigenetic Landscape Modulator.International journal of molecular sciences · 2018
    Review
  15. Article
  16. Article
  17. Review
  18. 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

9 authors at 2 institutions in 1 country.

Traci L MarinDivisions of Biochemistry and Molecular Biology and Biomedical Sciences, University of California, Riverside, CA, 92521-0121, USA. tmarin@llu.edu.
Brendan GongolDivisions of Biochemistry and Molecular Biology and Biomedical Sciences, University of California, Riverside, CA, 92521-0121, USA. brengong@gmail.com.
Marcy MartinDivisions of Biochemistry and Molecular Biology and Biomedical Sciences, University of California, Riverside, CA, 92521-0121, USA. mam085@ucsd.edu.
Stephanie J KingDivisions of Biochemistry and Molecular Biology and Biomedical Sciences, University of California, Riverside, CA, 92521-0121, USA. sking009@ucr.edu.
Lemar SmithDivisions of Biochemistry and Molecular Biology and Biomedical Sciences, University of California, Riverside, CA, 92521-0121, USA. lsmit004@ucr.edu.
David A JohnsonDivisions of Biochemistry and Molecular Biology and Biomedical Sciences, University of California, Riverside, CA, 92521-0121, USA. david.johnson@ucr.edu.
Shankar SubramaniamDivision of Physiology, Department of Medicine, University of California, San Diego, La Jolla, CA, 92093, USA. shankar@ucsd.edu.
Shu ChienDivision of Physiology, Department of Medicine, University of California, San Diego, La Jolla, CA, 92093, USA. shuchien@ucsd.edu.
John Y-J ShyyDivisions of Biochemistry and Molecular Biology and Biomedical Sciences, University of California, Riverside, CA, 92521-0121, USA. jshyy@ucsd.edu.
University of California, Riverside · USUniversity of California San Diego · US

Funding

Systems Biology Analyses for Hemodynamic Regulation of Vascular HomeostasisR01HL108735 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHIEN, SHU, SHYY, JOHN YJ · 2012 to 2024
$13.4M
Training In Cardiovascular Physiology & PharmacologyT32HL007444 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Ju Chen, Robert Scott Ross · 1985 to 2026
$11.1M
Shear Stress, AMPK, and Endothelial FunctionsR01HL089940 · NHLBI · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI SHYY, JOHN YJ · 2009 to 2013
$1.9M
NHLBI NIH HHS HL108735NHLBI NIH HHS HL89940NHLBI NIH HHS R01 HL089940NHLBI NIH HHS R01 HL108735NHLBI NIH HHS T32 HL007444
6 · The paper itself

Abstract

backgroundAMP-activated protein kinase (AMPK) is a heterotrimeric serine/threonine protein kinase that is activated by cellular perturbations associated with ATP depletion or stress. While AMPK modulates the activity of a variety of targets containing a specific phosphorylation consensus sequence, the number of AMPK targets and their influence over cellular processes is currently thought to be limited.

resultsWe queried the human and the mouse proteomes for proteins containing AMPK phosphorylation consensus sequences. Integration of this database into Gaggle software facilitated the construction of probable AMPK-regulated networks based on known and predicted molecular associations. In vitro kinase assays were conducted for preliminary validation of 12 novel AMPK targets across a variety of cellular functional categories, including transcription, translation, cell migration, protein transport, and energy homeostasis. Following initial validation, pathways that include NAD synthetase 1 (NADSYN1) and protein kinase B (AKT2) were hypothesized and experimentally tested to provide a mechanistic basis for AMPK regulation of cell migration and maintenance of cellular NAD(+) concentrations during catabolic processes.

conclusionsThis study delineates an approach that encompasses both in silico procedures and in vitro experiments to produce testable hypotheses for AMPK regulation of cellular processes.

Indexed as

Consensus SequenceProteomicsSystems BiologyAMP-Activated Protein KinasesAnimalsBiological TransportCalciumCell CycleChromatinCircadian RhythmEndoplasmic Reticulum StressEnzyme ActivationEpigenesis, GeneticGlucoseHomeostasisHumansAMP-Activated Protein KinasesCalciumChromatinGlucoseInsulinRNA, Messenger

Identifiers

PMID25890336
PMCPMC4357066
OpenAlexW2021613801

What OpenQuestion holds

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LicenceCC BY
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.