Evidence map›Paper›PMID 30837283›Full record

ArticleJournal of cell science2019

Phosphorylation at distinct subcellular locations underlies specificity in mTORC2-mediated activation of SGK1 and Akt.

Catherine E Gleason, Juan A Oses-Prieto, Kathy H Li, Bidisha Saha, Gavin Situ, Alma L Burlingame, David Pearce

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cell science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

37 citing papers in PubMed, 61 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Inhibition of mTORC1 by rapamycin results in feedback activation of AktbioRxiv : the preprint server for biology · 2025
    Article
  8. Review
  9. Pathology oncology research : POR · 2024
    Article
  10. Article
  11. Review
  12. ROS signaling-induced mitochondrial Sgk1 expression regulates epithelial cell renewal.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. Review
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

7 authors at 1 institution in 1 country.

Catherine E GleasonDepartment of Medicine, Division of Nephrology, UCSF, San Francisco, CA 94143, USA catie@circlepharma.com.ORCID 0000-0002-0063-0729
Juan A Oses-PrietoDepartments of Chemistry and Pharmaceutical Chemistry, UCSF, San Francisco, CA 94143, USA.
Kathy H LiDepartments of Chemistry and Pharmaceutical Chemistry, UCSF, San Francisco, CA 94143, USA.
Bidisha SahaDepartment of Medicine, Division of Nephrology, UCSF, San Francisco, CA 94143, USA.
Gavin SituDepartment of Medicine, Division of Nephrology, UCSF, San Francisco, CA 94143, USA.
Alma L BurlingameDepartments of Chemistry and Pharmaceutical Chemistry, UCSF, San Francisco, CA 94143, USA.
David PearceDepartment of Medicine, Division of Nephrology, UCSF, San Francisco, CA 94143, USA.
University of California, San Francisco · US

Funding

SGK Regulation of Epithelial Sodium TransportR01DK056695 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI DAVID PEARCE · 2000 to 2026
$8.1M
Academic Training Program in NephrologyT32DK007219 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HSU, CHI-YUAN · 1986 to 2022
$7.3M
Bio-Organic Biomedical Mass Spectromy ResourceP41GM103481 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BURLINGAME, ALMA L · 2012 to 2015
$6.4M
Howard Hughes Medical InstituteNIDDK NIH HHS R01 DK056695NIDDK NIH HHS T32 DK007219NIGMS NIH HHS P41 GM103481
6 · The paper itself

Abstract

mTORC2 lies at the intersection of signaling pathways that control metabolism and ion transport through phosphorylation of the AGC-family kinases, the Akt and SGK1 proteins. How mTORC2 targets these functionally distinct downstream effectors in a context-specific manner is not known. Here, we show that the salt- and blood pressure-regulatory hormone, angiotensin II (AngII) stimulates selective mTORC2-dependent phosphorylation of SGK1 (S422) but not Akt (S473 and equivalent sites). Conventional PKC (cPKC), a critical mediator of the angiotensin type I receptor (AT

Indexed as

PhosphorylationHEK293 CellsHumansImmediate-Early ProteinsMechanistic Target of Rapamycin Complex 2Protein Serine-Threonine KinasesProto-Oncogene Proteins c-aktSerum-Glucocorticoid Regulated KinasesSignal TransductionAKT1 protein, humanImmediate-Early ProteinsMechanistic Target of Rapamycin Complex 2Protein Serine-Threonine KinasesProto-Oncogene Proteins c-aktSerum-Glucocorticoid Regulated KinasesAktAngiotensinmTORC2PKCSGKSIN1

Identifiers

PMID30837283
PMCPMC6467483
OpenAlexW2918312708

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.