Evidence map›Paper›PMID 28325868›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Inositol phosphates and phosphoinositides activate insulin-degrading enzyme, while phosphoinositides also mediate binding to endosomes.

Eun Suk Song, HyeIn Jang, Hou-Fu Guo, Maria A Juliano, Luiz Juliano, Andrew J Morris, Emilia Galperin, David W Rodgers, Louis B Hersh

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

19 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Disorder-to-order active site capping regulates the rate-limiting step of the inositol pathway.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Targeting Insulin-Degrading Enzyme in Insulin Clearance.International journal of molecular sciences · 2021
    Review
  14. Review
  15. Review
  16. Article
  17. The cell biology of systemic insulin function.The Journal of cell biology · 2018
    Review
  18. Article
  19. 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 2 countries.

Eun Suk SongDepartment of Molecular and Cellular Biochemistry, University of Kentucky, Lexington, KY 40536.
HyeIn JangDepartment of Molecular and Cellular Biochemistry, University of Kentucky, Lexington, KY 40536.
Hou-Fu GuoDepartment of Molecular and Cellular Biochemistry, University of Kentucky, Lexington, KY 40536.
Maria A JulianoDepartment of Biophysics, Escola Paulista de Medicina, Universidade Federal de Sao Paulo, 04044-020 Sao Paulo, Brazil.
Luiz JulianoDepartment of Biophysics, Escola Paulista de Medicina, Universidade Federal de Sao Paulo, 04044-020 Sao Paulo, Brazil.
Andrew J MorrisDivision of Cardiovascular Medicine, University of Kentucky College of Medicine, Lexington, KY 40536.
Emilia GalperinDepartment of Molecular and Cellular Biochemistry, University of Kentucky, Lexington, KY 40536.
David W RodgersDepartment of Molecular and Cellular Biochemistry, University of Kentucky, Lexington, KY 40536; david.rodgers@uky.edu lhersh@uky.edu.
Louis B HershDepartment of Molecular and Cellular Biochemistry, University of Kentucky, Lexington, KY 40536; david.rodgers@uky.edu lhersh@uky.edu.
University of Kentucky · USUniversidade Federal de São Paulo · BR

Funding

The role of IKKß in linking obesity to adipose tissue inflammation and adipogeneP20GM103527 · NIGMS · UNIVERSITY OF KENTUCKY · PI CASSIS, LISA A · 2012 to 2017
$13.7M
Center for Biomedical Research Excellence in the Molecular Basis of Human DiseaseP20GM103486 · NIGMS · UNIVERSITY OF KENTUCKY · PI LOUIS HERSH, LOUIS HERSH LOUIS HERSH · 2012 to 2013
$4.2M
Supplement to Deciphering the molecular mechanisms underlying active scaffoldingR01GM113087 · NIGMS · UNIVERSITY OF KENTUCKY · PI GALPERIN, EMILIA · 2015 to 2019
$2.0M
Neuropeptidase FunctionR01NS038041 · NINDS · UNIVERSITY OF KENTUCKY · PI RODGERS, DAVID W · 2001 to 2004
$1.0M
Neuropeptidase FunctionR56NS038041 · NINDS · UNIVERSITY OF KENTUCKY · PI RODGERS, DAVID W · 2007 to 2007
$330k
NIGMS NIH HHS P20 GM103486NIGMS NIH HHS P20 GM103527NIGMS NIH HHS R01 GM113087NINDS NIH HHS R01 NS038041NINDS NIH HHS R56 NS038041
6 · The paper itself

Abstract

Insulin-degrading enzyme (IDE) hydrolyzes bioactive peptides, including insulin, amylin, and the amyloid β peptides. Polyanions activate IDE toward some substrates, yet an endogenous polyanion activator has not yet been identified. Here we report that inositol phosphates (InsPs) and phosphatdidylinositol phosphates (PtdInsPs) serve as activators of IDE. InsPs and PtdInsPs interact with the polyanion-binding site located on an inner chamber wall of the enzyme. InsPs activate IDE by up to ∼95-fold, affecting primarily

Indexed as

AndrostadienesAnimalsBinding SitesChlorocebus aethiopsCOS CellsEndosomesEnzyme ActivationEnzymes, ImmobilizedHydrogen-Ion ConcentrationInositol PhosphatesInsulysinLiposomesMutationPhosphatidylinositolsWortmanninAndrostadienesEnzymes, ImmobilizedInositol PhosphatesInsulysinLiposomesPhosphatidylinositolsWortmanninactivationinositolsinsulin-degrading enzymephosphatidylinositolssubcellular localization

Identifiers

PMID28325868
PMCPMC5389272
OpenAlexW2599273336

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.