Evidence map›Paper›PMID 23922959›Full record

ArticlePloS one2013

Nucleotidyl cyclase activity of particulate guanylyl cyclase A: comparison with particulate guanylyl cyclases E and F, soluble guanylyl cyclase and bacterial adenylyl cyclases CyaA and edema factor.

Kerstin Y Beste, Corinna M Spangler, Heike Burhenne, Karl-Wilhelm Koch, Yuequan Shen, Wei-Jen Tang, Volkhard Kaever, Roland Seifert

Open access · goldAbstract readComparative Study
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
6.7field-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

20 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Recent progress in the field of cIMP research.Naunyn-Schmiedeberg's archives of pharmacology · 2016
    Article
  12. Article
  13. Review
  14. cCMP and cUMP occur in vivo.Biochemical and biophysical research communications · 2015
    Article
  15. PDE and sGC hand in hand to see the light.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  16. Article
  17. Article
  18. Is cIMP a second messenger with functions opposite to those of cGMP?Naunyn-Schmiedeberg's archives of pharmacology · 2014
    Article
  19. Tissues cIMPly do not lie.Naunyn-Schmiedeberg's archives of pharmacology · 2014
    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

8 authors at 4 institutions in 3 countries.

Kerstin Y BesteInstitute of Pharmacology, Hannover Medical School, Hannover, Germany.
Corinna M Spangler
Heike Burhenne
Karl-Wilhelm Koch
Yuequan Shen
Wei-Jen Tang
Volkhard Kaever
Roland Seifert
Medizinische Hochschule Hannover · DECarl von Ossietzky Universität Oldenburg · DENankai University · CNUniversity of Chicago · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Guanylyl cyclases (GCs) regulate many physiological processes by catalyzing the synthesis of the second messenger cGMP. The GC family consists of seven particulate GCs (pGCs) and a nitric oxide-activated soluble GC (sGC). Rat sGC α1β1 possesses much broader substrate specificity than previously assumed. Moreover, the exotoxins CyaA from Bordetella pertussis and edema factor (EF) from Bacillus anthracis possess nucleotidyl cyclase (NC) activity. pGC-A is a natriuretic peptide-activated homodimer with two catalytic sites that act cooperatively. Here, we studied the NC activity of rat pGC-A in membranes of stably transfected HEK293 cells using a highly sensitive and specific HPLC-MS/MS technique. GTP and ITP were effective, and ATP and XTP were only poor, pGC-A substrates. In contrast to sGC, pGC-A did not use CTP and UTP as substrates. pGC-E and pGC-F expressed in bovine rod outer segment membranes used only GTP as substrate. In intact HEK293 cells, pGC-A generated only cGMP. In contrast to pGCs, EF and CyaA showed very broad substrate-specificity. In conclusion, NCs exhibit different substrate-specificities, arguing against substrate-leakiness of enzymes and pointing to distinct physiological functions of cyclic purine and pyrimidine nucleotides.

Indexed as

Adenylate Cyclase ToxinAnimalsAntigens, BacterialBacterial ToxinsCell LineCell MembraneCyclic GMPEnzyme ActivationGuanylate CyclaseHEK293 CellsHumansKineticsRatsReceptors, Atrial Natriuretic FactorReceptors, Cytoplasmic and NuclearSoluble Guanylyl CyclaseAdenylate Cyclase Toxinanthrax toxinAntigens, Bacterialatrial natriuretic factor receptor ABacterial ToxinsCyclic GMPGuanylate CyclaseReceptors, Atrial Natriuretic FactorReceptors, Cytoplasmic and NuclearSoluble Guanylyl Cyclase

Identifiers

PMID23922959
PMCPMC3726482
OpenAlexW2027354362

What OpenQuestion holds

Textmetadata
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.