Evidence map›Paper›PMID 1848015›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1991

Drosophila stimulatory G protein alpha subunit activates mammalian adenylyl cyclase but interacts poorly with mammalian receptors: implications for receptor-G protein interaction.

F Quan, L Thomas, M Forte

Open access · greenAbstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1991. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.7field-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

12 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Modulation of the light response by cAMP in Drosophila photoreceptors.The Journal of neuroscience : the official journal of the Society for Neuroscience · 1999
    Article
  9. Activation of protein kinase A-independent pathways by Gs alpha in Drosophila.Proceedings of the National Academy of Sciences of the United States of America · 1996
    Article
  10. Article
  11. Review
  12. 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

3 authors at 1 institution in 1 country.

F QuanVollum Institute for Advanced Biomedical Research, Oregon Health Sciences University, Portland 97201.
L Thomas
M Forte
Vollum Institute · US

Funding

Role of PACS proteins in polycystin-2 trafficking and ADPKDR01DK037274 · NIDDK · OREGON HEALTH & SCIENCE UNIVERSITY · PI THOMAS, GARY · 1986 to 2010
$3.3M
NIDDK NIH HHS DK37274
6 · The paper itself

Abstract

Heterotrimeric guanine nucleotide binding proteins (G proteins) transduce signals from cell-surface receptors to intracellular effector proteins. Two forms of stimulatory G protein (Gs) alpha-like subunit have been described in Drosophila melanogaster. To examine the function of these subunits we have used vaccinia virus vectors to express both proteins in cyc- cells, a murine S49 cell line deficient for Gs alpha activity. Receptor-independent activation of each Drosophila Gs alpha has demonstrated that both forms are capable of activating mammalian adenylyl cyclase and thus have the activity expected of stimulatory G proteins. However, the Drosophila Gs alpha subunits interact poorly with mammalian Gs-coupled receptors. These observations have helped to identify a region of high variability in Gs alpha proteins that may be important for receptor interactions.

Indexed as

Adenylyl CyclasesAmino Acid SequenceAnimalsAntisense Elements (Genetics)Base SequenceCell LineCholera ToxinCloning, MolecularDrosophilaEnzyme ActivationGenetic VectorsGTP-Binding ProteinsKineticsMacromolecular SubstancesMolecular Sequence DataMutagenesis, Site-DirectedAdenylyl CyclasesAntisense Elements (Genetics)Cholera ToxinGTP-Binding ProteinsMacromolecular SubstancesReceptors, Cell SurfaceRecombinant Proteins

Identifiers

PMID1848015
PMCPMC51133
OpenAlexW2034057052

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.