Evidence map›Paper›PMID 29249607›Full record

ArticleStructure (London, England : 1993)2018

Intracellular Transfer of Na

Owen N Vickery, Catarina A Carvalheda, Saheem A Zaidi, Andrei V Pisliakov, Vsevolod Katritch, Ulrich Zachariae

Open access · bronzeAbstract read
In one paragraph

Article in Structure (London, England : 1993), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

54 citing papers in PubMed, 98 citations in OpenAlex.

  1. Review
  2. Article
  3. The role of the tryptophan-rich allosteric network and sodium egress in GPCR activation.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  4. Article
  5. Review
  6. Constant-pH Simulation of the Human βJournal of chemical information and modeling · 2025
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. pJournal of chemical information and modeling · 2024
    Article
  15. Article
  16. Review
  17. Sodium regulates PLC and IPPhysiological reports · 2023
    Article
  18. The World of GPCR dimers - Mapping dopamine receptor DComputational and structural biotechnology journal · 2023
    Article
  19. Protons taken hostage: Dynamic H-bond networks of the pH-sensing GPR68.Computational and structural biotechnology journal · 2023
    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

6 authors at 2 institutions in 2 countries.

Owen N VickerySchool of Life Sciences, University of Dundee, Dundee DD1 5EH, UK; School of Science and Engineering, University of Dundee, Dundee DD1 4NH, UK.
Catarina A CarvalhedaSchool of Life Sciences, University of Dundee, Dundee DD1 5EH, UK; School of Science and Engineering, University of Dundee, Dundee DD1 4NH, UK.
Saheem A ZaidiDepartment of Biological Sciences, Bridge Institute, University of Southern California, Los Angeles, CA 90089, USA.
Andrei V PisliakovSchool of Life Sciences, University of Dundee, Dundee DD1 5EH, UK; School of Science and Engineering, University of Dundee, Dundee DD1 4NH, UK.
Vsevolod KatritchDepartment of Biological Sciences, Bridge Institute, University of Southern California, Los Angeles, CA 90089, USA; Department of Chemistry, Bridge Institute, University of Southern California, Los Angeles, CA 90089, USA.
Ulrich ZachariaeSchool of Life Sciences, University of Dundee, Dundee DD1 5EH, UK; School of Science and Engineering, University of Dundee, Dundee DD1 4NH, UK. Electronic address: u.zachariae@dundee.ac.uk.
University of Dundee · GBUniversity of Southern California · US

Funding

Structure-Function of Opioid ReceptorsP01DA035764 · NIDA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CHEREZOV, VADIM, ROTH, BRYAN L. · 2014 to 2018
$7.1M
Rational discovery of new DOR chemotypes to prevent addiction and overdoseR33DA038858 · NIDA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI KATRITCH, VSEVOLOD · 2017 to 2018
$719k
Biotechnology and Biological Sciences Research Council BB/J013072/1NIDA NIH HHS P01 DA035764NIDA NIH HHS R33 DA038858
6 · The paper itself

Abstract

Playing a central role in cell signaling, G-protein-coupled receptors (GPCRs) are the largest superfamily of membrane proteins and form the majority of drug targets in humans. How extracellular agonist binding triggers the activation of GPCRs and associated intracellular effector proteins remains, however, poorly understood. Structural studies have revealed that inactive class A GPCRs harbor a conserved binding site for Na

Indexed as

Amino Acid MotifsBinding SitesCarbacholCations, MonovalentHumansHydrophobic and Hydrophilic InteractionsIon Channel GatingIon TransportKineticsLigandsMolecular Dynamics SimulationPhosphatidylcholinesProtein BindingProtein Conformation, alpha-HelicalProtein Interaction Domains and MotifsReceptor, Muscarinic M21-palmitoyl-2-oleoylphosphatidylcholineCarbacholCations, MonovalentCHRM2 protein, humanLigandsPhosphatidylcholinesReceptor, Muscarinic M2Sodiumfree energy profilesGPCRGPCR activationion channelsmembrane surface receptorspK(a)polar networkprotonation statesignal transductionsodium

Identifiers

PMID29249607
PMCPMC5805466
OpenAlexW2952263612

What OpenQuestion holds

Textmetadata
LicenceTDM
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.