Evidence map›Paper›PMID 28760974›Full record

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

Structural basis of subunit selectivity for competitive NMDA receptor antagonists with preference for GluN2A over GluN2B subunits.

Genevieve E Lind, Tung-Chung Mou, Lucia Tamborini, Martin G Pomper, Carlo De Micheli, Paola Conti, Andrea Pinto, Kasper B Hansen

Open access · bronzeAbstract 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 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

32 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
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  7. Review
  8. Discovery of GluN2A subtype-selectiveActa pharmaceutica Sinica. B · 2024
    Review
  9. Multi-target Phenylpropanoids Against Epilepsy.Current neuropharmacology · 2024
    Review
  10. Selective Cell-Surface Expression of Triheteromeric NMDA Receptors.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  11. Therapeutic potential of N-methyl-D-aspartate receptor modulators in psychiatry.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Review
  12. Review
  13. Review
  14. Structural insights into NMDA receptor pharmacology.Biochemical Society transactions · 2023
    Review
  15. Review
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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 3 institutions in 2 countries.

Genevieve E LindDepartment of Biomedical and Pharmaceutical Sciences, University of Montana, Missoula, MT 59812.
Tung-Chung MouCenter for Biomolecular Structure and Dynamics, University of Montana, Missoula, MT 59812.
Lucia TamboriniDepartment of Pharmaceutical Sciences, University of Milan, 20133 Milan, Italy.
Martin G PomperRussell H. Morgan Department of Radiology and Radiological Science, Johns Hopkins Medical School, Baltimore, MD 21205.
Carlo De MicheliDepartment of Pharmaceutical Sciences, University of Milan, 20133 Milan, Italy.
Paola ContiDepartment of Pharmaceutical Sciences, University of Milan, 20133 Milan, Italy.
Andrea PintoDepartment of Food, Environmental and Nutritional Science, University of Milan, 20133 Milan, Italy kasper.hansen@mso.umt.edu andrea.pinto@unimi.it.
Kasper B HansenDepartment of Biomedical and Pharmaceutical Sciences, University of Montana, Missoula, MT 59812; kasper.hansen@mso.umt.edu andrea.pinto@unimi.it.ORCID 0000-0002-3303-4819
University of Milan · ITUniversity of Montana · USJohns Hopkins University · US

Funding

Surveillance genome sequencing to detect SARS-CoV-2 virus variants in MontanaP20GM103546 · NIGMS · UNIVERSITY OF MONTANA · PI BOWLER, BRUCE E · 2012 to 2021
$19.2M
Structural and functional investigation of negative allosteric NMDA receptor modulationR01NS097536 · NINDS · UNIVERSITY OF MONTANA · PI Kasper Boe Hansen · 2016 to 2026
$3.4M
NIGMS NIH HHS P20 GM103546NINDS NIH HHS R01 NS097536
6 · The paper itself

Abstract

NMDA-type glutamate receptors are ligand-gated ion channels that contribute to excitatory neurotransmission in the central nervous system (CNS). Most NMDA receptors comprise two glycine-binding GluN1 and two glutamate-binding GluN2 subunits (GluN2A-D). We describe highly potent (

Indexed as

AnimalsBinding, CompetitiveCrystallography, X-RayExcitatory Amino Acid AntagonistsFemaleGlutamic AcidHumansModels, MolecularOocytesPatch-Clamp TechniquesProtein DomainsProtein MultimerizationProtein SubunitsQuinoxalinesRatsReceptors, N-Methyl-D-Aspartate5-(alpha-methyl-4-bromobenzylamino)phosphonomethyl-1,4-dihydroquinoxaline-2,3-dioneExcitatory Amino Acid AntagonistsGlutamic AcidNR2B NMDA receptorProtein SubunitsQuinoxalinesReceptors, N-Methyl-D-Aspartatekinetic modelingPEAQXSchild analysissynaptic transmissionX-ray crystallography

Identifiers

PMID28760974
PMCPMC5565460
OpenAlexW2741991262

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.