Evidence map›Paper›PMID 41008633›Full record

ArticleBiomolecules2025

Bile Acids Are Potential Negative Allosteric Modulators of M1 Muscarinic Receptors.

Wenbo Yu, Alexander D MacKerell, David J Weber, Jean-Pierre Raufman

Abstract read
In one paragraph

Article in Biomolecules, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

4 authors.

Wenbo YuComputer-Aided Drug Design Center, Department of Pharmaceutical Sciences, School of Pharmacy, University of Maryland Baltimore, Baltimore, MD 21201, USA.ORCID 0000-0001-6962-5314
Alexander D MacKerellComputer-Aided Drug Design Center, Department of Pharmaceutical Sciences, School of Pharmacy, University of Maryland Baltimore, Baltimore, MD 21201, USA.ORCID 0000-0001-8287-6804
David J WeberInstitute for Bioscience and Biotechnology Research (IBBR), Rockville, MD 20850, USA.ORCID 0000-0002-8824-1110
Jean-Pierre RaufmanDepartment of Biochemistry and Molecular Biology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.ORCID 0000-0002-6340-4382

Funding

Macromolecular Conformational HeterogeneityR35GM131710 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE · PI ALEXANDER D MACKERELL · 2019 to 2026
$6.2M
Signal Propagation in Protein Allostery: Mechanism and EvolutionR01GM129327 · NIGMS · UNIV OF MARYLAND, COLLEGE PARK · PI WEBER, DAVID JOSEPH · 2019 to 2022
$1.3M
BLRD VA I01 BX004890NIGMS NIH HHS R01 GM129327NIGMS NIH HHS R35 GM131710NIH HHS 5R01GM129327-04NIH HHS 5R35GM131710-07United States Department of Veterans Affairs BX004890
6 · The paper itself

Abstract

The proposed physiological roles of bile acids have expanded beyond the digestion of fats to encompass cell signaling via the activation of a variety of nuclear and plasma membrane receptors in multiple organ systems. The current in silico study was inspired by previous observations from our group and others that bile acids interact functionally with cardiac, pulmonary, and gastrointestinal muscarinic receptors and more recent work demonstrating allosteric binding of cholesterol, the parent molecule for bile acid synthesis, to M

Indexed as

Bile Acids and SaltsReceptor, Muscarinic M1Allosteric RegulationAllosteric SiteBinding SitesHumansMolecular Dynamics SimulationProtein BindingBile Acids and SaltsReceptor, Muscarinic M1allosteric bindingbile acidscholinergic signalingdockingmolecular dynamicsmuscarinic receptorssite identification by ligand competitive saturation

Identifiers

PMID41008633
PMCPMC12467027

What Socratic 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 Socratic graph.