Evidence map›Paper›PMID 34884716›Full record

ArticleInternational journal of molecular sciences2021

State-Targeting Stabilization of Adenosine A

Masaya Mitsumoto, Kanna Sugaya, Kazuki Kazama, Ryosuke Nakano, Takahiro Kosugi, Takeshi Murata, Nobuyasu Koga

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 50% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Hot-Spot-Guided Generative Deep Learning for Drug-Like PPI Inhibitor Design.Interdisciplinary sciences, computational life sciences · 2026
    Article
  2. 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

7 authors at 2 institutions in 1 country.

Masaya MitsumotoDepartment of Structural Molecular Science, School of Physical Sciences, SOKENDAI, The Graduate University for Advanced Studies, Shonan Village, Hayama 240-0193, Kanagawa, Japan.ORCID 0000-0003-4926-1757
Kanna SugayaDepartment of Chemistry, Graduate School of Science, Chiba University, Chiba 263-8522, Japan.
Kazuki KazamaDepartment of Chemistry, Graduate School of Science, Chiba University, Chiba 263-8522, Japan.
Ryosuke NakanoDepartment of Chemistry, Graduate School of Science, Chiba University, Chiba 263-8522, Japan.
Takahiro KosugiDepartment of Structural Molecular Science, School of Physical Sciences, SOKENDAI, The Graduate University for Advanced Studies, Shonan Village, Hayama 240-0193, Kanagawa, Japan.
Takeshi MurataDepartment of Chemistry, Graduate School of Science, Chiba University, Chiba 263-8522, Japan.ORCID 0000-0002-5748-4670
Nobuyasu KogaDepartment of Structural Molecular Science, School of Physical Sciences, SOKENDAI, The Graduate University for Advanced Studies, Shonan Village, Hayama 240-0193, Kanagawa, Japan.ORCID 0000-0001-8457-0809
Chiba University · JPNational Institutes of Natural Sciences · JP

Funding

Japan Society for the Promotion of Science 18H05420Japan Society for the Promotion of Science 18H05425
6 · The paper itself

Abstract

G-protein coupled receptors (GPCRs) are known for their low stability and large conformational changes upon transitions between multiple states. A widely used method for stabilizing these receptors is to make chimeric receptors by fusing soluble proteins (i.e., fusion partner proteins) into the intracellular loop 3 (ICL3) connecting the transmembrane helices 5 and 6 (TM5 and TM6). However, this fusion approach requires experimental trial and error to identify appropriate soluble proteins, residue positions, and linker lengths for making the fusion. Moreover, this approach has not provided state-targeting stabilization of GPCRs. Here, to rationally stabilize a class A GPCR, adenosine A

Indexed as

AdenosineAdenosine A2 Receptor AgonistsHumansLigandsModels, MolecularMolecular Dynamics SimulationProtein Conformation, alpha-HelicalProteinsReceptor, Adenosine A2ARecombinant Fusion ProteinsAdenosineAdenosine A2 Receptor AgonistsLigandsProteinsReceptor, Adenosine A2ARecombinant Fusion Proteinsadenosine A2A receptorcomputational protein designde novo designed proteinfusion partner proteinG-protein coupled receptorprotein stabilization

Identifiers

PMID34884716
PMCPMC8657880
OpenAlexW3215837282

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.