Evidence map›Paper›PMID 39565315›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

Molecular basis for chemokine recognition and activation of XCR1.

Xuan Zhang, Roman R Schlimgen, Stephanie Singh, Michael P Tomani, Brian F Volkman, Cheng Zhang

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
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.

Xuan Zhang *Department of Pharmacology and Chemical Biology, School of Medicine, University of Pittsburgh, Pittsburgh, PA 15261.ORCID 0000-0002-4276-6464
Roman R Schlimgen *Department of Biochemistry, Medical College of Wisconsin, Milwaukee, WI 53226.ORCID 0000-0003-3395-5519
Stephanie SinghDepartment of Pharmacology and Chemical Biology, School of Medicine, University of Pittsburgh, Pittsburgh, PA 15261.
Michael P TomaniDepartment of Pharmacology and Chemical Biology, School of Medicine, University of Pittsburgh, Pittsburgh, PA 15261.
Brian F VolkmanDepartment of Biochemistry, Medical College of Wisconsin, Milwaukee, WI 53226.ORCID 0000-0002-6681-5179
Cheng ZhangDepartment of Pharmacology and Chemical Biology, School of Medicine, University of Pittsburgh, Pittsburgh, PA 15261.ORCID 0000-0001-9042-4007

Funding

Structure, pharmacology and signaling of G protein-coupled receptors (GPCRs) in inflammationR35GM128641 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CHENG ZHANG · 2018 to 2026
$3.5M
Structural Basis for Chemokine FunctionR37AI058072 · NIAID · MEDICAL COLLEGE OF WISCONSIN · PI Brian F Volkman · 2020 to 2026
$2.8M
Evolution and design of metamorphic fold-switching proteinsR01AI168423 · NIAID · MEDICAL COLLEGE OF WISCONSIN · PI Brian F Volkman · 2023 to 2026
$2.3M
Cryo-electron microscopeS10OD025009 · OD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CONWAY, JAMES F. · 2018 to 2018
$2.0M
Direct electron detecting (DED) cameraS10OD019995 · OD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CONWAY, JAMES F. · 2015 to 2015
$548k
HHS | NIH | National Institute of Allergy and Infectious Diseases (NIAID) R01AI168423HHS | NIH | National Institute of Allergy and Infectious Diseases (NIAID) R37AI058072HHS | NIH | National Institute of General Medical Sciences (NIGMS) R35GM128641NIAID NIH HHS R01 AI168423NIAID NIH HHS R37 AI058072NIGMS NIH HHS R35 GM128641NIH HHS S10 OD019995NIH HHS S10 OD025009
6 · The paper itself

Abstract

The X-C motif chemokine receptor XCR1, which selectively binds to the chemokine XCL1, is highly expressed in conventional dendritic cells subtype 1 (cDC1s) and crucial for their activation. Modulating XCR1 signaling in cDC1s could offer novel opportunities in cancer immunotherapy and vaccine development by enhancing the antigen presentation function of cDC1s. To investigate the molecular mechanism of XCL-induced XCR1 signaling, we determined a high-resolution structure of the human XCR1 and G

Indexed as

Chemokines, CCryoelectron MicroscopyReceptors, G-Protein-CoupledBinding SitesDendritic CellsHumansModels, MolecularProtein BindingReceptors, ChemokineSignal TransductionChemokines, CReceptors, ChemokineReceptors, G-Protein-CoupledXCL1 protein, humanXCR1 protein, humanchemokine receptorsconventional dendritic cells subtype 1cryo-electron microscopy (cryo-EM)XCL1XCR1

Identifiers

PMID39565315
PMCPMC11621518

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.