Evidence map›Paper›PMID 38332368›Full record

ArticleNature structural & molecular biology2024

Constitutive activation mechanism of a class C GPCR.

Jinwoo Shin, Junhyeon Park, Jieun Jeong, Jordy Homing Lam, Xingyu Qiu, Di Wu, Kuglae Kim, Joo-Youn Lee, Carol V Robinson, Jaekyung Hyun and 3 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature structural & molecular biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. A rare variant inProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Article
  7. Article
  8. 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

13 authors at 7 institutions in 3 countries.

Jinwoo Shin *Department of Life Sciences, Pohang University of Science and Technology, Pohang, Republic of Korea.ORCID http://orcid.org/0000-0003-4303-2419
Junhyeon Park *Department of Life Sciences, Pohang University of Science and Technology, Pohang, Republic of Korea.ORCID http://orcid.org/0000-0003-1069-1813
Jieun JeongDepartment of Applied Chemistry, Global Center for Pharmaceutical Ingredient Materials, Kyung Hee University, Yongin, Republic of Korea.
Jordy Homing LamDepartment of Quantitative and Computational Biology, University of Southern California, Los Angeles, CA, USA.
Xingyu QiuDepartment of Chemistry, University of Oxford, Oxford, UK.
Di WuDepartment of Chemistry, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0001-9748-4408
Kuglae KimDepartment of Pharmacy, Yonsei University, Incheon, Republic of Korea.
Joo-Youn LeeTherapeutics and Biotechnology Division, Korea Research Institute of Chemical Technology, 141 Gajeong-ro, Yuseong-gu, Daejeon, Republic of Korea.
Carol V RobinsonDepartment of Chemistry, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0001-7829-5505
Jaekyung HyunSchool of Pharmacy, Sungkyunkwan University, Suwon, Republic of Korea.ORCID http://orcid.org/0000-0003-2914-537X
Vsevolod KatritchDepartment of Quantitative and Computational Biology, University of Southern California, Los Angeles, CA, USA.ORCID http://orcid.org/0000-0003-3883-4505
Kwang Pyo KimDepartment of Applied Chemistry, Global Center for Pharmaceutical Ingredient Materials, Kyung Hee University, Yongin, Republic of Korea. kimkp@khu.ac.kr.ORCID http://orcid.org/0000-0003-0095-3787
Yunje ChoDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, Republic of Korea. yunje@postech.ac.kr.ORCID http://orcid.org/0000-0001-6481-1716
Pohang University of Science and Technology · KRUniversity of Oxford · GBUniversity of Southern California · USYonsei University · KRKorea Research Institute of Chemical Technology · KRKyung Hee University · KRSungkyunkwan University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Class C G-protein-coupled receptors (GPCRs) are activated through binding of agonists to the large extracellular domain (ECD) followed by rearrangement of the transmembrane domains (TMDs). GPR156, a class C orphan GPCR, is unique because it lacks an ECD and exhibits constitutive activity. Impaired GPR156-G

Indexed as

Receptors, G-Protein-CoupledSignal TransductionCryoelectron MicroscopyGTP-Binding ProteinsHumansPhospholipidsGTP-Binding ProteinsPhospholipidsReceptors, G-Protein-Coupled

Identifiers

PMID38332368
OpenAlexW4391653155

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.