Evidence map›Paper›PMID 31554800›Full record

ArticleNature communications2019

Purified F-ATP synthase forms a Ca

Andrea Urbani, Valentina Giorgio, Andrea Carrer, Cinzia Franchin, Giorgio Arrigoni, Chimari Jiko, Kazuhiro Abe, Shintaro Maeda, Kyoko Shinzawa-Itoh, Janna F M Bogers and 4 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 113 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
113citing papers in PubMed, 1 pooled it
10.2field-weighted citation impact, top 1% 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

113 citing papers in PubMed, 1 synthesis or guideline pooled it, 173 citations in OpenAlex.

  1. Pooled it
  2. ATP synthase subunits e and g are essential for CaCell death and differentiation · 2026
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53 more citing papers are in PubMed but not listed here.

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

14 authors at 7 institutions in 4 countries.

Andrea UrbaniDepartment of Biomedical Sciences, University of Padova, 35131, Padova, Italy.ORCID http://orcid.org/0000-0002-3935-6907
Valentina GiorgioDepartment of Biomedical Sciences, University of Padova, 35131, Padova, Italy.ORCID http://orcid.org/0000-0002-4229-3054
Andrea CarrerDepartment of Biomedical Sciences, University of Padova, 35131, Padova, Italy.
Cinzia FranchinDepartment of Biomedical Sciences, University of Padova, 35131, Padova, Italy.
Giorgio ArrigoniDepartment of Biomedical Sciences, University of Padova, 35131, Padova, Italy.
Chimari JikoInstitute for Integrated Radiation and Nuclear Science, Kyoto University, Kyoto, Japan.
Kazuhiro AbeCellular and Structural Physiology Institute, Nagoya University, Nagoya, Japan.ORCID http://orcid.org/0000-0003-2681-5921
Shintaro MaedaDepartment of Integrative Structural and Computational Biology, Scripps Research Institute, La Jolla, CA, 92037, USA.
Kyoko Shinzawa-ItohDepartment of Life Science, Graduate School of Life Science, University of Hyogo, Hyogo, 678-1297, Japan.
Janna F M BogersDepartment of Biotechnology, Delft University of Technology, 2629 HZ, Delft, The Netherlands.
Duncan G G McMillanDepartment of Biotechnology, Delft University of Technology, 2629 HZ, Delft, The Netherlands.ORCID http://orcid.org/0000-0001-6614-4494
Christoph GerleInstitute for Protein Research, Osaka University, Suita, Osaka, Japan. gerle.christoph@protein.osaka-u.ac.jp.ORCID http://orcid.org/0000-0002-7265-2804
Ildikò SzabòConsiglio Nazionale delle Ricerche Neuroscience Institute, 35131, Padova, Italy. ildi@bio.unipd.it.
Paolo BernardiDepartment of Biomedical Sciences, University of Padova, 35131, Padova, Italy. bernardi@bio.unipd.it.ORCID http://orcid.org/0000-0001-9187-3736
University of Padua · ITDelft University of Technology · NLJapan Agency for Medical Research and Development · JPKyoto University · JPNagoya University · JPScripps Research Institute · USUniversity of Hyogo · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The molecular identity of the mitochondrial megachannel (MMC)/permeability transition pore (PTP), a key effector of cell death, remains controversial. By combining highly purified, fully active bovine F-ATP synthase with preformed liposomes we show that Ca

Indexed as

Adenosine TriphosphateAnimalsCalciumCattleCryoelectron MicroscopyHydrolysisMagnesiumMembrane Potential, MitochondrialMitochondria, HeartMitochondrial Membrane Transport ProteinsMitochondrial Permeability Transition PoreMitochondrial Proton-Translocating ATPasesMitochondrial Transmembrane Permeability-Driven NecrosisProtein MultimerizationProtein SubunitsAdenosine TriphosphateCalciumMagnesiumMitochondrial Membrane Transport ProteinsMitochondrial Permeability Transition PoreMitochondrial Proton-Translocating ATPasesProtein Subunits

Identifiers

PMID31554800
PMCPMC6761146
OpenAlexW2976241964

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.