Evidence map›Paper›PMID 31661432›Full record

ArticleeLife2019

The lysosomal transporter MFSD1 is essential for liver homeostasis and critically depends on its accessory subunit GLMP.

David Massa López, Melanie Thelen, Felix Stahl, Christian Thiel, Arne Linhorst, Marc Sylvester, Irm Hermanns-Borgmeyer, Renate Lüllmann-Rauch, Winnie Eskild, Paul Saftig and 1 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 18% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Orphan lysosomal solute carrier MFSD1 facilitates highly selective dipeptide transport.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  10. Article
  11. Essential role of MFSD1-GLMP-GIMAP5 in lymphocyte survival and liver homeostasis.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  12. Article
  13. Article
  14. [Lysosomal membrane proteinNan fang yi ke da xue xue bao = Journal of Southern Medical University · 2023
    Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. 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

11 authors at 6 institutions in 2 countries.

David Massa LópezInstitute of Biochemistry, Christian-Albrechts-University Kiel, Kiel, Germany.
Melanie ThelenInstitute for Biochemistry and Molecular Biology, Rheinische-Friedrich-Wilhelms-University, Bonn, Germany.
Felix StahlInstitute of Clinical Chemistry and Laboratory Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0002-7443-8967
Christian ThielCenter for Child and Adolescent Medicine, Department of Pediatrics I, University of Heidelberg, Heidelberg, Germany.
Arne LinhorstInstitute of Biochemistry, Christian-Albrechts-University Kiel, Kiel, Germany.
Marc SylvesterInstitute for Biochemistry and Molecular Biology, Rheinische-Friedrich-Wilhelms-University, Bonn, Germany.
Irm Hermanns-BorgmeyerCenter for Molecular Neurobiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Renate Lüllmann-RauchInstitute for Anatomy, Christian-Albrechts-University Kiel, Kiel, Germany.
Winnie EskildDepartment of Bioscience, University of Oslo, Oslo, Norway.
Paul SaftigInstitute of Biochemistry, Christian-Albrechts-University Kiel, Kiel, Germany.
Markus DammeInstitute of Biochemistry, Christian-Albrechts-University Kiel, Kiel, Germany.ORCID 0000-0002-9699-9351
Christian-Albrechts-Universität zu Kiel · DEUniversität Hamburg · DEUniversity of Bonn · DEBielefeld University · DEHeidelberg University · DEUniversity of Oslo · NO

Funding

Deutsche Forschungsgemeinschaft DA 1785-1European Commission 607446 Euroclast
6 · The paper itself

Abstract

Lysosomes are major sites for intracellular, acidic hydrolase-mediated proteolysis and cellular degradation. The export of low-molecular-weight catabolic end-products is facilitated by polytopic transmembrane proteins mediating secondary active or passive transport. A number of these lysosomal transporters, however, remain enigmatic. We present a detailed analysis of MFSD1, a hitherto uncharacterized lysosomal family member of the major facilitator superfamily. MFSD1 is not N-glycosylated. It contains a dileucine-based sorting motif needed for its transport to lysosomes.

Indexed as

AnimalsHomeostasisLiverLysosomesMembrane ProteinsMembrane Transport ProteinsMice, KnockoutProtein BindingMembrane ProteinsMembrane Transport ProteinsMFSD1 protein, mouseNCU-G1 protein, mouseaccessory subunitbiochemistrycell biologychemical biologyGLMPlysosomalmajor facilitator superfamilyMFSD1mousetransporter

Identifiers

PMID31661432
PMCPMC6819133
OpenAlexW2982361520

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.