Evidence map›Paper›PMID 28425917›Full record

ArticleeLife2017

TAPBPR bridges UDP-glucose:glycoprotein glucosyltransferase 1 onto MHC class I to provide quality control in the antigen presentation pathway.

Andreas Neerincx, Clemens Hermann, Robin Antrobus, Andy van Hateren, Huan Cao, Nico Trautwein, Stefan Stevanović, Tim Elliott, Janet E Deane, Louise H Boyle

Open access · goldAbstract read
In one paragraph

Article in eLife, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
9.3field-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

39 citing papers in PubMed, 95 citations in OpenAlex.

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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

10 authors at 5 institutions in 3 countries.

Andreas NeerincxDepartment of Pathology, University of Cambridge, Cambridge, United Kingdom.
Clemens HermannDepartment of Pathology, University of Cambridge, Cambridge, United Kingdom.
Robin AntrobusCambridge Institute for Medical Research, University of Cambridge, Cambridge, United Kingdom.
Andy van HaterenFaculty of Medicine, University of Southampton, Southampton, United Kingdom.ORCID 0000-0002-3915-0239
Huan CaoDivision of Applied Medicine, Institute of Medical Sciences, University of Aberdeen, Aberdeen, United Kingdom.
Nico TrautweinDepartment of Immunology, Eberhard Karls University Tübingen, Tübingen, Germany.
Stefan StevanovićDepartment of Immunology, Eberhard Karls University Tübingen, Tübingen, Germany.
Tim ElliottFaculty of Medicine, University of Southampton, Southampton, United Kingdom.
Janet E DeaneCambridge Institute for Medical Research, University of Cambridge, Cambridge, United Kingdom.ORCID 0000-0002-4863-0330
Louise H BoyleDepartment of Pathology, University of Cambridge, Cambridge, United Kingdom.ORCID 0000-0002-3105-6555
University of Cambridge · GBUniversity of Southampton · GBUniversity of Tübingen · DEUniversity of Aberdeen · GBUniversity of Cape Town · ZA

Funding

Cancer Research UK 16997Cancer Research UK C7056AWellcome TrustWellcome Trust 089563Wellcome Trust 104647Wellcome Trust WT094847MA
6 · The paper itself

Abstract

Recently, we revealed that TAPBPR is a peptide exchange catalyst that is important for optimal peptide selection by MHC class I molecules. Here, we asked whether any other co-factors associate with TAPBPR, which would explain its effect on peptide selection. We identify an interaction between TAPBPR and UDP-glucose:glycoprotein glucosyltransferase 1 (UGT1), a folding sensor in the calnexin/calreticulin quality control cycle that is known to regenerate the Glc

Indexed as

Antigen PresentationCell LineGlucosyltransferasesHistocompatibility Antigens Class IHumansImmunoglobulinsMembrane ProteinsProtein Interaction MappingProtein MultimerizationUDP-Galactose TranslocatorsGlucosyltransferasesHistocompatibility Antigens Class IImmunoglobulinsMembrane ProteinsTAPBPL protein, humanUDP-Galactose TranslocatorsUGGT1 protein, humanantigen processing & presentationcell biologyHLAhumanimmunologyMHCTAPBPLTAPBPR

Identifiers

PMID28425917
PMCPMC5441866
OpenAlexW2606007585

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.