Evidence map›Paper›PMID 37258918›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2023

Prediction of TAP Transport of Peptides with Variable Length Using TAPREG.

Hector F Pelaez-Prestel, Sara Alonso Fernandez, Laura Ballesteros-Sanabria, Pedro A Reche

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

4 authors at 1 institution in 1 country.

Hector F Pelaez-PrestelSchool of Medicine, Department of Immunology, Complutense University of Madrid, Madrid, Spain.
Sara Alonso FernandezSchool of Medicine, Department of Immunology, Complutense University of Madrid, Madrid, Spain.
Laura Ballesteros-SanabriaSchool of Medicine, Department of Immunology, Complutense University of Madrid, Madrid, Spain.
Pedro A RecheSchool of Medicine, Department of Immunology, Complutense University of Madrid, Madrid, Spain. parecheg@med.ucm.es.
Universidad Complutense de Madrid · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CD8 T cells recognize short peptides, more frequently of nine residues, presented by class I major histocompatibility complex (MHC I) molecules in the cell surface of antigen-presenting cells. These epitope peptides are loaded onto MHC I molecules in the endoplasmic reticulum, where they are shuttled from the cytosol by the transporter associated with antigen processing (TAP) as such or as N-terminal extended precursors of up to 16 residues. In this chapter, we describe the use of TAPREG, a tool for predicting TAP binding affinity that has been enhanced to identify potential CD8 T cell epitope precursors transported by TAP. TAPREG is available for free public use at http://imed.med.ucm.es/Tools/tapreg/ .

Indexed as

ATP-Binding Cassette TransportersPeptidesAntigen PresentationHistocompatibility Antigens Class IMembrane Transport ProteinsATP-Binding Cassette TransportersHistocompatibility Antigens Class IMembrane Transport ProteinsPeptidesEpitope predictionPeptide transportTAPTAPREG

Identifiers

PMID37258918
OpenAlexW4378801483

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.