Evidence map›Paper›PMID 33374958›Full record

ArticleInternational journal of molecular sciences2020

MHCII3D-Robust Structure Based Prediction of MHC II Binding Peptides.

Josef Laimer, Peter Lackner

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

4 citing papers in PubMed, 19 citations in OpenAlex.

  1. Current medicinal chemistry · 2024
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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

2 authors at 1 institution in 1 country.

Josef LaimerDepartment of Biosciences, University of Salzburg, 5020 Salzburg, Austria.ORCID 0000-0001-6413-4268
Peter LacknerDepartment of Biosciences, University of Salzburg, 5020 Salzburg, Austria.ORCID 0000-0003-4681-6307
University of Salzburg · AT

Funding

Austrian Science Fund P30042Austrian Science Fund FWF P 30042
6 · The paper itself

Abstract

Knowledge of MHC II binding peptides is highly desired in immunological research, particularly in the context of cancer, autoimmune diseases, or allergies. The most successful prediction methods are based on machine learning methods trained on sequences of experimentally characterized binding peptides. Here, we describe a complementary approach called MHCII3D, which is based on structural scaffolds of MHC II-peptide complexes and statistical scoring functions (SSFs). The MHC II alleles reported in the Immuno Polymorphism Database are processed in a dedicated 3D-modeling pipeline providing a set of scaffold complexes for each distinct allotype sequence. Antigen protein sequences are threaded through the scaffolds and evaluated by optimized SSFs. We compared the predictive power of MHCII3D with different sequence-based machine learning methods. The Pearson correlation to experimentally determine IC

Indexed as

AlgorithmsAllelesComputational BiologyEpitopesHistocompatibility Antigens Class IIHLA-DRB1 ChainsHumansInternetMachine LearningPeptidesReproducibility of ResultsSoftwareEpitopesHistocompatibility Antigens Class IIHLA-DRB1 ChainsPeptidesbioinformaticsMHC II peptide bindingstatistical scoring functionstructure based binding prediction

Identifiers

PMID33374958
PMCPMC7792572
OpenAlexW3118132248

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.