MHC Motif Atlas

MHC Motif Atlas catalogs binding specificities and curated ligand datasets for Major Histocompatibility Complex (MHC) molecules to support analysis of MHC–peptide binding and T-cell epitope presentation.


Key Features:

  • Coverage: Comprehensive data on thousands of class I and class II MHC molecules.
  • Binding motifs: Detailed binding motifs characterizing MHC–peptide interactions.
  • Peptide length distributions: Empirical peptide length distributions across MHC ligands.
  • Phosphorylated ligands: Motifs and annotations associated with phosphorylated ligands.
  • Multiple specificities: Annotations of multiple specificities observed for certain MHC alleles.
  • Structural integration: Links to X-ray crystallography structures to relate motifs to atomic-level interactions.
  • Curated ligand datasets: Curated collections of MHC ligands comprising over a million entries.

Scientific Applications:

  • T-cell epitope analysis: Mapping how pathogen- or cancer-derived peptides bind and are presented by MHC molecules for T-cell recognition.
  • Vaccine design: Informing selection of candidate peptides for personalized cancer vaccine development.
  • Adoptive cell therapy: Supporting identification of target peptides for adoptive T-cell therapy development.
  • Structure–function studies: Correlating peptide-binding motifs with X-ray crystallography data to study atomic-level MHC–peptide interactions.

Methodology:

The provided description does not specify computational methods, algorithms, or processing pipelines used.

Topics

Details

Cost:
Free of charge
Tool Type:
web application
Operating Systems:
Mac, Linux, Windows
Added:
2/8/2023
Last Updated:
11/24/2024

Operations

Publications

Tadros DM, Eggenschwiler S, Racle J, Gfeller D. The MHC Motif Atlas: a database of MHC binding specificities and ligands. Nucleic Acids Research. 2022;51(D1):D428-D437. doi:10.1093/nar/gkac965. PMID:36318236. PMCID:PMC9825574.

PMID: 36318236
PMCID: PMC9825574
Funding: - Swiss Cancer Research Foundation: KFS-4104-02-2017