Out of Commission

Note, as of July 8, 2014 peptide binding predictions can be made using either NetMHCpan version 2.8, or NetMHCpan version 2.7 (the earlier default)

Version 2.8 can be found at NetMHCpan-2.8

NetMHCpan has been updated further til NetMHCpan-4.1

Article abstracts

Main reference:

MHCcluster, a method for functional clustering of MHC molecules.
Thomsen M1, Lundegaard C1,3, Buus S4, Lund O1, Nielsen M1,2,
Immunogenetics. 2013, Jun 18.

1Center for Biological Sequence Analysis, Technical University of Denmark, DK-2800 Lyngby, Denmark
2Instituto de Investigaciones Biotecnolo#gicas, Universidad Nacional de San Martin, San Martin, Buenos Aires, Argentina,
2ALK, Boege Alle 6, DK-2970 Hoersholm, Denmark,
4Division of Experimental Immunology, Institute of Medical Microbiology and Immunology, University of Copenhagen, Denmark

The identification of peptides binding to major histocompatibility complexes (MHC) is a critical step in the understanding of T cell immune responses. The human MHC genomic region (HLA) is extremely polymorphic comprising several thousand alleles, many encoding a distinct molecule. The potentially unique specificities remain experimentally uncharacterized for the vast majority of HLA molecules. Likewise, for nonhuman species, only a minor fraction of the known MHC molecules have been characterized. Here, we describe a tool, MHCcluster, to functionally cluster MHC molecules based on their predicted binding specificity. The method has a flexible web interface that allows the user to include any MHC of interest in the analysis. The output consists of a static heat map and graphical tree-based visualizations of the functional relationship between MHC variants and a dynamic TreeViewer interface where both the functional relationship and the individual binding specificities of MHC molecules are visualized. We demonstrate that conventional sequence-based clustering will fail to identify the functional relationship between molecules, when applied to MHC system, and only through the use of the predicted binding specificity can a correct clustering be found. Clustering of prevalent HLA-A and HLA-B alleles using MHCcluster confirms the presence of 12 major specificity groups (supertypes) some however with highly divergent specificities. Importantly, some HLA molecules are shown not to fit any supertype classification. Also, we use MHCcluster to show that chimpanzee MHC class I molecules have a reduced functional diversity compared to that of HLA class I molecules. MHCcluster is available at www.cbs.dtu.dk/services/MHCcluster-2.0 .

PMID: 23775223

Full text