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A HLA-DRB supertype chart with potential overlapping peptide binding function
HLA-DRB alleles are class II alleles that are associated with CD4+ T-cell immune response. DRB alleles are polymorphic and currently there are about 622 named in the IMGT/HLA sequence database. Each allele binds short peptides with high sensitivity and specificity. However, it has been suggested tha...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Biomedical Informatics Publishing Group
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2957767/ https://www.ncbi.nlm.nih.gov/pubmed/20978603 |
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author | Mohanapriya, Arumugam Nandagond, Satish Shapshak, Paul Kangueane, Uma Kangueane, Pandjassarame |
author_facet | Mohanapriya, Arumugam Nandagond, Satish Shapshak, Paul Kangueane, Uma Kangueane, Pandjassarame |
author_sort | Mohanapriya, Arumugam |
collection | PubMed |
description | HLA-DRB alleles are class II alleles that are associated with CD4+ T-cell immune response. DRB alleles are polymorphic and currently there are about 622 named in the IMGT/HLA sequence database. Each allele binds short peptides with high sensitivity and specificity. However, it has been suggested that majority of HLA alleles can be covered within few HLA supertypes, where different members of a supertype bind similar peptides showing distinct repertoires. Definition of DRB supertypes using binding data is limited to few (about 29) known alleles (≪ 5% of all known DRB alleles). Hence, we describe a strategy using structurally defined virtual pockets to group all known DRB alleles with regard to their overlapping peptide binding specificity. |
format | Text |
id | pubmed-2957767 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Biomedical Informatics Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-29577672010-10-26 A HLA-DRB supertype chart with potential overlapping peptide binding function Mohanapriya, Arumugam Nandagond, Satish Shapshak, Paul Kangueane, Uma Kangueane, Pandjassarame Bioinformation Hypothesis HLA-DRB alleles are class II alleles that are associated with CD4+ T-cell immune response. DRB alleles are polymorphic and currently there are about 622 named in the IMGT/HLA sequence database. Each allele binds short peptides with high sensitivity and specificity. However, it has been suggested that majority of HLA alleles can be covered within few HLA supertypes, where different members of a supertype bind similar peptides showing distinct repertoires. Definition of DRB supertypes using binding data is limited to few (about 29) known alleles (≪ 5% of all known DRB alleles). Hence, we describe a strategy using structurally defined virtual pockets to group all known DRB alleles with regard to their overlapping peptide binding specificity. Biomedical Informatics Publishing Group 2010-01-20 /pmc/articles/PMC2957767/ /pubmed/20978603 Text en © 2010 Biomedical Informatics Publishing Group This is an open-access article, which permits unrestricted use, distribution, and reproduction in any medium, for non-commercial purposes, provided the original author and source are credited. |
spellingShingle | Hypothesis Mohanapriya, Arumugam Nandagond, Satish Shapshak, Paul Kangueane, Uma Kangueane, Pandjassarame A HLA-DRB supertype chart with potential overlapping peptide binding function |
title | A HLA-DRB supertype chart with potential overlapping peptide binding function |
title_full | A HLA-DRB supertype chart with potential overlapping peptide binding function |
title_fullStr | A HLA-DRB supertype chart with potential overlapping peptide binding function |
title_full_unstemmed | A HLA-DRB supertype chart with potential overlapping peptide binding function |
title_short | A HLA-DRB supertype chart with potential overlapping peptide binding function |
title_sort | hla-drb supertype chart with potential overlapping peptide binding function |
topic | Hypothesis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2957767/ https://www.ncbi.nlm.nih.gov/pubmed/20978603 |
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