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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...

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Autores principales: Mohanapriya, Arumugam, Nandagond, Satish, Shapshak, Paul, Kangueane, Uma, Kangueane, Pandjassarame
Formato: Texto
Lenguaje:English
Publicado: Biomedical Informatics Publishing Group 2010
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.
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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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