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dc.contributor.authorLuscher, Mark A
dc.contributor.authorMacDonald, Kelly S
dc.contributor.authorBwayo, JJ
dc.contributor.authorPlummer, FA
dc.contributor.authorBarber, Brian H
dc.date.accessioned2013-07-26T08:26:42Z
dc.date.available2013-07-26T08:26:42Z
dc.date.issued2001
dc.identifier.citationImmunogenetics February 2001, Volume 53, Issue 1, pp 10-14en
dc.identifier.issn0093-7711
dc.identifier.issn1432-1211
dc.identifier.urihttp://link.springer.com/article/10.1007/s002510100299
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/51521
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/11261925.
dc.description.abstractAs part of the ongoing study of natural HIV-1 resistance in the women of the Nairobi Sex Workers' study, we have examined a resistance-associated HLA class I allele at the molecular level. Typing by polymerase chain reaction using sequence-specific primers determined that this molecule is closely related to HLA-A*0214, one of a family of HLA-A2 supertype alleles which correlate with HIV-1 resistance in this population. Direct nucleotide sequencing shows that this molecule differs from A*0214, having a silent nucleotide substitution. We therefore propose to designate it HLA-A*02142. We have determined the peptide-binding motif of HLA-A*0214/02142 by peptide elution and bulk Edman degradative sequencing. The resulting motif, X-[Q,V]-X-X-X-K-X-X-[V,L], includes lysine as an anchor at position 6. The data complement available information on the peptide-binding characteristics of this molecule, and will be of use in identifying antigenic peptides from HIV-1 and other pathogensen
dc.language.isoenen
dc.publisherSpringer-Verlagen
dc.titleSequence and peptide-binding motif for a variant of HLA-A*0214 (A*02142) in an HIV-1-resistant individual from the Nairobi Sex Worker cohorten
dc.typeArticleen
local.publisherDepartment of Medicine, University of Toronto, Toronto, Canada,en
local.publisherDepartment of Microbiology, Mount Sinai Hospital, Room 1484, 600 University Ave., Toronto, Ontario, M5G 1X5, Canada,en
local.publisherDepartment of Microbiology, University of Nairobi, Nairobi, Kenya,en
local.publisherDepartment of Medical Microbiology University of Manitoba, Winnipeg, Canadaen
local.publisherDepartment of Immunology, University of Toronto, Toronto, Canada,en


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