Highlights d TAPBPR exhibits a binding preference for HLA-A molecules over HLA-B and -C d HLA-A2 and -A24 superfamily members are the strongest TAPBPR binders d F pocket architecture impacts MHC I susceptibility to TAPBPR-mediated peptide editing
HLA‐DPA1 intralocus recombination between DPA1*04:01:01:03 and DPA1*01:03:01:27, or closely related other alleles, results in a novel allele HLA‐DPA1*01:03:43.
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