PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
16148127-7	2005	Structural analysis of peptides in which anchor residues were substituted with beta-amino acids revealed the basis for enhanced MHC binding and retention of immunogenicity observed for these analogs and paves the way for future vaccine design using beta-amino acids.	beta-amino acids	79-95	major histocompatibility complex, class I, C	Homo sapiens	128-131	
16148127-7	2005	Structural analysis of peptides in which anchor residues were substituted with beta-amino acids revealed the basis for enhanced MHC binding and retention of immunogenicity observed for these analogs and paves the way for future vaccine design using beta-amino acids.	beta-amino acids	249-265	major histocompatibility complex, class I, C	Homo sapiens	128-131	
11966446-9	2002	This article reviews the rapidly expanding applications of beta-amino acids in the design of bioactive peptide analogues ranging from receptor agonists and antagonists, MHC-binding peptides, antimicrobial peptides and peptidase inhibitors.	beta-amino acids	59-75	major histocompatibility complex, class I, C	Homo sapiens	169-172