From:  Exploratory proteomic and bioinformatics analysis unveils epitope pairing between IGHV3-64 and K-Ras for polyclonal drug conjugation in colorectal cancer

 Predicted and curated epitope regions identified in IGHV3-64 and K-Ras.

IEDB IDEpitopesPeptide sequence positionAntigenOrganism
IGHV3-64
722846RQAPGKGLEY58–67 AAIGHV 3-64 (UniProt: A0A075B6Q5)Homo sapiens
2260399EVQLVESGEG21–30 AA
2260400EVQLVESGEGLVQPG21–35 AA
2260401EVQLVESGEGLVQPGG21–36 AA
K-Ras
1275428SEDVPMVLV106–114 AAGTPase K-Ras (UniProt: P01116)Homo sapiens
2226767TEYKLVVVGAGGV2–14 AA
2268524KLVVVGAGGVGKS5–17 AA

This table summarizes epitope sequences identified within IGHV3-64 and K-Ras proteins, including epitope IDs, peptide sequences, AA positions, antigen names, and source organisms. Epitope information was retrieved from the IEDB and used to support epitope-level pairing analysis between circulating immunoglobulin variable regions and oncogenic K-Ras. These epitopes were evaluated for spatial compatibility and proximity-guided targeting potential and do not imply direct inhibition of K-Ras signaling or immune activation. AA: amino acid; IEDB: Immune Epitope Database; IGHV3-64: immunoglobulin heavy variable 3-64; K-Ras: Kirsten rat sarcoma viral oncogene homolog.