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. 2012 Mar 1;8(3):e1002412. doi: 10.1371/journal.pcbi.1002412

Table 1. Summary of all the average self/nonself overlaps obtained using peptides predicted to be presented on HLA molecules.

Recognized peptide positions
Self P1–9 P1 and P3–8 P3–8
percentage (complete) (non-anchor) (middle)
Exact 100 0.15%* 0.41% 2.7%*
50 0.09% 0.25% 1.6%
Degenerate 100 0.7% 5.2% 29%*

Overlaps were determined using all positions of the peptide (P1–9), the non-anchor positions (P1 and P3–8) or the middle positions between the anchors (P3–8). Further, overlaps were determined as exact, i.e. every position should be identical, or as degenerate, i.e. with 1 or 2 substitutions being allowed to mimic T-cell recognition (see Methods). Finally, overlaps with 100% or (a randomly chosen) 50% of the human proteome are shown. Self/nonself overlaps indicated with a star (*) are shown per HLA molecule in Figure 2.