Table 3.
Segments of PrP sequence | Mutations | Modification sites |
SNQNNFVHDCVNITIKQHTF | D178N, V180I, T183A | N-Glycozylation 181–184 Kinase C 183–185 Disulfide 179–214 |
KMMERVVEQMCITQYER | R208H, V210I, E211Q, Q212P, Q217R | Kinase II 216–219 Disulfide 179–214 |
SPPVILLISFLIFLIVG | P238S |
Column 1: Human prion protein (P04156), segments 170–188, 204–220, and 237–253. Underlined amino acids are those of column 2. Columns 2 and 3: Pathologenic point mutations and potential protein modifications according to UniProtKB.