2005, PrionDB.
This data was extracted from Medline abstracts and full texts (when available) in an automated manner.
The table below describes the selected point mutation and provides links to other documents. The sentence(s) where the point mutation P105L was found are listed after the table.
The mutated residues are also indicated in the family sequence alignments and hyperlinked to the corresponding mutation pages.
| Point mutation: | P105L | |
| Domain: | Not determined | |
| General numbering (PrionDB): | - | |
| Protein: | PRIO_HUMAN (PRNP) | Swiss-Prot Cross-reference table Family page |
| Other point mutations / same protein / same position | Point mutations at position 105 in PRIO_HUMAN | |
| Other point mutations / same protein | List of mutations in PRIO_HUMAN | |
| Family alignments |
Mammalian prion proteins Prion proteins (PRP, PRNP) | |
| Other point mutations / same position |
Position 105 in Mammalian prion proteins family Position 105 in Prion proteins (PRP, PRNP) family | |
| Reference: | Prion proteins with different conformations accumulate in Gerstmann-Straussler-Scheinker disease caused by A117V and F198S mutations. Piccardo P, Liepnieks JJ, William A, Dlouhy SR, Farlow MR, Young K, Nochlin D, Bird TD, Nixon RR, Ball MJ, DeCarli C, Bugiani O, Tagliavini F, Benson MD, Ghetti B Am J Pathol 2001 Jun;158(6):2201-7. | Medline |
| Other point mutations / same article | List | |
| Text source | HTML full text | |
| Validation status | True positive |
Relevant sentences:
P105L
cmbi.ru.nl), 22-Aug-2005