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 N171S 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.
|General numbering (PrionDB):||-|
|Other point mutations / same protein / same position||Point mutations at position 171 in PRIO_HUMAN|
|Other point mutations / same protein||List of mutations in PRIO_HUMAN|
Mammalian prion proteins|
Prion proteins (PRP, PRNP)
|Other point mutations / same position||
Position 171 in Mammalian prion proteins family |
Position 171 in Prion proteins (PRP, PRNP) family
|Reference:||The prion Peptide forms ion channels in planar lipid bilayers.|
Berest V, Rutkowski M, Rolka K, LEgowska A, Debska G, Stepkowski D, Szewczyk A
Cell Mol Biol Lett 2003;8(2):353-62.
|Other point mutations / same article||List|
|Validation status||True positive|