PrionDB: Extraction of mutation data from the literature

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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 T188R 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 T188R in PRIO_HUMAN

Point mutation:T188R
Domain:Not determined
General numbering (PrionDB): -
Protein:PRIO_HUMAN (PRNP)Swiss-Prot
Cross-reference table
Family page
Other point mutations / same protein / same positionPoint mutations at position 188 in PRIO_HUMAN
Other point mutations / same proteinList of mutations in PRIO_HUMAN
Family alignments Mammalian prion proteins
Prion proteins (PRP, PRNP)
Other point mutations / same position Position 188 in Mammalian prion proteins family
Position 188 in Prion proteins (PRP, PRNP) family
Reference:A cluster of familial Creutzfeldt-Jakob disease mutations recapitulate conserved residues in Doppel: a case of molecular mimicry?
Mastrangelo P, Serpell L, Dafforn T, Lesk A, Fraser P, Westaway D
FEBS Lett 2002 Dec 4;532(1-2):21-6.
Medline
Other point mutations / same articleList
Text sourcePDF full text
Validation statusTrue positive

Relevant sentences:

T188R


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F.Horn (priondbcmbi.ru.nl), 22-Aug-2005