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 E200K 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: | E200K | |
| 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 200 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 200 in Mammalian prion proteins family Position 200 in Prion proteins (PRP, PRNP) family | |
| Reference: | When sporadic disease is not sporadic: the potential for genetic etiology. Goldman JS, Miller BL, Safar J, de Tourreil S, Martindale JL, Prusiner SB, Geschwind MD Arch Neurol 2004 Feb;61(2):213-6. | Medline |
| Other point mutations / same article | List | |
| Text source | abstract | |
| Validation status | Not yet checked |
Relevant sentences:
E200K
cmbi.ru.nl), 22-Aug-2005