The Eukaryotic Linear Motif resource for
Functional Sites in Proteins

o  Instance

Accession Acc. Gene-, NameStartEndSubsequenceLogic PDB OrganismLength
ELMI000600 P04156 PRNP
PRIO_HUMAN
196 201 VTTTTKGENFTETDVKMMER TP --- Homo sapiens (Human) 253

o  Instance evidence

Evidence classPSI-MIMethodBioSourcePubMedLogicReliabilityNotes
not annotated not specified Gauczynski,2002 not specified not specified

o  Pathways

The sequence P04156 is implicated in the following 1 Pathway: (color codes: This sequence=red, interacting sequence=orange)

o  Diseases

  • Sequence Variation VAR_008749 (Pos 196) has been implicated in Creutzfeldt-jakob Disease; Cjd (OMIM:123400).
  • Sequence Variation VAR_006473 (Pos 200) has been implicated in Creutzfeldt-jakob Disease; Cjd (OMIM:123400).
  • Sequence Variation VAR_006472 (Pos 198) has been implicated in Gerstmann-straussler Disease; Gsd (OMIM:137440).
Please cite: ELM 2016-data update and new functionality of the eukaryotic linear motif resource. (PMID:26615199)

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