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

KEGG: The sequence P04156 is implicated in the following 3 Pathways: (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-the Eukaryotic Linear Motif resource-2024 update. (PMID:37962385)

ELM data can be downloaded & distributed for non-commercial use according to the ELM Software License Agreement
feedback@elm.eu.org