VWF C1099P (764-1605) [extracellular region]

Stable Identifier
R-HSA-9852778
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
von Willebrand factor C1099P (764-1605), vWF C1099P
VWF C1099P (764-1605) [extracellular region] icon
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
VWF, F8VWF
Chain
signal peptide:1-22, chain:23-763, chain:764-2813
Participates
Other forms of this molecule
Modified Residues
Name
L-cysteine 1099 replaced with L-proline
Coordinate
1099
PsiMod
A protein modification that effectively removes or replaces an L-cysteine.
A protein modification that effectively converts a source amino acid residue to L-proline.
Disease
Name Identifier Synonyms
blood platelet disease DOID:2218 platelet disorder, Thrombocytopathy
Interactors (6)
Accession #Entities Entities Confidence Score Evidence (IntAct)
 UniProt:P04275 VWF  20 0.868 21
 UniProt:Q76LX8 ADAMTS13  7 0.789 19
 UniProt:P00451 F8  20 0.623 2
 UniProt:P07359 GP1BA  6 0.623 2
 UniProt:P00451-PRO_0000002967 F8      0.544 2
 UniProt:Q96CV9 OPTN  6 0.454 2
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