VWF K1794E (764-2813) [extracellular region]

Stable Identifier
R-HSA-9823657
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
vWF K1794E , von Willebrand factor
VWF K1794E (764-2813) [extracellular region] icon
Locations in the PathwayBrowser
Literature References
PubMed ID Title Journal Year
34758185 Von Willebrand disease type 2M: Correlation between genotype and phenotype

Maas, DPMSM, Atiq, F, Blijlevens, NMA, Brons, PPT, Krouwel, S, Laros-van Gorkom, BAP, Leebeek, FWG, Nieuwenhuizen, L, Schoormans, SCM, Simons, A, Meijer, D, van Heerde, WL, Schols, SEM

J Thromb Haemost 2022
Participates
Other forms of this molecule
Modified Residues
Name
L-lysine 1794 replaced with L-glutamic acid
Coordinate
1794
PsiMod
A protein modification that effectively converts a source amino acid residue to an L-glutamic acid.
A protein modification that effectively removes or replaces an L-lysine.
Disease
Name Identifier Synonyms
blood platelet disease DOID:2218 platelet disorder, Thrombocytopathy
Cross References
OpenTargets
Mondo
ZINC - Substances
ZINC target
PRO
GlyGen
GeneCards
VWF
Pharos - Targets
Orphanet
VWF
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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