VWF W1745C (764-2813) [extracellular region]

Stable Identifier
R-HSA-9823611
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
vWF W1745C, von Willebrand factor
VWF W1745C (764-2813) [extracellular region] icon
Locations in the PathwayBrowser
Literature References
PubMed ID Title Journal Year
19687512 Characterization of W1745C and S1783A: 2 novel mutations causing defective collagen binding in the A3 domain of von Willebrand factor

Riddell, AF, Gomez, K, Millar, CM, Mellars, G, Gill, S, Brown, SA, Sutherland, M, Laffan, MA, McKinnon, TA

Blood 2009
Participates
Other forms of this molecule
Modified Residues
Name
L-tryptophan 1745 replaced with L-cysteine
Coordinate
1745
PsiMod
A protein modification that effectively converts a source amino acid residue to an L-cysteine.
A protein modification that effectively removes or replaces an L-tryptophan.
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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