F8 Q2106E [extracellular region]

Stable Identifier
R-HSA-9668161
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
FVIII Q2106E
F8 Q2106E [extracellular region] icon
Locations in the PathwayBrowser
Literature References
PubMed ID Title Journal Year
10910913 Hemophilic factor VIII C1- and C2-domain missense mutations and their modeling to the 1.5-angstrom human C2-domain crystal structure

Fujikawa, K, Nakaya, S, Pratt, KP, Davie, EW, Stoddard, BL, Shen, BW, Thompson, AR, Liu, ML

Blood 2000
External Reference Information
External Reference
Gene Names
F8, F8C
Chain
signal peptide:1-19, chain:20-2351, chain:20-1332, chain:20-759, chain:760-1332, chain:1668-2351
Participates
Other forms of this molecule
Modified Residues
Name
L-glutamine 2106 replaced with L-glutamic acid
Coordinate
2106
PsiMod
A protein modification that effectively removes or replaces an L-glutamine.
A protein modification that effectively converts a source amino acid residue to an L-glutamic acid.
Disease
Name Identifier Synonyms
factor VIII deficiency DOID:12134 Congenital factor VIII disorder, Subhemophilia, Hemophilia A
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