Homo sapiens Protein: F10
Summary
InnateDB Protein IDBP-52277.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol F10
Protein Name coagulation factor X
Synonyms FX; FXA;
Species Homo sapiens
Ensembl Protein ENSP00000364709
InnateDB Gene IDBG-52275 (F10)
Protein Structure
UniProt Annotation
Function Factor Xa is a vitamin K-dependent glycoprotein that converts prothrombin to thrombin in the presence of factor Va, calcium and phospholipid during blood clotting.
Subcellular Localization Secreted.
Disease Associations Factor X deficiency (FA10D) [MIM:227600]: A hemorrhagic disease with variable presentation. Affected individuals can manifest prolonged nasal and mucosal hemorrhage, menorrhagia, hematuria, and occasionally hemarthrosis. Some patients do not have clinical bleeding diathesis. {ECO:0000269PubMed:10468877, ECO:0000269PubMed:10746568, ECO:0000269PubMed:11248282, ECO:0000269PubMed:11728527, ECO:0000269PubMed:12945883, ECO:0000269PubMed:15650540, ECO:0000269PubMed:17393015, ECO:0000269PubMed:19135706, ECO:0000269PubMed:1973167, ECO:0000269PubMed:1985698, ECO:0000269PubMed:2790181, ECO:0000269PubMed:7669671, ECO:0000269PubMed:7860069, ECO:0000269PubMed:8529633, ECO:0000269PubMed:8845463, ECO:0000269PubMed:8910490}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Plasma; synthesized in the liver. {ECO:0000269PubMed:6587384}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 16 experimentally validated interaction(s) in this database.
Experimentally validated
Total 16 [view]
Protein-Protein 15 [view]
Protein-DNA 1 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0003824 catalytic activity
GO:0004252 serine-type endopeptidase activity
GO:0005509 calcium ion binding
GO:0005515 protein binding
GO:0005543 phospholipid binding
Biological Process
GO:0006508 proteolysis
GO:0007596 blood coagulation
GO:0007597 blood coagulation, intrinsic pathway
GO:0007598 blood coagulation, extrinsic pathway
GO:0017187 peptidyl-glutamic acid carboxylation
GO:0030335 positive regulation of cell migration
GO:0043687 post-translational protein modification
GO:0044267 cellular protein metabolic process
GO:0051897 positive regulation of protein kinase B signaling
Cellular Component
GO:0005576 extracellular region
GO:0005788 endoplasmic reticulum lumen
GO:0005796 Golgi lumen
GO:0005886 plasma membrane
GO:0016020 membrane
GO:0031233 intrinsic to external side of plasma membrane
GO:0043231 intracellular membrane-bounded organelle
Protein Structure and Domains
PDB ID
InterPro IPR000294 Gamma-carboxyglutamic acid-rich (GLA) domain
IPR000742 Epidermal growth factor-like domain
IPR001254 Peptidase S1
IPR001314 Peptidase S1A, chymotrypsin-type
IPR001881 EGF-like calcium-binding domain
IPR009003 Trypsin-like cysteine/serine peptidase domain
IPR012224 Peptidase S1A, coagulation factor VII/IX/X/C/Z
PFAM PF00594
PF00008
PF00089
PF07645
PRINTS PR00001
PR00722
PIRSF PIRSF001143
SMART SM00069
SM00181
SM00020
SM00179
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P00742
PhosphoSite PhosphoSite-P00742
TrEMBL Q5JVE7
UniProt Splice Variant
Entrez Gene 2159
UniGene Hs.702204
RefSeq NP_000495
HUGO HGNC:3528
OMIM 613872
CCDS CCDS9530
HPRD 01966
IMGT
EMBL AF503510 AK313798 BC046125 CH471085 EF445049 K01886 K03194 L00390 L00391 L00392 L00393 L00394 L00395 L00396 M22613 M33297 M57285 N00045
GenPept AAA51984 AAA52421 AAA52486 AAA52490 AAA52636 AAA52764 AAH46125 AAM19347 ACA06104 BAG36534 EAX09184