Homo sapiens Protein: F11
Summary
InnateDB Protein IDBP-294810.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol F11
Protein Name coagulation factor XI
Synonyms FXI;
Species Homo sapiens
Ensembl Protein ENSP00000384957
InnateDB Gene IDBG-47627 (F11)
Protein Structure
UniProt Annotation
Function Factor XI triggers the middle phase of the intrinsic pathway of blood coagulation by activating factor IX.
Subcellular Localization Secreted.
Disease Associations Factor XI deficiency (FA11D) [MIM:612416]: A hemorrhagic disease characterized by reduced levels and activity of factor XI resulting in moderate bleeding symptoms, usually occurring after trauma or surgery. Patients usually do not present spontaneous bleeding but women can present with menorrhagia. Hemorrhages are usually moderate. {ECO:0000269PubMed:10027710, ECO:0000269PubMed:10606881, ECO:0000269PubMed:11895778, ECO:0000269PubMed:15026311, ECO:0000269PubMed:15180874, ECO:0000269PubMed:1547342, ECO:0000269PubMed:15953011, ECO:0000269PubMed:16607084, ECO:0000269PubMed:18005151, ECO:0000269PubMed:21457405, ECO:0000269PubMed:21668437, ECO:0000269PubMed:21999818, ECO:0000269PubMed:22016685, ECO:0000269PubMed:22159456, ECO:0000269PubMed:22322133, ECO:0000269PubMed:2813350, ECO:0000269PubMed:7669672, ECO:0000269PubMed:7888672, ECO:0000269PubMed:9401068, ECO:0000269PubMed:9787168}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Isoform 2 is produced by platelets and megakaryocytes but absent from other blood cells.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 8 experimentally validated interaction(s) in this database.
Experimentally validated
Total 8 [view]
Protein-Protein 6 [view]
Protein-DNA 2 [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:0005515 protein binding
GO:0008201 heparin binding
GO:0070009 serine-type aminopeptidase activity
Biological Process
GO:0006508 proteolysis
GO:0007596 blood coagulation
GO:0007597 blood coagulation, intrinsic pathway
GO:0030193 regulation of blood coagulation
GO:0031639 plasminogen activation
GO:0045087 innate immune response (InnateDB)
GO:0051919 positive regulation of fibrinolysis
Cellular Component
GO:0005576 extracellular region
GO:0005615 extracellular space
GO:0005886 plasma membrane
GO:0016020 membrane
GO:0070062 extracellular vesicular exosome
Protein Structure and Domains
PDB ID
InterPro IPR000177 Apple domain
IPR001254 Peptidase S1
IPR001314 Peptidase S1A, chymotrypsin-type
IPR003014 PAN-1 domain
IPR003609 Apple-like
IPR009003 Trypsin-like cysteine/serine peptidase domain
PFAM PF00089
PF00024
PRINTS PR00005
PR00722
PIRSF
SMART SM00223
SM00020
SM00473
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P03951
PhosphoSite PhosphoSite-P03951
TrEMBL Q9UEG0
UniProt Splice Variant
Entrez Gene 2160
UniGene
RefSeq NP_000119
HUGO HGNC:3529
OMIM 264900
CCDS CCDS3847
HPRD 07524
IMGT
EMBL AB004057 AC110771 AF045649 AY191837 BC119014 BC122863 CH471056 M13142 M18296 M18298 M18299 M18300 M18301 M18302 M18303 M18304 M19417 M20217 M20218 M21184
GenPept AAA51985 AAA52487 AAC24506 AAI19015 AAI22864 AAN85554 AAY40901 BAA20295 EAX04621