Factor XI

F11
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 1XX9, 1XXD, 1XXF, 1ZHM, 1ZHP, 1ZHR, 1ZJD, 1ZLR, 1ZMJ, 1ZML, 1ZMN, 1ZOM, 1ZPB, 1ZPC, 1ZPZ, 1ZRK, 1ZSJ, 1ZSK, 1ZSL, 1ZTJ, 1ZTK, 1ZTL, 2F83, 2FDA, 2J8J, 2J8L, 3BG8, 3SOR, 3SOS, 4CR5, 4CR9, 4CRA, 4CRB, 4CRC, 4CRD, 4CRE, 4CRF, 4CRG, 4NA7, 4NA8, 4TY6, 4TY7, 4WXI, 4X6M, 4X6N, 4X6O, 4X6P, 4Y8X, 4Y8Y, 4Y8Z, 4D7F, 5E2O, 5E2P, 4D76, 4D7G, 5EXL, 5I25, 5EXM, 5EOD, 5EXN, 5EOK
Identifiers
Aliases	F11, FXI, coagulation factor XI, PTA
External IDs	OMIM: 264900 MGI: 99481 HomoloGene: 86654 GeneCards: F11
Gene location (Human) Chr. Chromosome 4 (human)[1] Band 4q35.2 Start 186,266,189 bp[1] End 186,289,681 bp[1]
Gene location (Mouse) Chr. Chromosome 8 (mouse)[2] Band 8 B1.1|8 25.14 cM Start 45,694,211 bp[2] End 45,715,068 bp[2]
RNA expression pattern Bgee Top expressed in Right lobe of liver liver Body of pancreas pancreas kidney duodenum gallbladder renal cortex lung More reference expression data BioGPS More reference expression data
Gene ontology Molecular function serine-type aminopeptidase activity peptidase activity heparin binding serine-type endopeptidase activity serine-type peptidase activity GO:0001948 protein binding hydrolase activity identical protein binding Cellular component extracellular region plasma membrane extracellular exosome membrane extracellular space Biological process hemostasis blood coagulation, intrinsic pathway plasminogen activation regulation of blood coagulation proteolysis positive regulation of fibrinolysis blood coagulation Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	2160	109821
Ensembl	ENSG00000088926	ENSMUSG00000031645
UniProt	P03951	Q91Y47
RefSeq (mRNA)	NM_000128 NM_019559 NM_001354804	NM_028066
RefSeq (protein)	NP_000119 NP_001341733	NP_082342
Location (UCSC)	Chr 4: 186.27 – 186.29 Mb	Chr 8: 45.69 – 45.72 Mb
PubMed search	[3]	[4]
Wikidata
View/Edit Human View/Edit Mouse

Factor XI or plasma thromboplastin antecedent is the zymogen form of factor XIa, one of the enzymes of the coagulation cascade. Like many other coagulation factors, it is a serine protease. In humans, Factor XI is encoded by the F11 gene.^[5][6][7][8]

Function[]

Factor XI (FXI) is produced by the liver and circulates as a homo-dimer in its inactive form.^[9] The plasma half-life of FXI is approximately 52 hours. The zymogen factor is activated into factor XIa by factor XIIa (FXIIa), thrombin, and FXIa itself; due to its activation by FXIIa, FXI is a member of the "contact pathway" (which includes HMWK, prekallikrein, factor XII, factor XI, and factor IX).^[10]

Factor XIa activates factor IX by selectively cleaving arg-ala and arg-val peptide bonds. Factor IXa, in turn, forms a complex with Factor VIIIa (FIXa-FVIIIa) and activates factor X.

Inhibitors of factor XIa include protein Z-dependent protease inhibitor (ZPI, a member of the serine protease inhibitor/serpin class of proteins), which is independent of protein Z (its action on factor X, however, is protein Z-dependent, hence its name).

Structure[]

Although synthesized as a single polypeptide chain, FXI circulates as a homodimer. Every chain has a relative molecular mass of approximately 80000. Typical plasma concentrations of FXI are 5 μg/mL, corresponding to a plasma concentration (of FXI dimers) of approximately 30 nM. The FXI gene is 23kb in length, has 15 exons, and is found on chromosome 4q32-35.^[6][7]

Factor XI consists of four apple domains, that create a disk-like platform around the base of a fifth, catalytic serine protease domain. One contains a binding site for thrombin, another for high molecular weight kininogen, a third one for factor IX, heparin and glycoprotein Ib and the fourth is implicated in forming the factor XI homodimer, including a cysteine residue that creates a disulfide bond.

In the homodimer, the apple domains create two disk-like platforms connected together at an angle, with the catalytic domains sticking out at each side of the dimer.

Activation by thrombin or factor XIIa is achieved by cleavage of Arg369-Ile370 peptide bonds on both subunits of the dimer. This results in a partial detachment of the catalytic domain from the disk-like apple domains, still linked to the fourth domain with a disulfide bond, but now farther from the third domain. This is thought that this exposes the factor IX binding site of the third apple domain, allowing factor XI's protease activity on it. ^[11]

Role in disease[]

Deficiency of factor XI causes the rare hemophilia C; this mainly occurs in Ashkenazi Jews and is believed to affect approximately 8% of that population. Less commonly, hemophilia C can be found in Jews of Iraqi ancestry and in Israeli Arabs. The condition has been described in other populations at around 1% of cases. It is an autosomal recessive disorder. There is little spontaneous bleeding, but surgical procedures may cause excessive blood loss, and prophylaxis is required.^[12]

Low levels of factor XI also occur in many other disease states, including Noonan syndrome.

High levels of factor XI have been implicated in thrombosis, although it is uncertain what determines these levels and how serious the procoagulant state is.

See also[]

• Contact activation pathway (also known as the intrinsic pathway)
• Tissue factor pathway (also known as the extrinsic pathway)

References[]

Further reading[]

External links[]

• The MEROPS online database for peptidases and their inhibitors: S01.213