Homo sapiens Protein: FGB
Summary
InnateDB Protein IDBP-42023.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol FGB
Protein Name fibrinogen beta chain
Synonyms HEL-S-78p;
Species Homo sapiens
Ensembl Protein ENSP00000306099
InnateDB Gene IDBG-42021 (FGB)
Protein Structure
UniProt Annotation
Function Fibrinogen has a double function: yielding monomers that polymerize into fibrin and acting as a cofactor in platelet aggregation.
Subcellular Localization Secreted.
Disease Associations Congenital afibrinogenemia (CAFBN) [MIM:202400]: Rare autosomal recessive disorder is characterized by bleeding that varies from mild to severe and by complete absence or extremely low levels of plasma and platelet fibrinogen. {ECO:0000269PubMed:10666208, ECO:0000269PubMed:11468164}. Note=The disease is caused by mutations affecting the gene represented in this entry. Patients with congenital fibrinogen abnormalities can manifest different clinical pictures. Some cases are clinically silent, some show a tendency toward bleeding and some show a predisposition for thrombosis with or without bleeding.
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 34 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 34 [view]
Protein-Protein 34 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005102 receptor binding
GO:0005198 structural molecule activity
GO:0005515 protein binding
GO:0030674 protein binding, bridging
GO:0050839 cell adhesion molecule binding
GO:0051087 chaperone binding
Biological Process
GO:0002576 platelet degranulation
GO:0007160 cell-matrix adhesion
GO:0007165 signal transduction
GO:0007596 blood coagulation
GO:0030168 platelet activation
GO:0030198 extracellular matrix organization
GO:0034116 positive regulation of heterotypic cell-cell adhesion
GO:0043623 cellular protein complex assembly
GO:0044320 cellular response to leptin stimulus
GO:0045907 positive regulation of vasoconstriction
GO:0045921 positive regulation of exocytosis
GO:0050714 positive regulation of protein secretion
GO:0051258 protein polymerization
GO:0051592 response to calcium ion
GO:0070374 positive regulation of ERK1 and ERK2 cascade
GO:0070527 platelet aggregation
GO:0071347 cellular response to interleukin-1
GO:0090277 positive regulation of peptide hormone secretion
GO:1900026 positive regulation of substrate adhesion-dependent cell spreading
GO:1902042 negative regulation of extrinsic apoptotic signaling pathway via death domain receptors
GO:2000352 negative regulation of endothelial cell apoptotic process
Cellular Component
GO:0005576 extracellular region
GO:0005577 fibrinogen complex
GO:0005615 extracellular space
GO:0005737 cytoplasm
GO:0005886 plasma membrane
GO:0005938 cell cortex
GO:0009897 external side of plasma membrane
GO:0009986 cell surface
GO:0031091 platelet alpha granule
GO:0031093 platelet alpha granule lumen
GO:0070062 extracellular vesicular exosome
GO:0072562 blood microparticle
Protein Structure and Domains
PDB ID
InterPro IPR002181 Fibrinogen, alpha/beta/gamma chain, C-terminal globular domain
IPR012290 Fibrinogen, alpha/beta/gamma chain, coiled coil domain
PFAM PF00147
PF08702
PRINTS
PIRSF
SMART SM00186
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P02675
PhosphoSite PhosphoSite-P02675
TrEMBL V9HVY1
UniProt Splice Variant
Entrez Gene 2244
UniGene Hs.300774
RefSeq NP_005132
HUGO HGNC:3662
OMIM 134830
CCDS CCDS3786
HPRD 00620
IMGT
EMBL AC107385 AF388026 AH002694 AK303788 AK312972 BC007030 BC106760 BC107766 CH471056 EU668333 J00129 J00130 J00131 J00132 J00133 M64983 X05018
GenPept AAA18024 AAA52429 AAA52445 AAA98115 AAA98116 AAH07030 AAI06761 AAI07767 AAK62470 ACF94486 BAG35810 BAG64745 CAA28674 EAX04932 EAX04934 EAX04939