Homo sapiens Protein: CFP
Summary
InnateDB Protein IDBP-61797.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol CFP
Protein Name complement factor properdin
Synonyms BFD; PFC; PFD; PROPERDIN;
Species Homo sapiens
Ensembl Protein ENSP00000247153
InnateDB Gene IDBG-61793 (CFP)
Protein Structure
UniProt Annotation
Function A positive regulator of the alternate pathway of complement. It binds to and stabilizes the C3- and C5-convertase enzyme complexes. {ECO:0000269PubMed:20382442}.
Subcellular Localization Secreted.
Disease Associations Properdin deficiency (PFD) [MIM:312060]: Results in higher susceptibility to bacterial infections; especially to meningococcal infections. Three phenotypes have been reported: complete deficiency (type I), incomplete deficiency (type II), and dysfunction of properdin (type III). {ECO:0000269PubMed:10909851, ECO:0000269PubMed:8871668, ECO:0000269PubMed:9710744}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 4 experimentally validated interaction(s) in this database.
Experimentally validated
Total 4 [view]
Protein-Protein 4 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
Biological Process
GO:0006955 immune response
GO:0006956 complement activation
GO:0006957 complement activation, alternative pathway
GO:0030449 regulation of complement activation
GO:0042742 defense response to bacterium
GO:0045087 innate immune response (InnateDB)
Cellular Component
GO:0005576 extracellular region
GO:0005615 extracellular space
GO:0031012 extracellular matrix
Protein Structure and Domains
PDB ID
InterPro IPR000884 Thrombospondin, type 1 repeat
PFAM PF00090
PRINTS
PIRSF
SMART SM00209
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P27918
PhosphoSite PhosphoSite-P27918
TrEMBL E9PAQ1
UniProt Splice Variant
Entrez Gene 5199
UniGene Hs.53155
RefSeq NP_002612
HUGO HGNC:8864
OMIM 300383
CCDS CCDS14282
HPRD 02308
IMGT
EMBL AF005664 AF005665 AF005666 AF005667 AF005668 AL009172 AY297813 BC015756 M83652 X57748 X70872
GenPept AAA36489 AAB62886 AAB63279 AAB63280 AAC51626 AAH15756 AAP43692 CAA15658 CAA40914 CAA50220