InnateDB Protein
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IDBP-61797.6
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Last Modified
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2014-10-13 [Report errors or provide feedback]
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Gene Symbol
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CFP
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Protein Name
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complement factor properdin
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Synonyms
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BFD; PFC; PFD; PROPERDIN;
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Species
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Homo sapiens
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Ensembl Protein
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ENSP00000247153
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InnateDB Gene
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IDBG-61793 (CFP)
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Protein Structure
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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}.
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Subcellular Localization |
Secreted.
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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.
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Tissue Specificity |
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Comments |
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Number of Interactions
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This gene and/or its encoded proteins are associated with 4 experimentally validated interaction(s) in this database.
Experimentally validated |
Total |
4
[view]
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Protein-Protein |
4
[view]
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Protein-DNA |
0
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Protein-RNA |
0
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DNA-DNA |
0
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RNA-RNA |
0
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DNA-RNA |
0
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Molecular Function |
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Biological Process |
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Cellular Component |
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PDB ID |
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InterPro |
IPR000884
Thrombospondin, type 1 repeat
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PFAM |
PF00090
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PRINTS |
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PIRSF |
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SMART |
SM00209
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TIGRFAMs |
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Modification |
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SwissProt |
P27918
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PhosphoSite |
PhosphoSite-P27918
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TrEMBL |
E9PAQ1
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UniProt Splice Variant |
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Entrez Gene |
5199
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UniGene |
Hs.53155
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RefSeq |
NP_002612
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HUGO |
HGNC:8864
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OMIM |
300383
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CCDS |
CCDS14282
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HPRD |
02308
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IMGT |
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EMBL |
AF005664
AF005665
AF005666
AF005667
AF005668
AL009172
AY297813
BC015756
M83652
X57748
X70872
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GenPept |
AAA36489
AAB62886
AAB63279
AAB63280
AAC51626
AAH15756
AAP43692
CAA15658
CAA40914
CAA50220
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