Homo sapiens Protein: CP
Summary
InnateDB Protein IDBP-60597.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol CP
Protein Name ceruloplasmin (ferroxidase)
Synonyms CP-2;
Species Homo sapiens
Ensembl Protein ENSP00000264613
InnateDB Gene IDBG-60595 (CP)
Protein Structure
UniProt Annotation
Function Ceruloplasmin is a blue, copper-binding (6-7 atoms per molecule) glycoprotein. It has ferroxidase activity oxidizing Fe(2+) to Fe(3+) without releasing radical oxygen species. It is involved in iron transport across the cell membrane. Provides Cu(2+) ions for the ascorbate-mediated deaminase degradation of the heparan sulfate chains of GPC1. May also play a role in fetal lung development or pulmonary antioxidant defense (By similarity). {ECO:0000250}.
Subcellular Localization Secreted. Note=Colocalizes with GCP1 in secretory intracellular compartments. {ECO:0000250}.
Disease Associations Aceruloplasminemia (ACERULOP) [MIM:604290]: An autosomal recessive disorder of iron metabolism characterized by iron accumulation in the brain as well as visceral organs. Clinical features consist of the triad of retinal degeneration, diabetes mellitus and neurological disturbances. Note=The disease is caused by mutations affecting the gene represented in this entry.Note=Ceruloplasmin levels are decreased in Wilson disease, in which copper cannot be incorporated into ceruloplasmin in liver because of defects in the copper-transporting ATPase 2.
Tissue Specificity Expressed by the liver and secreted in plasma.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 7 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 7 [view]
Protein-Protein 6 [view]
Protein-DNA 0
Protein-RNA 1 [view]
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0004322 ferroxidase activity
GO:0005507 copper ion binding
GO:0016491 oxidoreductase activity
GO:0051087 chaperone binding
Biological Process
GO:0006825 copper ion transport
GO:0006879 cellular iron ion homeostasis
GO:0055085 transmembrane transport
GO:0055114 oxidation-reduction process
Cellular Component
GO:0005576 extracellular region
GO:0005615 extracellular space
GO:0005765 lysosomal membrane
GO:0070062 extracellular vesicular exosome
GO:0072562 blood microparticle
Protein Structure and Domains
PDB ID
InterPro IPR001117 Multicopper oxidase, type 1
IPR008972 Cupredoxin
IPR011706 Multicopper oxidase, type 2
IPR011707 Multicopper oxidase, type 3
PFAM PF00394
PF07731
PF07732
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P00450
PhosphoSite PhosphoSite-P00450
TrEMBL
UniProt Splice Variant
Entrez Gene 1356
UniGene Hs.732558
RefSeq NP_000087
HUGO HGNC:2295
OMIM 117700
CCDS CCDS3141
HPRD 00317
IMGT
EMBL AF132978 D00025 D45045 DQ314867 J05506 M13536 M13699 X04135 X04136 X04137 X04138
GenPept AAA51975 AAA51976 AAF02483 ABC40726 BAA00019 BAA08085 CAA27752 CAA27753 CAA27754 CAA27755