CP and MPO

Number of citations of the paper that reports this interaction (PubMedID 9097926)
27

Data Source:
HPRD (in vitro)

		CP	MPO
Description		ceruloplasmin	myeloperoxidase
Image
GO Annotations	Cellular Component	Extracellular Region Extracellular Space Cell Lysosomal Membrane Endoplasmic Reticulum Lumen Plasma Membrane Extracellular Exosome Blood Microparticle	Extracellular Region Extracellular Space Cell Nucleus Nucleoplasm Cytoplasm Lysosome Secretory Granule Azurophil Granule Lumen Azurophil Granule Intracellular Membrane-bounded Organelle Extracellular Exosome Phagocytic Vesicle Lumen
	Molecular Function	Ferroxidase Activity Copper Ion Binding Oxidoreductase Activity Chaperone Binding	Chromatin Binding Peroxidase Activity Heparin Binding Heme Binding Metal Ion Binding
	Biological Process	Copper Ion Transport Iron Ion Transport Cellular Iron Ion Homeostasis Post-translational Protein Modification Cellular Protein Metabolic Process Iron Ion Homeostasis Oxidation-reduction Process	Response To Yeast Hypochlorous Acid Biosynthetic Process Respiratory Burst Involved In Defense Response Defense Response Response To Oxidative Stress Aging Response To Mechanical Stimulus Removal Of Superoxide Radicals Response To Food Response To Lipopolysaccharide Low-density Lipoprotein Particle Remodeling Defense Response To Bacterium Hydrogen Peroxide Catabolic Process Negative Regulation Of Apoptotic Process Neutrophil Degranulation Cell Redox Homeostasis Defense Response To Fungus Oxidation-reduction Process Response To Gold Nanoparticle
Pathways		Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) Metal ion SLC transporters Defective SLC40A1 causes hemochromatosis 4 (HFE4) (macrophages) Defective CP causes aceruloplasminemia (ACERULOP) Post-translational protein phosphorylation Iron uptake and transport	Neutrophil degranulation Events associated with phagocytolytic activity of PMN cells
Drugs		Drotrecogin alfa Calcium Iron Zinc	Mesalazine Cefdinir L-Carnitine Melatonin Nomifensine
Diseases			Other phagocyte defects, including the following eight diseases: Chediak-Higashi syndrome; Griscelli syndrome, type 1 (GS1); Griscelli syndrome, type 2 (GS2); Griscelli syndrome, type 3 (GS3); beta-actin deficiency; Neutrophil-specific granule deficiency; Myeloperoxidase deficiency; Glucose 6-phosphate dehydrogenase deficiency; Shwachman syndrome
GWAS		Subcutaneous adipose tissue ( 22589738)	Blood protein levels ( 30072576 29875488) Blood protein levels in cardiovascular risk ( 28369058) Circulating myeloperoxidase levels (plasma) ( 23620142) Granulocyte count ( 27863252) Granulocyte percentage of myeloid white cells ( 27863252) Monocyte count ( 27863252) Monocyte percentage of white cells ( 27863252) Multiple sclerosis ( 31604244) Myeloid white cell count ( 27863252) Neutrophil count ( 27863252) Neutrophil percentage of white cells ( 27863252) Post bronchodilator FEV1/FVC ratio in COPD ( 26634245) Sum basophil neutrophil counts ( 27863252) Sum neutrophil eosinophil counts ( 27863252) White blood cell count ( 27863252)
Interacting Genes		7 interacting genes: ATP7A BTRC GAST LTF MPO PLG PROC	1 interacting genes: CP
Entrez ID		1356	4353
HPRD ID		00317	06102
Ensembl ID		ENSG00000047457	ENSG00000005381
Uniprot IDs		A5PL27 P00450	P05164
PDB IDs		1KCW 2J5W 4EJX 4ENZ	1CXP 1D2V 1D5L 1D7W 1DNU 1DNW 1MHL 1MYP 3F9P 3ZS0 3ZS1 4C1M 4DL1 4EJX 5FIW 5MFA 5UZU 6AZP 6BMT
Enriched GO Terms of Interacting Partners?
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