ATP7A and CP

Number of citations of the paper that reports this interaction (PubMedID 11040994)
1

Data Source:
HPRD (in vitro)

		ATP7A	CP
Description		ATPase copper transporting alpha	ceruloplasmin
Image
GO Annotations	Cellular Component	Cell Nucleus Late Endosome Endoplasmic Reticulum Golgi Apparatus Trans-Golgi Network Cytosol Plasma Membrane Microvillus Membrane Integral Component Of Membrane Basolateral Plasma Membrane Apical Plasma Membrane Trans-Golgi Network Transport Vesicle Secretory Granule Phagocytic Vesicle Membrane Cell Leading Edge Brush Border Membrane Neuron Projection Neuronal Cell Body Perikaryon Membrane Raft Perinuclear Region Of Cytoplasm	Extracellular Region Extracellular Space Cell Lysosomal Membrane Endoplasmic Reticulum Lumen Plasma Membrane Extracellular Exosome Blood Microparticle
	Molecular Function	Copper Ion Transmembrane Transporter Activity Copper Ion Binding Protein Binding ATP Binding Superoxide Dismutase Copper Chaperone Activity Copper-dependent Protein Binding Copper-transporting ATPase Activity Rac GTPase Binding Chaperone Binding Cuprous Ion Binding	Ferroxidase Activity Copper Ion Binding Oxidoreductase Activity Chaperone Binding
	Biological Process	Blood Vessel Development In Utero Embryonic Development Liver Development Blood Vessel Remodeling Regulation Of Oxidative Phosphorylation Tryptophan Metabolic Process Catecholamine Metabolic Process Copper Ion Transport Cellular Copper Ion Homeostasis Mitochondrion Organization Lactation Locomotory Behavior Response To Iron(III) Ion Response To Manganese Ion Response To Zinc Ion Detoxification Of Copper Ion Regulation Of Gene Expression Positive Regulation Of Lamellipodium Assembly Copper Ion Import Peptidyl-lysine Modification Removal Of Superoxide Radicals Antimicrobial Humoral Response Cerebellar Purkinje Cell Differentiation Pyramidal Neuron Development Central Nervous System Neuron Development Extracellular Matrix Organization Collagen Fibril Organization Hair Follicle Morphogenesis Ion Transmembrane Transport Negative Regulation Of Iron Ion Transmembrane Transport Cellular Response To Platelet-derived Growth Factor Stimulus T-helper Cell Differentiation Epinephrine Metabolic Process Norepinephrine Metabolic Process Dopamine Metabolic Process Serotonin Metabolic Process Positive Regulation Of Catalytic Activity Negative Regulation Of Catalytic Activity Pigmentation Skin Development Positive Regulation Of Cell Size Elastic Fiber Assembly Lung Alveolus Development Neuron Projection Morphogenesis Positive Regulation Of Epithelial Cell Proliferation Cartilage Development Positive Regulation Of Oxidoreductase Activity Elastin Biosynthetic Process Copper Ion Export Cellular Response To Amino Acid Stimulus Cellular Response To Antibiotic Cellular Response To Cadmium Ion Cellular Response To Cobalt Ion Cellular Response To Copper Ion Cellular Response To Iron Ion Cellular Response To Lead Ion Cellular Response To Hypoxia Divalent Inorganic Cation Transport Positive Regulation Of Response To Wounding Positive Regulation Of Vascular Associated Smooth Muscle Cell Migration Regulation Of Cytochrome-c Oxidase Activity	Copper Ion Transport Iron Ion Transport Cellular Iron Ion Homeostasis Post-translational Protein Modification Cellular Protein Metabolic Process Iron Ion Homeostasis Oxidation-reduction Process
Pathways		Detoxification of Reactive Oxygen Species Ion influx/efflux at host-pathogen interface Ion transport by P-type ATPases	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
Drugs			Drotrecogin alfa Calcium Iron Zinc
Diseases		Spinal muscular atrophy (SMA), including: SMA type I (SMA1) / Werdning-Hoffman disease; SMA type II (SMA2); SMA type III (SMA3) / Kugeleberg-Welander disease; SMA type IV (SMA4); X-linked SMA 2 (SMAX2); X-linked distal SMA 3 (DSMAX); Distal SMA autosomal recessive type 4 (DSMA4); Congenital distal spinal muscular atrophy (SMAL); SMA proximal adult autosomal dominant (SMAPAD) Distal hereditary motor neuropathies (dHMN) Menkes disease (MD); Menkes kinky hair syndrome Cutis laxa, including: Autosomal dominant cutis laxa (ADCL); Autosomal recessive cutis laxa I (ARCL1); Autosomal recessive cutis laxa II (ARCL2); X-linked recessive cutis laxa (XRCL); Wrinkly skin syndrome
GWAS		Height ( 31562340)	Subcutaneous adipose tissue ( 22589738)
Interacting Genes		3 interacting genes: ATOX1 CP PDZD11	7 interacting genes: ATP7A BTRC GAST LTF MPO PLG PROC
Entrez ID		538	1356
HPRD ID		02054	00317
Ensembl ID		ENSG00000165240	ENSG00000047457
Uniprot IDs		B4DRW0 Q04656 Q762B6	A5PL27 P00450
PDB IDs		1AW0 1KVI 1KVJ 1Q8L 1S6O 1S6U 1Y3J 1Y3K 1YJR 1YJT 1YJU 1YJV 2AW0 2G9O 2GA7 2K1R 2KIJ 2KMV 2KMX 3CJK 5T7L	1KCW 2J5W 4EJX 4ENZ
Enriched GO Terms of Interacting Partners?
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