ATP7A and PDZD11

Data Source:
HPRD (two hybrid, in vivo)

		ATP7A	PDZD11
Description		ATPase copper transporting alpha	PDZ domain containing 11
Image			No pdb structure
GO Annotations	Cellular Component	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 Cytosol Cell-cell Junction Adherens Junction Basolateral Plasma Membrane Synapse Pore Complex Presynapse
	Molecular Function	Copper Ion Transmembrane Transporter Activity Copper Ion Binding Protein Binding ATP Binding Superoxide Dismutase Copper Chaperone Activity Copper-dependent Protein Binding P-type Divalent Copper Transporter Activity Chaperone Binding Cuprous Ion Binding	Protein 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 Female Pregnancy 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 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 Inorganic Cation Transmembrane Transport Positive Regulation Of Response To Wounding Positive Regulation Of Vascular Associated Smooth Muscle Cell Migration Regulation Of Cytochrome-c Oxidase Activity	Biotin Metabolic Process Neurotransmitter Secretion Pantothenate Metabolic Process Antimicrobial Humoral Response Ion Transmembrane Transport Maintenance Of Epithelial Cell Apical/basal Polarity Pore Complex Assembly Transmembrane Transport Protein Localization To Basolateral Plasma Membrane
Pathways		Detoxification of Reactive Oxygen Species Ion influx/efflux at host-pathogen interface Ion transport by P-type ATPases	Biotin transport and metabolism Vitamin B5 (pantothenate) metabolism Transport of vitamins, nucleosides, and related molecules Ion influx/efflux at host-pathogen interface Ion transport by P-type ATPases
Drugs
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)
Interacting Genes		3 interacting genes: ATOX1 CP PDZD11	5 interacting genes: ATP2B2 ATP7A MAGI2 PLEKHA5 SIGMAR1
Entrez ID		538	51248
HPRD ID		02054	06622
Ensembl ID		ENSG00000165240	ENSG00000120509
Uniprot IDs		B4DRW0 Q04656 Q762B6	Q5EBL8
PDB IDs		1AW0 1KVI 1KVJ 1Q8L 1S6O 1S6U 1Y3J 1Y3K 1YJR 1YJT 1YJU 1YJV 2AW0 2G9O 2GA7 2K1R 2KIJ 2KMV 2KMX 3CJK 5T7L
Enriched GO Terms of Interacting Partners?
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