PLEKHA5 and PDZD11

Number of citations of the paper that reports this interaction (PMID 25416956)
0

Data Source:
BioGRID (two hybrid)

		PLEKHA5	PDZD11
Gene Name		pleckstrin homology domain containing, family A member 5	PDZ domain containing 11
Image			No pdb structure
Gene Ontology Annotations	Cellular Component	Cytosol Membrane	Extracellular Region Cytosol Cell-cell Junction Basolateral Plasma Membrane Synapse
	Molecular Function	Protein Binding 1-phosphatidylinositol Binding Phosphatidylinositol-5-phosphate Binding Phosphatidylinositol-3-phosphate Binding Phosphatidylinositol-4-phosphate Binding Phosphatidylinositol-3,5-bisphosphate Binding	Protein Binding Protein C-terminus Binding
	Biological Process	Biological_process Reproductive System Development	Vitamin Metabolic Process Water-soluble Vitamin Metabolic Process Biotin Metabolic Process Exocytosis Neurotransmitter Secretion Asymmetric Protein Localization Pantothenate Metabolic Process Ion Transmembrane Transport Small Molecule Metabolic Process Maintenance Of Epithelial Cell Apical/basal Polarity Transmembrane Transport Protein Localization To Basolateral Plasma Membrane
Pathways			Metabolism of vitamins and cofactors Defective CD320 causes methylmalonic aciduria Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF Defective BTD causes biotidinase deficiency Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC Defective MTR causes methylmalonic aciduria and homocystinuria type cblG SLC-mediated transmembrane transport Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE Ion transport by P-type ATPases Defective AMN causes hereditary megaloblastic anemia 1 Ion channel transport Transport of vitamins, nucleosides, and related molecules Defects in cobalamin (B12) metabolism Defective GIF causes intrinsic factor deficiency Vitamin B5 (pantothenate) metabolism Defective HLCS causes multiple carboxylase deficiency Defective MMAB causes methylmalonic aciduria type cblB Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD Defective MMAA causes methylmalonic aciduria type cblA Defective CUBN causes hereditary megaloblastic anemia 1 Defective MUT causes methylmalonic aciduria mut type Metabolism of water-soluble vitamins and cofactors Defects in biotin (Btn) metabolism Defective TCN2 causes hereditary megaloblastic anemia Biotin transport and metabolism Defects in vitamin and cofactor metabolism
Drugs
Diseases
GWAS
Protein-Protein Interactions		30 interactors: ARHGEF9 BLOC1S6 CCDC186 CCDC88B CCDC92 CEP250 CEP350 DES EVPL EXTL3 KANSL1 KIF3A KRT19 KRT20 KTN1 LAMB2 LSM4 MAX PDZD11 PLEC PLEKHA6 PPP1R13B PROM1 SH3BP5L SOGA1 SPTAN1 SPTBN1 UPF1 WASH2P YWHAG	4 interactors: ATP2B2 ATP7A PLEKHA5 SIGMAR1
Entrez ID		54477	51248
HPRD ID		09684	06622
Ensembl ID		ENSG00000052126	ENSG00000120509
Uniprot IDs		Q9HAU0	Q5EBL8
PDB IDs		2DKP
Enriched GO Terms of Interacting Partners?		Apoptotic Process Programmed Cell Death Cell Death Death Hemidesmosome Assembly Glomerular Visceral Epithelial Cell Differentiation Regulation Of Protein Complex Disassembly Cellular Localization Regulation Of Cellular Component Organization Movement Of Cell Or Subcellular Component Cellular Process Retina Development In Camera-type Eye Organelle Organization Generation Of Neurons Cell Differentiation Involved In Kidney Development Neuron Differentiation Cytoskeleton Organization Regulation Of Actin Filament Polymerization Microtubule-based Process Neurogenesis Metanephric Glomerular Basement Membrane Development Axon Extension Involved In Regeneration Regulation Of Actin Polymerization Or Depolymerization Regulation Of Actin Filament Length Cell-substrate Junction Assembly Actin Filament Capping Membrane Organization Regulation Of Cytoskeleton Organization Glomerulus Development Cellular Component Disassembly Involved In Execution Phase Of Apoptosis Negative Regulation Of Actin Filament Depolymerization Epithelial Cell Differentiation Regulation Of Organelle Organization Metanephric Glomerular Visceral Epithelial Cell Development Response To Axon Injury Protein Localization Neuron Development Regulation Of Actin Filament Depolymerization Execution Phase Of Apoptosis Negative Regulation Of Actin Filament Polymerization Sensory Organ Development Glomerular Parietal Epithelial Cell Differentiation Positive Regulation Of Nephron Tubule Epithelial Cell Differentiation Regulation Of Centriole-centriole Cohesion Response To Insulin Establishment Of Localization In Cell Microtubule-based Movement Intracellular Transport Negative Regulation Of Protein Polymerization Post-Golgi Vesicle-mediated Transport	Cerebellar Purkinje Cell Differentiation Serotonin Metabolic Process Cerebellar Purkinje Cell Layer Morphogenesis Cerebellar Cortex Formation Cell Differentiation In Hindbrain Cerebellar Purkinje Cell Layer Development Cerebellar Cortex Morphogenesis Cerebellum Morphogenesis Hindbrain Morphogenesis Lactation Cerebellar Cortex Development Regulation Of Oxidoreductase Activity Phenol-containing Compound Metabolic Process Body Fluid Secretion Cerebellum Development Elastin Biosynthetic Process Negative Regulation Of Citrulline Biosynthetic Process Negative Regulation Of Cardiac Muscle Hypertrophy In Response To Stress Negative Regulation Of Arginine Catabolic Process Calcium Ion Import Across Plasma Membrane Plasma Membrane Copper Ion Transport Otolith Mineralization Negative Regulation Of The Force Of Heart Contraction Metencephalon Development Mammary Gland Development Hindbrain Development Calcium Ion Import Into Cell Copper Ion Export Negative Regulation Of Adrenergic Receptor Signaling Pathway Involved In Heart Process Negative Regulation Of Cardiac Muscle Adaptation Elastin Metabolic Process Detoxification Of Copper Ion Negative Regulation Of Adrenergic Receptor Signaling Pathway Central Nervous System Neuron Differentiation Locomotory Behavior Regulation Of Neuron Apoptotic Process Response To Iron(III) Ion Epinephrine Metabolic Process Negative Regulation Of Nitric Oxide Mediated Signal Transduction Epidermis Development Negative Regulation Of Peptidyl-cysteine S-nitrosylation Positive Regulation Of CAMP-dependent Protein Kinase Activity Regulation Of Neuron Death Norepinephrine Biosynthetic Process Negative Regulation Of Metalloenzyme Activity Regulation Of Adrenergic Receptor Signaling Pathway Negative Regulation Of Calcineurin-NFAT Signaling Cascade Ribonucleotide Metabolic Process System Development Purine Nucleotide Metabolic Process
Tagcloud ?		a375 a375br a375p aberrantly barrier bbb brain cerebrotropic constructed differentially extra homing immunofluorescence knock mediators melanoma metastases metastasis metastatic overwhelming parental passage profiles profiling propensity subjected transmigration viability yumul
Tagcloud (Difference) ?		a375 a375br a375p aberrantly barrier bbb brain cerebrotropic constructed differentially extra homing immunofluorescence knock mediators melanoma metastases metastasis metastatic overwhelming parental passage profiles profiling propensity subjected transmigration viability yumul
Tagcloud (Intersection) ?