EIF2D and HEXB

Number of citations of the paper that reports this interaction (PMID 7299841)
2

Data Source:
HPRD (in vitro)

		EIF2D	HEXB
Gene Name		eukaryotic translation initiation factor 2D	hexosaminidase B (beta polypeptide)
Image		No pdb structure
Gene Ontology Annotations	Cellular Component	Nucleus Nucleoplasm Cytoplasm Cytosolic Small Ribosomal Subunit	Acrosomal Vesicle Membrane Lysosomal Lumen Extracellular Vesicular Exosome
	Molecular Function	Translation Initiation Factor Activity Receptor Activity	Beta-N-acetylhexosaminidase Activity Protein Homodimerization Activity Protein Heterodimerization Activity
	Biological Process	Formation Of Translation Preinitiation Complex IRES-dependent Translational Initiation Intracellular Protein Transport Ribosome Disassembly	Skeletal System Development Carbohydrate Metabolic Process Sphingolipid Metabolic Process Glycosphingolipid Metabolic Process Ganglioside Catabolic Process Cellular Calcium Ion Homeostasis Lysosome Organization Penetration Of Zona Pellucida Sensory Perception Of Sound Locomotory Behavior Male Courtship Behavior Regulation Of Cell Shape Phospholipid Biosynthetic Process Oligosaccharide Catabolic Process Pathogenesis Lipid Storage Glycosaminoglycan Metabolic Process Chondroitin Sulfate Metabolic Process Chondroitin Sulfate Catabolic Process Hyaluronan Metabolic Process Hyaluronan Catabolic Process Keratan Sulfate Metabolic Process Keratan Sulfate Catabolic Process Myelination Astrocyte Cell Migration Cellular Protein Metabolic Process Small Molecule Metabolic Process Positive Regulation Of Transcription From RNA Polymerase II Promoter Oogenesis Neuromuscular Process Controlling Balance
Pathways			MPS IIIB - Sanfilippo syndrome B Diseases of glycosylation Metabolism of lipids and lipoproteins Defective B4GALT7 causes EDS, progeroid type Keratan sulfate/keratin metabolism MPS I - Hurler syndrome MPS IX - Natowicz syndrome Chondroitin sulfate/dermatan sulfate metabolism Defective SLC26A2 causes chondrodysplasias Glycosaminoglycan metabolism CS/DS degradation Hyaluronan uptake and degradation Defective B4GALT1 causes B4GALT1-CDG (CDG-2d) Defective CHST14 causes EDS, musculocontractural type Defective PAPSS2 causes SEMD-PA MPS IIIA - Sanfilippo syndrome A Myoclonic epilepsy of Lafora Hyaluronan metabolism Defective CHST6 causes MCDC1 MPS IIID - Sanfilippo syndrome D Glycogen storage diseases MPS IIIC - Sanfilippo syndrome C Sphingolipid metabolism Diseases associated with glycosaminoglycan metabolism Mucopolysaccharidoses Keratan sulfate degradation Glycosphingolipid metabolism Defective EXT2 causes exostoses 2 MPS II - Hunter syndrome Defective CHST3 causes SEDCJD Defective B3GAT3 causes JDSSDHD Defective EXT1 causes exostoses 1, TRPS2 and CHDS MPS IV - Morquio syndrome A MPS IV - Morquio syndrome B Defective CHSY1 causes TPBS MPS VII - Sly syndrome Metabolism of carbohydrates MPS VI - Maroteaux-Lamy syndrome
Drugs			2-Acetamido-2-Deoxy-D-Glucono-1,5-Lactone 3ar,5r,6s,7r,7ar-5-Hydroxymethyl-2-Methyl-5,6,7,7a-Tetrahydro-3ah-Pyrano[3,2-D]Thiazole-6,7-Diol (2r,3r,4s,5r)-2-Acetamido-3,4-Dihydroxy-5-Hydroxymethyl-Piperidinium
Diseases
GWAS
Protein-Protein Interactions		2 interactors: ACHE HEXB	2 interactors: CSNK2B EIF2D
Entrez ID		1939	3074
HPRD ID		01057	06043
Ensembl ID		ENSG00000143486	ENSG00000049860
Uniprot IDs		P41214	P07686 Q5URX0
PDB IDs			1NOU 1NOW 1NP0 1O7A 1QBD 2GJX 2GK1 3LMY
Enriched GO Terms of Interacting Partners?		Male Courtship Behavior Negative Regulation Of Synaptic Transmission, Cholinergic Neurotransmitter Receptor Biosynthetic Process Phospholipid Biosynthetic Process Acetylcholine Catabolic Process Acetylcholine Catabolic Process In Synaptic Cleft Phospholipid Metabolic Process Receptor Biosynthetic Process Male Mating Behavior Penetration Of Zona Pellucida Astrocyte Cell Migration Regulation Of Synaptic Transmission, Cholinergic Ganglioside Catabolic Process Lipid Biosynthetic Process Oligosaccharide Catabolic Process Neurotransmitter Receptor Metabolic Process Keratan Sulfate Catabolic Process Neurotransmitter Catabolic Process Hyaluronan Catabolic Process Synaptic Transmission, Cholinergic Chondroitin Sulfate Catabolic Process Neurotransmitter Biosynthetic Process Ganglioside Metabolic Process Glycosphingolipid Catabolic Process Glycolipid Catabolic Process Amyloid Precursor Protein Metabolic Process Ceramide Catabolic Process Cellular Lipid Metabolic Process Organophosphate Metabolic Process Phosphatidylcholine Biosynthetic Process Neurotransmitter Metabolic Process Sphingolipid Catabolic Process Regulation Of Receptor Recycling Keratan Sulfate Metabolic Process Osteoblast Development Membrane Lipid Catabolic Process Mating Behavior Lipid Metabolic Process Lipid Storage Hyaluronan Metabolic Process Receptor Internalization Oligosaccharide Metabolic Process Mating Lysosome Organization Phosphatidylcholine Metabolic Process Glycosaminoglycan Catabolic Process Chondroitin Sulfate Metabolic Process Negative Regulation Of Synaptic Transmission Glial Cell Migration Catabolic Process	IRES-dependent Translational Initiation Cap-independent Translational Initiation Ribosome Disassembly Positive Regulation Of Activin Receptor Signaling Pathway Adiponectin-activated Signaling Pathway Cellular Macromolecular Complex Assembly Cytoplasmic Translational Initiation Endothelial Tube Morphogenesis Cytoplasmic Translation Negative Regulation Of Blood Vessel Endothelial Cell Migration Formation Of Translation Preinitiation Complex Regulation Of Activin Receptor Signaling Pathway Negative Regulation Of Endothelial Cell Migration Organelle Disassembly Positive Regulation Of Pathway-restricted SMAD Protein Phosphorylation Regulation Of Blood Vessel Endothelial Cell Migration Negative Regulation Of Epithelial Cell Migration Regulation Of Pathway-restricted SMAD Protein Phosphorylation Cellular Component Assembly Regulation Of DNA Binding Endothelium Development
Tagcloud ?			1404delt 26g admitted ataxia atrophy boy cerebellar confirming cranial dysarthria fluorometric fsx62 gait ganglia heterozygote hexosaminidase juvenile leukocytes mri mrs mutation neuroimaging nmol p468p psychomotor retrospectively sandhoff slowly thalamus
Tagcloud (Difference) ?			1404delt 26g admitted ataxia atrophy boy cerebellar confirming cranial dysarthria fluorometric fsx62 gait ganglia heterozygote hexosaminidase juvenile leukocytes mri mrs mutation neuroimaging nmol p468p psychomotor retrospectively sandhoff slowly thalamus
Tagcloud (Intersection) ?