GLUL and TAT

Number of citations of the paper that reports this interaction (PubMedID 25910212)
127

Data Source:
BioGRID (two hybrid)

		GLUL	TAT
Description		glutamate-ammonia ligase	tyrosine aminotransferase
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GO Annotations	Cellular Component	Nucleus Mitochondrion Rough Endoplasmic Reticulum Cytosol Plasma Membrane Protein-containing Complex Perikaryon Myelin Sheath Axon Terminus Extracellular Exosome Glial Cell Projection	Cellular_component Mitochondrion Cytosol
	Molecular Function	Magnesium Ion Binding Glutamate-ammonia Ligase Activity Protein Binding ATP Binding Glutamate Binding Protein-cysteine S-palmitoyltransferase Activity Manganese Ion Binding Identical Protein Binding Dynein Light Chain Binding	L-tyrosine:2-oxoglutarate Aminotransferase Activity Protein Binding Amino Acid Binding Pyridoxal Phosphate Binding Identical Protein Binding
	Biological Process	Neurotransmitter Uptake Angiogenesis Glutamate Catabolic Process Glutamine Biosynthetic Process Cell Proliferation Cellular Amino Acid Biosynthetic Process Cellular Response To Starvation Response To Glucose Regulation Of Endothelial Cell Migration Protein Palmitoylation Ammonia Assimilation Cycle Positive Regulation Of Insulin Secretion Ribosome Biogenesis Positive Regulation Of Epithelial Cell Proliferation Positive Regulation Of Synaptic Transmission, Glutamatergic Regulation Of Sprouting Angiogenesis Regulation Of Protein Localization To Nucleolus	2-oxoglutarate Metabolic Process Glutamate Metabolic Process L-phenylalanine Catabolic Process Tyrosine Catabolic Process Response To Oxidative Stress Biosynthetic Process Response To Mercury Ion Response To Glucocorticoid
Pathways		Astrocytic Glutamate-Glutamine Uptake And Metabolism Glutamate and glutamine metabolism	Tyrosine catabolism
Drugs		L-Glutamine Glutamic Acid	Pyridoxal Phosphate L-Phenylalanine L-Tyrosine Glutamic Acid
Diseases		Congenital systemic glutamine deficiency (CSGD); Glutamine synthetase deficiency	Tyrosinemia; Tyrosinemia, type I; Tyrosinemia, type II; Tyrosinemia, type III; Hawkinsinuria
GWAS		Cardiovascular heart disease in diabetics ( 23982368) Morning person ( 30696823)	Chronotype ( 30696823) Metabolite levels ( 22286219 22916037) Morning person ( 30696823) Urate levels ( 31578528)
Interacting Genes		22 interacting genes: CASP8AP2 CRBN CYP39A1 DYNLL1 EP300 HIPK1 HIPK3 HSD17B10 HTR2A MT-ND5 NFKB1 NUDT18 PIAS1 PIAS2 PIAS3 PLEKHF2 PPARD RABEPK RBBP6 SKIL TAT UBE2I	3 interacting genes: GLUL GRN UBE3A
Entrez ID		2752	6898
HPRD ID		00701	11776
Ensembl ID		ENSG00000135821	ENSG00000198650
Uniprot IDs		A8YXX4 P15104	A0A140VKB7 P17735
PDB IDs		2OJW 2QC8	3DYD
Enriched GO Terms of Interacting Partners?
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