PPT1

Description		palmitoyl-protein thioesterase 1
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GO Annotations	Cellular Component	Extracellular Region Extracellular Space Nucleus Lysosome Lysosomal Membrane Endoplasmic Reticulum Golgi Apparatus Cytosol Synaptic Vesicle Membrane Axon Dendrite Synaptic Vesicle Membrane Neuronal Cell Body Lysosomal Lumen Membrane Raft Extracellular Exosome Presynaptic Cytosol
	Molecular Function	Protein Binding Palmitoyl-(protein) Hydrolase Activity Hydrolase Activity Phospholipase A2 Inhibitor Activity Lysophosphatidic Acid Binding Long-chain Fatty Acyl-CoA Hydrolase Activity Palmitoyl Hydrolase Activity Sulfatide Binding
	Biological Process	Protein Depalmitoylation Endocytosis Receptor-mediated Endocytosis Pinocytosis Lysosome Organization Lysosomal Lumen Acidification Neurotransmitter Secretion Nervous System Development Brain Development Visual Perception Grooming Behavior Associative Learning Adult Locomotory Behavior Macromolecule Catabolic Process Protein Transport Lipid Catabolic Process Sphingolipid Catabolic Process Protein Catabolic Process Negative Regulation Of Cell Growth Membrane Raft Organization Toll-like Receptor 9 Signaling Pathway Negative Regulation Of Toll-like Receptor 9 Signaling Pathway Negative Regulation Of Apoptotic Process Negative Regulation Of Neuron Apoptotic Process Fatty-acyl-CoA Biosynthetic Process Positive Regulation Of Receptor-mediated Endocytosis Positive Regulation Of Pinocytosis Neuron Development Regulation Of Synapse Structure Or Activity
Pathways		Fatty acyl-CoA biosynthesis
Drugs		Hexadecanesulfonyl fluoride Palmitic Acid
Diseases		Progressive myoclonic epilepsy (PME), including: Lafora disease (LBD); Unverricht-Lundborg disease (ULD); Neuronal ceroid lipofuscinoses (NCL); Type I sialidosis; Action myoclonus-renal failure syndrome (AMRF); Type III Gaucher disease (GD) Neuronal ceroid lipofuscinosis, including: Infantile Neuronal Ceroid Lipofuscinosis (INCL)/ Santavuori-Haltia Disease (CLN1); Late-Infantile Neuronal Ceroid Lipofuscinosis (LINCL)/ Jansky-Bielschowsky Disease (CLN2); Juvenile Neuronal Ceroid Lipofuscinosis (JNCL)/Batten Disease/ Spielmeyer-Vogt Disease (CLN3); Adult Neuronal Ceroid Lipofuscinosis (ANCL)/ Kufs Disease (CLN4); LINCL variant (CLN5, CLN6, CLN7, CLN8); Batten Disease variant (CLN9); Congenital NCL (CLN10)
GWAS		Blood protein levels ( 30072576) Platelet count ( 32888494)
Novel Interacting Genes		3 novel interacting genes: COL6A3 EPS15 RLF
Interacting Genes		2 interacting genes: GNAQ LCOR
Entrez ID		5538
HPRD ID		07203
Ensembl ID		ENSG00000131238
Uniprot IDs		P50897 Q5T0S4
PDB IDs		3GRO
Enriched GO Terms of Interacting Partners?
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