Literature summary extracted from

Vesa, J.; Hellsten, E.; Verkruyse, L.A.; Camp, L.A.; Rapola, J.; Santavuori, P.; Hofmann, S.L.; Peltonen, L.
Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis (1995), Nature, 376, 584-587.

Localization

EC Number	Localization	Comment	Organism	GeneOntology No.	Textmining
3.1.2.22	intracellular	the most common mutation results in intracellular accumulation of the enzyme polypeptide and undetectable activity in the brain	Homo sapiens	5622	-

Organism

EC Number	Organism	UniProt	Comment	Textmining
3.1.2.22	Homo sapiens	-	-	-

Source Tissue

EC Number	Source Tissue	Comment	Organism	Textmining
3.1.2.22	additional information	the most common mutation results in intracellular accumulationof the enzyme polypeptide and undetectable activity in the brain	Homo sapiens	-

Substrates and Products (Substrate)

EC Number	Substrates	Comment Substrates	Organism	Products	Comment (Products)	Rev.	Reac.
3.1.2.22	palmitoyl-[protein] + H2O	-	Homo sapiens	palmitate + protein	-	?

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Release 2023.1 (January 2023)