Any feedback?
Please rate this page
(literature.php)
(0/150)

BRENDA support

Literature summary for 3.1.2.22 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.
    View publication on PubMed

Localization

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

Organism

Organism UniProt Comment Textmining
Homo sapiens
-
-
-

Source Tissue

Source Tissue Comment Organism Textmining
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)

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