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Literature summary for 3.1.2.22 extracted from

  • Salonen, T.; Jarvela, I.; Peltonen, L.; Jalanko, A.
    Detection of eight novel palmitoyl protein thioesterase (PPT) mutations underlying infantile neuronal ceroid lipofuscinosis (INCL;CLN1) (2000), Hum. Mutat., 15, 273-279.
    View publication on PubMed

Cloned(Commentary)

Cloned (Comment) Organism
gene ppt, DNA sequence determnation and analysis, identification of 8 natural mutations of different origins leading to enzyme deficiency Homo sapiens

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
additional information Homo sapiens enzyme deficiency causes the infantile form of neuronal ceroid lipofuscinosis INCL, a progressive encephalopathyof children ?
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?

Organism

Organism UniProt Comment Textmining
Homo sapiens
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Reaction

Reaction Comment Organism Reaction ID
palmitoyl[protein] + H2O = palmitate + protein specific for long-chain thioesters of fatty acids from S-acylated residues in proteins, palmitoyl cysteine and palmitoyl-CoA Homo sapiens

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
additional information enzyme deficiency causes the infantile form of neuronal ceroid lipofuscinosis INCL, a progressive encephalopathyof children Homo sapiens ?
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?
palmitoyl-[protein] + H2O
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Homo sapiens palmitate + protein
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?

Synonyms

Synonyms Comment Organism
palmitoyl protein thioesterase
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Homo sapiens
PPT
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Homo sapiens