Literature summary for 4.1.1.37 extracted from

Tavazzi, D.; Di Montemuros, F.M.; Fargion, S.; Fracanzani, A.L.; Fiorelli, G.; Cappellini, M.D.
Levels of uroporphyrinogen decarboxylase (URO-D) in erythrocytes of Italian porphyria cutanea tarda patients (2002), Cell. Mol. Biol., 48, 27-32.

Search for more literature for 4.1.1.37

Application

Application	Comment	Organism
medicine	PCT is a human metabolic disorder, due to the acquired or genetic impairment of uroporphyrinogen decarboxylase activity	Homo sapiens

Natural Substrates/ Products (Substrates)

Natural Substrates	Organism	Comment (Nat. Sub.)	Natural Products	Comment (Nat. Pro.)	Rev.	Reac.
Uroporphyrinogen III	Homo sapiens	fifth enzyme of the heme biosynthetic pathway	Coproporphyrinogen III + 4 CO2	-	?

Organism

Organism	UniProt	Comment	Textmining
Homo sapiens	-	human, italian porphyria cutanea tarda patients	-

Source Tissue

Source Tissue	Comment	Organism	Textmining

Substrates and Products (Substrate)

Substrates	Comment Substrates	Organism	Products	Comment (Products)	Rev.	Reac.
Uroporphyrinogen III	-	Homo sapiens	Coproporphyrinogen III + 4 CO2	-	?
Uroporphyrinogen III	fifth enzyme of the heme biosynthetic pathway	Homo sapiens	Coproporphyrinogen III + 4 CO2	-	?

Synonyms

Synonyms	Comment	Organism
URO-D	-	Homo sapiens
uroporphyrinogen decarboxylase	-	Homo sapiens

Use of this online version of BRENDA is free under the CC BY 4.0 license. See terms of use for full details.

Release 2023.1 (January 2023)