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Literature summary for 1.3.3.3 extracted from

  • Lambie, D.; Florkowski, C.; Sies, C.; Raizis, A.; Siu, W.K.; Towns, C.
    A case of hereditary coproporphyria with posterior reversible encephalopathy and novel coproporphyrinogen oxidase gene mutation c.863T>G (p.Leu288Trp) (2018), Ann. Clin. Biochem., 55, 616-619 .
    View publication on PubMed
Search for more literature for 1.3.3.3

Protein Variants

Protein Variants Comment Organism
L288W the mutation is associated with hereditary coproporphyria with posterior reversible encephalopathy Homo sapiens

Localization

Localization Comment Organism GeneOntology No. Textmining
mitochondrion
-
 Homo sapiens 5739
-

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
coproporphyrinogen III + O2 + 2 H+ Homo sapiens
-
 protoporphyrinogen-IX + 2 CO2 + 2 H2O
-
 ?

Organism

Organism UniProt Comment Textmining
Homo sapiens
-
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
coproporphyrinogen III + O2 + 2 H+
-
 Homo sapiens protoporphyrinogen-IX + 2 CO2 + 2 H2O
-
 ?

Synonyms

Synonyms Comment Organism
CPOX
-
 Homo sapiens