Coproporphyrinogen III oxidase

Coproporphyrinogen-III oxidase, mitochondrial (abbreviated as CPOX) is an enzyme that in humans is encoded by the CPOX gene. A genetic defect in the enzyme results in a reduced production of heme in animals. The medical condition associated with this enzyme defect is called hereditary coproporphyria.

CPOX
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesCPOX, CPO, CPX, HCP, coproporphyrinogen oxidase, COX, HARPO
External IDsOMIM: 612732 MGI: 104841 HomoloGene: 76 GeneCards: CPOX
EC number1.3.3.3
Orthologs
SpeciesHumanMouse
Entrez

1371

12892

Ensembl

n/a

ENSMUSG00000022742

UniProt

P36551

P36552

RefSeq (mRNA)

NM_000097

NM_007757

RefSeq (protein)

NP_000088

NP_031783

Location (UCSC)n/aChr 16: 58.49 – 58.54 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse
Coprogen oxidase
coproporphyrinogen iii oxidase from leishmania major
Identifiers
SymbolCoprogen oxidase
PfamPF01218
InterProIPR001260
PROSITEPDOC00783
Available protein structures:
Pfam  structures / ECOD  
PDBRCSB PDB; PDBe; PDBj
PDBsumstructure summary

CPOX, the sixth enzyme of the haem biosynthetic pathway, converts coproporphyrinogen III to protoporphyrinogen IX through two sequential steps of oxidative decarboxylation. The activity of the CPOX enzyme, located in the mitochondrial membrane, is measured in lymphocytes.

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