Species Human Entrez 5498 Gene ontology 0070818 | Human Mouse Ensembl ENSG00000143224 | |
 | ||
Aliases PPOX, PPO, V290M, VP, protoporphyrinogen oxidase External IDs OMIM: 600923 MGI: 104968 HomoloGene: 262 GeneCards: PPOX | ||
Protoporphyrinogen oxidase physiology biochemistry and organic mechanism
Protoporphyrinogen oxidase is an enzyme that in humans is encoded by the PPOX gene.
Contents
- Protoporphyrinogen oxidase physiology biochemistry and organic mechanism
- Medical vocabulary what does protoporphyrinogen oxidase mean
- Gene
- Function
- Heme biosynthetic pathway
- Clinical significance
- References
Protoporphyrinogen oxidase is responsible for the seventh step in biosynthesis of protoporphyrin IX. This porphyrin is the precursor to hemoglobin, the oxygen carrier in animals, and chlorophyll, the dye in plants. The enzyme catalyzes the dehydrogenation (removal of hydrogen atoms) of protoporphyrinogen IX (the product of the sixth step in the production of heme) to form protoporphyrin IX. One additional enzyme must modify protoporphyrin IX before it becomes heme. Inhibition of this enzyme is a strategy used in certain herbicides.
Medical vocabulary what does protoporphyrinogen oxidase mean
Gene
The PPOX gene is located on the long (q) arm of chromosome 1 at position 22, from base pair 157,949,266 to base pair 157,954,082.
Function
This gene encodes the penultimate enzyme of heme biosynthesis, which catalyzes the 6-electron oxidation of protoporphyrinogen IX to form protoporphyrin IX. This protein is a flavoprotein associated with the outer surface of the inner mitochondrial membrane.
Heme biosynthetic pathway
The following genes encode enzymes that catalyze the various steps in the heme biosynthetic pathway:
Clinical significance
Variegate porphyria is caused by mutations in the PPOX gene. More than 100 mutations that can cause variegate porphyria have been identified in the PPOX gene. One mutation, a substitution of the amino acid tryptophan for arginine at position 59 (also written as Arg59Trp or R59W), is found in about 95 percent of South African families with variegate porphyria. Mutations in the PPOX gene reduce the activity of the enzyme made by the gene, allowing byproducts of heme production to build up in the body. This buildup, in combination with nongenetic factors (such as certain drugs, alcohol and dieting), causes this type of porphyria.