Protoporphyrinogen oxidase: Difference between revisions
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'''Protoporphyrinogen oxidase''' ( | {{Short description|An enzyme involved in heme biosynthesis}} | ||
{{Enzyme}} | |||
==Protoporphyrinogen oxidase== | |||
[[File:Heme_synthesis.png|thumb|right|300px|Overview of heme synthesis, showing the role of protoporphyrinogen oxidase.]] | |||
'''Protoporphyrinogen oxidase''' (PPOX) is an enzyme that plays a crucial role in the [[biosynthesis]] of [[heme]], an essential component of [[hemoglobin]], [[myoglobin]], and various [[cytochrome]]s. This enzyme catalyzes the oxidation of [[protoporphyrinogen IX]] to [[protoporphyrin IX]], a key step in the heme synthesis pathway. | |||
==Function== | ==Function== | ||
Protoporphyrinogen oxidase | Protoporphyrinogen oxidase is located in the [[mitochondrial membrane]] and is responsible for the seventh step in the heme biosynthetic pathway. The enzyme facilitates the conversion of protoporphyrinogen IX, a colorless compound, into protoporphyrin IX, a colored compound, by removing six hydrogen atoms. This reaction is crucial for the subsequent incorporation of [[iron]] to form heme. | ||
== | ==Structure== | ||
PPOX is a flavoprotein, meaning it contains a [[flavin adenine dinucleotide]] (FAD) cofactor that is essential for its enzymatic activity. The enzyme is encoded by the PPOX gene, which is located on chromosome 1 in humans. Mutations in this gene can lead to disorders such as [[variegate porphyria]]. | |||
== | ==Clinical significance== | ||
Deficiencies or malfunctions in protoporphyrinogen oxidase can result in a group of disorders known as [[porphyrias]]. These are metabolic disorders characterized by an accumulation of porphyrins or porphyrin precursors, leading to a variety of symptoms including skin photosensitivity, abdominal pain, and neurological complications. | |||
== | ==Related pages== | ||
* [[Heme | * [[Heme]] | ||
* [[ | * [[Porphyria]] | ||
* [[ | * [[Cytochrome]] | ||
* [[ | * [[Hemoglobin]] | ||
* [[Myoglobin]] | |||
[[Category:Enzymes]] | [[Category:Enzymes]] | ||
[[Category: | [[Category:Heme biosynthesis]] | ||
[[Category:Flavoproteins]] | |||
Latest revision as of 14:07, 16 February 2025
An enzyme involved in heme biosynthesis
Protoporphyrinogen oxidase
Protoporphyrinogen oxidase[edit]

Protoporphyrinogen oxidase (PPOX) is an enzyme that plays a crucial role in the biosynthesis of heme, an essential component of hemoglobin, myoglobin, and various cytochromes. This enzyme catalyzes the oxidation of protoporphyrinogen IX to protoporphyrin IX, a key step in the heme synthesis pathway.
Function[edit]
Protoporphyrinogen oxidase is located in the mitochondrial membrane and is responsible for the seventh step in the heme biosynthetic pathway. The enzyme facilitates the conversion of protoporphyrinogen IX, a colorless compound, into protoporphyrin IX, a colored compound, by removing six hydrogen atoms. This reaction is crucial for the subsequent incorporation of iron to form heme.
Structure[edit]
PPOX is a flavoprotein, meaning it contains a flavin adenine dinucleotide (FAD) cofactor that is essential for its enzymatic activity. The enzyme is encoded by the PPOX gene, which is located on chromosome 1 in humans. Mutations in this gene can lead to disorders such as variegate porphyria.
Clinical significance[edit]
Deficiencies or malfunctions in protoporphyrinogen oxidase can result in a group of disorders known as porphyrias. These are metabolic disorders characterized by an accumulation of porphyrins or porphyrin precursors, leading to a variety of symptoms including skin photosensitivity, abdominal pain, and neurological complications.