CYP20A1 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Aliases | CYP20A1 , CYP-M, cytochrome P450 family 20 subfamily A member 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | MGI: 1925201 HomoloGene: 18584 GeneCards: CYP20A1 | ||||||||||||||||||||||||||||||||||||||||||||||||||
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Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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CYP20A1 (cytochrome P450, family 20, subfamily A, polypeptide 1) is a protein which in humans is encoded by the CYP20A1 gene. [5]
This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases that catalyze many reactions involved in pollutant and drug metabolism and the synthesis of cholesterol, steroids, and other lipids. CYP20A1 lacks one amino acid of the conserved heme binding site. It also lacks the conserved I-helix motif AGX(D,E)T, suggesting that its substrate may carry its own oxygen. [6]
CYP20A1 has no identified substrate or biological role and is considered an "orphan" P450.
Cytochrome P450 2A6 is a member of the cytochrome P450 mixed-function oxidase system, which is involved in the metabolism of xenobiotics in the body. CYP2A6 is the primary enzyme responsible for the oxidation of nicotine and cotinine. It is also involved in the metabolism of several pharmaceuticals, carcinogens, and a number of coumarin-type alkaloids. CYP2A6 is the only enzyme in the human body that appreciably catalyzes the 7-hydroxylation of coumarin, such that the formation of the product of this reaction, 7-hydroxycoumarin, is used as a probe for CYP2A6 activity.
Cytochrome P450 1A2, a member of the cytochrome P450 mixed-function oxidase system, is involved in the metabolism of xenobiotics in the human body. In humans, the CYP1A2 enzyme is encoded by the CYP1A2 gene.
Cytochrome P450 1B1 is an enzyme that in humans is encoded by the CYP1B1 gene.
Steroid 21-hydroxylase is an enzyme that hydroxylates steroids at the C21 position and is involved in biosynthesis of aldosterone and cortisol. The enzyme converts progesterone and 17α-hydroxyprogesterone into 11-deoxycorticosterone and 11-deoxycortisol, respectively, within metabolic pathways that ultimately lead to aldosterone and cortisol. Deficiency in the enzyme may cause congenital adrenal hyperplasia.
Steroid 11β-hydroxylase, also known as steroid 11β-monooxygenase, is a steroid hydroxylase found in the zona glomerulosa and zona fasciculata of the adrenal cortex. Named officially the cytochrome P450 11B1, mitochondrial, it is a protein that in humans is encoded by the CYP11B1 gene. The enzyme is involved in the biosynthesis of adrenal corticosteroids by catalyzing the addition of hydroxyl groups during oxidation reactions.
Cytochrome P450 2C18 is a protein that in humans is encoded by the CYP2C18 gene.
Cytochrome P450 4B1 is a protein that in humans is encoded by the CYP4B1 gene.
Cytochrome P450 2A13 is a protein that in humans is encoded by the CYP2A13 gene.
Cytochrome P450 3A43 is a protein that in humans is encoded by the CYP3A43 gene.
Cytochrome P450 2F1 is a protein that in humans is encoded by the CYP2F1 gene.
Cytochrome P450 4F12 is a protein that in humans is encoded by the CYP4F12 gene.
Cytochrome P450 26B1 is a protein that in humans is encoded by the CYP26B1 gene.
CYP39A1 also known as oxysterol 7-α-hydroxylase 2 is a protein that in humans is encoded by the CYP39A1 gene.
CYP26C1 is a protein which in humans is encoded by the CYP26C1gene.
CYP8B1 also known as sterol 12-alpha-hydroxylase is a protein which in humans is encoded by the CYP8B1 gene.
CYP4X1 is a protein which in humans is encoded by the CYP4X1 gene.
CYP4F22 is a protein that in humans is encoded by the CYP4F22 gene.
CYP2W1 is a protein that in humans is encoded by the CYP2W1 gene.
CYP2U1 is a protein that in humans is encoded by the CYP2U1 gene
CYP2A7 is a protein that in humans is encoded by the CYP2A7 gene.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.