Category:Drug-metabolizing enzymes - Revision history

MDElliottMD: Category:Drug-metabolizing enzymes: repoint the 11 enzyme links onto the Enzyme: namespace; correct the stale sandbox note (task #24)

2026-05-22T16:57:28Z

Category:Drug-metabolizing enzymes: repoint the 11 enzyme links onto the Enzyme: namespace; correct the stale sandbox note (task #24)

MDElliottMD: Add Category:CuratedCategoryPage marker tag per interface-claude 2026-05-20. This marker lets MediaWiki:Common.css suppress MediaWiki's auto-generated 'Pages in category' list, which otherwise renders the member list a second time (machine-formatted) below the curated 'Enzymes indexed' section. Marker is the general non-MedCategory equivalent of the existing MedCategoryFull marker. No prose change.

2026-05-19T23:18:14Z

Add Category:CuratedCategoryPage marker tag per interface-claude 2026-05-20. This marker lets MediaWiki:Common.css suppress MediaWiki's auto-generated 'Pages in category' list, which otherwise renders the member list a second time (machine-formatted) below the curated 'Enzymes indexed' section. Marker is the general non-MedCategory equivalent of the existing MedCategoryFull marker. No prose change.

← Older revision		Revision as of 23:18, 19 May 2026
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	[[Category:Pharmacogenomics]]		[[Category:Pharmacogenomics]]
			[[Category:CuratedCategoryPage]]

MDElliottMD: Rewrite category intro: replace the wiki-plumbing lead with a descriptive, history-first account of what a drug-metabolizing enzyme is. Covers the cytochrome P450 naming (Omura and Sato 1964, the 450 nm absorption peak, PMID 14209971), the phase-I / phase-II framework, the mixed-function-oxidase mechanism, the enzyme families, and the detoxification-versus-bioactivation duality (Pott 1775 chimney-sweep scrotal cancer as the historical thread; CYP1A/CYP3A4/CYP2E1 carcinogen activation as the m...

2026-05-19T23:01:24Z

Rewrite category intro: replace the wiki-plumbing lead with a descriptive, history-first account of what a drug-metabolizing enzyme is. Covers the cytochrome P450 naming (Omura and Sato 1964, the 450 nm absorption peak, PMID 14209971), the phase-I / phase-II framework, the mixed-function-oxidase mechanism, the enzyme families, and the detoxification-versus-bioactivation duality (Pott 1775 chimney-sweep scrotal cancer as the historical thread; CYP1A/CYP3A4/CYP2E1 carcinogen activation as the m...

← Older revision		Revision as of 23:01, 19 May 2026
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	~~This category collects the wiki's~~ '''drug-metabolizing-enzyme ~~entity pages~~''': the ~~pharmacogenomics-layer reference pages for~~ the ~~enzymes that metabolize~~, ~~activate~~, ~~or inactivate medicines in~~ the ~~human~~ body. ~~Each page follows~~ a ~~common structure (history-first opening~~, ~~tissue distribution~~, ~~substrate spectrum with~~ a ~~sortable substrate table, phenotype categories, major variants, inhibitors, inducers, clinical implications,~~ and ~~authoritative external resources)~~ and ~~each is the human-readable companion~~ to the ~~machine~~-~~level~~ <~~code~~>~~pk_inhibit_via_<ENZYME&gt~~;</~~code~~> ~~and <code>pk_induce_via_<ENZYME></code> interaction edges in~~ the wiki's ~~pharmacogenomic interaction layer~~.		A '''drug-metabolizing enzyme''' is one of the enzymes by which the body chemically transforms a medicine, after it has been taken, into something the body can use, inactivate, and ultimately excrete. The largest and most important family of these enzymes carries a name taken directly from a laboratory measurement. In the early 1960s, working at Osaka University, Tsuneo Omura and Ryo Sato studied a pigment in the microsomal fraction of liver cells and found that when it was chemically reduced and allowed to bind carbon monoxide it absorbed light sharply at a wavelength of 450 nanometres. They named the pigment for that absorption peak, and cytochrome P-450 has been called that ever since.<ref name="omura1964">Omura T, Sato R. The carbon monoxide-binding pigment of liver microsomes. I. Evidence for its hemoprotein nature. ''Journal of Biological Chemistry''. 1964 Jul;239:2370-2378. PMID: 14209971.</ref> This category collects the wiki's reference pages for the cytochromes P450 and for the other enzyme families that share their work.

	~~These pages currently live as drafting sandboxes under~~ the <~~code~~>~~Pharmacopedia~~:~~</code> project namespace~~ (~~titled <code>Pharmacogenomics sandbox/Enzyme <NAME>~~</~~code~~>); ~~their permanent home will be~~ the ~~dedicated~~ <~~code~~>~~Enzyme~~:</~~code~~> ~~namespace once~~ it is ~~registered~~. The ~~closely related transporter~~, ~~variant~~, and ~~phenotype~~ pages ~~will live under <code>Transporter~~:</~~code~~>, <~~code~~>~~Variant~~:</~~code~~>, and <~~code>Phenotype:<~~/~~code~~> ~~respectively~~, and are not ~~collected here~~.		The body does not, at the molecular level, distinguish a medicine from any other foreign organic chemical: a plant alkaloid, an industrial solvent, a combustion product are all, to the liver, the same kind of problem. The general term for such a substance is a xenobiotic, and the same enzyme systems process all of them. Pharmacologists describe that processing in two stages.<ref name="sheweita2000">Sheweita SA. Drug-metabolizing enzymes: mechanisms and functions. ''Current Drug Metabolism''. 2000 Sep;1(2):107-132. PMID: 11465078.</ref> '''Phase I''' reactions, principally oxidation but also reduction and hydrolysis, introduce or expose a chemically reactive group on the molecule. '''Phase II''' reactions, the conjugations, attach a bulky water-soluble group, glucuronic acid, sulfate, glutathione, or an acetyl group, to that reactive handle, producing a metabolite polar enough to leave the body in bile or urine. The two phases usually run in sequence: phase I prepares the molecule, phase II finishes it.

			The phase-I oxidations are dominated by the '''cytochromes P450''', a multigene family of heme-containing enzymes classified, by the homology of their amino-acid sequences, into families and subfamilies; in human medicine the CYP1, CYP2, and CYP3 groups carry most of the load.<ref name="zanger2013">Zanger UM, Schwab M. Cytochrome P450 enzymes in drug metabolism: regulation of gene expression, enzyme activities, and impact of genetic variation. ''Pharmacology and Therapeutics''. 2013 Apr;138(1):103-141. PMID: 23333322.</ref> A cytochrome P450 does not act alone: it is the terminal oxidase of a small electron-transport assembly, the mixed-function oxidase or monooxygenase system, which draws electrons from NADPH through a flavoprotein partner, NADPH-cytochrome P450 reductase, and inserts one atom of molecular oxygen into the substrate while the other atom is reduced to water.<ref name="sheweita2000" /> The phase-II conjugations are carried out by a separate set of enzyme families: the UDP-glucuronosyltransferases, the sulfotransferases, the glutathione S-transferases, the N-acetyltransferases, and others. The eleven pages collected here cover both phases: eight cytochromes P450, and three phase-II and related enzymes.

			A drug-metabolizing enzyme is usually described as part of the body's detoxification machinery, and most of the time the description holds: the metabolite is less active than the medicine, and the body is rid of it. But the same chemistry that inactivates one molecule can activate another. When a phase-I oxidation places its reactive group onto the wrong kind of substrate, the product is not a harmless handle for conjugation but a reactive, electrophilic species that binds to DNA and protein. This is '''metabolic activation''', or bioactivation, and it is the molecular basis of a large part of chemical carcinogenesis.<ref name="sheweita2000" /> The recognition that foreign substances could cause disease in this way is older than the enzymology that explains it: in 1775 the London surgeon Percival Pott traced the scrotal cancers he saw in chimney sweeps to the soot of their trade, the first clear account of an environmental cause of human cancer.<ref name="pott1775">Pott P. ''Chirurgical Observations Relative to the Cataract, the Polypus of the Nose, the Cancer of the Scrotum, the Different Kinds of Ruptures, and the Mortification of the Toes and Feet''. London: Hawes, Clarke and Collins; 1775.</ref> Two centuries later the mechanism was filled in. The polycyclic aromatic hydrocarbons of soot and tobacco smoke are activated to DNA-binding carcinogens by CYP1A enzymes; aflatoxin is activated by CYP3A4; the nitrosamines by CYP2E1. The same enzyme that safely clears a prescribed medicine can, presented with a different substrate, manufacture a carcinogen. Whether an enzyme detoxifies or activates a given chemical is a property of the specific pairing, and individual susceptibility to chemical injury depends in part on the balance between the activating cytochromes P450 and the detoxifying conjugating enzymes.<ref name="sheweita2000" />

			This balance, and the enzymes that strike it, are not the same in every person. Drug-metabolizing enzymes vary in activity from one individual to the next, partly through inherited genetic variation, partly through induction and inhibition by diet, by other medicines, by tobacco smoke, and by disease. Two patients given the same dose of the same medicine may therefore reach very different blood concentrations of it. That variation is the subject of pharmacogenomics, and it is the reason this wiki maintains a dedicated reference page for each drug-metabolizing enzyme of clinical importance.

	== Enzymes indexed ==		== Enzymes indexed ==
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	== Notes on scope ==		== Notes on scope ==
	The boundary of this category is "enzyme that metabolizes medicines," not "every gene relevant to pharmacogenomics." Drug '''transporters''' (such as SLCO1B1 and ABCB1) move medicines across membranes rather than chemically transforming them, and they are collected separately. The pharmacogenomically important '''non-enzyme variant''' loci (such as the HLA-B alleles that govern severe hypersensitivity reactions) are likewise collected separately. Some loci sit at the edge of the boundary: VKORC1, the warfarin target, is a reductase enzyme and may be indexed here when its page is built; G6PD and DPYD are enzymes and belong here when built.		The boundary of this category is "enzyme that metabolizes medicines," not "every gene relevant to pharmacogenomics." Drug '''transporters''' (such as SLCO1B1 and ABCB1) move medicines across membranes rather than chemically transforming them, and they are collected separately. The pharmacogenomically important '''non-enzyme variant''' loci (such as the HLA-B alleles that govern severe hypersensitivity reactions) are likewise collected separately. Some loci sit at the edge of the boundary: VKORC1, the warfarin target, is a reductase enzyme and may be indexed here when its page is built; G6PD and DPYD are enzymes and belong here when built.

			== About these pages ==
			Each enzyme page follows a common structure: a history-first opening, tissue distribution, the substrate spectrum with a sortable substrate table, phenotype categories, major genetic variants, inhibitors, inducers, clinical implications, and authoritative external resources. Each page is also the human-readable companion to the machine-level <code>pk_inhibit_via_<ENZYME></code> and <code>pk_induce_via_<ENZYME></code> interaction edges in the wiki's pharmacogenomic interaction layer.

			These pages currently live as drafting sandboxes under the <code>Pharmacopedia:</code> project namespace (titled <code>Pharmacogenomics sandbox/Enzyme <NAME></code>); their permanent home will be the dedicated <code>Enzyme:</code> namespace once it is registered. The closely related transporter, variant, and phenotype pages will live under <code>Transporter:</code>, <code>Variant:</code>, and <code>Phenotype:</code> respectively.

			== References ==

			<references/>

	[[Category:Pharmacogenomics]]		[[Category:Pharmacogenomics]]

MDElliottMD: Create Category:Drug-metabolizing enzymes: curated index of the 11 enzyme entity pages (8 CYPs + UGT1A1 + TPMT + NUDT15) at their canonical Pharmacopedia: sandbox location, grouped by enzyme family, with scope notes distinguishing enzymes from transporters and non-enzyme variant loci. Parent Category:Pharmacogenomics.

2026-05-19T22:39:14Z

Create Category:Drug-metabolizing enzymes: curated index of the 11 enzyme entity pages (8 CYPs + UGT1A1 + TPMT + NUDT15) at their canonical Pharmacopedia: sandbox location, grouped by enzyme family, with scope notes distinguishing enzymes from transporters and non-enzyme variant loci. Parent Category:Pharmacogenomics.

New page

This category collects the wiki's '''drug-metabolizing-enzyme entity pages''': the pharmacogenomics-layer reference pages for the enzymes that metabolize, activate, or inactivate medicines in the human body. Each page follows a common structure (history-first opening, tissue distribution, substrate spectrum with a sortable substrate table, phenotype categories, major variants, inhibitors, inducers, clinical implications, and authoritative external resources) and each is the human-readable companion to the machine-level <code>pk_inhibit_via_<ENZYME></code> and <code>pk_induce_via_<ENZYME></code> interaction edges in the wiki's pharmacogenomic interaction layer.

These pages currently live as drafting sandboxes under the <code>Pharmacopedia:</code> project namespace (titled <code>Pharmacogenomics sandbox/Enzyme <NAME></code>); their permanent home will be the dedicated <code>Enzyme:</code> namespace once it is registered. The closely related transporter, variant, and phenotype pages will live under <code>Transporter:</code>, <code>Variant:</code>, and <code>Phenotype:</code> respectively, and are not collected here.

== Enzymes indexed ==

'''Cytochrome P450 (CYP) enzymes''', the hemoprotein monooxygenases responsible for the majority of phase-I oxidative drug metabolism:
* [[Pharmacopedia:Pharmacogenomics sandbox/Enzyme CYP1A2|CYP1A2]] (caffeine probe; clozapine, olanzapine, theophylline, tizanidine; the tobacco-smoke induction story)
* [[Pharmacopedia:Pharmacogenomics sandbox/Enzyme CYP2B6|CYP2B6]] (efavirenz, methadone, bupropion, cyclophosphamide bioactivation)
* [[Pharmacopedia:Pharmacogenomics sandbox/Enzyme CYP2C8|CYP2C8]] (paclitaxel, repaglinide, the glitazones; the gemfibrozil interaction)
* [[Pharmacopedia:Pharmacogenomics sandbox/Enzyme CYP2C9|CYP2C9]] (warfarin, phenytoin, NSAIDs, sulfonylureas)
* [[Pharmacopedia:Pharmacogenomics sandbox/Enzyme CYP2C19|CYP2C19]] (clopidogrel, proton pump inhibitors, several SSRIs, voriconazole)
* [[Pharmacopedia:Pharmacogenomics sandbox/Enzyme CYP2D6|CYP2D6]] (codeine and tramadol activation, tricyclic antidepressants, many antipsychotics, metoprolol, tamoxifen)
* [[Pharmacopedia:Pharmacogenomics sandbox/Enzyme CYP2E1|CYP2E1]] (ethanol, acetaminophen bioactivation, the halogenated anesthetics)
* [[Pharmacopedia:Pharmacogenomics sandbox/Enzyme CYP3A4|CYP3A4]] (the single most clinically consequential drug-metabolizing enzyme; roughly half of all medicines in clinical use)

'''Phase-II and other non-CYP enzymes''':
* [[Pharmacopedia:Pharmacogenomics sandbox/Enzyme UGT1A1|UGT1A1]] (UDP-glucuronosyltransferase; bilirubin, irinotecan, atazanavir)
* [[Pharmacopedia:Pharmacogenomics sandbox/Enzyme TPMT|TPMT]] (thiopurine S-methyltransferase; azathioprine, mercaptopurine, thioguanine)
* [[Pharmacopedia:Pharmacogenomics sandbox/Enzyme NUDT15|NUDT15]] (nudix hydrolase; the parallel thiopurine-safety gene with a complementary ancestry distribution to TPMT)

== Notes on scope ==
The boundary of this category is "enzyme that metabolizes medicines," not "every gene relevant to pharmacogenomics." Drug '''transporters''' (such as SLCO1B1 and ABCB1) move medicines across membranes rather than chemically transforming them, and they are collected separately. The pharmacogenomically important '''non-enzyme variant''' loci (such as the HLA-B alleles that govern severe hypersensitivity reactions) are likewise collected separately. Some loci sit at the edge of the boundary: VKORC1, the warfarin target, is a reductase enzyme and may be indexed here when its page is built; G6PD and DPYD are enzymes and belong here when built.

[[Category:Pharmacogenomics]]

← Older revision		Revision as of 16:57, 22 May 2026
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	'''Cytochrome P450 (CYP) enzymes''', the hemoprotein monooxygenases responsible for the majority of phase-I oxidative drug metabolism:		'''Cytochrome P450 (CYP) enzymes''', the hemoprotein monooxygenases responsible for the majority of phase-I oxidative drug metabolism:
	* [[~~Pharmacopedia~~:~~Pharmacogenomics sandbox/Enzyme~~ CYP1A2\|CYP1A2]] (caffeine probe; clozapine, olanzapine, theophylline, tizanidine; the tobacco-smoke induction story)		* [[Enzyme:CYP1A2\|CYP1A2]] (caffeine probe; clozapine, olanzapine, theophylline, tizanidine; the tobacco-smoke induction story)
	* [[~~Pharmacopedia~~:~~Pharmacogenomics sandbox/Enzyme~~ CYP2B6\|CYP2B6]] (efavirenz, methadone, bupropion, cyclophosphamide bioactivation)		* [[Enzyme:CYP2B6\|CYP2B6]] (efavirenz, methadone, bupropion, cyclophosphamide bioactivation)
	* [[~~Pharmacopedia~~:~~Pharmacogenomics sandbox/Enzyme~~ CYP2C8\|CYP2C8]] (paclitaxel, repaglinide, the glitazones; the gemfibrozil interaction)		* [[Enzyme:CYP2C8\|CYP2C8]] (paclitaxel, repaglinide, the glitazones; the gemfibrozil interaction)
	* [[~~Pharmacopedia~~:~~Pharmacogenomics sandbox/Enzyme~~ CYP2C9\|CYP2C9]] (warfarin, phenytoin, NSAIDs, sulfonylureas)		* [[Enzyme:CYP2C9\|CYP2C9]] (warfarin, phenytoin, NSAIDs, sulfonylureas)
	* [[~~Pharmacopedia~~:~~Pharmacogenomics sandbox/Enzyme~~ CYP2C19\|CYP2C19]] (clopidogrel, proton pump inhibitors, several SSRIs, voriconazole)		* [[Enzyme:CYP2C19\|CYP2C19]] (clopidogrel, proton pump inhibitors, several SSRIs, voriconazole)
	* [[~~Pharmacopedia~~:~~Pharmacogenomics sandbox/Enzyme~~ CYP2D6\|CYP2D6]] (codeine and tramadol activation, tricyclic antidepressants, many antipsychotics, metoprolol, tamoxifen)		* [[Enzyme:CYP2D6\|CYP2D6]] (codeine and tramadol activation, tricyclic antidepressants, many antipsychotics, metoprolol, tamoxifen)
	* [[~~Pharmacopedia~~:~~Pharmacogenomics sandbox/Enzyme~~ CYP2E1\|CYP2E1]] (ethanol, acetaminophen bioactivation, the halogenated anesthetics)		* [[Enzyme:CYP2E1\|CYP2E1]] (ethanol, acetaminophen bioactivation, the halogenated anesthetics)
	* [[~~Pharmacopedia~~:~~Pharmacogenomics sandbox/Enzyme~~ CYP3A4\|CYP3A4]] (the single most clinically consequential drug-metabolizing enzyme; roughly half of all medicines in clinical use)		* [[Enzyme:CYP3A4\|CYP3A4]] (the single most clinically consequential drug-metabolizing enzyme; roughly half of all medicines in clinical use)

	'''Phase-II and other non-CYP enzymes''':		'''Phase-II and other non-CYP enzymes''':
	* [[~~Pharmacopedia~~:~~Pharmacogenomics sandbox/Enzyme~~ UGT1A1\|UGT1A1]] (UDP-glucuronosyltransferase; bilirubin, irinotecan, atazanavir)		* [[Enzyme:UGT1A1\|UGT1A1]] (UDP-glucuronosyltransferase; bilirubin, irinotecan, atazanavir)
	* [[~~Pharmacopedia~~:~~Pharmacogenomics sandbox/Enzyme~~ TPMT\|TPMT]] (thiopurine S-methyltransferase; azathioprine, mercaptopurine, thioguanine)		* [[Enzyme:TPMT\|TPMT]] (thiopurine S-methyltransferase; azathioprine, mercaptopurine, thioguanine)
	* [[~~Pharmacopedia~~:~~Pharmacogenomics sandbox/Enzyme~~ NUDT15\|NUDT15]] (nudix hydrolase; the parallel thiopurine-safety gene with a complementary ancestry distribution to TPMT)		* [[Enzyme:NUDT15\|NUDT15]] (nudix hydrolase; the parallel thiopurine-safety gene with a complementary ancestry distribution to TPMT)

	== Notes on scope ==		== Notes on scope ==
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	Each enzyme page follows a common structure: a history-first opening, tissue distribution, the substrate spectrum with a sortable substrate table, phenotype categories, major genetic variants, inhibitors, inducers, clinical implications, and authoritative external resources. Each page is also the human-readable companion to the machine-level <code>pk_inhibit_via_<ENZYME></code> and <code>pk_induce_via_<ENZYME></code> interaction edges in the wiki's pharmacogenomic interaction layer.		Each enzyme page follows a common structure: a history-first opening, tissue distribution, the substrate spectrum with a sortable substrate table, phenotype categories, major genetic variants, inhibitors, inducers, clinical implications, and authoritative external resources. Each page is also the human-readable companion to the machine-level <code>pk_inhibit_via_<ENZYME></code> and <code>pk_induce_via_<ENZYME></code> interaction edges in the wiki's pharmacogenomic interaction layer.

	These pages ~~currently~~ live ~~as drafting sandboxes under the <code>Pharmacopedia:</code> project namespace (titled <code>Pharmacogenomics sandbox/Enzyme <NAME></code>); their permanent home will be~~ the dedicated <code>Enzyme:</code> namespace ~~once it is registered~~. The closely related transporter, variant, and phenotype pages will live under <code>Transporter:</code>, <code>Variant:</code>, and <code>Phenotype:</code> respectively.		These pages live in the dedicated <code>Enzyme:</code> namespace. The closely related transporter, variant, and phenotype pages will live under <code>Transporter:</code>, <code>Variant:</code>, and <code>Phenotype:</code> respectively.

	== References ==		== References ==