CYP2C9: Difference between revisions
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{{protein |
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{{PBB_Controls |
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| update_page = yes |
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| require_manual_inspection = no |
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| update_protein_box = yes |
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| update_summary = no |
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|AltSymbols=CYP2C10 |
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| update_citations = yes |
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|EntrezGene=1559 |
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}} |
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|RefSeq=NM_000771 |
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<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. --> |
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|UniProt=P11712 |
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{{GNF_Protein_box |
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|PDB= |
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|Chromosome=10 |
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| PDB = {{PDB2|1og2}}, {{PDB2|1og5}}, {{PDB2|1r9o}} |
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|Arm=q |
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|Band=24.1 |
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|LocusSupplementaryData= |
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| AltSymbols =; CYP2C; CPC9; CYP2C10; MGC149605; MGC88320; P450 MP-4; P450 PB-1; P450IIC9 |
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| Homologene = 86657 |
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| MGIid = 103238 |
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| GeneAtlas_image1 = PBB_GE_CYP2C9_214421_x_at_tn.png |
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| GeneAtlas_image2 = PBB_GE_CYP2C9_216025_x_at_tn.png |
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| GeneAtlas_image3 = PBB_GE_CYP2C9_216661_x_at_tn.png |
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| Function = {{GNF_GO|id=GO:0005506 |text = iron ion binding}} {{GNF_GO|id=GO:0016712 |text = oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen}} {{GNF_GO|id=GO:0018675 |text = (S)-limonene 6-monooxygenase activity}} {{GNF_GO|id=GO:0018676 |text = (S)-limonene 7-monooxygenase activity}} {{GNF_GO|id=GO:0020037 |text = heme binding}} {{GNF_GO|id=GO:0046872 |text = metal ion binding}} |
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| Component = {{GNF_GO|id=GO:0005783 |text = endoplasmic reticulum}} {{GNF_GO|id=GO:0005792 |text = microsome}} {{GNF_GO|id=GO:0016020 |text = membrane}} |
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| Process = {{GNF_GO|id=GO:0006118 |text = electron transport}} |
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| Orthologs = {{GNF_Ortholog_box |
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| Hs_EntrezGene = 1559 |
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| Hs_Ensembl = ENSG00000138109 |
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| Hs_RefseqProtein = NP_000762 |
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| Hs_RefseqmRNA = NM_000771 |
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| Hs_GenLoc_db = |
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| Hs_GenLoc_chr = 10 |
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| Hs_GenLoc_start = 96688418 |
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| Hs_GenLoc_end = 96739137 |
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| Hs_Uniprot = P11712 |
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| Mm_EntrezGene = 13095 |
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| Mm_Ensembl = ENSMUSG00000003053 |
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| Mm_RefseqmRNA = NM_007815 |
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| Mm_RefseqProtein = NP_031841 |
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| Mm_GenLoc_db = |
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| Mm_GenLoc_chr = 19 |
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| Mm_GenLoc_start = 39340422 |
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| Mm_GenLoc_end = 39384010 |
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| Mm_Uniprot = Q3UEF2 |
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}} |
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}} |
}} |
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'''Cytochrome P450 2C9''' (abbreviated '''CYP2C9'''), a member of the [[cytochrome P450]] mixed-function oxidase system, is involved in the metabolism of [[xenobiotic]]s in the body. It is involved in the metabolism of several important groups of drugs including many [[non-steroidal anti-inflammatory drug]]s (NSAIDs) and [[sulfonylurea]]s. |
'''Cytochrome P450 2C9''' (abbreviated '''CYP2C9'''), a member of the [[cytochrome P450]] mixed-function oxidase system, is involved in the metabolism of [[xenobiotic]]s in the body. It is involved in the metabolism of several important groups of drugs including many [[non-steroidal anti-inflammatory drug]]s (NSAIDs) and [[sulfonylurea]]s. |
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== See also == |
== See also == |
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*[[Cytochrome P450 oxidase]] |
*[[Cytochrome P450 oxidase]] |
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==References== |
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{{reflist}} |
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==Further reading== |
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{{refbegin | 2}} |
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{{PBB_Further_reading |
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| citations = |
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*{{cite journal | author=Goldstein JA, de Morais SM |title=Biochemistry and molecular biology of the human CYP2C subfamily. |journal=Pharmacogenetics |volume=4 |issue= 6 |pages= 285-99 |year= 1995 |pmid= 7704034 |doi= }} |
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*{{cite journal | author=Miners JO, Birkett DJ |title=Cytochrome P4502C9: an enzyme of major importance in human drug metabolism. |journal=British journal of clinical pharmacology |volume=45 |issue= 6 |pages= 525-38 |year= 1998 |pmid= 9663807 |doi= }} |
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*{{cite journal | author=Smith G, Stubbins MJ, Harries LW, Wolf CR |title=Molecular genetics of the human cytochrome P450 monooxygenase superfamily. |journal=Xenobiotica |volume=28 |issue= 12 |pages= 1129-65 |year= 1999 |pmid= 9890157 |doi= }} |
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*{{cite journal | author=Henderson RF |title=Species differences in the metabolism of olefins: implications for risk assessment. |journal=Chem. Biol. Interact. |volume=135-136 |issue= |pages= 53-64 |year= 2001 |pmid= 11397381 |doi= }} |
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*{{cite journal | author=Xie HG, Prasad HC, Kim RB, Stein CM |title=CYP2C9 allelic variants: ethnic distribution and functional significance. |journal=Adv. Drug Deliv. Rev. |volume=54 |issue= 10 |pages= 1257-70 |year= 2003 |pmid= 12406644 |doi= }} |
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*{{cite journal | author=Palkimas MP, Skinner HM, Gandhi PJ, Gardner AJ |title=Polymorphism induced sensitivity to warfarin: a review of the literature. |journal=J. Thromb. Thrombolysis |volume=15 |issue= 3 |pages= 205-12 |year= 2004 |pmid= 14739630 |doi= 10.1023/B:THRO.0000011376.12309.af }} |
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*{{cite journal | author=Daly AK, Aithal GP |title=Genetic regulation of warfarin metabolism and response. |journal=Seminars in vascular medicine |volume=3 |issue= 3 |pages= 231-8 |year= 2004 |pmid= 15199455 |doi= 10.1055/s-2003-44458 }} |
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*{{cite journal | author=García-Martín E, Martínez C, Ladero JM, Agúndez JA |title=Interethnic and intraethnic variability of CYP2C8 and CYP2C9 polymorphisms in healthy individuals. |journal=Molecular diagnosis & therapy |volume=10 |issue= 1 |pages= 29-40 |year= 2007 |pmid= 16646575 |doi= }} |
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}} |
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{{refend}} |
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{{Cytochrome P450}} |
{{Cytochrome P450}} |
Revision as of 23:18, 10 November 2007
Cytochrome P450 2C9 (abbreviated CYP2C9), a member of the cytochrome P450 mixed-function oxidase system, is involved in the metabolism of xenobiotics in the body. It is involved in the metabolism of several important groups of drugs including many non-steroidal anti-inflammatory drugs (NSAIDs) and sulfonylureas.
Genetic polymorphism exists for CYP2C9 expression, with approximately 1–3% of Caucasian populations being poor metabolisers with no CYP2C9 function.
CYP2C9 Ligands
Substrates | Inhibitors | Inducers |
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Often mentioned [6]:
Less often mentioned[6]: |
Strong [7]:
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Often mentioned [6]:
Less often mentioned:
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See also
References
- ^ a b c GRCh38: Ensembl release 89: ENSG00000138109 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000067231 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ Where classes of agents are listed, there may be exceptions within the class
- ^ a b c Mentioned both in the reference named FASS and were previously mentioned in Wikipedia. Further contributions may follow other systems
- ^ Swedish environmental classification of pharmaceuticals Facts for prescribers (Fakta för förskrivare)