KEGG   PATHWAY: dpol00982
Entry
dpol00982                   Pathway                                
Name
Drug metabolism - cytochrome P450 - Dreissena polymorpha (zebra mussel)
Class
Metabolism; Xenobiotics biodegradation and metabolism
Pathway map
dpol00982  Drug metabolism - cytochrome P450
dpol00982

Organism
Dreissena polymorpha (zebra mussel) [GN:dpol]
Gene
127850751  flavin-containing monooxygenase 5-like [KO:K00485] [EC:1.14.13.8 1.8.1.-]
127834388  flavin-containing monooxygenase 5-like isoform X1 [KO:K00485] [EC:1.14.13.8 1.8.1.-]
127874645  flavin-containing monooxygenase 5-like [KO:K00485] [EC:1.14.13.8 1.8.1.-]
127838903  flavin-containing monooxygenase 5-like isoform X1 [KO:K00485] [EC:1.14.13.8 1.8.1.-]
127838906  flavin-containing monooxygenase 5-like [KO:K00485] [EC:1.14.13.8 1.8.1.-]
127858434  flavin-containing monooxygenase 5-like [KO:K00485] [EC:1.14.13.8 1.8.1.-]
127844130  glutathione S-transferase omega-1-like [KO:K00799] [EC:2.5.1.18]
127844144  probable glutathione S-transferase 7 [KO:K00799] [EC:2.5.1.18]
127845100  pyrimidodiazepine synthase-like [KO:K00799] [EC:2.5.1.18]
127865039  S-crystallin SL11-like [KO:K00799] [EC:2.5.1.18]
127865042  glutathione S-transferase 1-like isoform X1 [KO:K00799] [EC:2.5.1.18]
127865043  glutathione S-transferase 1-like [KO:K00799] [EC:2.5.1.18]
127882287  glutathione S-transferase A-like [KO:K00799] [EC:2.5.1.18]
127882438  glutathione S-transferase A-like isoform X1 [KO:K00799] [EC:2.5.1.18]
127882447  glutathione S-transferase A-like isoform X1 [KO:K00799] [EC:2.5.1.18]
127882449  glutathione S-transferase A-like [KO:K00799] [EC:2.5.1.18]
127845277  probable glutathione S-transferase 7 [KO:K00799] [EC:2.5.1.18]
127846583  glutathione S-transferase theta-3-like isoform X1 [KO:K00799] [EC:2.5.1.18]
127867177  glutathione S-transferase 1-like [KO:K00799] [EC:2.5.1.18]
127867940  glutathione S-transferase 1-like [KO:K00799] [EC:2.5.1.18]
127868904  glutathione S-transferase Mu 4-like [KO:K00799] [EC:2.5.1.18]
127868983  glutathione S-transferase Mu 4-like [KO:K00799] [EC:2.5.1.18]
127850715  microsomal glutathione S-transferase 3-like isoform X1 [KO:K00799] [EC:2.5.1.18]
127871422  microsomal glutathione S-transferase 3-like [KO:K00799] [EC:2.5.1.18]
127831548  glutathione S-transferase A-like [KO:K00799] [EC:2.5.1.18]
127871640  glutathione S-transferase theta-1-like isoform X1 [KO:K00799] [EC:2.5.1.18]
127874805  glutathione S-transferase theta-1-like [KO:K00799] [EC:2.5.1.18]
127837130  glutathione S-transferase theta-1-like [KO:K00799] [EC:2.5.1.18]
127837149  uncharacterized protein LOC127837149 [KO:K00799] [EC:2.5.1.18]
127876588  microsomal glutathione S-transferase 2-like isoform X1 [KO:K00799] [EC:2.5.1.18]
127876589  microsomal glutathione S-transferase 2-like [KO:K00799] [EC:2.5.1.18]
127839253  microsomal glutathione S-transferase 1-like [KO:K00799] [EC:2.5.1.18]
127859852  probable glutathione S-transferase 7 [KO:K00799] [EC:2.5.1.18]
127860789  probable glutathione S-transferase 7 isoform X1 [KO:K00799] [EC:2.5.1.18]
127879357  glutathione S-transferase 3-like [KO:K00799] [EC:2.5.1.18]
127879507  microsomal glutathione S-transferase 1-like [KO:K00799] [EC:2.5.1.18]
127852352  glutathione S-transferase P 1-like [KO:K23790] [EC:2.5.1.18]
127852353  glutathione S-transferase P 1-like [KO:K23790] [EC:2.5.1.18]
127852354  glutathione S-transferase P 1-like [KO:K23790] [EC:2.5.1.18]
127853433  glutathione S-transferase P 1-like [KO:K23790] [EC:2.5.1.18]
127854132  glutathione S-transferase P-like [KO:K23790] [EC:2.5.1.18]
127881506  glutathione S-transferase kappa 1-like [KO:K13299] [EC:2.5.1.18]
127832115  glutathione S-transferase kappa 1-like isoform X1 [KO:K13299] [EC:2.5.1.18]
127842373  glutathione S-transferase kappa 1-like [KO:K13299] [EC:2.5.1.18]
127864226  glutathione S-transferase 1-like [KO:K04097] [EC:5.3.99.2 2.5.1.18]
127844668  probable glutathione S-transferase 7 [KO:K04097] [EC:5.3.99.2 2.5.1.18]
127865041  glutathione S-transferase 1-like [KO:K04097] [EC:5.3.99.2 2.5.1.18]
127865295  probable glutathione S-transferase 9 [KO:K04097] [EC:5.3.99.2 2.5.1.18]
127850713  glutathione S-transferase-like [KO:K04097] [EC:5.3.99.2 2.5.1.18]
127832641  glutathione S-transferase 3-like [KO:K04097] [EC:5.3.99.2 2.5.1.18]
127836223  glutathione S-transferase-like [KO:K04097] [EC:5.3.99.2 2.5.1.18]
127879229  glutathione S-transferase-like [KO:K04097] [EC:5.3.99.2 2.5.1.18]
127879372  glutathione S-transferase class-mu 28 kDa isozyme-like [KO:K04097] [EC:5.3.99.2 2.5.1.18]
127868073  alcohol dehydrogenase class-3-like [KO:K00121] [EC:1.1.1.284 1.1.1.1]
127881352  aldehyde dehydrogenase family 3 member B1-like [KO:K00129] [EC:1.2.1.5]
127834923  aldehyde dehydrogenase family 3 member B1-like isoform X1 [KO:K00129] [EC:1.2.1.5]
127868780  probable flavin-containing monoamine oxidase A [KO:K00274] [EC:1.4.3.4]
127868781  probable flavin-containing monoamine oxidase A [KO:K00274] [EC:1.4.3.4]
127836326  amine oxidase [flavin-containing] B-like [KO:K00274] [EC:1.4.3.4]
Compound
C01471  Acrolein
C01516  Morphine
C05011  Hydroxytamoxifen
C06174  Codeine
C06754  Chloroacetaldehyde
C06868  Carbamazepine
C07047  Ifosfamide
C07073  Lidocaine
C07108  Tamoxifen
C07163  Methadone
C07185  Valproic acid
C07492  Oxcarbazepine
C07493  10-Hydroxycarbazepine
C07495  Dihydroxycarbazepine
C07496  Carbamazepine-10,11-epoxide
C07501  Felbamate
C07572  Citalopram
C07643  4-Hydroxycyclophosphamide
C07644  4-Ketocyclophosphamide
C07645  Aldophosphamide
C07646  Carboxyphosphamide
C07647  Phosphoramide mustard
C07888  Cyclophosphamide
C08012  Levomethadyl acetate
C11004  2,6-Dimethylaniline
C11583  4-Glutathionyl cyclophosphamide
C11785  Normorphine
C16544  alpha-Hydroxytamoxifen
C16545  Tamoxifen N-oxide
C16546  N-Desmethyltamoxifen
C16547  Endoxifen
C16548  N,N-Didesmethyltamoxifen
C16549  alpha-Hydroxy-N-desmethyltamoxifen
C16550  Dechloroethylcyclophosphamide
C16551  Alcophosphamide
C16552  Nornitrogen mustard
C16553  4-Hydroxyifosfamide
C16554  4-Ketoifosfamide
C16555  2-Dechloroethylifosfamide
C16556  Aldoifosfamide
C16557  Carboxyifosfamide
C16558  Alcoifosfamide
C16559  Isophosphoramide mustard
C16560  3-Hydroxylidocaine
C16561  Monoethylglycinexylidide
C16569  Glycinexylidide
C16570  4-Hydroxy-2,6-dimethylaniline
C16571  2-Amino-3-methylbenzoate
C16572  3-Hydroxymonoethylglycinexylidide
C16576  Norcodeine
C16577  Codeine-6-glucuronide
C16578  Morphine-6-glucuronide
C16582  2-Hydroxyfelbamate
C16584  p-Hydroxyfelbamate
C16586  2-Phenyl-1,3-propanediol monocarbamate
C16587  3-Carbamoyl-2-phenylpropionaldehyde
C16591  3-Carbamoyl-2-phenylpropionic acid
C16592  Atropaldehyde
C16595  4-Hydroxy-5-phenyltetrahydro-1,3-oxazin-2-one
C16596  5-Phenyl-1,3-oxazinane-2,4-dione
C16601  2-Hydroxycarbamazepine
C16602  3-Hydroxycarbamazepine
C16603  2,3-Dihydroxycarbamazepine
C16604  2-Hydroxyiminostilbene
C16605  2H-Dibenz[b,f]azepin-2-one
C16606  Carbamazepine-o-quinone
C16607  Citalopram N-oxide
C16608  Demethylcitalopram
C16609  Didemethylcitalopram
C16610  Citalopram propionic acid
C16612  Citalopram aldehyde
C16643  Morphine-3-glucuronide
C16648  2-n-Propyl-4-pentenoic acid
C16649  4-Hydroxyvalproic acid
C16650  5-Hydroxyvalproic acid
C16651  3-Hydroxyvalproic acid
C16652  3-Oxovalproic acid
C16653  2-n-Propyl-2-pentenoic acid
C16654  2-n-Propyl-3-pentenoic acid
C16655  2-n-Propyl-4-oxopentanoic acid
C16656  2-Propyl-2,4-pentadienoic acid
C16657  2-Propylsuccinic acid
C16658  2-Propylglutaric acid
C16659  2-Ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine
C16660  2-Ethyl-5-methyl-3,3-diphenyl-1-pyrroline
C16661  L-alpha-Acetyl-N-normethadol
C16662  L-alpha-Acetyl-N,N-dinormethadol
D00195  Codeine (USP)
D00252  Carbamazepine (JP18/USP/INN)
D00343  Ifosfamide (JAN/USP/INN)
D00358  Lidocaine (JP18/USP/INN)
D00399  Valproic acid (USP)
D00533  Oxcarbazepine (JAN/USP/INN)
D00536  Felbamate (USPINN)
D04716  Levomethadyl acetate (USAN)
D07704  Citalopram (USP/INN)
D07760  Cyclophosphamide (INN)
D08195  Methadone (BAN)
D08233  Morphine (BAN)
D08559  Tamoxifen (INN)
Reference
  Authors
Kato R, Kamatari T (eds).
  Title
[Drug Metabolism] (In Japanese)
  Journal
Tokyo Kagaku Dojin (2000)
Reference
  Authors
Gjerde J, Kisanga ER, Hauglid M, Holm PI, Mellgren G, Lien EA.
  Title
Identification and quantification of tamoxifen and four metabolites in serum by liquid chromatography-tandem mass spectrometry.
  Journal
J Chromatogr A 1082:6-14 (2005)
DOI:10.1016/j.chroma.2005.01.004
Reference
  Authors
Buck MB, Coller JK, Murdter TE, Eichelbaum M, Knabbe C.
  Title
TGFbeta2 and TbetaRII are valid molecular biomarkers for the antiproliferative effects of tamoxifen and tamoxifen metabolites in breast cancer cells.
  Journal
Breast Cancer Res Treat 107:15-24 (2008)
DOI:10.1007/s10549-007-9526-7
Reference
  Authors
Rodriguez-Antona C, Ingelman-Sundberg M.
  Title
Cytochrome P450 pharmacogenetics and cancer.
  Journal
Oncogene 25:1679-91 (2006)
DOI:10.1038/sj.onc.1209377
Reference
  Authors
Zhang J, Tian Q, Yung Chan S, Chuen Li S, Zhou S, Duan W, Zhu YZ.
  Title
Metabolism and transport of oxazaphosphorines and the clinical implications.
  Journal
Drug Metab Rev 37:611-703 (2005)
DOI:10.1080/03602530500364023
Reference
  Authors
Kosel M, Amey M, Aubert AC, Baumann P.
  Title
In vitro metabolism of citalopram by monoamine oxidase B in human blood.
  Journal
Eur Neuropsychopharmacol 11:75-8 (2001)
DOI:10.1016/S0924-977X(00)00128-0
Reference
  Authors
Olesen OV, Linnet K.
  Title
Studies on the stereoselective metabolism of citalopram by human liver microsomes and cDNA-expressed cytochrome P450 enzymes.
  Journal
Pharmacology 59:298-309 (1999)
DOI:10.1159/000028333
Reference
PMID:9698084
  Authors
Rochat B, Kosel M, Boss G, Testa B, Gillet M, Baumann P.
  Title
Stereoselective biotransformation of the selective serotonin reuptake inhibitor citalopram and its demethylated metabolites by monoamine oxidases in human liver.
  Journal
Biochem Pharmacol 56:15-23 (1998)
DOI:10.1016/S0006-2952(98)00008-2
Reference
  Authors
David AW, Thomas LL, William OF.
  Title
Foye's Principles of Medicinal Chemistry (5th ed)
  Journal
Lippincott Williams & Wilkins (2002)
Reference
  Authors
Oda Y, Kharasch ED.
  Title
Metabolism of methadone and levo-alpha-acetylmethadol (LAAM) by human intestinal cytochrome P450 3A4 (CYP3A4): potential contribution of intestinal metabolism to presystemic clearance and bioactivation.
  Journal
J Pharmacol Exp Ther 298:1021-32 (2001)
Reference
  Authors
Wang JS, Backman JT, Taavitsainen P, Neuvonen PJ, Kivisto KT.
  Title
Involvement of CYP1A2 and CYP3A4 in lidocaine N-deethylation and 3-hydroxylation in humans.
  Journal
Drug Metab Dispos 28:959-65 (2000)
Reference
  Authors
Dieckhaus CM, Thompson CD, Roller SG, Macdonald TL.
  Title
Mechanisms of idiosyncratic drug reactions: the case of felbamate.
  Journal
Chem Biol Interact 142:99-117 (2002)
DOI:10.1016/S0009-2797(02)00057-1
Reference
  Authors
Pearce RE, Lu W, Wang Y, Uetrecht JP, Correia MA, Leeder JS
  Title
Pathways of carbamazepine bioactivation in vitro. III. The role of human cytochrome P450 enzymes in the formation of 2,3-dihydroxycarbamazepine.
  Journal
Drug Metab Dispos 36:1637-49 (2008)
DOI:10.1124/dmd.107.019562
Reference
  Authors
Pearce RE, Vakkalagadda GR, Leeder JS.
  Title
Pathways of carbamazepine bioactivation in vitro I. Characterization of human cytochromes P450 responsible for the formation of 2- and 3-hydroxylated metabolites.
  Journal
Drug Metab Dispos 30:1170-9 (2002)
DOI:10.1124/dmd.30.11.1170
Reference
  Authors
Kumar S, Wong H, Yeung SA, Riggs KW, Abbott FS, Rurak DW.
  Title
Disposition of valproic acid in maternal, fetal, and newborn sheep. II: metabolism and renal elimination.
  Journal
Drug Metab Dispos 28:857-64 (2000)
Reference
  Authors
Bernad T, Joachim M.
  Title
Hydrolysis in Drug and Prodrug Metabolism: Chemistry, Biochemistry, and Enzymology
  Journal
Wiley-VCH (2003)
KO pathway
ko00982   
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