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Volumn 49, Issue 2, 2002, Pages 216-231

Impact of incorporating the 2C5 crystal structure into comparative models of cytochrome P450 2D6

Author keywords

Binding determinants; Model validation; Molecular modeling; Principal component analysis; Substrate specificity

Indexed keywords

1,2,3,6 TETRAHYDRO 1 METHYL 4 PHENYLPYRIDINE; ASPARTIC ACID; CODEINE; CYTOCHROME P450; CYTOCHROME P450 2D6; GLUTAMINE;

EID: 0036836542     PISSN: 08873585     EISSN: None     Source Type: Journal    
DOI: 10.1002/prot.10192     Document Type: Article
Times cited : (66)

References (79)
  • 3
    • 0030834058 scopus 로고    scopus 로고
    • Human cytochrome P450 enzymes: A status report summarizing their reactions, substrates, inducers, and inhibitors
    • Rendic S, Di Carlo FJ. Human cytochrome P450 enzymes: a status report summarizing their reactions, substrates, inducers, and inhibitors. Drug Metab Rev 1997;29:413-580.
    • (1997) Drug Metab Rev , vol.29 , pp. 413-580
    • Rendic, S.1    Di Carlo, F.J.2
  • 4
    • 0031877729 scopus 로고    scopus 로고
    • The CYP2 family: Models, mutants and interactions
    • Lewis DF. The CYP2 family: models, mutants and interactions. Xenobiotica 1998;28:617-661.
    • (1998) Xenobiotica , vol.28 , pp. 617-661
    • Lewis, D.F.1
  • 5
    • 0030867858 scopus 로고    scopus 로고
    • Identification of the cytochrome P450 isoforms involved in the O-demethylation of 4-nitroanisole in human liver microsomes
    • Jones BC, Tyman CA, Smith DA. Identification of the cytochrome P450 isoforms involved in the O-demethylation of 4-nitroanisole in human liver microsomes. Xenobiotica 1997;27:1025-1037.
    • (1997) Xenobiotica , vol.27 , pp. 1025-1037
    • Jones, B.C.1    Tyman, C.A.2    Smith, D.A.3
  • 7
    • 0018714764 scopus 로고
    • Influence of the defective metabolism of sparteine on its pharmacokinetics
    • Eichelbaum M, Spannbrucker N, Dengler HJ. Influence of the defective metabolism of sparteine on its pharmacokinetics. Eur J Clin Pharmacol 1979;16:189-194.
    • (1979) Eur J Clin Pharmacol , vol.16 , pp. 189-194
    • Eichelbaum, M.1    Spannbrucker, N.2    Dengler, H.J.3
  • 10
    • 0022885696 scopus 로고
    • Genetics of drug transformation
    • Kalow W. Genetics of drug transformation. Clin Biochem 1986;19: 76-82.
    • (1986) Clin Biochem , vol.19 , pp. 76-82
    • Kalow, W.1
  • 11
    • 0024500321 scopus 로고
    • Polymorphism of cytochrome P-450 in humans
    • Guengerich FP. Polymorphism of cytochrome P-450 in humans. Trends Pharmacol Sci 1989;10:107-109.
    • (1989) Trends Pharmacol Sci , vol.10 , pp. 107-109
    • Guengerich, F.P.1
  • 12
    • 0024818411 scopus 로고
    • Polymorphic drug metabolism
    • Relling MV. Polymorphic drug metabolism. Clin Pharm. 1989;8: 852-863.
    • (1989) Clin Pharm , vol.8 , pp. 852-863
    • Relling, M.V.1
  • 13
    • 0025639014 scopus 로고
    • Genetic polymorphisms of drug metabolism
    • Meyer UA. Genetic polymorphisms of drug metabolism. Fundam Clin Pharmacol 1990;4:595-615.
    • (1990) Fundam Clin Pharmacol , vol.4 , pp. 595-615
    • Meyer, U.A.1
  • 15
    • 0022899555 scopus 로고
    • The molecular mechanisms of two common polymorphisms of drug oxidation-evidence for functional changes in cytochrome P-450 isozymes catalysing bufuralol and mephenytoin oxidation
    • Meyer UA, Gut J, Kronbach T, Skoda C, Meier UT, Catin T, Dayer P. The molecular mechanisms of two common polymorphisms of drug oxidation-evidence for functional changes in cytochrome P-450 isozymes catalysing bufuralol and mephenytoin oxidation. Xenobiotica 1986;16:449-464.
    • (1986) Xenobiotica , vol.16 , pp. 449-464
    • Meyer, U.A.1    Gut, J.2    Kronbach, T.3    Skoda, C.4    Meier, U.T.5    Catin, T.6    Dayer, P.7
  • 16
    • 0026046988 scopus 로고
    • A threedimensional molecular template for substrates of human cytochrome P450 involved in debrisoquine 4-hydroxylation
    • Islam SA, Wolf CR, Lennard MS, Sternberg MJ. A threedimensional molecular template for substrates of human cytochrome P450 involved in debrisoquine 4-hydroxylation. Carcinogenesis 1991;12:2211-2219.
    • (1991) Carcinogenesis , vol.12 , pp. 2211-2219
    • Islam, S.A.1    Wolf, C.R.2    Lennard, M.S.3    Sternberg, M.J.4
  • 18
    • 0030914738 scopus 로고    scopus 로고
    • Molecular modelling of cytochrome P4502D6 (CYP2D6) based on an alignment with CYP102: Structural studies on specific CYP2D6 substrate metabolism
    • Lewis DF, Eddershaw PJ, Goldfarb PS, Tarbit MH. Molecular modelling of cytochrome P4502D6 (CYP2D6) based on an alignment with CYP102: structural studies on specific CYP2D6 substrate metabolism. Xenobiotica 1997;27:319-339.
    • (1997) Xenobiotica , vol.27 , pp. 319-339
    • Lewis, D.F.1    Eddershaw, P.J.2    Goldfarb, P.S.3    Tarbit, M.H.4
  • 20
    • 0029995711 scopus 로고    scopus 로고
    • A three-dimensional protein model for human cytochrome P450 2D6 based on the crystal structures of P450 101, P450 102, and P450 108
    • de Groot MJ, Vermeulen NP, Kramer JD, van Acker FA, Donne-Op den Kelder GM. A three-dimensional protein model for human cytochrome P450 2D6 based on the crystal structures of P450 101, P450 102, and P450 108. Chem Res Toxicol 1996;9:1079-1091.
    • (1996) Chem Res Toxicol , vol.9 , pp. 1079-1091
    • De Groot, M.J.1    Vermeulen, N.P.2    Kramer, J.D.3    Van Acker, F.A.4    Donne-Op den Kelder, G.M.5
  • 21
    • 0032080291 scopus 로고    scopus 로고
    • Determinants of the substrate specificity of human cytochrome P-450 CYP2D6: Design and construction of a mutant with testosterone hydroxylase activity
    • Smith G, Modi S, Pillai I, Lian LY, Sutcliffe MJ, Pritchard MP, Friedberg T, Roberts GC, Wolf CR. Determinants of the substrate specificity of human cytochrome P-450 CYP2D6: design and construction of a mutant with testosterone hydroxylase activity. Biochem J 1998;331:783-792.
    • (1998) Biochem J , vol.331 , pp. 783-792
    • Smith, G.1    Modi, S.2    Pillai, I.3    Lian, L.Y.4    Sutcliffe, M.J.5    Pritchard, M.P.6    Friedberg, T.7    Roberts, G.C.8    Wolf, C.R.9
  • 22
    • 0030963409 scopus 로고    scopus 로고
    • 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine as a substrate of cytochrome P450 2D6: Allosteric effects of NADPH-cytochrome P450 reductase
    • Modi S, Gilham DE, Sutcliffe MJ, Lian LY, Primrose WU, Wolf CR, Roberts GC. 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine as a substrate of cytochrome P450 2D6: allosteric effects of NADPH-cytochrome P450 reductase. Biochemistry 1997;36:4461-4470.
    • (1997) Biochemistry , vol.36 , pp. 4461-4470
    • Modi, S.1    Gilham, D.E.2    Sutcliffe, M.J.3    Lian, L.Y.4    Primrose, W.U.5    Wolf, C.R.6    Roberts, G.C.7
  • 26
    • 0028267490 scopus 로고
    • Crystal structure and refinement of cytochrome P450terp at 2.3 A resolution
    • Hasemann CA, Ravichandran KG, Peterson JA, Deisenhofer J. Crystal structure and refinement of cytochrome P450terp at 2.3 A resolution. J Mol Biol 1994;236:1169-1185.
    • (1994) J Mol Biol , vol.236 , pp. 1169-1185
    • Hasemann, C.A.1    Ravichandran, K.G.2    Peterson, J.A.3    Deisenhofer, J.4
  • 27
    • 0029586252 scopus 로고
    • Structure of cytochrome P450eryF involved in erythromycin biosynthesis
    • Cupp-Vickery JR, Poulos TL. Structure of cytochrome P450eryF involved in erythromycin biosynthesis. Nat. Struct. Biol 1995;2: 144-153.
    • (1995) Nat Struct Biol , vol.2 , pp. 144-153
    • Cupp-Vickery, J.R.1    Poulos, T.L.2
  • 28
    • 0027136282 scopus 로고
    • Comparative protein modelling by satisfaction of spatial restraints
    • Sali A, Blundell TL. Comparative protein modelling by satisfaction of spatial restraints. J Mol Biol 1993;234:779-815.
    • (1993) J Mol Biol , vol.234 , pp. 779-815
    • Sali, A.1    Blundell, T.L.2
  • 29
    • 0027968068 scopus 로고
    • CLUSTAL W: Improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice
    • Thompson JD, Higgins DG, Gibson TJ. CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res 1994;22:4673-4680.
    • (1994) Nucleic Acids Res , vol.22 , pp. 4673-4680
    • Thompson, J.D.1    Higgins, D.G.2    Gibson, T.J.3
  • 30
    • 0023023246 scopus 로고
    • Physical methods in the study of the active site geometry of cytochromes P-450
    • Lewis DF. Physical methods in the study of the active site geometry of cytochromes P-450. Drug. Metab. Rev. 1986;17:1-66.
    • (1986) Drug Metab Rev , vol.17 , pp. 1-66
    • Lewis, D.F.1
  • 31
    • 0020997912 scopus 로고
    • Dictionary of protein secondary structure: Pattern recognition of hydrogen-bonded and geometrical features
    • Kabsch W, Sander C. Dictionary of protein secondary structure: pattern recognition of hydrogen-bonded and geometrical features. Biopolymers 1983;22:2577-2637.
    • (1983) Biopolymers , vol.22 , pp. 2577-2637
    • Kabsch, W.1    Sander, C.2
  • 32
    • 0033578684 scopus 로고    scopus 로고
    • Protein secondary structure prediction based on positionspecific scoring matrices
    • Jones DT. Protein secondary structure prediction based on positionspecific scoring matrices. J Mol Biol 1999;292:195-202.
    • (1999) J Mol Biol , vol.292 , pp. 195-202
    • Jones, D.T.1
  • 33
    • 0034738973 scopus 로고    scopus 로고
    • Microsomal cytochrome P450 2C5: Comparison to microbial P450s and unique features
    • Williams PA, Cosme J, Sridhar V, Johnson EF, McRee DE. Microsomal cytochrome P450 2C5: comparison to microbial P450s and unique features. J Inorg Biochem 2000;81:183-190.
    • (2000) J Inorg Biochem , vol.81 , pp. 183-190
    • Williams, P.A.1    Cosme, J.2    Sridhar, V.3    Johnson, E.F.4    McRee, D.E.5
  • 34
    • 0029918694 scopus 로고    scopus 로고
    • The FSSP database: Fold classification based on structure-structure alignment of proteins
    • Holm L, Sander C. The FSSP database: fold classification based on structure-structure alignment of proteins. Nucleic Acids Res 1996;24:206-209.
    • (1996) Nucleic Acids Res , vol.24 , pp. 206-209
    • Holm, L.1    Sander, C.2
  • 35
    • 0027169515 scopus 로고
    • Main-chain bond lengths and bond angles in protein structures
    • Laskowski RA, Moss DS, Thornton JM. Main-chain bond lengths and bond angles in protein structures. J Mol Biol 1993;231:1049-1067.
    • (1993) J Mol Biol , vol.231 , pp. 1049-1067
    • Laskowski, R.A.1    Moss, D.S.2    Thornton, J.M.3
  • 36
    • 0027180507 scopus 로고
    • Verification of protein structures: Patterns of nonbonded atomic interactions
    • Colovos C, Yeates TO. Verification of protein structures: patterns of nonbonded atomic interactions. Protein Sci 1993;2:1511-1519.
    • (1993) Protein Sci , vol.2 , pp. 1511-1519
    • Colovos, C.1    Yeates, T.O.2
  • 37
    • 0026610767 scopus 로고
    • Assessment of protein models with three-dimensional profiles
    • Luthy R, Bowie JU, Eisenberg D. Assessment of protein models with three-dimensional profiles. Nature 1992;356:83-85.
    • (1992) Nature , vol.356 , pp. 83-85
    • Luthy, R.1    Bowie, J.U.2    Eisenberg, D.3
  • 38
    • 0031301954 scopus 로고    scopus 로고
    • Criteria for evaluating protein structures derived from comparative modeling
    • Venclovas C, Zemla A, Fidelis K, Moult J. Criteria for evaluating protein structures derived from comparative modeling. Proteins 1997;Suppl.:7-13.
    • (1997) Proteins , Issue.SUPPL. , pp. 7-13
    • Venclovas, C.1    Zemla, A.2    Fidelis, K.3    Moult, J.4
  • 39
    • 0021871375 scopus 로고
    • A computational procedure for determining energetically favorable binding sites on biologically important macromolecules
    • Goodford PJ. A computational procedure for determining energetically favorable binding sites on biologically important macromolecules. J Med Chem 1985;28:849-857.
    • (1985) J Med Chem , vol.28 , pp. 849-857
    • Goodford, P.J.1
  • 40
    • 0028101464 scopus 로고
    • Comparative molecular field analysis using GRID force-field and GOLPE variable selection methods in a study of inhibitors of glycogen phosphorylase b
    • Cruciani G, Watson KA. Comparative molecular field analysis using GRID force-field and GOLPE variable selection methods in a study of inhibitors of glycogen phosphorylase b. J Med Chem 1994;37:2589-2601.
    • (1994) J Med Chem , vol.37 , pp. 2589-2601
    • Cruciani, G.1    Watson, K.A.2
  • 41
    • 0026750647 scopus 로고
    • The human hepatic cytochromes P450 involved in drug metabolism
    • Wrighton SA, Stevens JC. The human hepatic cytochromes P450 involved in drug metabolism. Crit Rev Toxicol 1992;22:1-21.
    • (1992) Crit Rev Toxicol , vol.22 , pp. 1-21
    • Wrighton, S.A.1    Stevens, J.C.2
  • 42
    • 0031552362 scopus 로고    scopus 로고
    • Development and validation of a genetic algorithm for flexible docking
    • Jones G, Willett P, Glen RC, Leach AR, Taylor R. Development and validation of a genetic algorithm for flexible docking. J Mol Biol 1997;267:727-748.
    • (1997) J Mol Biol , vol.267 , pp. 727-748
    • Jones, G.1    Willett, P.2    Glen, R.C.3    Leach, A.R.4    Taylor, R.5
  • 43
    • 0022919721 scopus 로고
    • Crystal structure of substratefree Pseudomonas putida cytochrome P-450
    • Poulos TL, Finzel BC, Howard AJ. Crystal structure of substratefree Pseudomonas putida cytochrome P-450. Biochemistry 1986;25: 5314-5322.
    • (1986) Biochemistry , vol.25 , pp. 5314-5322
    • Poulos, T.L.1    Finzel, B.C.2    Howard, A.J.3
  • 45
    • 0034724310 scopus 로고    scopus 로고
    • Crystal structures of ligand complexes of P450eryF exhibiting homotropic cooperativity
    • Cupp-Vickery J, Anderson R, Hatziris Z. Crystal structures of ligand complexes of P450eryF exhibiting homotropic cooperativity. Proc. Natl. Acad. Sci U S A 2000;97:3050-3055.
    • (2000) Proc Natl Acad Sci U S A , vol.97 , pp. 3050-3055
    • Cupp-Vickery, J.1    Anderson, R.2    Hatziris, Z.3
  • 47
    • 0022706389 scopus 로고
    • The relation between the divergence of sequence and structure in proteins
    • Chothia C, Lesk AM. The relation between the divergence of sequence and structure in proteins. EMBO J 1986;5:823-826.
    • (1986) EMBO J , vol.5 , pp. 823-826
    • Chothia, C.1    Lesk, A.M.2
  • 48
    • 0010459708 scopus 로고
    • A new approach to the display of local molecular surface
    • Brickmann J. A new approach to the display of local molecular surface. J Comp Aid Mol Des 1993;7:503.
    • (1993) J Comp Aid Mol Des , vol.7 , pp. 503
    • Brickmann, J.1
  • 49
    • 0025103215 scopus 로고
    • Polymorphic formation of morphine from codeine in poor and extensive metabolizers of dextromethorphan: Relationship to the presence of immunoidentified cytochrome P-450IID1
    • Mortimer O, Persson K, Ladona MG, Spalding D, Zanger UM, Meyer UA, Rane A. Polymorphic formation of morphine from codeine in poor and extensive metabolizers of dextromethorphan: relationship to the presence of immunoidentified cytochrome P-450IID1. Clin Pharmacol Ther 1990;47:27-35.
    • (1990) Clin Pharmacol Ther , vol.47 , pp. 27-35
    • Mortimer, O.1    Persson, K.2    Ladona, M.G.3    Spalding, D.4    Zanger, U.M.5    Meyer, U.A.6    Rane, A.7
  • 51
    • 0025820318 scopus 로고
    • Differential foetal development of the O- and N-demethylation of codeine and dextromethorphan in man
    • Ladona MG, Lindstrom B, Thyr C, Dun-Ren P, Rane A. Differential foetal development of the O- and N-demethylation of codeine and dextromethorphan in man. Br J Clin Pharmacol 1991;32:295-302.
    • (1991) Br J Clin Pharmacol , vol.32 , pp. 295-302
    • Ladona, M.G.1    Lindstrom, B.2    Thyr, C.3    Dun-Ren, P.4    Rane, A.5
  • 52
    • 0033669346 scopus 로고    scopus 로고
    • Influence of N-substitution of 7-methoxy-4-(aminomethyl)-coumarin on cytochrome P450 metabolism and selectivity
    • Venhorst J, Onderwater RC, Meerman JH, Commandeur JN, Vermeulen NP. Influence of N-substitution of 7-methoxy-4-(aminomethyl)-coumarin on cytochrome P450 metabolism and selectivity. Drug Metab Dispos 2000;28:1524-1532.
    • (2000) Drug Metab Dispos , vol.28 , pp. 1524-1532
    • Venhorst, J.1    Onderwater, R.C.2    Meerman, J.H.3    Commandeur, J.N.4    Vermeulen, N.P.5
  • 53
    • 0033529017 scopus 로고    scopus 로고
    • Novel approach to predicting P450-mediated drug metabolism: Development of a combined protein and pharmacophore model for CYP2D6
    • de Groot MJ, Ackland MJ, Horne VA, Alex AA, Jones BC. Novel approach to predicting P450-mediated drug metabolism: development of a combined protein and pharmacophore model for CYP2D6. J Med Chem 1999:42:1515-1524.
    • (1999) J Med Chem , vol.42 , pp. 1515-1524
    • De Groot, M.J.1    Ackland, M.J.2    Horne, V.A.3    Alex, A.A.4    Jones, B.C.5
  • 54
    • 0035883891 scopus 로고    scopus 로고
    • Heterologous expression of cytochrome P450 2D6 mutants, electron transfer and catalysis of bufuralol hydroxylation: The role of aspartate 301 in structural integrity
    • Hanna IH, Kim M-S, Guengerich FP. Heterologous expression of cytochrome P450 2D6 mutants, electron transfer and catalysis of bufuralol hydroxylation: The role of aspartate 301 in structural integrity. Arch Biochem Biophys 2001;393:255-261.
    • (2001) Arch Biochem Biophys , vol.393 , pp. 255-261
    • Hanna, I.H.1    Kim, M.-S.2    Guengerich, F.P.3
  • 55
    • 0010459709 scopus 로고    scopus 로고
    • http://www.icgeb.trieste.it/∼p450srv/
  • 56
    • 0025164996 scopus 로고
    • The rat P450 IID subfamily: Complete sequences of four closely linked genes and evidence that gene conversions maintained sequence homogeneity at the heme-binding region of the cytochrome P450 active site
    • Matsunaga E, Umeno M, Gonzalez FJ. The rat P450 IID subfamily: complete sequences of four closely linked genes and evidence that gene conversions maintained sequence homogeneity at the heme-binding region of the cytochrome P450 active site. J Mol Evol 1990;30:155-169.
    • (1990) J Mol Evol , vol.30 , pp. 155-169
    • Matsunaga, E.1    Umeno, M.2    Gonzalez, F.J.3
  • 57
    • 0026671134 scopus 로고
    • Characterization of the cytochrome P-450IID subfamily in bovine liver. Nucleotide sequences and microheterogeneity
    • Tsuneoka Y, Matsuo Y, Higuchi R, Ichikawa Y. Characterization of the cytochrome P-450IID subfamily in bovine liver. Nucleotide sequences and microheterogeneity. Eur J Biochem 1992;208:739-746.
    • (1992) Eur J Biochem , vol.208 , pp. 739-746
    • Tsuneoka, Y.1    Matsuo, Y.2    Higuchi, R.3    Ichikawa, Y.4
  • 60
    • 0027739383 scopus 로고
    • A major role for cytochrome P450TB (CYP2C subfamily) in the actions of nonsteroidal antiinflammatory drugs
    • Leemann TD, Transon C, Bonnabry P, Dayer P. A major role for cytochrome P450TB (CYP2C subfamily) in the actions of nonsteroidal antiinflammatory drugs. Drugs Exp Clin Res 1993;19: 189-195.
    • (1993) Drugs Exp Clin Res , vol.19 , pp. 189-195
    • Leemann, T.D.1    Transon, C.2    Bonnabry, P.3    Dayer, P.4
  • 61
    • 0022869269 scopus 로고
    • Complementary DNA and protein sequences of ethanol-inducible rat and human cytochrome P-450s. Transcriptional and post-transcriptional regulation of the rat enzyme
    • Song BJ, Gelboin HV, Park SS, Yang CS, Gonzalez FJ. Complementary DNA and protein sequences of ethanol-inducible rat and human cytochrome P-450s. Transcriptional and post-transcriptional regulation of the rat enzyme. J Biol Chem 1986;261:16689-16697.
    • (1986) J Biol Chem , vol.261 , pp. 16689-16697
    • Song, B.J.1    Gelboin, H.V.2    Park, S.S.3    Yang, C.S.4    Gonzalez, F.J.5
  • 62
    • 0022980836 scopus 로고
    • The cDNA and protein sequence of a phenobarbital-induced chicken cytochrome P-450
    • Hobbs AA, Mattschoss LA, May BK, Williams KE, Elliott WH. The cDNA and protein sequence of a phenobarbital-induced chicken cytochrome P-450. J Biol Chem 1986;261:9444-9449.
    • (1986) J Biol Chem , vol.261 , pp. 9444-9449
    • Hobbs, A.A.1    Mattschoss, L.A.2    May, B.K.3    Williams, K.E.4    Elliott, W.H.5
  • 64
    • 0022455516 scopus 로고
    • Structure of a bovine gene for P-450c21 (steroid 21-hydroxylase) defines a novel cytochrome P-450 gene family
    • Chung BC, Matteson KJ, Miller WL. Structure of a bovine gene for P-450c21 (steroid 21-hydroxylase) defines a novel cytochrome P-450 gene family. Proc Natl Acad Sci USA 1986;83:4243-4247.
    • (1986) Proc Natl Acad Sci USA , vol.83 , pp. 4243-4247
    • Chung, B.C.1    Matteson, K.J.2    Miller, W.L.3
  • 65
    • 0028276386 scopus 로고
    • Complete cDNA sequence of a human dioxin-inducible mRNA identifies a new gene subfamily of cytochrome P450 that maps to chromosome 2
    • Sutter TR, Tang YM, Hayes CL, Wo YY, Jabs EW, Li X, Yin H, Cody, CW, Greenlee WF. Complete cDNA sequence of a human dioxin-inducible mRNA identifies a new gene subfamily of cytochrome P450 that maps to chromosome 2. J Biol Chem 1994;269: 13092-13099.
    • (1994) J Biol Chem , vol.269 , pp. 13092-13099
    • Sutter, T.R.1    Tang, Y.M.2    Hayes, C.L.3    Wo, Y.Y.4    Jabs, E.W.5    Li, X.6    Yin, H.7    Cody, C.W.8    Greenlee, W.F.9
  • 66
    • 0012293592 scopus 로고
    • Cytochrome P450c17 (steroid 17 alpha-hydroxylase/17,20 lyase): Cloning of human adrenal and testis cDNAs indicates the same gene is expressed in both tissues
    • Chung BC, Picado-Leonard J, Haniu M, Bienkowski M, Hall PF, Shively JE, Miller WL. Cytochrome P450c17 (steroid 17 alpha- hydroxylase/17,20 lyase): cloning of human adrenal and testis cDNAs indicates the same gene is expressed in both tissues. Proc Natl Acad Sci USA 1987;84:407-411.
    • (1987) Proc Natl Acad Sci USA , vol.84 , pp. 407-411
    • Chung, B.C.1    Picado-Leonard, J.2    Haniu, M.3    Bienkowski, M.4    Hall, P.F.5    Shively, J.E.6    Miller, W.L.7
  • 67
    • 0025301127 scopus 로고
    • Sequence analysis of ripening-related cytochrome P-450 cDNAS from avocado fruit
    • Bozak KR, Yu H, Sirevag R, Christoffersen RE. Sequence analysis of ripening-related cytochrome P-450 cDNAS from avocado fruit. Proc Natl Acad Sci USA 1990;87:3904-3908.
    • (1990) Proc Natl Acad Sci USA , vol.87 , pp. 3904-3908
    • Bozak, K.R.1    Yu, H.2    Sirevag, R.3    Christoffersen, R.E.4
  • 68
    • 0028848836 scopus 로고
    • Expression of a cytochrome P450 gene family in maize
    • Frey M, Kliem R, Saedler H, Gierl A. Expression of a cytochrome P450 gene family in maize. Mol Gen Genet 1995;246:100-109.
    • (1995) Mol Gen Genet , vol.246 , pp. 100-109
    • Frey, M.1    Kliem, R.2    Saedler, H.3    Gierl, A.4
  • 69
    • 0023154962 scopus 로고
    • Debrisoquine 4-hydroxylase: Characterization of a new P450 gene subfamily, regulation, chromosomal mapping, and molecular analysis of the DA rat polymorphism
    • Gonzalez FJ, Matsunaga T, Nagata K, Meyer UA, Nebert DW, Pastewka J, Kozak CA, Gillette J, Gelboin HV, Hardwick, JP. Debrisoquine 4-hydroxylase: characterization of a new P450 gene subfamily, regulation, chromosomal mapping, and molecular analysis of the DA rat polymorphism. DNA 1987;6:149-161.
    • (1987) DNA , vol.6 , pp. 149-161
    • Gonzalez, F.J.1    Matsunaga, T.2    Nagata, K.3    Meyer, U.A.4    Nebert, D.W.5    Pastewka, J.6    Kozak, C.A.7    Gillette, J.8    Gelboin, H.V.9    Hardwick, J.P.10
  • 70
    • 0024416946 scopus 로고
    • The CYP2D gene subfamily: Analysis of the molecular basis of the debrisoquine 4-hydroxylase deficiency in DA rats
    • Matsunaga E, Zanger UM, Hardwick, JP, Gelboin HV, Meyer UA, Gonzalez FJ. The CYP2D gene subfamily: analysis of the molecular basis of the debrisoquine 4-hydroxylase deficiency in DA rats. Biochemistry 1989;28:7349-7355.
    • (1989) Biochemistry , vol.28 , pp. 7349-7355
    • Matsunaga, E.1    Zanger, U.M.2    Hardwick, J.P.3    Gelboin, H.V.4    Meyer, U.A.5    Gonzalez, F.J.6
  • 71
    • 0028834385 scopus 로고
    • The primary sequence of cytochrome P450tyr, the multifunctional N-hydroxylase catalyzing the conversion of L-tyrosine to p-hydroxyphenylacetaldehyde oxime in the biosynthesis of the cyanogenic glucoside dhurrin in Sorghum bicolor (L.) Moench
    • Koch BM, Sibbesen O, Halkier BA, Svendsen I, Moller BL. The primary sequence of cytochrome P450tyr, the multifunctional N-hydroxylase catalyzing the conversion of L-tyrosine to p- hydroxyphenylacetaldehyde oxime in the biosynthesis of the cyanogenic glucoside dhurrin in Sorghum bicolor (L.) Moench Arch Biochem Biophys 1995;323:177-186.
    • (1995) Arch Biochem Biophys , vol.323 , pp. 177-186
    • Koch, B.M.1    Sibbesen, O.2    Halkier, B.A.3    Svendsen, I.4    Moller, B.L.5
  • 72
    • 0029314739 scopus 로고
    • A cDNA encoding a novel cytochrome P450-dependent monooxygenase from Arabidopsis thaliana
    • Chapple CC. A cDNA encoding a novel cytochrome P450- dependent monooxygenase from Arabidopsis thaliana. Plant Physiol 1995;108:875-876.
    • (1995) Plant Physiol , vol.108 , pp. 875-876
    • Chapple, C.C.1
  • 73
    • 0027243314 scopus 로고
    • Isolation and sequence of a cDNA encoding the Jerusalem artichoke cinnamate 4-hydroxylase, a major plant cytochrome P450 involved in the general phenylpropanoid pathway
    • Teutsch HG, Hasenfratz MP, Lesot A, Stoltz C, Garnier JM, Jeltsch JM, Durst F, Werck-Reichhart D. Isolation and sequence of a cDNA encoding the Jerusalem artichoke cinnamate 4-hydroxy- lase, a major plant cytochrome P450 involved in the general phenylpropanoid pathway. Proc Natl Acad Sci USA 1993;90:4102- 4106.
    • (1993) Proc Natl Acad Sci USA , vol.90 , pp. 4102-4106
    • Teutsch, H.G.1    Hasenfratz, M.P.2    Lesot, A.3    Stoltz, C.4    Garnier, J.M.5    Jeltsch, J.M.6    Durst, F.7    Werck-Reichhart, D.8
  • 74
    • 0027303672 scopus 로고
    • Molecular cloning and sequencing of a cDNA encoding mung bean cytochrome P450 (P450C4H) possessing cinnamate 4-hydroxylase activity
    • Mizutani M, Ward E, DiMaio J, Ohta D, Ryals J, Sato R. Molecular cloning and sequencing of a cDNA encoding mung bean cytochrome P450 (P450C4H) possessing cinnamate 4-hydroxylase activity. Biochem Biophys Res Commun 1993;190:875-880.
    • (1993) Biochem Biophys Res Commun , vol.190 , pp. 875-880
    • Mizutani, M.1    Ward, E.2    DiMaio, J.3    Ohta, D.4    Ryals, J.5    Sato, R.6
  • 75
    • 0027186054 scopus 로고
    • Stress responses in alfalfa (Medicago sativa L.). XVIII: Molecular cloning and expression of the elicitorinducible cinnamic acid 4-hydroxylase cytochrome P450
    • Fahrendorf T, Dixon RA. Stress responses in alfalfa (Medicago sativa L.). XVIII: Molecular cloning and expression of the elicitorinducible cinnamic acid 4-hydroxylase cytochrome P450. Arch Biochem Biophys 1993;305:509-515.
    • (1993) Arch Biochem Biophys , vol.305 , pp. 509-515
    • Fahrendorf, T.1    Dixon, R.A.2
  • 76
    • 0028786298 scopus 로고
    • Cinnamate 4-hydroxylase from Catharanthus roseus and a strategy for the functional expression of plant cytochrome P450 proteins as translational fusions with P450 reductase in Escherichia coli
    • Hotze M, Schroder G, Schroder J. Cinnamate 4-hydroxylase from Catharanthus roseus and a strategy for the functional expression of plant cytochrome P450 proteins as translational fusions with P450 reductase in Escherichia coli. FEBS Lett 1995;374:345-350.
    • (1995) FEBS Lett , vol.374 , pp. 345-350
    • Hotze, M.1    Schroder, G.2    Schroder, J.3
  • 77
    • 0030111330 scopus 로고    scopus 로고
    • Cloning of wound-induced cytochrome P450 monooxygenases expressed in pea
    • Frank MR, Deyneka JM, Schuler MA. Cloning of wound-induced cytochrome P450 monooxygenases expressed in pea. Plant Physiol 1996;110:1035-1046.
    • (1996) Plant Physiol , vol.110 , pp. 1035-1046
    • Frank, M.R.1    Deyneka, J.M.2    Schuler, M.A.3
  • 78
    • 0032859019 scopus 로고    scopus 로고
    • Expression and molecular cloning of human liver leukotriene B4 omega-hydroxylase (CYP4F2) gene
    • Kikuta Y, Miyauchi Y, Kusunose E, Kusunose M. Expression and molecular cloning of human liver leukotriene B4 omega-hydroxylase (CYP4F2) gene. DNA Cell Biol 1999;18:723-730.
    • (1999) DNA Cell Biol , vol.18 , pp. 723-730
    • Kikuta, Y.1    Miyauchi, Y.2    Kusunose, E.3    Kusunose, M.4


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