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Volumn 54, Issue 3, 2014, Pages 857-869

Elucidating substrate promiscuity in the human cytochrome 3A4

Author keywords

[No Author keywords available]

Indexed keywords

BIOCHEMISTRY; CRYSTALS; ENZYMES; LIGANDS; METABOLISM;

EID: 84896986979     PISSN: 15499596     EISSN: 1549960X     Source Type: Journal    
DOI: 10.1021/ci4006782     Document Type: Article
Times cited : (20)

References (70)
  • 1
    • 79955601786 scopus 로고    scopus 로고
    • Trial watch: Phase II failures: 2008-2010
    • Arrowsmith, J. Trial watch: Phase II failures: 2008-2010 Nat. Rev. Drug Discovery 2011, 10, 328-9
    • (2011) Nat. Rev. Drug Discovery , vol.10 , pp. 328-329
    • Arrowsmith, J.1
  • 2
    • 79551575056 scopus 로고    scopus 로고
    • Trial watch: Phase III and submission failures: 2007-2010
    • Arrowsmith, J. Trial watch: Phase III and submission failures: 2007-2010 Nat. Rev. Drug Discovery 2011, 10, 87
    • (2011) Nat. Rev. Drug Discovery , vol.10 , pp. 87
    • Arrowsmith, J.1
  • 4
    • 33645050104 scopus 로고    scopus 로고
    • Cytochrome P450s and other enzymes in drug metabolism and toxicity
    • Guengerich, F. P. Cytochrome P450s and other enzymes in drug metabolism and toxicity AAPS J. 2006, 8, E101-11
    • (2006) AAPS J. , vol.8 , pp. 101-111
    • Guengerich, F.P.1
  • 7
    • 3042645255 scopus 로고    scopus 로고
    • Computer-assisted design of selective imidazole inhibitors for cytochrome p450 enzymes
    • Verras, A.; Kuntz, I. D.; Ortiz de Montellano, P. R. Computer-assisted design of selective imidazole inhibitors for cytochrome p450 enzymes J. Med. Chem. 2004, 47, 3572-9
    • (2004) J. Med. Chem. , vol.47 , pp. 3572-3579
    • Verras, A.1    Kuntz, I.D.2    Ortiz De Montellano, P.R.3
  • 8
    • 0033199227 scopus 로고    scopus 로고
    • Cytochrome P450 and the individuality of species
    • Nelson, D. R. Cytochrome P450 and the individuality of species Arch. Biochem. Biophys. 1999, 369, 1-10
    • (1999) Arch. Biochem. Biophys. , vol.369 , pp. 1-10
    • Nelson, D.R.1
  • 11
    • 84971201043 scopus 로고    scopus 로고
    • Drug Metabolsim
    • 7 th ed. Lemke, T. Williams, D. A. Roche, V. F. Zito, S. W. Lippincott Williams & Wilkins: Baltimore, MD
    • Williams, D. A. Drug Metabolsim. In Foyes Principles of Medicinal Chemistry, 7 th ed.; Lemke, T.; Williams, D. A.; Roche, V. F.; Zito, S. W., Eds.; Lippincott Williams & Wilkins: Baltimore, MD, 2013; pp 106-90.
    • (2013) Foyes Principles of Medicinal Chemistry , pp. 106-190
    • Williams, D.A.1
  • 12
    • 33645460847 scopus 로고    scopus 로고
    • 3 rd ed. Ortiz de Montellano, P. R. Kluwer Academic/Plenum Publishers: New York
    • Guengerich, F. P. In Cytochrome P450: Structure, Mechanism, and Biochemistry, 3 rd ed.; Ortiz de Montellano, P. R., Ed.; Kluwer Academic/Plenum Publishers: New York, 2005; pp 377-530.
    • (2005) Cytochrome P450: Structure, Mechanism, and Biochemistry , pp. 377-530
    • Guengerich, F.P.1
  • 13
    • 6944221357 scopus 로고    scopus 로고
    • Drug-drug interactions for UDP-glucuronosyltransferase substrates: A pharmacokinetic explanation for typically observed low exposure (AUCi/AUC) ratios
    • Williams, J. A.; Hyland, R.; Jones, B. C.; Smith, D. A.; Hurst, S.; Goosen, T. C.; Peterkin, V.; Koup, J. R.; Ball, S. E. Drug-drug interactions for UDP-glucuronosyltransferase substrates: A pharmacokinetic explanation for typically observed low exposure (AUCi/AUC) ratios Drug Metab. Dispos. 2004, 32, 1201-8
    • (2004) Drug Metab. Dispos. , vol.32 , pp. 1201-1208
    • Williams, J.A.1    Hyland, R.2    Jones, B.C.3    Smith, D.A.4    Hurst, S.5    Goosen, T.C.6    Peterkin, V.7    Koup, J.R.8    Ball, S.E.9
  • 14
    • 0025273823 scopus 로고
    • Enzymatic oxidation of xenobiotic chemicals
    • Guengerich, F. P. Enzymatic oxidation of xenobiotic chemicals Crit. Rev. Biochem. Mol. Biol. 1990, 25, 97-153
    • (1990) Crit. Rev. Biochem. Mol. Biol. , vol.25 , pp. 97-153
    • Guengerich, F.P.1
  • 15
    • 34147112191 scopus 로고    scopus 로고
    • Cooperativity in cytochrome P450 3A4: Linkages in substrate binding, spin state, uncoupling, and product formation
    • Denisov, I. G.; Baas, B. J.; Grinkova, Y. V.; Sligar, S. G. Cooperativity in cytochrome P450 3A4: Linkages in substrate binding, spin state, uncoupling, and product formation J. Biol. Chem. 2007, 282, 7066-76
    • (2007) J. Biol. Chem. , vol.282 , pp. 7066-7076
    • Denisov, I.G.1    Baas, B.J.2    Grinkova, Y.V.3    Sligar, S.G.4
  • 16
    • 0032924934 scopus 로고    scopus 로고
    • Cytochrome P-450 3A4: Regulation and role in drug metabolism
    • Guengerich, F. P. Cytochrome P-450 3A4: Regulation and role in drug metabolism Annu. Rev. Pharmacol. Toxicol. 1999, 39, 1-17
    • (1999) Annu. Rev. Pharmacol. Toxicol. , vol.39 , pp. 1-17
    • Guengerich, F.P.1
  • 17
    • 33748802003 scopus 로고    scopus 로고
    • Structural basis for ligand promiscuity in cytochrome P450 3A4
    • Ekroos, M.; Sjogren, T. Structural basis for ligand promiscuity in cytochrome P450 3A4 Proc. Natl. Acad. Sci. U.S.A. 2006, 103, 13682-7
    • (2006) Proc. Natl. Acad. Sci. U.S.A. , vol.103 , pp. 13682-13687
    • Ekroos, M.1    Sjogren, T.2
  • 18
    • 78649885201 scopus 로고    scopus 로고
    • Structure and mechanism of the complex between cytochrome P4503A4 and ritonavir
    • Sevrioukova, I. F.; Poulos, T. L. Structure and mechanism of the complex between cytochrome P4503A4 and ritonavir Proc. Natl. Acad. Sci. U.S.A. 2010, 107, 18422-7
    • (2010) Proc. Natl. Acad. Sci. U.S.A. , vol.107 , pp. 18422-18427
    • Sevrioukova, I.F.1    Poulos, T.L.2
  • 19
    • 84856266049 scopus 로고    scopus 로고
    • Structural and mechanistic insights into the interaction of cytochrome P4503A4 with bromoergocryptine, A type i ligand
    • Sevrioukova, I. F.; Poulos, T. L. Structural and mechanistic insights into the interaction of cytochrome P4503A4 with bromoergocryptine, A type I ligand J. Biol. Chem. 2012, 287, 3510-7
    • (2012) J. Biol. Chem. , vol.287 , pp. 3510-3517
    • Sevrioukova, I.F.1    Poulos, T.L.2
  • 20
    • 84877717752 scopus 로고    scopus 로고
    • Pyridine-substituted desoxyritonavir is a more potent inhibitor of cytochrome P450 3A4 than ritonavir
    • Sevrioukova, I. F.; Poulos, T. L. Pyridine-substituted desoxyritonavir is a more potent inhibitor of cytochrome P450 3A4 than ritonavir J. Med. Chem. 2013, 56, 3733-41
    • (2013) J. Med. Chem. , vol.56 , pp. 3733-3741
    • Sevrioukova, I.F.1    Poulos, T.L.2
  • 21
    • 84880150381 scopus 로고    scopus 로고
    • Dissecting cytochrome P450 3A4-ligand interactions using ritonavir analogues
    • Sevrioukova, I. F.; Poulos, T. L. Dissecting cytochrome P450 3A4-ligand interactions using ritonavir analogues Biochemistry 2013, 52, 4474-81
    • (2013) Biochemistry , vol.52 , pp. 4474-4481
    • Sevrioukova, I.F.1    Poulos, T.L.2
  • 22
    • 84859353403 scopus 로고    scopus 로고
    • Interaction of human cytochrome P4503A4 with ritonavir analogs
    • Sevrioukova, I. F.; Poulos, T. L. Interaction of human cytochrome P4503A4 with ritonavir analogs Arch. Biochem. Biophys. 2012, 520, 108-16
    • (2012) Arch. Biochem. Biophys. , vol.520 , pp. 108-116
    • Sevrioukova, I.F.1    Poulos, T.L.2
  • 23
    • 4644301430 scopus 로고    scopus 로고
    • The structure of human microsomal cytochrome P450 3A4 determined by X-ray crystallography to 2.05-Å resolution
    • Yano, J. K.; Wester, M. R.; Schoch, G. A.; Griffin, K. J.; Stout, C. D.; Johnson, E. F. The structure of human microsomal cytochrome P450 3A4 determined by X-ray crystallography to 2.05-Å resolution J. Biol. Chem. 2004, 279, 38091-4
    • (2004) J. Biol. Chem. , vol.279 , pp. 38091-38094
    • Yano, J.K.1    Wester, M.R.2    Schoch, G.A.3    Griffin, K.J.4    Stout, C.D.5    Johnson, E.F.6
  • 24
    • 75749127293 scopus 로고    scopus 로고
    • Role of water in molecular docking simulations of cytochrome P450 2D6
    • Santos, R.; Hritz, J.; Oostenbrink, C. Role of water in molecular docking simulations of cytochrome P450 2D6 J. Chem. Inf. Model. 2010, 50, 146-54
    • (2010) J. Chem. Inf. Model. , vol.50 , pp. 146-154
    • Santos, R.1    Hritz, J.2    Oostenbrink, C.3
  • 26
    • 77956060951 scopus 로고    scopus 로고
    • Analysis of binding modes of ligands to multiple conformations of CYP3A4
    • Teixeira, V. H.; Ribeiro, V.; Martel, P. J. Analysis of binding modes of ligands to multiple conformations of CYP3A4 Biochim. Biophys. Acta 2010, 1804, 2036-45
    • (2010) Biochim. Biophys. Acta , vol.1804 , pp. 2036-2045
    • Teixeira, V.H.1    Ribeiro, V.2    Martel, P.J.3
  • 27
    • 0037212102 scopus 로고    scopus 로고
    • LigandFit: A novel method for the shape-directed rapid docking of ligands to protein active sites
    • Venkatachalam, C. M.; Jiang, X.; Oldfield, T.; Waldman, M. LigandFit: A novel method for the shape-directed rapid docking of ligands to protein active sites J. Mol. Graphics Modell. 2003, 21, 289-307
    • (2003) J. Mol. Graphics Modell. , vol.21 , pp. 289-307
    • Venkatachalam, C.M.1    Jiang, X.2    Oldfield, T.3    Waldman, M.4
  • 28
    • 0031552362 scopus 로고    scopus 로고
    • Development and validation of a genetic algorithm for flexible docking
    • Jones, G.; Willett, P.; Glen, R. C.; Leach, A. R.; Taylor, R. Development and validation of a genetic algorithm for flexible docking J. Mol. Biol. 1997, 267, 727-48
    • (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
  • 32
    • 1642310340 scopus 로고    scopus 로고
    • Glide: A new approach for rapid, accurate docking and scoring. 2. Enrichment factors in database screening
    • Halgren, T. A.; Murphy, R. B.; Friesner, R. A.; Beard, H. S.; Frye, L. L.; Pollard, W. T.; Banks, J. L. Glide: A new approach for rapid, accurate docking and scoring. 2. Enrichment factors in database screening J. Med. Chem. 2004, 47, 1750-9
    • (2004) J. Med. Chem. , vol.47 , pp. 1750-1759
    • Halgren, T.A.1    Murphy, R.B.2    Friesner, R.A.3    Beard, H.S.4    Frye, L.L.5    Pollard, W.T.6    Banks, J.L.7
  • 33
    • 33745088619 scopus 로고    scopus 로고
    • Use of an induced fit receptor structure in virtual screening
    • Sherman, W.; Beard, H. S.; Farid, R. Use of an induced fit receptor structure in virtual screening Chem. Biol. Drug Des. 2006, 67, 83-4
    • (2006) Chem. Biol. Drug Des. , vol.67 , pp. 83-84
    • Sherman, W.1    Beard, H.S.2    Farid, R.3
  • 34
    • 31544450787 scopus 로고    scopus 로고
    • Novel procedure for modeling ligand/receptor induced fit effects
    • Sherman, W.; Day, T.; Jacobson, M. P.; Friesner, R. A.; Farid, R. Novel procedure for modeling ligand/receptor induced fit effects J. Med. Chem. 2006, 49, 534-53
    • (2006) J. Med. Chem. , vol.49 , pp. 534-553
    • Sherman, W.1    Day, T.2    Jacobson, M.P.3    Friesner, R.A.4    Farid, R.5
  • 35
    • 33644967111 scopus 로고    scopus 로고
    • New insights about HERG blockade obtained from protein modeling, potential energy mapping, and docking studies
    • Farid, R.; Day, T.; Friesner, R. A.; Pearlstein, R. A. New insights about HERG blockade obtained from protein modeling, potential energy mapping, and docking studies Bioorg. Med. Chem. 2006, 14, 3160-73
    • (2006) Bioorg. Med. Chem. , vol.14 , pp. 3160-3173
    • Farid, R.1    Day, T.2    Friesner, R.A.3    Pearlstein, R.A.4
  • 36
    • 13944260141 scopus 로고    scopus 로고
    • Prediction of binding modes for ligands in the cytochromes P450 and other heme-containing proteins
    • Kirton, S. B.; Murray, C. W.; Verdonk, M. L.; Taylor, R. D. Prediction of binding modes for ligands in the cytochromes P450 and other heme-containing proteins Proteins 2005, 58, 836-44
    • (2005) Proteins , vol.58 , pp. 836-844
    • Kirton, S.B.1    Murray, C.W.2    Verdonk, M.L.3    Taylor, R.D.4
  • 37
    • 84896913945 scopus 로고    scopus 로고
    • Cambridge Crystallographic Data Centre: Cambridge, United Kingdom
    • GOLD 5.1; Cambridge Crystallographic Data Centre: Cambridge, United Kingdom, 2005-2011.
    • (2005) GOLD 5.1
  • 38
  • 39
    • 84896968576 scopus 로고    scopus 로고
    • version 9.2.112; Schrodinger, LLC: New York, NY
    • Maestro, version 9.2.112; Schrodinger, LLC: New York, NY, 2011.
    • (2011) Maestro
  • 41
  • 42
    • 57749122048 scopus 로고    scopus 로고
    • Structures of human cytochrome P-450 2E1. Insights into the binding of inhibitors and both small molecular weight and fatty acid substrates
    • Porubsky, P. R.; Meneely, K. M.; Scott, E. E. Structures of human cytochrome P-450 2E1. Insights into the binding of inhibitors and both small molecular weight and fatty acid substrates J. Biol. Chem. 2008, 283, 33698-707
    • (2008) J. Biol. Chem. , vol.283 , pp. 33698-33707
    • Porubsky, P.R.1    Meneely, K.M.2    Scott, E.E.3
  • 43
    • 84986505827 scopus 로고
    • Validation of the general purpose QUANTA 3.2/CHARMm force field
    • Momany, F. A.; Rone, R. Validation of the general purpose QUANTA 3.2/CHARMm force field J. Comput. Chem. 1992, 13, 888-900
    • (1992) J. Comput. Chem. , vol.13 , pp. 888-900
    • Momany, F.A.1    Rone, R.2
  • 44
    • 80052585054 scopus 로고    scopus 로고
    • Drug Interactions
    • Cytochrome P450. In; Therapeutic Research Center: Stockton, CA
    • Cytochrome P450 Drug Interactions. In Pharmacists Letter/Prescribers Letter; Therapeutic Research Center: Stockton, CA, 2011; Vol. 22, p 220233.
    • (2011) Pharmacists Letter/Prescribers Letter , vol.22 , pp. 220233
  • 46
    • 0036310711 scopus 로고    scopus 로고
    • On the role of the crystal environment in determining protein side-chain conformations
    • Jacobson, M. P.; Friesner, R. A.; Xiang, Z.; Honig, B. On the role of the crystal environment in determining protein side-chain conformations J. Mol. Biol. 2002, 320, 597-608
    • (2002) J. Mol. Biol. , vol.320 , pp. 597-608
    • Jacobson, M.P.1    Friesner, R.A.2    Xiang, Z.3    Honig, B.4
  • 48
    • 0033970047 scopus 로고    scopus 로고
    • Mammalian microsomal cytochrome P450 monooxygenase: Structural adaptations for membrane binding and functional diversity
    • Williams, P. A.; Cosme, J.; Sridhar, V.; Johnson, E. F.; McRee, D. E. Mammalian microsomal cytochrome P450 monooxygenase: structural adaptations for membrane binding and functional diversity Mol. Cell 2000, 5, 121-31
    • (2000) Mol. Cell , vol.5 , pp. 121-131
    • Williams, P.A.1    Cosme, J.2    Sridhar, V.3    Johnson, E.F.4    McRee, D.E.5
  • 49
    • 0037076392 scopus 로고    scopus 로고
    • Single-molecule height measurements on microsomal cytochrome P450 in nanometer-scale phospholipid bilayer disks
    • Bayburt, T. H.; Sligar, S. G. Single-molecule height measurements on microsomal cytochrome P450 in nanometer-scale phospholipid bilayer disks Proc. Natl. Acad. Sci. U.S.A. 2002, 99, 6725-30
    • (2002) Proc. Natl. Acad. Sci. U.S.A. , vol.99 , pp. 6725-6730
    • Bayburt, T.H.1    Sligar, S.G.2
  • 50
    • 70349509736 scopus 로고    scopus 로고
    • Theoretical characterization of substrate access/exit channels in the human cytochrome P450 3A4 enzyme: Involvement of phenylalanine residues in the gating mechanism
    • Fishelovitch, D.; Shaik, S.; Wolfson, H. J.; Nussinov, R. Theoretical characterization of substrate access/exit channels in the human cytochrome P450 3A4 enzyme: involvement of phenylalanine residues in the gating mechanism J. Phys. Chem. B. 2009, 113, 13018-25
    • (2009) J. Phys. Chem. B. , vol.113 , pp. 13018-13025
    • Fishelovitch, D.1    Shaik, S.2    Wolfson, H.J.3    Nussinov, R.4
  • 51
    • 0027497950 scopus 로고
    • Expression of truncated forms of liver microsomal P450 cytochromes 2B4 and 2E1 in Escherichia coli: Influence of NH2-terminal region on localization in cytosol and membranes
    • Pernecky, S. J.; Larson, J. R.; Philpot, R. M.; Coon, M. J. Expression of truncated forms of liver microsomal P450 cytochromes 2B4 and 2E1 in Escherichia coli: influence of NH2-terminal region on localization in cytosol and membranes Proc. Natl. Acad. Sci. U.S.A. 1993, 90, 2651-5
    • (1993) Proc. Natl. Acad. Sci. U.S.A. , vol.90 , pp. 2651-2655
    • Pernecky, S.J.1    Larson, J.R.2    Philpot, R.M.3    Coon, M.J.4
  • 52
    • 0026088436 scopus 로고
    • The expression of a catalytically active cholesterol 7 alpha-hydroxylase cytochrome P450 in Escherichia coli
    • Li, Y. C.; Chiang, J. Y. The expression of a catalytically active cholesterol 7 alpha-hydroxylase cytochrome P450 in Escherichia coli J. Biol. Chem. 1991, 266, 19186-91
    • (1991) J. Biol. Chem. , vol.266 , pp. 19186-19191
    • Li, Y.C.1    Chiang, J.Y.2
  • 53
    • 0027199068 scopus 로고
    • Expression in Escherichia coli of functional cytochrome P450c17 lacking its hydrophobic amino-terminal signal anchor
    • Sagara, Y.; Barnes, H. J.; Waterman, M. R. Expression in Escherichia coli of functional cytochrome P450c17 lacking its hydrophobic amino-terminal signal anchor Arch. Biochem. Biophys. 1993, 304, 272-8
    • (1993) Arch. Biochem. Biophys. , vol.304 , pp. 272-278
    • Sagara, Y.1    Barnes, H.J.2    Waterman, M.R.3
  • 54
    • 80053539881 scopus 로고    scopus 로고
    • Conformational selection or induced fit? 50 years of debate resolved
    • Changeux, J. P.; Edelstein, S. Conformational selection or induced fit? 50 years of debate resolved F1000 Biol. Rep. 2011, 3, 19
    • (2011) F1000 Biol. Rep. , vol.3 , pp. 19
    • Changeux, J.P.1    Edelstein, S.2
  • 55
    • 0001858251 scopus 로고
    • Application of a theory of enzyme specificity to protein synthesis
    • Koshland, D. E. Application of a theory of enzyme specificity to protein synthesis Proc. Natl. Acad. Sci. U.S.A. 1958, 44, 98-104
    • (1958) Proc. Natl. Acad. Sci. U.S.A. , vol.44 , pp. 98-104
    • Koshland, D.E.1
  • 56
    • 49149089445 scopus 로고    scopus 로고
    • Flexibility of human cytochromes P450: Molecular dynamics reveals differences between CYPs 3A4, 2C9, and 2A6, which correlate with their substrate preferences
    • Skopalik, J.; Anzenbacher, P.; Otyepka, M. Flexibility of human cytochromes P450: Molecular dynamics reveals differences between CYPs 3A4, 2C9, and 2A6, which correlate with their substrate preferences J. Phys. Chem. B. 2008, 112, 8165-73
    • (2008) J. Phys. Chem. B. , vol.112 , pp. 8165-8173
    • Skopalik, J.1    Anzenbacher, P.2    Otyepka, M.3
  • 57
    • 84857473710 scopus 로고    scopus 로고
    • Peripheral ligand-binding site in cytochrome P450 3A4 located with fluorescence resonance energy transfer (FRET)
    • Davydov, D. R.; Rumfeldt, J. A.; Sineva, E. V.; Fernando, H.; Davydova, N. Y.; Halpert, J. R. Peripheral ligand-binding site in cytochrome P450 3A4 located with fluorescence resonance energy transfer (FRET) J. Biol. Chem. 2012, 287, 6797-809
    • (2012) J. Biol. Chem. , vol.287 , pp. 6797-6809
    • Davydov, D.R.1    Rumfeldt, J.A.2    Sineva, E.V.3    Fernando, H.4    Davydova, N.Y.5    Halpert, J.R.6
  • 58
    • 1642540577 scopus 로고    scopus 로고
    • Evaluation of docking performance: Comparative data on docking algorithms
    • Kontoyianni, M.; McClellan, L. M.; Sokol, G. S. Evaluation of docking performance: comparative data on docking algorithms J. Med. Chem. 2004, 47, 558-65
    • (2004) J. Med. Chem. , vol.47 , pp. 558-565
    • Kontoyianni, M.1    McClellan, L.M.2    Sokol, G.S.3
  • 59
    • 11144255694 scopus 로고    scopus 로고
    • Evaluation of library ranking efficacy in virtual screening
    • Kontoyianni, M.; Sokol, G. S.; McClellan, L. M. Evaluation of library ranking efficacy in virtual screening J. Comput. Chem. 2005, 26, 11-22
    • (2005) J. Comput. Chem. , vol.26 , pp. 11-22
    • Kontoyianni, M.1    Sokol, G.S.2    McClellan, L.M.3
  • 61
    • 61449104961 scopus 로고    scopus 로고
    • Fragment-based identification of druggable "hot spots" of proteins using Fourier domain correlation techniques
    • Brenke, R.; Kozakov, D.; Chuang, G. Y.; Beglov, D.; Hall, D.; Landon, M. R.; Mattos, C.; Vajda, S. Fragment-based identification of druggable "hot spots" of proteins using Fourier domain correlation techniques Bioinformatics 2009, 25, 621-7
    • (2009) Bioinformatics , vol.25 , pp. 621-627
    • Brenke, R.1    Kozakov, D.2    Chuang, G.Y.3    Beglov, D.4    Hall, D.5    Landon, M.R.6    Mattos, C.7    Vajda, S.8
  • 63
    • 17144368025 scopus 로고    scopus 로고
    • Binding mode prediction of cytochrome p450 and thymidine kinase protein-ligand complexes by consideration of water and rescoring in automated docking
    • de Graaf, C.; Pospisil, P.; Pos, W.; Folkers, G.; Vermeulen, N. P. Binding mode prediction of cytochrome p450 and thymidine kinase protein-ligand complexes by consideration of water and rescoring in automated docking J. Med. Chem. 2005, 48, 2308-18
    • (2005) J. Med. Chem. , vol.48 , pp. 2308-2318
    • De Graaf, C.1    Pospisil, P.2    Pos, W.3    Folkers, G.4    Vermeulen, N.P.5
  • 64
    • 27444443492 scopus 로고    scopus 로고
    • Cooperative binding of midazolam with testosterone and alpha-naphthoflavone within the CYP3A4 active site: A NMR T1 paramagnetic relaxation study
    • Cameron, M. D.; Wen, B.; Allen, K. E.; Roberts, A. G.; Schuman, J. T.; Campbell, A. P.; Kunze, K. L.; Nelson, S. D. Cooperative binding of midazolam with testosterone and alpha-naphthoflavone within the CYP3A4 active site: A NMR T1 paramagnetic relaxation study Biochemistry 2005, 44, 14143-51
    • (2005) Biochemistry , vol.44 , pp. 14143-14151
    • Cameron, M.D.1    Wen, B.2    Allen, K.E.3    Roberts, A.G.4    Schuman, J.T.5    Campbell, A.P.6    Kunze, K.L.7    Nelson, S.D.8
  • 65
    • 34548432500 scopus 로고    scopus 로고
    • Understanding cooperativity in human p450 mediated drug-drug interactions
    • Sligar, S. G.; Denisov, I. G. Understanding cooperativity in human p450 mediated drug-drug interactions Drug Metab. Rev. 2007, 39, 567-79
    • (2007) Drug Metab. Rev. , vol.39 , pp. 567-579
    • Sligar, S.G.1    Denisov, I.G.2
  • 66
    • 52949113775 scopus 로고    scopus 로고
    • Multiple substrate binding by cytochrome P450 3A4: Estimation of the number of bound substrate molecules
    • Kapelyukh, Y.; Paine, M. J.; Marechal, J. D.; Sutcliffe, M. J.; Wolf, C. R.; Roberts, G. C. Multiple substrate binding by cytochrome P450 3A4: Estimation of the number of bound substrate molecules Drug Metab. Dispos. 2008, 36, 2136-44
    • (2008) Drug Metab. Dispos. , vol.36 , pp. 2136-2144
    • Kapelyukh, Y.1    Paine, M.J.2    Marechal, J.D.3    Sutcliffe, M.J.4    Wolf, C.R.5    Roberts, G.C.6
  • 67
  • 68
    • 84858450938 scopus 로고    scopus 로고
    • Structural differences between soluble and membrane bound cytochrome P450s
    • Denisov, I. G.; Shih, A. Y.; Sligar, S. G. Structural differences between soluble and membrane bound cytochrome P450s J. Inorg. Biochem. 2012, 108, 150-8
    • (2012) J. Inorg. Biochem. , vol.108 , pp. 150-158
    • Denisov, I.G.1    Shih, A.Y.2    Sligar, S.G.3
  • 69
    • 84873620874 scopus 로고    scopus 로고
    • Understanding the mechanism of cytochrome P450 3A4: Recent advances and remaining problems
    • Sevrioukova, I. F.; Poulos, T. L. Understanding the mechanism of cytochrome P450 3A4: recent advances and remaining problems Dalton Trans 2013, 42 (9) 3116-26
    • (2013) Dalton Trans , vol.42 , Issue.9 , pp. 3116-3126
    • Sevrioukova, I.F.1    Poulos, T.L.2
  • 70
    • 84857861034 scopus 로고    scopus 로고
    • A novel type of allosteric regulation: Functional cooperativity in monomeric proteins
    • Denisov, I. G.; Sligar, S. G. A novel type of allosteric regulation: functional cooperativity in monomeric proteins Arch. Biochem. Biophys. 2012, 519, 91-102
    • (2012) Arch. Biochem. Biophys. , vol.519 , pp. 91-102
    • Denisov, I.G.1    Sligar, S.G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.