-
1
-
-
38949094492
-
Cytochrome P450 and chemical toxicology
-
Guengerich, F. P. (2008) Cytochrome P450 and chemical toxicology Chem. Res. Toxicol. 21, 70-83
-
(2008)
Chem. Res. Toxicol.
, vol.21
, pp. 70-83
-
-
Guengerich, F.P.1
-
2
-
-
34548432500
-
Understanding cooperativity in human P450 mediated drug-drug interactions
-
Sligar, S. G. and Denisov, I. G. (2007) Understanding cooperativity in human P450 mediated drug-drug interactions Drug Metab. Rev. 39, 567-579
-
(2007)
Drug Metab. Rev.
, vol.39
, pp. 567-579
-
-
Sligar, S.G.1
Denisov, I.G.2
-
3
-
-
58149199796
-
Allosteric P450 mechanisms: Multiple binding sites, multiple conformers or both?
-
Davydov, D. R. and Halpert, J. R. (2008) Allosteric P450 mechanisms: Multiple binding sites, multiple conformers or both? Expert Opin. Drug Metab. Toxicol. 4, 1523-1535
-
(2008)
Expert Opin. Drug Metab. Toxicol.
, vol.4
, pp. 1523-1535
-
-
Davydov, D.R.1
Halpert, J.R.2
-
4
-
-
33750535207
-
Atypical cytochrome P450 kinetics: Implications for drug discovery
-
Tracy, T. S. (2006) Atypical cytochrome P450 kinetics: Implications for drug discovery Drugs R&D 7, 349-363
-
(2006)
Drugs R&D
, vol.7
, pp. 349-363
-
-
Tracy, T.S.1
-
5
-
-
0037048522
-
Pyrene-pyrene complexes at the active site of cytochrome P450 3A4: Evidence for a multiple substrate binding site
-
Dabrowski, M. J., Schrag, M. L., Wienkers, L. C., and Atkins, W. M. (2002) Pyrene-pyrene complexes at the active site of cytochrome P450 3A4: Evidence for a multiple substrate binding site J. Am. Chem. Soc. 124, 11866-11867
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 11866-11867
-
-
Dabrowski, M.J.1
Schrag, M.L.2
Wienkers, L.C.3
Atkins, W.M.4
-
6
-
-
33748802003
-
Structural basis for ligand promiscuity in cytochrome P450 3A4
-
Ekroos, M. and Sjogren, T. (2006) Structural basis for ligand promiscuity in cytochrome P450 3A4 Proc. Natl. Acad. Sci. U.S.A. 103, 13682-13687
-
(2006)
Proc. Natl. Acad. Sci. U.S.A.
, vol.103
, pp. 13682-13687
-
-
Ekroos, M.1
Sjogren, T.2
-
7
-
-
33846135094
-
Mechanism of interactions of α-naphthoflavone with cytochrome P450 3A4 explored with an engineered enzyme bearing a fluorescent probe
-
Tsalkova, T. N., Davydova, N. Y., Halpert, J. R., and Davydov, D. R. (2007) Mechanism of interactions of α-naphthoflavone with cytochrome P450 3A4 explored with an engineered enzyme bearing a fluorescent probe Biochemistry 46, 106-119
-
(2007)
Biochemistry
, vol.46
, pp. 106-119
-
-
Tsalkova, T.N.1
Davydova, N.Y.2
Halpert, J.R.3
Davydov, D.R.4
-
8
-
-
84857473710
-
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., and Halpert, J. R. (2012) Peripheral ligand-binding site in cytochrome P450 3A4 located with fluorescence resonance energy transfer (FRET) J. Biol. Chem. 287, 6797-6809
-
(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
-
9
-
-
33646942269
-
Kinetics and thermodynamics of ligand binding by cytochrome P450 3A4
-
Isin, E. M. and Guengerich, F. P. (2006) Kinetics and thermodynamics of ligand binding by cytochrome P450 3A4 J. Biol. Chem. 281, 9127-9136
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 9127-9136
-
-
Isin, E.M.1
Guengerich, F.P.2
-
10
-
-
84858976886
-
Three-dimensional structure of steroid 21-hydroxylase (cytochrome P450 21A2) with two substrates reveals locations of disease-associated variants
-
Zhao, B., Lei, L., Kagawa, N., Sundaramoorthy, M., Banerjee, S., Nagy, L. D., Guengerich, F. P., and Waterman, M. R. (2012) Three-dimensional structure of steroid 21-hydroxylase (cytochrome P450 21A2) with two substrates reveals locations of disease-associated variants J. Biol. Chem. 287, 10613-10622
-
(2012)
J. Biol. Chem.
, vol.287
, pp. 10613-10622
-
-
Zhao, B.1
Lei, L.2
Kagawa, N.3
Sundaramoorthy, M.4
Banerjee, S.5
Nagy, L.D.6
Guengerich, F.P.7
Waterman, M.R.8
-
11
-
-
33646854265
-
Structure of microsomal cytochrome P450 2B4 complexed with the antifungal drug bifonazole: Insight into P450 conformational plasticity and membrane interaction
-
Zhao, Y., White, M. A., Muralidhara, B. K., Sun, L., Halpert, J. R., and Stout, C. D. (2006) Structure of microsomal cytochrome P450 2B4 complexed with the antifungal drug bifonazole: Insight into P450 conformational plasticity and membrane interaction J. Biol. Chem. 281, 5973-5981
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 5973-5981
-
-
Zhao, Y.1
White, M.A.2
Muralidhara, B.K.3
Sun, L.4
Halpert, J.R.5
Stout, C.D.6
-
12
-
-
84866389270
-
Conformational adaptation of human cytochrome P450 2B6 and rabbit cytochrome P450 2B4 revealed upon binding multiple amlodipine molecules
-
Shah, M. B., Wilderman, P. R., Pascual, J., Zhang, Q., Stout, C. D., and Halpert, J. R. (2012) Conformational adaptation of human cytochrome P450 2B6 and rabbit cytochrome P450 2B4 revealed upon binding multiple amlodipine molecules Biochemistry 51, 7225-7238
-
(2012)
Biochemistry
, vol.51
, pp. 7225-7238
-
-
Shah, M.B.1
Wilderman, P.R.2
Pascual, J.3
Zhang, Q.4
Stout, C.D.5
Halpert, J.R.6
-
13
-
-
34547424283
-
Crystal structures and catalytic mechanism of cytochrome P450 stap that produces the indolocarbazole skeleton
-
Makino, M., Sugimoto, H., Shiro, Y., Asamizu, S., Onaka, H., and Nagano, S. (2007) Crystal structures and catalytic mechanism of cytochrome P450 stap that produces the indolocarbazole skeleton Proc. Natl. Acad. Sci. U.S.A. 104, 11591-11596
-
(2007)
Proc. Natl. Acad. Sci. U.S.A.
, vol.104
, pp. 11591-11596
-
-
Makino, M.1
Sugimoto, H.2
Shiro, Y.3
Asamizu, S.4
Onaka, H.5
Nagano, S.6
-
14
-
-
38949099990
-
Mechanism-based inactivation of human cytochromes P450s: Experimental characterization, reactive intermediates, and clinical implications
-
Hollenberg, P. F., Kent, U. M., and Bumpus, N. N. (2008) Mechanism-based inactivation of human cytochromes P450s: Experimental characterization, reactive intermediates, and clinical implications Chem. Res. Toxicol. 21, 189-205
-
(2008)
Chem. Res. Toxicol.
, vol.21
, pp. 189-205
-
-
Hollenberg, P.F.1
Kent, U.M.2
Bumpus, N.N.3
-
15
-
-
79958024314
-
Structural analysis of mammalian cytochrome P450 2B4 covalently bound to the mechanism-based inactivator tert-butylphenylacetylene: Insight into partial enzymatic activity
-
Gay, S. C., Zhang, H., Wilderman, P. R., Roberts, A. G., Liu, T., Li, S., Lin, H. L., Zhang, Q., Woods, V. L., Jr., Stout, C. D., Hollenberg, P. F., and Halpert, J. R. (2011) Structural analysis of mammalian cytochrome P450 2B4 covalently bound to the mechanism-based inactivator tert-butylphenylacetylene: Insight into partial enzymatic activity Biochemistry 50, 4903-4911
-
(2011)
Biochemistry
, vol.50
, pp. 4903-4911
-
-
Gay, S.C.1
Zhang, H.2
Wilderman, P.R.3
Roberts, A.G.4
Liu, T.5
Li, S.6
Lin, H.L.7
Zhang, Q.8
Woods Jr., V.L.9
Stout, C.D.10
Hollenberg, P.F.11
Halpert, J.R.12
-
16
-
-
70350457938
-
Tert-butylphenylacetylene is a potent mechanism-based inactivator of cytochrome P450 2B4: Inhibition of cytochrome P450 catalysis by steric hindrance
-
Zhang, H., Lin, H. L., Walker, V. J., Hamdane, D., and Hollenberg, P. F. (2009) Tert-butylphenylacetylene is a potent mechanism-based inactivator of cytochrome P450 2B4: Inhibition of cytochrome P450 catalysis by steric hindrance Mol. Pharmacol. 76, 1011-1018
-
(2009)
Mol. Pharmacol.
, vol.76
, pp. 1011-1018
-
-
Zhang, H.1
Lin, H.L.2
Walker, V.J.3
Hamdane, D.4
Hollenberg, P.F.5
-
17
-
-
77957579589
-
A quantitative high-throughput 96-well plate fluorescence assay for mechanism-based inactivators of cytochromes P450 exemplified using CYP2B6
-
Kenaan, C., Zhang, H., and Hollenberg, P. F. (2010) A quantitative high-throughput 96-well plate fluorescence assay for mechanism-based inactivators of cytochromes P450 exemplified using CYP2B6 Nat. Protoc. 5, 1652-1658
-
(2010)
Nat. Protoc.
, vol.5
, pp. 1652-1658
-
-
Kenaan, C.1
Zhang, H.2
Hollenberg, P.F.3
-
18
-
-
0004114084
-
-
CRC Press, Boca Raton, FL
-
Kuby, S. A. (1991) A study of enzymes, Volume I, Enzyme Catalysis, Kinetics, and Substrate Binding, CRC Press, Boca Raton, FL.
-
(1991)
A Study of Enzymes, Volume I, Enzyme Catalysis, Kinetics, and Substrate Binding
-
-
Kuby, S.A.1
-
19
-
-
0030923680
-
Mechanism-based inactivation of cytochrome P450 2B1 by n-benzyl-1-aminobenzotriazole
-
Kent, U. M., Bend, J. R., Chamberlin, B. A., Gage, D. A., and Hollenberg, P. F. (1997) Mechanism-based inactivation of cytochrome P450 2B1 by n-benzyl-1-aminobenzotriazole Chem. Res. Toxicol. 10, 600-608
-
(1997)
Chem. Res. Toxicol.
, vol.10
, pp. 600-608
-
-
Kent, U.M.1
Bend, J.R.2
Chamberlin, B.A.3
Gage, D.A.4
Hollenberg, P.F.5
-
20
-
-
70350028665
-
Effect of conformational dynamics on substrate recognition and specificity as probed by the introduction of a de novo disulfide bond into cytochrome P450 2B1
-
Zhang, H., Kenaan, C., Hamdane, D., Hoa, G. H., and Hollenberg, P. F. (2009) Effect of conformational dynamics on substrate recognition and specificity as probed by the introduction of a de novo disulfide bond into cytochrome P450 2B1 J. Biol. Chem. 284, 25678-25686
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 25678-25686
-
-
Zhang, H.1
Kenaan, C.2
Hamdane, D.3
Hoa, G.H.4
Hollenberg, P.F.5
-
21
-
-
34447508216
-
Phaser crystallographic software
-
McCoy, A. J., Grosse-Kunstleve, R. W., Adams, P. D., Winn, M. D., Storoni, L. C., and Read, R. J. (2007) Phaser crystallographic software J. Appl. Crystallogr. 40, 658-674
-
(2007)
J. Appl. Crystallogr.
, vol.40
, pp. 658-674
-
-
McCoy, A.J.1
Grosse-Kunstleve, R.W.2
Adams, P.D.3
Winn, M.D.4
Storoni, L.C.5
Read, R.J.6
-
22
-
-
14244272868
-
Phenix: Building new software for automated crystallographic structure determination
-
Adams, P. D., Grosse-Kunstleve, R. W., Hung, L. W., Ioerger, T. R., McCoy, A. J., Moriarty, N. W., Read, R. J., Sacchettini, J. C., Sauter, N. K., and Terwilliger, T. C. (2002) Phenix: Building new software for automated crystallographic structure determination Acta Crystallogr. D58, 1948-1954
-
(2002)
Acta Crystallogr.
, vol.58
, pp. 1948-1954
-
-
Adams, P.D.1
Grosse-Kunstleve, R.W.2
Hung, L.W.3
Ioerger, T.R.4
McCoy, A.J.5
Moriarty, N.W.6
Read, R.J.7
Sacchettini, J.C.8
Sauter, N.K.9
Terwilliger, T.C.10
-
23
-
-
77949535720
-
Features and development of Coot
-
Emsley, P., Lohkamp, B., Scott, W., and Cowtan, K. (2010) Features and development of Coot Acta Crystallogr. D66, 486-501
-
(2010)
Acta Crystallogr.
, vol.66
, pp. 486-501
-
-
Emsley, P.1
Lohkamp, B.2
Scott, W.3
Cowtan, K.4
-
24
-
-
84860290638
-
Jligand: A graphical tool for the CCP4 template-restraint library
-
Lebedev, A. A., Young, P., Isupov, M. N., Moroz, O. V., Vagin, A. A., and Murshudov, G. N. (2012) Jligand: A graphical tool for the CCP4 template-restraint library Acta Crystallogr. D68, 431-440
-
(2012)
Acta Crystallogr.
, vol.68
, pp. 431-440
-
-
Lebedev, A.A.1
Young, P.2
Isupov, M.N.3
Moroz, O.V.4
Vagin, A.A.5
Murshudov, G.N.6
-
25
-
-
0000756628
-
The molar light absorption of pyridine ferroprotoporphyrin (pyridine hemochromogen)
-
Paul, K. G., Theorell, H., and Akeson, A. (1953) The molar light absorption of pyridine ferroprotoporphyrin (pyridine hemochromogen) Acta Chem. Scand. 7, 1284-1287
-
(1953)
Acta Chem. Scand.
, vol.7
, pp. 1284-1287
-
-
Paul, K.G.1
Theorell, H.2
Akeson, A.3
-
26
-
-
0030203710
-
Distributed automated docking of flexible ligands to proteins: Parallel applications of Autodock 2.4
-
Morris, G. M., Goodsell, D. S., Huey, R., and Olson, A. J. (1996) Distributed automated docking of flexible ligands to proteins: Parallel applications of Autodock 2.4 J. Comput.-Aided Mol. Des. 10, 293-304
-
(1996)
J. Comput.-Aided Mol. Des.
, vol.10
, pp. 293-304
-
-
Morris, G.M.1
Goodsell, D.S.2
Huey, R.3
Olson, A.J.4
-
27
-
-
23444454552
-
The Amber biomolecular simulation programs
-
Case, D. A., Cheatham, T. E., III, Darden, T., Gohlke, H., Luo, R., Merz, K. M., Jr., Onufriev, A., Simmerling, C., Wang, B., and Woods, R. J. (2005) The Amber biomolecular simulation programs J. Comput. Chem. 26, 1668-1688
-
(2005)
J. Comput. Chem.
, vol.26
, pp. 1668-1688
-
-
Case, D.A.1
Cheatham Iii, T.E.2
Darden, T.3
Gohlke, H.4
Luo, R.5
Merz Jr., K.M.6
Onufriev, A.7
Simmerling, C.8
Wang, B.9
Woods, R.J.10
-
28
-
-
0037464481
-
Construction and assessment of models of CYP2E1: Predictions of metabolism from docking, molecular dynamics, and density functional theoretical calculations
-
Park, J. Y. and Harris, D. (2003) Construction and assessment of models of CYP2E1: Predictions of metabolism from docking, molecular dynamics, and density functional theoretical calculations J. Med. Chem. 46, 1645-1660
-
(2003)
J. Med. Chem.
, vol.46
, pp. 1645-1660
-
-
Park, J.Y.1
Harris, D.2
-
29
-
-
0032499691
-
Analysis of human cytochrome P450 3A4 cooperativity: Construction and characterization of a site-directed mutant that displays hyperbolic steroid hydroxylation kinetics
-
Harlow, G. R. and Halpert, J. R. (1998) Analysis of human cytochrome P450 3A4 cooperativity: Construction and characterization of a site-directed mutant that displays hyperbolic steroid hydroxylation kinetics Proc. Natl. Acad. Sci. U.S.A. 95, 6636-6641
-
(1998)
Proc. Natl. Acad. Sci. U.S.A.
, vol.95
, pp. 6636-6641
-
-
Harlow, G.R.1
Halpert, J.R.2
-
30
-
-
84866461533
-
CYP2E1 metabolism of styrene involves allostery
-
Hartman, J. H., Boysen, G., and Miller, G. P. (2012) CYP2E1 metabolism of styrene involves allostery Drug Metab. Dispos. 40, 1976-1983
-
(2012)
Drug Metab. Dispos.
, vol.40
, pp. 1976-1983
-
-
Hartman, J.H.1
Boysen, G.2
Miller, G.P.3
-
31
-
-
41849114583
-
Cooperativity in oxidation reactions catalyzed by cytochrome P450 1A2: Highly cooperative pyrene hydroxylation and multiphasic kinetics of ligand binding
-
Sohl, C. D., Isin, E. M., Eoff, R. L., Marsch, G. A., Stec, D. F., and Guengerich, F. P. (2008) Cooperativity in oxidation reactions catalyzed by cytochrome P450 1A2: Highly cooperative pyrene hydroxylation and multiphasic kinetics of ligand binding J. Biol. Chem. 283, 7293-7308
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 7293-7308
-
-
Sohl, C.D.1
Isin, E.M.2
Eoff, R.L.3
Marsch, G.A.4
Stec, D.F.5
Guengerich, F.P.6
-
32
-
-
70350443423
-
Mechanism-based inactivation of CYP2B1 and its F-helix mutant by two tert-butyl acetylenic compounds: Covalent modification of prosthetic heme versus apoprotein
-
Lin, H. L., Zhang, H., Noon, K. R., and Hollenberg, P. F. (2009) Mechanism-based inactivation of CYP2B1 and its F-helix mutant by two tert-butyl acetylenic compounds: Covalent modification of prosthetic heme versus apoprotein J. Pharmacol. Exp. Ther. 331, 392-403
-
(2009)
J. Pharmacol. Exp. Ther.
, vol.331
, pp. 392-403
-
-
Lin, H.L.1
Zhang, H.2
Noon, K.R.3
Hollenberg, P.F.4
-
33
-
-
0036151664
-
Effect of 17α-ethynylestradiol on activities of cytochrome P450 2B (P450 2B) enzymes: Characterization of inactivation of P450s 2B1 and 2B6 and identification of metabolites
-
Kent, U. M., Mills, D. E., Rajnarayanan, R. V., Alworth, W. L., and Hollenberg, P. F. (2002) Effect of 17α-ethynylestradiol on activities of cytochrome P450 2B (P450 2B) enzymes: Characterization of inactivation of P450s 2B1 and 2B6 and identification of metabolites J. Pharmacol. Exp. Ther. 300, 549-558
-
(2002)
J. Pharmacol. Exp. Ther.
, vol.300
, pp. 549-558
-
-
Kent, U.M.1
Mills, D.E.2
Rajnarayanan, R.V.3
Alworth, W.L.4
Hollenberg, P.F.5
-
34
-
-
0028930481
-
Mechanism-based enzyme inactivators
-
Silverman, R. B. (1995) Mechanism-based enzyme inactivators Methods Enzymol. 249, 240-283
-
(1995)
Methods Enzymol.
, vol.249
, pp. 240-283
-
-
Silverman, R.B.1
-
35
-
-
3242886389
-
Molprobity: Structure validation and all-atom contact analysis for nucleic acids and their complexes
-
Davis, I. W., Murray, L. W., Richardson, J. S., and Richardson, D. C. (2004) Molprobity: Structure validation and all-atom contact analysis for nucleic acids and their complexes Nucleic Acids Res. 32, W615-W619
-
(2004)
Nucleic Acids Res.
, vol.32
-
-
Davis, I.W.1
Murray, L.W.2
Richardson, J.S.3
Richardson, D.C.4
-
36
-
-
3042553224
-
Structure of mammalian cytochrome P450 2B4 complexed with 4-(4-chlorophenyl)imidazole at 1.9-Å resolution: Insight into the range of P450 conformations and the coordination of redox partner binding
-
Scott, E. E., White, M. A., He, Y. A., Johnson, E. F., Stout, C. D., and Halpert, J. R. (2004) Structure of mammalian cytochrome P450 2B4 complexed with 4-(4-chlorophenyl)imidazole at 1.9-Å resolution: Insight into the range of P450 conformations and the coordination of redox partner binding J. Biol. Chem. 279, 27294-27301
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 27294-27301
-
-
Scott, E.E.1
White, M.A.2
He, Y.A.3
Johnson, E.F.4
Stout, C.D.5
Halpert, J.R.6
-
37
-
-
0032479307
-
Identification of the binding site on cytochrome P450 2B4 for cytochrome b5 and cytochrome P450 reductase
-
Bridges, A., Gruenke, L., Chang, Y. T., Vakser, I. A., Loew, G., and Waskell, L. (1998) Identification of the binding site on cytochrome P450 2B4 for cytochrome b5 and cytochrome P450 reductase J. Biol. Chem. 273, 17036-17049
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 17036-17049
-
-
Bridges, A.1
Gruenke, L.2
Chang, Y.T.3
Vakser, I.A.4
Loew, G.5
Waskell, L.6
-
38
-
-
76149134076
-
Defining the structural consequences of mechanism-based inactivation of mammalian cytochrome P450 2B4 using resonance Raman spectroscopy
-
Mak, P. J., Zhang, H., Hollenberg, P. F., and Kincaid, J. R. (2010) Defining the structural consequences of mechanism-based inactivation of mammalian cytochrome P450 2B4 using resonance Raman spectroscopy J. Am. Chem. Soc. 132, 1494-1495
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 1494-1495
-
-
Mak, P.J.1
Zhang, H.2
Hollenberg, P.F.3
Kincaid, J.R.4
-
39
-
-
79951566203
-
Targeting of the highly conserved threonine 302 residue of cytochromes P450 2B family during mechanism-based inactivation by aryl acetylenes
-
Zhang, H., Lin, H. L., Kenaan, C., and Hollenberg, P. F. (2011) Targeting of the highly conserved threonine 302 residue of cytochromes P450 2B family during mechanism-based inactivation by aryl acetylenes Arch. Biochem. Biophys. 507, 135-143
-
(2011)
Arch. Biochem. Biophys.
, vol.507
, pp. 135-143
-
-
Zhang, H.1
Lin, H.L.2
Kenaan, C.3
Hollenberg, P.F.4
-
40
-
-
0038637141
-
Threonine-205 in the F helix of P450 2B1 contributes to androgen 16β-hydroxylation activity and mechanism-based inactivation
-
Lin, H. L., Zhang, H., Waskell, L., and Hollenberg, P. F. (2003) Threonine-205 in the F helix of P450 2B1 contributes to androgen 16β-hydroxylation activity and mechanism-based inactivation J. Pharmacol. Exp. Ther. 306, 744-751
-
(2003)
J. Pharmacol. Exp. Ther.
, vol.306
, pp. 744-751
-
-
Lin, H.L.1
Zhang, H.2
Waskell, L.3
Hollenberg, P.F.4
-
41
-
-
84863685665
-
Conformational dynamics of CYP3A4 demonstrate the important role of Arg212 coupled with the opening of ingress, egress and solvent channels to dehydrogenation of 4-hydroxy-tamoxifen
-
Shahrokh, K., Cheatham, T. E., III, and Yost, G. S. (2012) Conformational dynamics of CYP3A4 demonstrate the important role of Arg212 coupled with the opening of ingress, egress and solvent channels to dehydrogenation of 4-hydroxy-tamoxifen Biochim. Biophys. Acta 1820, 1605-1617
-
(2012)
Biochim. Biophys. Acta
, vol.1820
, pp. 1605-1617
-
-
Shahrokh, K.1
Cheatham Iii, T.E.2
Yost, G.S.3
-
43
-
-
0031041652
-
Alanine-scanning mutagenesis of a putative substrate recognition site in human cytochrome P450 3A4. Role of residues 210 and 211 in flavonoid activation and substrate specificity
-
Harlow, G. R. and Halpert, J. R. (1997) Alanine-scanning mutagenesis of a putative substrate recognition site in human cytochrome P450 3A4. Role of residues 210 and 211 in flavonoid activation and substrate specificity J. Biol. Chem. 272, 5396-5402
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 5396-5402
-
-
Harlow, G.R.1
Halpert, J.R.2
-
44
-
-
0028264896
-
Structural determinants of cytochrome P450 2B1 specificity: Evidence for five substrate recognition sites
-
He, Y., Luo, Z., Klekotka, P. A., Burnett, V. L., and Halpert, J. R. (1994) Structural determinants of cytochrome P450 2B1 specificity: Evidence for five substrate recognition sites Biochemistry 33, 4419-4424
-
(1994)
Biochemistry
, vol.33
, pp. 4419-4424
-
-
He, Y.1
Luo, Z.2
Klekotka, P.A.3
Burnett, V.L.4
Halpert, J.R.5
-
45
-
-
0026801607
-
Role of residue 478 as a determinant of the substrate specificity of cytochrome P450 2B1
-
He, Y. A., Balfour, C. A., Kedzie, K. M., and Halpert, J. R. (1992) Role of residue 478 as a determinant of the substrate specificity of cytochrome P450 2B1 Biochemistry 31, 9220-9226
-
(1992)
Biochemistry
, vol.31
, pp. 9220-9226
-
-
He, Y.A.1
Balfour, C.A.2
Kedzie, K.M.3
Halpert, J.R.4
-
46
-
-
80054782748
-
Mechanism-based inactivation of human cytochrome P450 2B6 by clopidogrel: Involvement of both covalent modification of cysteinyl residue 475 and loss of heme
-
Zhang, H., Amunugama, H., Ney, S., Cooper, N., and Hollenberg, P. F. (2011) Mechanism-based inactivation of human cytochrome P450 2B6 by clopidogrel: Involvement of both covalent modification of cysteinyl residue 475 and loss of heme Mol. Pharmacol. 80, 839-847
-
(2011)
Mol. Pharmacol.
, vol.80
, pp. 839-847
-
-
Zhang, H.1
Amunugama, H.2
Ney, S.3
Cooper, N.4
Hollenberg, P.F.5
-
47
-
-
0345687195
-
An open conformation of mammalian cytochrome P450 2B4 at 1.6-Å resolution
-
Scott, E. E., He, Y. A., Wester, M. R., White, M. A., Chin, C. C., Halpert, J. R., Johnson, E. F., and Stout, C. D. (2003) An open conformation of mammalian cytochrome P450 2B4 at 1.6-Å resolution Proc. Natl. Acad. Sci. U.S.A. 100, 13196-13201
-
(2003)
Proc. Natl. Acad. Sci. U.S.A.
, vol.100
, pp. 13196-13201
-
-
Scott, E.E.1
He, Y.A.2
Wester, M.R.3
White, M.A.4
Chin, C.C.5
Halpert, J.R.6
Johnson, E.F.7
Stout, C.D.8
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