-
1
-
-
54949144309
-
Functional pharmacogenetics/genomics of human cytochromes P450 involved in drug biotransformation
-
Zanger, U. M., Turpeinen, M., Klein, K., and Schwab, M. (2008) Functional pharmacogenetics/genomics of human cytochromes P450 involved in drug biotransformation. Anal. Bioanal. Chem. 392, 1093-1108
-
(2008)
Anal. Bioanal. Chem.
, vol.392
, pp. 1093-1108
-
-
Zanger, U.M.1
Turpeinen, M.2
Klein, K.3
Schwab, M.4
-
2
-
-
77952301353
-
Pharmacogenetic biomarkers as tools for improved drug therapy; emphasis on the cytochrome P450 system
-
Ingelman-Sundberg, M., and Sim, S. C. (2010) Pharmacogenetic biomarkers as tools for improved drug therapy; emphasis on the cytochrome P450 system. Biochem. Biophys. Res. Commun. 396, 90-94
-
(2010)
Biochem. Biophys. Res. Commun.
, vol.396
, pp. 90-94
-
-
Ingelman-Sundberg, M.1
Sim, S.C.2
-
3
-
-
0028279041
-
Evidence that CYP2C19 is the major (S)-mephenytoin 4'-hydroxylase in humans
-
Goldstein, J. A., Faletto, M. B., Romkes-Sparks, M., Sullivan, T., Kitareewan, S., Raucy, J. L., Lasker, J. M., and Ghanayem, B. I. (1994) Evidence that CYP2C19 is the major (S)-mephenytoin 4′-hydroxylase in humans. Biochemistry 33, 1743-1752 (Pubitemid 24089701)
-
(1994)
Biochemistry
, vol.33
, Issue.7
, pp. 1743-1752
-
-
Goldstein, J.A.1
Faletto, M.B.2
Romkes-Sparks, M.3
Sullivan, T.4
Kitareewan, S.5
Raucy, J.L.6
Lasker, J.M.7
Ghanayem, B.I.8
-
4
-
-
36148976077
-
Influence of cytochrome P450 polymorphisms on drug therapies: Pharmacogenetic, pharmacoepigenetic and clinical aspects
-
DOI 10.1016/j.pharmthera.2007.09.004, PII S016372580700201X
-
Ingelman-Sundberg, M., Sim, S. C., Gomez, A., and Rodriguez-Antona, C. (2007) Influence of cytochrome P450 polymorphisms on drug therapies. Pharmacogenetic, pharmacoepigenetic, and clinical aspects. Pharmacol. Ther. 116, 496-526 (Pubitemid 350116943)
-
(2007)
Pharmacology and Therapeutics
, vol.116
, Issue.3
, pp. 496-526
-
-
Ingelman-Sundberg, M.1
Sim, S.C.2
Gomez, A.3
Rodriguez-Antona, C.4
-
5
-
-
48549093980
-
Clinically relevant pharmacokinetic drug interactions with second generation antidepressants. An update
-
Spina, E., Santoro, V., and D'Arrigo, C. (2008) Clinically relevant pharmacokinetic drug interactions with second generation antidepressants. An update. Clin. Ther. 30, 1206-1227
-
(2008)
Clin. Ther.
, vol.30
, pp. 1206-1227
-
-
Spina, E.1
Santoro, V.2
D'Arrigo, C.3
-
6
-
-
53249121028
-
Proton pump inhibitors. An update of their clinical use and pharmacokinetics
-
Shi, S., and Klotz, U. (2008) Proton pump inhibitors. An update of their clinical use and pharmacokinetics. Eur. J. Clin. Pharmacol. 64, 935-951
-
(2008)
Eur. J. Clin. Pharmacol.
, vol.64
, pp. 935-951
-
-
Shi, S.1
Klotz, U.2
-
7
-
-
84455194048
-
Effects of omeprazole and genetic polymorphism of CYP2C19 on the clopidogrel active metabolite
-
Boulenc, X., Djebli, N., Shi, J., Perrin, L., Brian, W., Van Horn, R., and Hurbin, F. (2012) Effects of omeprazole and genetic polymorphism of CYP2C19 on the clopidogrel active metabolite. Drug Metab. Dispos. 40, 187-197
-
(2012)
Drug Metab. Dispos.
, vol.40
, pp. 187-197
-
-
Boulenc, X.1
Djebli, N.2
Shi, J.3
Perrin, L.4
Brian, W.5
Van Horn, R.6
Hurbin, F.7
-
8
-
-
84865180550
-
Evaluation of six proton pump inhibitors as inhibitors of various human cytochromes P450. Focus on cytochrome P450 2C19
-
Zvyaga, T., Chang, S. Y., Chen, C., Yang, Z., Vuppugalla, R., Hurley, J., Thorndike, D., Wagner, A., Chimalakonda, A., and Rodrigues, A. D. (2012) Evaluation of six proton pump inhibitors as inhibitors of various human cytochromes P450. Focus on cytochrome P450 2C19. Drug Metab. Dispos. 40, 1698-1711
-
(2012)
Drug Metab. Dispos.
, vol.40
, pp. 1698-1711
-
-
Zvyaga, T.1
Chang, S.Y.2
Chen, C.3
Yang, Z.4
Vuppugalla, R.5
Hurley, J.6
Thorndike, D.7
Wagner, A.8
Chimalakonda, A.9
Rodrigues, A.D.10
-
9
-
-
70350325443
-
Comparison of mechanism-based inhibition of human cytochrome P450 2C19 by ticlopidine, clopidogrel, and prasugrel
-
Nishiya, Y., Hagihara, K., Kurihara, A., Okudaira, N., Farid, N. A., Okazaki, O., and Ikeda, T. (2009) Comparison of mechanism-based inhibition of human cytochrome P450 2C19 by ticlopidine, clopidogrel, and prasugrel. Xenobiotica 39, 836-843
-
(2009)
Xenobiotica
, vol.39
, pp. 836-843
-
-
Nishiya, Y.1
Hagihara, K.2
Kurihara, A.3
Okudaira, N.4
Farid, N.A.5
Okazaki, O.6
Ikeda, T.7
-
10
-
-
62249112083
-
Metabolic oxidative cleavage of thioesters. Evidence for the formation of sulfenic acid intermediates in the bioactivation of the antithrombotic prodrugs ticlopidine and clopidogrel
-
Dansette, P. M., Libraire, J., Bertho, G., and Mansuy, D. (2009) Metabolic oxidative cleavage of thioesters. Evidence for the formation of sulfenic acid intermediates in the bioactivation of the antithrombotic prodrugs ticlopidine and clopidogrel. Chem. Res. Toxicol. 22, 369-373
-
(2009)
Chem. Res. Toxicol.
, vol.22
, pp. 369-373
-
-
Dansette, P.M.1
Libraire, J.2
Bertho, G.3
Mansuy, D.4
-
11
-
-
73149119363
-
Identification of the human cytochrome P450 enzymes involved in the two oxidative steps in the bioactivation of clopidogrel to its pharmacologically active metabolite
-
Kazui, M., Nishiya, Y., Ishizuka, T., Hagihara, K., Farid, N. A., Okazaki, O., Ikeda, T., and Kurihara, A. (2010) Identification of the human cytochrome P450 enzymes involved in the two oxidative steps in the bioactivation of clopidogrel to its pharmacologically active metabolite. Drug Metab. Dispos. 38, 92-99
-
(2010)
Drug Metab. Dispos.
, vol.38
, pp. 92-99
-
-
Kazui, M.1
Nishiya, Y.2
Ishizuka, T.3
Hagihara, K.4
Farid, N.A.5
Okazaki, O.6
Ikeda, T.7
Kurihara, A.8
-
12
-
-
84859747728
-
Cytochromes P450 catalyze both steps of the major pathway of clopidogrel bioactivation, whereas paraoxonase catalyzes the formation of a minor thiol metabolite isomer
-
Dansette, P. M., Rosi, J., Bertho, G., and Mansuy, D. (2012) Cytochromes P450 catalyze both steps of the major pathway of clopidogrel bioactivation, whereas paraoxonase catalyzes the formation of a minor thiol metabolite isomer. Chem. Res. Toxicol. 25, 348-356
-
(2012)
Chem. Res. Toxicol.
, vol.25
, pp. 348-356
-
-
Dansette, P.M.1
Rosi, J.2
Bertho, G.3
Mansuy, D.4
-
13
-
-
58749090547
-
Genetic determinants of response to clopidogrel and cardiovascular events
-
French Registry of Acute ST-Elevation and Non-ST-Elevation Myocardial Infarction (FAST-MI) Investigators
-
Simon, T., Verstuyft, C., Mary-Krause, M., Quteineh, L., Drouet, E., Méneveau, N., Steg, P. G., Ferrières, J., Danchin, N., Becquemont, L., and French Registry of Acute ST-Elevation and Non-ST-Elevation Myocardial Infarction (FAST-MI) Investigators (2009) Genetic determinants of response to clopidogrel and cardiovascular events. N. Engl. J. Med. 360, 363-375
-
(2009)
N. Engl. J. Med.
, vol.360
, pp. 363-375
-
-
Simon, T.1
Verstuyft, C.2
Mary-Krause, M.3
Quteineh, L.4
Drouet, E.5
Méneveau, N.6
Steg, P.G.7
Ferrières, J.8
Danchin, N.9
Becquemont, L.10
-
14
-
-
84862249165
-
Recent advances in the pharmacogenetics of clopidogrel
-
Cuisset, T., Morange, P. E., and Alessi, M. C. (2012) Recent advances in the pharmacogenetics of clopidogrel. Hum. Genet. 5, 693-664
-
(2012)
Hum. Genet.
, vol.5
, pp. 693-1664
-
-
Cuisset, T.1
Morange, P.E.2
Alessi, M.C.3
-
15
-
-
77956353400
-
Protective effect of the CYP2C19*17 polymorphism with increased activation of clopidogrel on cardiovascular events
-
Tiroch, K. A., Sibbing, D., Koch, W., Roosen-Runge, T., Mehilli, J., Schömig, A., and Kastrati, A. (2010) Protective effect of the CYP2C19*17 polymorphism with increased activation of clopidogrel on cardiovascular events. Am. Heart J. 160, 506-512
-
(2010)
Am. Heart J.
, vol.160
, pp. 506-512
-
-
Tiroch, K.A.1
Sibbing, D.2
Koch, W.3
Roosen-Runge, T.4
Mehilli, J.5
Schömig, A.6
Kastrati, A.7
-
16
-
-
76349098199
-
Cytochrome 2C19*17 allelic variant, platelet aggregation, bleeding events, and stent thrombosis in clopidogrel-treated patients with coronary stent placement
-
Sibbing, D., Koch, W., Gebhard, D., Schuster, T., Braun, S., Stegherr, J., Morath, T., Schömig, A., von Beckerath, N., and Kastrati, A. (2010) Cytochrome 2C19*17 allelic variant, platelet aggregation, bleeding events, and stent thrombosis in clopidogrel-treated patients with coronary stent placement. Circulation 121, 512-518
-
(2010)
Circulation
, vol.121
, pp. 512-518
-
-
Sibbing, D.1
Koch, W.2
Gebhard, D.3
Schuster, T.4
Braun, S.5
Stegherr, J.6
Morath, T.7
Schömig, A.8
Von Beckerath, N.9
Kastrati, A.10
-
17
-
-
1542364450
-
Structure of human microsomal cytochrome P450 2C8: Evidence for a peripheral fatty acid binding site
-
DOI 10.1074/jbc.M312516200
-
Schoch, G. A., Yano, J. K., Wester, M. R., Griffin, K. J., Stout, C. D., and Johnson, E. F. (2004) Structure of human microsomal cytochrome P450 2C8. Evidence for a peripheral fatty acid-binding site. J. Biol. Chem. 279, 9497-9503 (Pubitemid 38296017)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.10
, pp. 9497-9503
-
-
Schoch, G.A.1
Yano, J.K.2
Wester, M.R.3
Griffin, K.J.4
Stout, C.D.5
Johnson, E.F.6
-
18
-
-
47749092044
-
Determinants of cytochrome P450 2C8 substrate binding. Structures of complexes with montelukast, troglitazone, felodipine, and 9-cis-retinoic acid
-
Schoch, G. A., Yano, J. K., Sansen, S., Dansette, P. M., Stout, C. D., and Johnson, E. F. (2008) Determinants of cytochrome P450 2C8 substrate binding. Structures of complexes with montelukast, troglitazone, felodipine, and 9-cis-retinoic acid. J. Biol. Chem. 283, 17227-17237
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 17227-17237
-
-
Schoch, G.A.1
Yano, J.K.2
Sansen, S.3
Dansette, P.M.4
Stout, C.D.5
Johnson, E.F.6
-
19
-
-
0042265520
-
Crystal structure of human cytochrome P450 2C9 with bound warfarin
-
DOI 10.1038/nature01862
-
Williams, P. A., Cosme, J., Ward, A., Angove, H. C., Matak Vinkoviæ, D., and Jhoti, H. (2003) Crystal structure of human cytochrome P450 2C9 with bound warfarin. Nature 424, 464-468 (Pubitemid 36917499)
-
(2003)
Nature
, vol.424
, Issue.6947
, pp. 464-468
-
-
Williams, P.A.1
Cosme, J.2
Ward, A.3
Angove, H.C.4
Vinkovic, D.M.5
Jhoti, H.6
-
20
-
-
4143143372
-
The structure of human cytochrome P450 2C9 complexed with flurbiprofen at 2.0-Å resolution
-
DOI 10.1074/jbc.M405427200
-
Wester, M. R., Yano, J. K., Schoch, G. A., Yang, C., Griffin, K. J., Stout, C. D., and Johnson, E. F. (2004) The structure of human microsomal cytochrome P450 2C9 complexed with flurbiprofen at 2.0 Å resolution. J. Biol. Chem. 279, 35630-35637 (Pubitemid 39100565)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.34
, pp. 35630-35637
-
-
Wester, M.R.1
Yano, J.K.2
Schoch, G.A.3
Yang, C.4
Griffin, K.J.5
Stout, C.D.6
Johnson, E.F.7
-
21
-
-
15844394255
-
Identification of residues 99, 220, and 221 of human cytochrome P450 2C19 as key determinants of omeprazole hydroxylase activity
-
DOI 10.1074/jbc.271.21.12496
-
Ibeanu, G. C., Ghanayem, B. I., Linko, P., Li, L., Pederson, L. G., and Goldstein, J. A. (1996) Identification of residues 99, 220, and 221 of human cytochrome P450 2C19 as key determinants of omeprazole hydroxylase activity. J. Biol. Chem. 271, 12496-12501 (Pubitemid 26160921)
-
(1996)
Journal of Biological Chemistry
, vol.271
, Issue.21
, pp. 12496-12501
-
-
Ibeanu, G.C.1
Ghanayem, B.I.2
Linko, P.3
Li, L.4
Pedersen, L.G.5
Goldstein, J.A.6
-
22
-
-
0032542015
-
Identification of amino acid substitutions that confer a high affinity for sulfaphenazole binding and a high catalytic efficiency for warfarin metabolism to P450 2C19
-
DOI 10.1021/bi981704c
-
Jung, F., Griffin, K. J., Song, W., Richardson, T. H., Yang, M., and Johnson, E. F. (1998) Identification of amino acid substitutions that confer a high affinity for sulfaphenazole binding and a high catalytic efficiency for warfarin metabolism to P450 2C19. Biochemistry 37, 16270-16279 (Pubitemid 28536263)
-
(1998)
Biochemistry
, vol.37
, Issue.46
, pp. 16270-16279
-
-
Jung, F.1
Griffin, K.J.2
Song, W.3
Richardson, T.H.4
Yang, M.5
Johnson, E.F.6
-
23
-
-
0032530108
-
Identification of residues 286 and 289 as critical for conferring substrate specificity of human CYP2C9 for diclofenac and ibuprofen
-
DOI 10.1006/abbi.1998.0826
-
Klose, T. S., Ibeanu, G. C., Ghanayem, B. I., Pedersen, L. G., Li, L., Hall, S. D., and Goldstein, J. A. (1998) Identification of residues 286 and 289 as critical for conferring substrate specificity of human CYP2C9 for diclofenac and ibuprofen. Arch. Biochem. Biophys. 357, 240-248 (Pubitemid 28419205)
-
(1998)
Archives of Biochemistry and Biophysics
, vol.357
, Issue.2
, pp. 240-248
-
-
Klose, T.S.1
Ibeanu, G.C.2
Ghanayem, B.I.3
Pedersen, L.G.4
Li, L.5
Hall, S.D.6
Goldstein, J.A.7
-
24
-
-
0035916224
-
Identification of human CYP2C19 residues that confer S-mephenytoin 4́-hydroxylation activity to CYP2C9
-
DOI 10.1021/bi001678u
-
Tsao, C. C., Wester, M. R., Ghanayem, B., Coulter, S. J., Chanas, B., Johnson, E. F., and Goldstein, J. A. (2001) Identification of human CYP2C19 residues that confer S-mephenytoin 4′-hydroxylation activity to CYP2C9. Biochemistry 40, 1937-1944 (Pubitemid 32165662)
-
(2001)
Biochemistry
, vol.40
, Issue.7
, pp. 1937-1944
-
-
Tsao, C.-C.1
Wester, M.R.2
Ghanayem, B.3
Coulter, S.J.4
Chanas, B.5
Johnson, E.F.6
Goldstein, J.A.7
-
25
-
-
52949150913
-
Important amino acid residues that confer CYP2C19 selective activity to CYP2C9
-
Wada, Y., Mitsuda, M., Ishihara, Y., Watanabe, M., Iwasaki, M., and Asahi, S. (2008) Important amino acid residues that confer CYP2C19 selective activity to CYP2C9. J. Biochem. 144, 323-333
-
(2008)
J. Biochem.
, vol.144
, pp. 323-333
-
-
Wada, Y.1
Mitsuda, M.2
Ishihara, Y.3
Watanabe, M.4
Iwasaki, M.5
Asahi, S.6
-
26
-
-
11144223711
-
Charge and substituent effects on affinity and metabolism of benzbromarone-based CYP2C19 inhibitors
-
DOI 10.1021/jm049605m
-
Locuson, C. W., 2nd, Suzuki, H., Rettie, A. E., and Jones, J. P. (2004) Charge and substituent effects on affinity and metabolism of benzbromarone-based CYP2C19 inhibitors. J. Med. Chem. 47, 6768-6776 (Pubitemid 40053765)
-
(2004)
Journal of Medicinal Chemistry
, vol.47
, Issue.27
, pp. 6768-6776
-
-
Locuson II, C.W.1
Suzuki, H.2
Rettie, A.E.3
Jones, J.P.4
-
27
-
-
0028846823
-
Universal approach to the expression of human and rabbit cytochrome P450s of the 2C subfamily in Escherichia coli
-
Richardson, T. H., Jung, F., Griffin, K. J., Wester, M., Raucy, J. L., Kemper, B., Bornheim, L. M., Hassett, C., Omiecinski, C. J., and Johnson, E. F. (1995) Universal approach to the expression of human and rabbit cytochrome P450s of the 2C subfamily in Escherichia coli. Arch. Biochem. Biophys. 323, 87-96
-
(1995)
Arch. Biochem. Biophys.
, vol.323
, pp. 87-96
-
-
Richardson, T.H.1
Jung, F.2
Griffin, K.J.3
Wester, M.4
Raucy, J.L.5
Kemper, B.6
Bornheim, L.M.7
Hassett, C.8
Omiecinski, C.J.9
Johnson, E.F.10
-
28
-
-
12244261584
-
Identification and functional characterization of new potentially defective alleles of human CYP2C19
-
DOI 10.1097/00008571-200212000-00004
-
Blaisdell, J., Mohrenweiser, H., Jackson, J., Ferguson, S., Coulter, S., Chanas, B., Xi, T., Ghanayem, B., and Goldstein, J. A. (2002) Identification and functional characterization of new potentially defective alleles of human CYP2C19. Pharmacogenetics 12, 703-711 (Pubitemid 36054937)
-
(2002)
Pharmacogenetics
, vol.12
, Issue.9
, pp. 703-711
-
-
Blaisdell, J.1
Mohrenweiser, H.2
Jackson, J.3
Ferguson, S.4
Coulter, S.5
Chanas, B.6
Xi, T.7
Ghanayem, B.8
Goldstein, J.A.9
-
29
-
-
79955036726
-
Evaluation of the effects of 20 nonsynonymous single nucleotide polymorphisms of CYP2C19 on S-mephenytoin 4′-hydroxylation and omeprazole 5′-hydroxylation
-
Wang, H., An, N., Wang, H., Gao, Y., Liu, D., Bian, T., Zhu, J., and Chen, C. (2011) Evaluation of the effects of 20 nonsynonymous single nucleotide polymorphisms of CYP2C19 on S-mephenytoin 4′-hydroxylation and omeprazole 5′-hydroxylation. Drug Metab. Dispos. 39, 830-837
-
(2011)
Drug Metab. Dispos.
, vol.39
, pp. 830-837
-
-
Wang, H.1
An, N.2
Wang, H.3
Gao, Y.4
Liu, D.5
Bian, T.6
Zhu, J.7
Chen, C.8
-
30
-
-
0034723195
-
Engineering microsomal cytochrome P450 2C5 to be a soluble, monomeric enzyme: Mutations that alter aggregation, phospholipid dependence of catalysis, and membrane binding
-
DOI 10.1074/jbc.275.4.2545
-
Cosme, J., and Johnson, E. F. (2000) Engineering microsomal cytochrome P450 2C5 to be a soluble, monomeric enzyme. Mutations that alter aggregation, phospholipid dependence of catalysis, and membrane binding. J. Biol. Chem. 275, 2545-2553 (Pubitemid 30082019)
-
(2000)
Journal of Biological Chemistry
, vol.275
, Issue.4
, pp. 2545-2553
-
-
Cosme, J.1
Johnson, E.F.2
-
31
-
-
34347235844
-
Adaptations for the oxidation of polycyclic aromatic hydrocarbons exhibited by the structure of human P450 1A2
-
DOI 10.1074/jbc.M611692200
-
Sansen, S., Yano, J. K., Reynald, R. L., Schoch, G. A., Griffin, K. J., Stout, C. D., and Johnson, E. F. (2007) Adaptations for the oxidation of polycyclic aromatic hydrocarbons exhibited by the structure of human P450 1A2. J. Biol. Chem. 282, 14348-14355 (Pubitemid 47100434)
-
(2007)
Journal of Biological Chemistry
, vol.282
, Issue.19
, pp. 14348-14355
-
-
Sansen, S.1
Yano, J.K.2
Reynald, R.L.3
Schoch, G.A.4
Griffin, K.J.5
Stout, C.D.6
Johnson, E.F.7
-
32
-
-
50449100139
-
The carbon monoxide-binding pigment of liver microsomes. II. Solubilization, purification, and properties
-
Omura, T., and Sato, R. (1964) The carbon monoxide-binding pigment of liver microsomes. II. Solubilization, purification, and properties. J. Biol. Chem. 239, 2379-2385
-
(1964)
J. Biol. Chem.
, vol.239
, pp. 2379-2385
-
-
Omura, T.1
Sato, R.2
-
34
-
-
23844546311
-
Likelihood-enhanced fast translation functions
-
DOI 10.1107/S0907444905001617
-
McCoy, A. J., Grosse-Kunstleve, R. W., Storoni, L. C., and Read, R. J. (2005) Likelihood-enhanced fast translation functions. Acta Crystallogr. D Biol. Crystallogr. 61, 458-464 (Pubitemid 43934606)
-
(2005)
Acta Crystallographica Section D: Biological Crystallography
, vol.61
, Issue.4
, pp. 458-464
-
-
McCoy, A.J.1
Grosse-Kunstleve, R.W.2
Storoni, L.C.3
Read, R.J.4
-
36
-
-
3543012707
-
Crystallography and NMR system. A new software suite for macromolecular structure determination
-
Brünger, A. T., Adams, P. D., Clore, G. M., DeLano, W. L., Gros, P., Grosse-Kunstleve, R. W., Jiang, J. S., Kuszewski, J., Nilges, M., Pannu, N. S., Read, R. J., Rice, L. M., Simonson, T., and Warren, G. L. (1998) Crystallography and NMR system. A new software suite for macromolecular structure determination. Acta Crystallogr. D Biol. Crystallogr. 54, 905-921
-
(1998)
Acta Crystallogr. D Biol. Crystallogr.
, vol.54
, pp. 905-921
-
-
Brünger, A.T.1
Adams, P.D.2
Clore, G.M.3
DeLano, W.L.4
Gros, P.5
Grosse-Kunstleve, R.W.6
Jiang, J.S.7
Kuszewski, J.8
Nilges, M.9
Pannu, N.S.10
Read, R.J.11
Rice, L.M.12
Simonson, T.13
Warren, G.L.14
-
37
-
-
0027995683
-
Detection, delineation, measurement and display of cavities in macromolecular structures
-
DOI 10.1107/S0907444993011333
-
Kleywegt, G. J., and Jones, T. A. (1994) Detection, delineation, measurement, and display of cavities in macromolecular structures. Acta Crystallogr. D Biol. Crystallogr. 50, 178-185 (Pubitemid 2054290)
-
(1994)
Acta Crystallographica Section D: Biological Crystallography
, vol.50
, Issue.2
, pp. 178-185
-
-
Kleywegt, G.J.1
Alwyn, J.T.2
-
38
-
-
84859500879
-
Crystal structure of human cytochrome P450 2D6 with prinomastat bound
-
Wang, A., Savas, U., Hsu, M. H., Stout, C. D., and Johnson, E. F. (2012) Crystal structure of human cytochrome P450 2D6 with prinomastat bound. J. Biol. Chem. 287, 10834-10843
-
(2012)
J. Biol. Chem.
, vol.287
, pp. 10834-10843
-
-
Wang, A.1
Savas, U.2
Hsu, M.H.3
Stout, C.D.4
Johnson, E.F.5
-
39
-
-
66749089988
-
CYP2C9 amino acid residues influencing phenytoin turnover and metabolite regio- and stereochemistry
-
Mosher, C. M., Tai, G., and Rettie, A. E. (2009) CYP2C9 amino acid residues influencing phenytoin turnover and metabolite regio- and stereochemistry. J. Pharmacol. Exp. Ther. 329, 938-944
-
(2009)
J. Pharmacol. Exp. Ther.
, vol.329
, pp. 938-944
-
-
Mosher, C.M.1
Tai, G.2
Rettie, A.E.3
-
40
-
-
0037636387
-
A new class of CYP2C9 inhibitors: Probing 2C9 specificity with high-affinity benzbromarone derivatives
-
DOI 10.1124/dmd.31.7.967
-
Locuson, C. W., 2nd, Wahlstrom, J. L., Rock, D. A., Rock, D. A., and Jones, J. P. (2003)Anew class of CYP2C9 inhibitors. Probing 2C9 specificity with high affinity benzbromarone derivatives. Drug Metab. Dispos. 31, 967-971 (Pubitemid 36759068)
-
(2003)
Drug Metabolism and Disposition
, vol.31
, Issue.7
, pp. 967-971
-
-
Locuson II, C.W.1
Wahlstrom, J.L.2
Rock, D.A.3
Rock, D.A.4
Jones, J.P.5
-
41
-
-
0034696808
-
Arginines 97 and 108 in CYP2C9 are important determinants of the catalytic function
-
DOI 10.1006/bbrc.2000.2538
-
Ridderström, M., Masimirembwa, C., Trump-Kallmeyer, S., Ahlefelt, M., Otter, C., and Andersson, T. B. (2000) Arginines 97 and 108 in CYP2C9 are important determinants of the catalytic function. Biochem. Biophys. Res. Commun. 270, 983-987 (Pubitemid 30444818)
-
(2000)
Biochemical and Biophysical Research Communications
, vol.270
, Issue.3
, pp. 983-987
-
-
Ridderstrom, M.1
Masimirembwa, C.2
Trump-Kallmeyer, S.3
Ahlefelt, M.4
Otter, C.5
Andersson, T.B.6
-
42
-
-
1842428730
-
Differential Roles of Arg97, Asp293, and Arg108 in Enzyme Stability and Substrate Specificity of CYP2C9
-
DOI 10.1124/mol.65.4.842
-
Dickmann, L. J., Locuson, C. W., Jones, J. P., and Rettie, A. E. (2004) Differential roles of Arg97, Asp293, and Arg108 in enzyme stability and substrate specificity of CYP2C9. Mol. Pharmacol. 65, 842-850 (Pubitemid 38420489)
-
(2004)
Molecular Pharmacology
, vol.65
, Issue.4
, pp. 842-850
-
-
Dickmann, L.J.1
Locuson, C.W.2
Jones, J.P.3
Rettie, A.E.4
-
43
-
-
0037672866
-
Structure of a substrate complex of mammalian cytochrome P450 2C5 at 2.3 Å resolution: Evidence for multiple substrate binding modes
-
DOI 10.1021/bi0273922
-
Wester, M. R., Johnson, E. F., Marques-Soares, C., Dansette, P. M., Mansuy, D., and Stout, C. D. (2003) The structure of a substrate complex of mammalian cytochrome P450 2C5 at 2.3 Å resolution. Evidence for multiple substrate binding modes. Biochemistry 42, 6370-6379 (Pubitemid 36665811)
-
(2003)
Biochemistry
, vol.42
, Issue.21
, pp. 6370-6379
-
-
Wester, M.R.1
Johnson, E.F.2
Marques-Soares, C.3
Dansette, P.M.4
Mansuy, D.5
Stout, C.D.6
-
44
-
-
0042573727
-
Structure of mammalian cytochrome P450 2C5 complexed with diclofenac at 2.1 Å resolution: Evidence for an induced fit model of substrate binding
-
DOI 10.1021/bi034556l
-
Wester, M. R., Johnson, E. F., Marques-Soares, C., Dijols, S., Dansette, P. M., Mansuy, D., and Stout, C. D. (2003) The structure of mammalian cytochrome P450 2C5 complexed with diclofenac at 2.1 Å resolution. Evidence for an induced fit model of substrate binding. Biochemistry 42, 9335-9345 (Pubitemid 36959241)
-
(2003)
Biochemistry
, vol.42
, Issue.31
, pp. 9335-9345
-
-
Wester, M.R.1
Johnson, E.F.2
Marques-Soares, C.3
Dijols, S.4
Dansette, P.M.5
Mansuy, D.6
Stout, C.D.7
-
45
-
-
74549178560
-
MolProbity: All-atom structure validation for macromolecular crystallography
-
Chen, V. B., Arendall, W. B., 3rd, Headd, J. J., Keedy, D. A., Immormino, R. M., Kapral, G. J., Murray, L. W., Richardson, J. S., and Richardson, D. C. (2010) MolProbity: all-atom structure validation for macromolecular crystallography. Acta Crystallogr. D Biol. Crystallgr. 66, (Pt. 1) 12-21
-
(2010)
Acta Crystallogr. D Biol. Crystallgr.
, vol.66
, Issue.PART. 1
, pp. 12-21
-
-
Chen, V.B.1
Arendall III, W.B.2
Headd, J.J.3
Keedy, D.A.4
Immormino, R.M.5
Kapral, G.J.6
Murray, L.W.7
Richardson, J.S.8
Richardson, D.C.9
|