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Cytochromes P450 substrate binding

Lewis DFV, Eddershaw PJ, Dickins M, Tarbit MH, Goldfarb PS. Structural determinants of cytochrome P450 substrate specificity, binding affinity and catalytic rate. Chem Bio Interact 1998 115 175-99. [Pg.459]

Interact., 117, 187 (1999). Erratum to Structural Determinants of Cytochrome P450 Substrate Specificity, Binding Affinity and Catalytic Rate. [Pg.397]

S Modi, MI Paine, MI Sutcliffe, L-Y Lian, WU Pnmi-ose, CR Wolfe, GCK Roberts. A model for human cytochrome P450 2d6 based on homology modeling and NMR studies of substrate binding. Biochemistry 35 4540-4550, 1996. [Pg.311]

Li S, LP Wackett (1993) Reductive dehalogenation by cytochrome P450(,j jy[ substrate binding and catalysis. Biochemistry 32 9355-9361. [Pg.141]

Liu J, Ericksen SS, Besspiata D et al (2003) Characterization of substrate binding to cytochrome P450 1A1 using molecular modeling and kinetic analyses case of residue 382. Drug Metab Dispos 31 412 -20... [Pg.63]

Dabrowski, M.J., Schrag, M.L., Wienkers, L.C. and Atkins, W.M. (2002) Pyrene-pyrene complexes at the active site of cytochrome P450 3 A4 evidence for a multiple substrate binding site. Journal of the American Chemical Society, 124 (40), 11866-11867. [Pg.237]

Korzekwa, K.R., Krishnamachary, N., Shou, M., Ogai, A., Parise, R.A., Rettie, A.E., Gonzalez, F.J. and Tracy, T.S. (1998) Evaluation of atypical cytochrome P450 kinetics with two-substrate models evidence that multiple substrates can simultaneously bind to cytochrome P450 active sites. Biochemistry, 37 (12), 4137-4147. [Pg.241]

Wester, M.R., Johnson, E.F., Marques-Soares, C., Dansette, P.M., Mansuy, D. and Stout, C.D. (2003) Structure of a substrate complex of mammalian cytochrome P450 2C 5 at 2.3 A resolution evidence for multiple substrate binding modes. Biochemistry, 42, 6370-6379. [Pg.263]

Nakayama K, Puchkaev A, Pikuleva lA. 2001. Membrane binding and substrate access merge in cytochrome P450 7A1, a key enzyme in degradation of cholesterol. J Biol... [Pg.87]

Fig. 14.8 Experimental ligand interactions with cytochrome P450 2C family. (A) X-ray structure ofthe sulfaphenazole derivate DMZ in rabbit CYP2C5 at 2.3 A resolution (PDB 1 N5B) from Wester et al. [191]. Only one ofthe two-ligand orientations for DMZ in accord with electron density is shown placing the benzylic methyl group in a 4.4 A distance to the heme iron. (B) X-ray structure of S-warfarin in human CYP2C9 at 2.55 A resolution (PDB 10G5) from Williams et al. [192]. The substrate is situated in a predominantly hydrophobic pocket. This binding mode places the 6- and 7-hydroxylation sites 10 A from the iron (arrow). Fig. 14.8 Experimental ligand interactions with cytochrome P450 2C family. (A) X-ray structure ofthe sulfaphenazole derivate DMZ in rabbit CYP2C5 at 2.3 A resolution (PDB 1 N5B) from Wester et al. [191]. Only one ofthe two-ligand orientations for DMZ in accord with electron density is shown placing the benzylic methyl group in a 4.4 A distance to the heme iron. (B) X-ray structure of S-warfarin in human CYP2C9 at 2.55 A resolution (PDB 10G5) from Williams et al. [192]. The substrate is situated in a predominantly hydrophobic pocket. This binding mode places the 6- and 7-hydroxylation sites 10 A from the iron (arrow).

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See also in sourсe #XX -- [ Pg.141 , Pg.142 ]




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