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NADPH-CYP reductase

Figure 9.1 CYP catalytic cycle. The sequential two-electron reduction of CYP and the various transient intermediates were first described in the late 1960s [206], The sequence of events that make up the CYP catalytic cycle is shown. The simplified CYP cycle begins with heme iron in the ferric state. In step (i), the substrate (R—H) binds to the enzyme, somewhere nearthe distal region of the heme group and disrupts the water lattice within the enzymes active site [207], The loss of water elicits a change in the heme iron spin state (from low spin to high spin) [208]. Step (ii) involves the transfers of an electron from NADPH via the accessory flavoprotein NADPH-CYP reductase, with the electron flow going from the reductase prosthetic group FAD to FMN to the CYP enzyme [206,209]. The... Figure 9.1 CYP catalytic cycle. The sequential two-electron reduction of CYP and the various transient intermediates were first described in the late 1960s [206], The sequence of events that make up the CYP catalytic cycle is shown. The simplified CYP cycle begins with heme iron in the ferric state. In step (i), the substrate (R—H) binds to the enzyme, somewhere nearthe distal region of the heme group and disrupts the water lattice within the enzymes active site [207], The loss of water elicits a change in the heme iron spin state (from low spin to high spin) [208]. Step (ii) involves the transfers of an electron from NADPH via the accessory flavoprotein NADPH-CYP reductase, with the electron flow going from the reductase prosthetic group FAD to FMN to the CYP enzyme [206,209]. The...
Cytochrome b5 affects the kinetics of drug metabolism by certain CYP enzymes hence, coexpression of this microsomal hemoprotein (together with NADPH-CYP reductase) can affect the catalytic efficiency of certain recombinant CYP enzymes (76,109). For example, the presence of cytochrome b5 tends to increase Fmax for reactions catalyzed by CYP3 A4, whereas it tends to decrease Km for reactions catalyzed by CYP2E1. In both cases, cytochrome b5 increases Vmax/Km, which is a measure of in vitro intrinsic clearance. The fact that some commercially available recombinant CYP enzymes are expressed with cytochrome b5 while others are not complicates the interpretation of results of studies performed with recombinant human CYP enzymes. [Pg.333]

Contains all liver microsomal CYP enzymes with physiological levels of cytochrome b5 and NADPH-CYP reductase. Establishes the degree of interindividual variation in metabolic formation or substrate disappearance. [Pg.335]

The absence of cytochrome bs and/or artificially high levels of NADPH-CYP reductase can alter the kinetics of CYP enzymes and/or introduce artifacts. [Pg.336]

Endothelial biotransformation (e.g, gamma-GTP, GST, NADPH-cyp reductase, MAO, UGT, alkaline phosphatase, epoxide hydrolases, AAD, COMT, BChE, etc)... [Pg.657]

Those include C-, N- and 5-oxidations, N-, 0- and 5-deaIkylation, deaminations, and certain dehalogenations. Under anaerobic conditions, it can also catalyze reductive reactions. The CYP monooxygenase system is a multien-zymatic complex constituted by the CYP hemoprotein, the flavoprotein enzyme NADPH CYP reductase, and the unsatnrated phospholipid phosphatidylcholine. The isoforms involved in xenobiotic metabolism are membrane bonnd enzymes situated in the endoplasmic reticnlnm. After... [Pg.676]

Activation by NADPH CYP reductase leading to formation of DNA adducts mutagenic and carcinogenic DNA intercalation inhibition of DNA polymerase, reverse transcriptase... [Pg.238]


See other pages where NADPH-CYP reductase is mentioned: [Pg.198]    [Pg.246]    [Pg.114]    [Pg.263]    [Pg.263]    [Pg.264]    [Pg.265]    [Pg.269]    [Pg.332]    [Pg.333]    [Pg.333]    [Pg.662]    [Pg.376]    [Pg.489]    [Pg.662]    [Pg.676]    [Pg.176]    [Pg.831]    [Pg.831]    [Pg.58]    [Pg.59]    [Pg.105]    [Pg.110]   
See also in sourсe #XX -- [ Pg.263 , Pg.264 ]

See also in sourсe #XX -- [ Pg.376 ]




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