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Cytochrome P-450 : multiplicity of isoforms, substrates, and catalytic and regulatory mechanisms

The Journal of biological chemistry, 1991-07, Vol.266 (21), p.13469-13472

1991

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Special issue: Cytochrome P450

Biochimica et biophysica acta. General subjects, 2007-03, Vol.1770 (3), p.313

Coon, M.J.

2007

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Steroid Metabolism by Rabbit Olfactory-Specific P450 2G1

Archives of biochemistry and biophysics, 1994-12, Vol.315 (2), p.454-459

1994

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Separate roles for FMN and FAD in catalysis by liver microsomal NADPH-cytochrome P-450 reductase

The Journal of biological chemistry, 1981-01, Vol.256 (1), p.266-277

1981

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Purified liver microsomal NADPH-cytochrome P-450 reductase. Spectral characterization of oxidation-reduction states

The Journal of biological chemistry, 1978-04, Vol.253 (8), p.2694-2704

1978

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Identification of the high and low potential flavins of liver microsomal NADPH-cytochrome P-450 reductase

The Journal of biological chemistry, 1978-12, Vol.253 (24), p.8812-8819

1978

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Interactions of cytochrome P-450, NADPH-cytochrome P-450 reductase, phospholipid, and substrate in the reconstituted liver microsomal enzyme system

The Journal of biological chemistry, 1980-05, Vol.255 (9), p.4112-4119

1980

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On the mechanism of action of cytochrome P-450. Evaluation of homolytic and heterolytic mechanisms of oxygen-oxygen bond cleavage during substrate hydroxylation by peroxides

The Journal of biological chemistry, 1981-12, Vol.256 (23), p.12127-12133

1981

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Specificity in the activation and inhibition by flavonoids of benzo[a]pyrene hydroxylation by cytochrome P-450 isozymes from rabbit liver microsomes

The Journal of biological chemistry, 1981-11, Vol.256 (21), p.10897-10901

1981

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Ronald W. Estabrook: gifted scientist with the same versatile, energetic, and colorful qualities as cytochrome P450

Archives of biochemistry and biophysics, 2003, Vol.409 (1), p.16-17

Coon, M.J

2003

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Evidence for a homolytic mechanism of peroxide oxygen--oxygen bond cleavage during substrate hydroxylation by cytochrome P-450

The Journal of biological chemistry, 1980-12, Vol.255 (23), p.11108-11111

1980

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Alcohol-inducible cytochrome P-450IIE1 lacking the hydrophobic NH2-terminal segment retains catalytic activity and is membrane-bound when expressed in Escherichia coli

The Journal of biological chemistry, 1991-04, Vol.266 (12), p.7321-7324

1991

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Subcellular localization, aggregation state, and catalytic activity of microsomal P450 cytochromes modified in the NH2-terminal region and expressed in Escherichia coli

Archives of biochemistry and biophysics, 1995-04, Vol.318 (2), p.446-456

1995

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Isolation and heterologous expression of cloned cDNAs for two rabbit nasal microsomal proteins, CYP2A10 and CYP2A11, that are related to nasal microsomal cytochrome P450 form a

The Journal of biological chemistry, 1993-08, Vol.268 (23), p.17253-17260

1993

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Oxidative Cleavage of Esters and Amides to Carbonyl Products by Cytochrome P450

Archives of biochemistry and biophysics, 1995-04, Vol.318 (2), p.333-339

1995

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Purification and characterization of 7 alpha-hydroxy-4-cholesten-3-one 12 alpha-hydroxylase

The Journal of biological chemistry, 1992-10, Vol.267 (30), p.21319-21323

1992

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Reductive β-Scission of the Hydroperoxides of Fatty Acids and Xenobiotics: Role of Alcohol-Inducible Cytochrome P-450

Proceedings of the National Academy of Sciences - PNAS, 1990-07, Vol.87 (14), p.5499-5503

1990

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Structure-Function Analysis of CYP2A10 and CYP2A11, P450 Cytochromes That Differ in Only Eight Amino Acids But Have Strikingly Different Activities toward Testosterone and Coumarin

Biochemical and biophysical research communications, 1994-08, Vol.203 (1), p.373-378

1994

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Subcellular Localization, Aggregation State, and Catalytic Activity of Microsomal P450 Cytochromes Modified in the NH 2-Terminal Region and Expressed in Escherichia coli

Archives of biochemistry and biophysics, 1995, Vol.318 (2), p.446-456

1995

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Membrane topology of microsomal cytochrome P-450: Saturation transfer EPR and freeze-fracture electron microscopy studies

Biochemical and biophysical research communications, 1990-08, Vol.171 (1), p.175-181

1990

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Intramolecular isotope effects favor a concerted mechanism for the cytochrome P-450-catalyzed oxidative deformylation of cyclohexane carboxaldehyde to give cyclohexene

FASEB Journal (Federation of American Societies for Experimental Biology); (United States), 1992, Vol.6:1

1992

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The NH2-Terminal Region of Rabbit CYP2E1 Is Not Essential for Interaction with NADPH-Cytochrome P450 Reductase

Biochemical and biophysical research communications, 1994-08, Vol.203 (1), p.156-161

1994

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Cytochrome P450 2E1 mRNA in the rat prostate: detection and quantitation by competitive reverse transcription and polymerase chain reaction

Molecular and cellular probes, 1998-10, Vol.12 (5), p.263-271

1998

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Properties of electrophoretically homogeneous constitutive forms of liver microsomal cytochrome P-450

The Journal of biological chemistry, 1981-01, Vol.256 (20), p.10704-10711

1981

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On the mechanism of action of cytochrome P-450. Spectral intermediates in the reaction of P-450LM2 with peroxy compounds

The Journal of biological chemistry, 1980-05, Vol.255 (9), p.4100-4111

1980

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Cytochrome P-450 : multiplicity of isoforms, substrates, and catalytic and regulatory mechanisms

Special issue: Cytochrome P450

Steroid Metabolism by Rabbit Olfactory-Specific P450 2G1

Separate roles for FMN and FAD in catalysis by liver microsomal NADPH-cytochrome P-450 reductase

Purified liver microsomal NADPH-cytochrome P-450 reductase. Spectral characterization of oxidation-reduction states

Identification of the high and low potential flavins of liver microsomal NADPH-cytochrome P-450 reductase

Interactions of cytochrome P-450, NADPH-cytochrome P-450 reductase, phospholipid, and substrate in the reconstituted liver microsomal enzyme system

On the mechanism of action of cytochrome P-450. Evaluation of homolytic and heterolytic mechanisms of oxygen-oxygen bond cleavage during substrate hydroxylation by peroxides

Specificity in the activation and inhibition by flavonoids of benzo[a]pyrene hydroxylation by cytochrome P-450 isozymes from rabbit liver microsomes

Ronald W. Estabrook: gifted scientist with the same versatile, energetic, and colorful qualities as cytochrome P450

Evidence for a homolytic mechanism of peroxide oxygen--oxygen bond cleavage during substrate hydroxylation by cytochrome P-450

Alcohol-inducible cytochrome P-450IIE1 lacking the hydrophobic NH2-terminal segment retains catalytic activity and is membrane-bound when expressed in Escherichia coli

Subcellular localization, aggregation state, and catalytic activity of microsomal P450 cytochromes modified in the NH2-terminal region and expressed in Escherichia coli

Isolation and heterologous expression of cloned cDNAs for two rabbit nasal microsomal proteins, CYP2A10 and CYP2A11, that are related to nasal microsomal cytochrome P450 form a

Oxidative Cleavage of Esters and Amides to Carbonyl Products by Cytochrome P450

Purification and characterization of 7 alpha-hydroxy-4-cholesten-3-one 12 alpha-hydroxylase

Reductive β-Scission of the Hydroperoxides of Fatty Acids and Xenobiotics: Role of Alcohol-Inducible Cytochrome P-450

Structure-Function Analysis of CYP2A10 and CYP2A11, P450 Cytochromes That Differ in Only Eight Amino Acids But Have Strikingly Different Activities toward Testosterone and Coumarin

Subcellular Localization, Aggregation State, and Catalytic Activity of Microsomal P450 Cytochromes Modified in the NH 2-Terminal Region and Expressed in Escherichia coli

Membrane topology of microsomal cytochrome P-450: Saturation transfer EPR and freeze-fracture electron microscopy studies

Intramolecular isotope effects favor a concerted mechanism for the cytochrome P-450-catalyzed oxidative deformylation of cyclohexane carboxaldehyde to give cyclohexene

The NH2-Terminal Region of Rabbit CYP2E1 Is Not Essential for Interaction with NADPH-Cytochrome P450 Reductase

Cytochrome P450 2E1 mRNA in the rat prostate: detection and quantitation by competitive reverse transcription and polymerase chain reaction

Properties of electrophoretically homogeneous constitutive forms of liver microsomal cytochrome P-450

On the mechanism of action of cytochrome P-450. Spectral intermediates in the reaction of P-450LM2 with peroxy compounds

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