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Volumn 271, Issue 42, 1996, Pages 25864-25872
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Secobarbital-mediated inactivation of cytochrome P450 2B1 and its active site mutants. Partitioning between heme and protein alkylation and epoxidation
a b b b a,c |
Author keywords
[No Author keywords available]
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Indexed keywords
CYTOCHROME P450;
HEMOPROTEIN;
N [5 (2 HYDROXYPROPYL) 5 (1 METHYLBUTYL)BARBITURIC ACID]PROTOPORPHYRIN;
PROTOPORPHYRIN;
SECOBARBITAL;
UNCLASSIFIED DRUG;
ALKYLATION;
ANIMAL CELL;
ARTICLE;
DNA ADDUCT;
ENZYME ACTIVE SITE;
ENZYME INACTIVATION;
ENZYME KINETICS;
EPOXIDATION;
MALE;
MOLECULAR DYNAMICS;
NONHUMAN;
PRIORITY JOURNAL;
PROTEIN LOCALIZATION;
PROTEIN MODIFICATION;
RAT;
SEQUENCE HOMOLOGY;
SITE DIRECTED MUTAGENESIS;
ALKYLATION;
ANIMALS;
BINDING SITES;
CHROMATOGRAPHY, HIGH PRESSURE LIQUID;
CYTOCHROME P-450 CYP2B1;
EPOXY COMPOUNDS;
HEME;
MALE;
MUTATION;
PROTEIN CONFORMATION;
RATS;
RATS, SPRAGUE-DAWLEY;
SECOBARBITAL;
SPECTROMETRY, MASS, MATRIX-ASSISTED LASER DESORPTION-IONIZATION;
SPECTROPHOTOMETRY, ATOMIC;
SPECTROPHOTOMETRY, ULTRAVIOLET;
STRUCTURE-ACTIVITY RELATIONSHIP;
ANIMALIA;
ESCHERICHIA COLI;
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EID: 0037905938
PISSN: 00219258
EISSN: None
Source Type: Journal
DOI: 10.1074/jbc.271.42.25864 Document Type: Article |
Times cited : (36)
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References (32)
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