Binding of 2-naphthols to D38E mutants of 3-oxo-Δ5-steroid isomerase: Variation of ligand ionization state with the nature of the electrophilic component

Biochemistry

Volumn 39, Issue 1, 2000, Pages 110-116

  Pollack, R M ^a,b  

^a UNIVERSITY OF MARYLAND BALTIMORE COUNTY   (United States)

^b UNIVERSITY OF MARYLAND BIOTECHNOLOGY INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

2 NAPHTHOL; ASPARTIC ACID; EQUILENIN; MUTANT PROTEIN; STEROID DELTA ISOMERASE; TYROSINE;

ARTICLE; CATALYSIS; DISSOCIATION CONSTANT; ENZYME BINDING; ENZYME MECHANISM; ENZYME SUBSTRATE COMPLEX; FLUORESCENCE SPECTROSCOPY; HYDROGEN BOND; IONIZATION; ISOMERISM; LIGAND BINDING; PKA; PRIORITY JOURNAL; ULTRAVIOLET SPECTROSCOPY;

EID: 0034635151     PISSN: 00062960     EISSN: None     Source Type: Journal    
DOI: 10.1021/bi9917838     Document Type: Article

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