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Volumn 31, Issue 5, 2000, Pages 365-371

Raman difference spectroscopic studies of dithiobenzoyl substrate and product analogs binding to the enzyme dehalogenase: π-electron polarization is prevented by the C=O to C=S substitution

(5) Dong, Jian a Luo, Lusong b Liang, Po Huang b Dunaway Mariano, Debra b Carey, Paul R a

a CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE (United States)

b UNIVERSITY OF NEW MEXICO (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DENSITY FUNCTIONAL THEORY; ELECTRONS; ENZYMES; POLARIZATION;

COENZYME A; DEHALOGENASE; DITHIOESTERS; ELECTRON POLARIZATION; ENZYME ACTIVE SITES; NORMAL MODES; PHENYL RINGS; PULLING FORCE; SPECTROSCOPIC STUDIES; Π-ELECTRONS;

SPECTROSCOPIC ANALYSIS;

4 CHLOROBENZOYLDITHIO COENZYME A; 4 HYDROXYBENZOYLDITHIO COENZYME A; COENZYME A; DEHALOGENASE; ENZYME; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; COMPLEX FORMATION; ELECTRON; ENZYME ACTIVE SITE; POLARIZATION; RAMAN SPECTROMETRY;

EID: 0033659999 PISSN: 03770486 EISSN: None Source Type: Journal
DOI: 10.1002/1097-4555(200005)31:5<365::AID-JRS516>3.0.CO;2-L Document Type: Article

Times cited : (14)

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