Catalytic mechanism of S-ribosylhomocysteinase (LuxS): Stereochemical course and kinetic isotope effect of proton transfer reactions

Biochemistry

Volumn 43, Issue 31, 2004, Pages 10166-10172

  Zhu, Jinge ^a   Patel, Reena ^a   Pei, Dehua ^a  

^a OHIO STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BACTERIA; CATALYSIS; ISOTOPES; MASS SPECTROMETRY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PROTONS;

KINETIC ISOTOPE EFFECTS; PROTON TRANSFER REACTIONS; REGIOCHEMISTRY; STEREOCHEMICAL COURSE;

REACTION KINETICS;

ACETYLACETONE; ACID; BASE; CARBONYL DERIVATIVE; DEUTERIUM; ENZYME; FERROUS ION; GLUTAMIC ACID; HOMOCYSTEINE; PROTON; RIBOSE; S RIBOSYLHOMOCYSTEINASE; SULFIDE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; ENZYME ACTIVE SITE; KINETICS; MASS SPECTROMETRY; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; PROTON TRANSPORT; STEREOCHEMISTRY;

BACILLUS SUBTILIS; BACTERIAL PROTEINS; BINDING SITES; CARBON-SULFUR LYASES; CATALYSIS; DEUTERIUM EXCHANGE MEASUREMENT; HOMOCYSTEINE; KINETICS; N-GLYCOSYL HYDROLASES; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; PROTEIN CONFORMATION; PROTONS; SUBSTRATE SPECIFICITY; VIBRIO;

BACTERIA (MICROORGANISMS);

EID: 3543138871     PISSN: 00062960     EISSN: None     Source Type: Journal    
DOI: 10.1021/bi0491088     Document Type: Article

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