Probing the active sites of butyrylcholinesterase and cholesterol esterase with isomalathion: Conserved stereoselective inactivation of serine hydrolases structurally related to acetylcholinesterase

Chemical Research in Toxicology

Volumn 14, Issue 7, 2001, Pages 807-813

  Doorn, J A ^a   Talley, T T ^b   Thompson, C M ^b   Richardson, R J ^a  

^a UNIVERSITY OF MICHIGAN   (United States)

^b UNIVERSITY OF MONTANA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLCHOLINESTERASE; CHOLESTEROL ESTERASE; CHOLINESTERASE; MALATHION; SERINE DEHYDRATASE;

ARTICLE; ENZYME ACTIVE SITE; ENZYME INACTIVATION; ENZYME INHIBITION; ENZYME STRUCTURE; ISOMER; STEREOCHEMISTRY;

ACETYLCHOLINESTERASE; ANIMALS; BINDING SITES; BUTYRYLCHOLINESTERASE; CATTLE; CHOLESTEROL ESTERASE; HORSES; HUMANS; KINETICS; MALATHION; MODELS, MOLECULAR; SERINE ENDOPEPTIDASES; STEREOISOMERISM; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 0034946676     PISSN: 0893228X     EISSN: None     Source Type: Journal    
DOI: 10.1021/tx015501s     Document Type: Article

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