Theoretical model for pyruvoyl-dependent enzymatic decarboxylation of α-amino acids

Journal of the American Chemical Society

Volumn 119, Issue 49, 1997, Pages 11725-11733

  Bach, Robert D ^a   Canepa, Carlo ^a  

^a UNIVERSITY OF DELAWARE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HISTIDINE DECARBOXYLASE;

AMINO ACID METABOLISM; ARTICLE; DECARBOXYLATION; ENZYME ACTIVE SITE; ENZYME ACTIVITY; ENZYME BINDING; IN VITRO STUDY; MODEL; MOLECULAR DYNAMICS; PROTON TRANSPORT; THERMODYNAMICS;

EID: 0031453841     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja963686x     Document Type: Article

References (3)

1. Bach, R. D.; Canepa, C. J. Org. Chem. 1996, 61, 6346.
2. Carboxylic acids with potential anionic leaving groups such as benisoxazole-3-carboxylate exhibit pronounced solvent effects. See, for example: (a) Ferris, D. C.; Drago, R. S. J. Am. Chem. Soc. 1994, 116, 7509. (b) Gao, J. J. Am. Chem. Soc. 1995, 117, 8600 and references therein.
3. Carboxylic acids with potential anionic leaving groups such as benisoxazole-3-carboxylate exhibit pronounced solvent effects. See, for example: (a) Ferris, D. C.; Drago, R. S. J. Am. Chem. Soc. 1994, 116, 7509. (b) Gao, J. J. Am. Chem. Soc. 1995, 117, 8600 and references therein.