Comparable rates for cleavage of amide and ester bonds through nucleophilic attack by carboxylate anion and general acid catalysis by metal-bound water in a carboxypeptidase A model

1992 ◽  
Vol 114 (13) ◽  
pp. 5141-5146 ◽  
Author(s):  
Junghun Suh ◽  
Tae Hoon Park ◽  
Byung Keun Hwang
2005 ◽  
Vol 127 (19) ◽  
pp. 7033-7040 ◽  
Author(s):  
Anthony J. Kirby ◽  
Neil Dutta-Roy ◽  
Davi da Silva ◽  
Jonathan M. Goodman ◽  
Marcelo F. Lima ◽  
...  

2006 ◽  
Vol 128 (51) ◽  
pp. 16944-16952 ◽  
Author(s):  
Anthony J. Kirby ◽  
Marcelo F. Lima ◽  
Davi da Silva ◽  
Christo D. Roussev ◽  
Faruk Nome

2005 ◽  
Vol 83 (9) ◽  
pp. 1629-1636 ◽  
Author(s):  
Anthony J Kirby ◽  
José Carlos Gesser ◽  
Florian Hollfelder ◽  
Jacks P Priebe ◽  
Faruk Nome

The mechanism of hydrolysis of 8-N,N-dimethylaminonaphthyl sulfate closely resembles that of the corresponding phosphate monoester. Nucleophilic attack by water on the sulfate group of the zwitterion is catalyzed by the neighbouring dimethylammonium group, acting as a particularly efficient general acid through the intramolecular hydrogen bond. This hydrogen bond is present in both reactant and product, but is strongest in the transition state. Transfer of the sulfuryl group to oxygen nucleophiles, including water and carboxylate anions, shows steric and electrostatic effects, and a sensitivity to basicity which is low, but significantly higher than expected for uncatalyzed transfer of the SO3– group.Key words: sulfate, sulfatase, intramolecular, general acid catalysis, promiscuity.


1965 ◽  
Vol 39 ◽  
pp. 75 ◽  
Author(s):  
A. J. Kresge ◽  
L. E. Hakka ◽  
S. Mylonakis ◽  
Y. Sato

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