Intermolecular Potentials of Mean Force of Amino Acid Side Chain Interactions in Aqueous Medium

2004 ◽  
Vol 108 (50) ◽  
pp. 19501-19509 ◽  
Author(s):  
Sergio A. Hassan
SynOpen ◽  
2017 ◽  
Vol 01 (01) ◽  
pp. 0059-0062
Author(s):  
Ikumi Otomo ◽  
Kanna Watanabe ◽  
Chiaki Kuroda ◽  
Kenichi Kobayashi

The reaction of five amphipathic-type thioesters, CH3(CH2) m COS(CH2) n COONa (m + n = 12), with cysteine hexyl, butyl, and ethyl esters were studied in aqueous medium. Compounds with the thioester group in close proximity to the carboxylate moiety (m = 10, n = 2) afforded amides in almost quantitative yield, whereas no reaction proceeded by using compounds with the thioester group distant from the carboxylate. In contrast, no clear difference in yield was observed among the five amphipathic-type thioesters upon reaction with valine hexyl ester. The results indicate that the reaction is affected by both the position of the thioester group and the hydrophilic/hydrophobic properties of the amino acid side chain.


Biopolymers ◽  
1992 ◽  
Vol 32 (12) ◽  
pp. 1623-1629 ◽  
Author(s):  
Paul E. Smith ◽  
B. Montgomery Pettitt

Amino Acids ◽  
2015 ◽  
Vol 47 (5) ◽  
pp. 885-898 ◽  
Author(s):  
Hsiou-Ting Kuo ◽  
Shing-Lung Liu ◽  
Wen-Chieh Chiu ◽  
Chun-Jen Fang ◽  
Hsien-Chen Chang ◽  
...  

2007 ◽  
Vol 14 (4) ◽  
pp. 379-386 ◽  
Author(s):  
Nicholas M. Llewellyn ◽  
Yanyan Li ◽  
Jonathan B. Spencer

Sign in / Sign up

Export Citation Format

Share Document