CH/π interactions involving aromatic amino acids: Refinement of the CHARMM tryptophan force field

2005 ◽  
Vol 26 (14) ◽  
pp. 1452-1463 ◽  
Author(s):  
Alba T. Macias ◽  
Alexander D. MacKerell
2015 ◽  
Vol 13 (29) ◽  
pp. 7961-7972 ◽  
Author(s):  
Ana A. Rodríguez-Sanz ◽  
Enrique M. Cabaleiro-Lago ◽  
Jesús Rodríguez-Otero

Phe, Tyr and Trp form parallel complexes with cation⋯π interactions. His complexes are the strongest, but without making contact with the aromatic cloud.


2015 ◽  
Vol 68 (3) ◽  
pp. 385 ◽  
Author(s):  
Hanzala B. Hussain ◽  
Katie A. Wilson ◽  
Stacey D. Wetmore

Despite many DNA–protein π-interactions in high-resolution crystal structures, only four X–H···π or X···π interactions were found between serine (Ser) or cysteine (Cys) and DNA nucleobase π-systems in over 100 DNA–protein complexes (where X = O for Ser and X = S for Cys). Nevertheless, 126 non-covalent contacts occur between Ser or Cys and the aromatic amino acids in many binding arrangements within proteins. Furthermore, Ser and Cys protein–protein π-interactions occur with similar frequencies and strengths. Most importantly, due to the great stability that can be provided to biological macromolecules (up to –20 kJ mol–1 for neutral π-systems or –40 kJ mol–1 for cationic π-systems), Ser and Cys π-interactions should be considered when analyzing protein stability and function.


2007 ◽  
Vol 137 (6) ◽  
pp. 1504S-1508S ◽  
Author(s):  
Dennis A. Dougherty

Molecules ◽  
2015 ◽  
Vol 20 (5) ◽  
pp. 9214-9228 ◽  
Author(s):  
Cristina Trujillo ◽  
Ana Rodriguez-Sanz ◽  
Isabel Rozas

2015 ◽  
Vol 290 (31) ◽  
pp. 19334-19342 ◽  
Author(s):  
Tao He ◽  
Anne Gershenson ◽  
Stephen J. Eyles ◽  
Yan-Jiun Lee ◽  
Wenshe R. Liu ◽  
...  

2012 ◽  
Vol 46 (4) ◽  
pp. 907-915 ◽  
Author(s):  
Christopher J. Pace ◽  
Jianmin Gao

2011 ◽  
Vol 13 (40) ◽  
pp. 18154 ◽  
Author(s):  
Elizabeth A. Ploetz ◽  
Paul E. Smith

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