High-Resolution NMR of Membrane Proteins: The Example of Bacteriorhodopsin

Author(s):  
M. Seigneuret
2016 ◽  
Vol 55 (35) ◽  
pp. 10518-10521 ◽  
Author(s):  
Mariusz Jaremko ◽  
Łukasz Jaremko ◽  
Saskia Villinger ◽  
Christian D. Schmidt ◽  
Christian Griesinger ◽  
...  

2010 ◽  
Vol 132 (16) ◽  
pp. 5628-5629 ◽  
Author(s):  
Zakhar O. Shenkarev ◽  
Ekaterina N. Lyukmanova ◽  
Alexander S. Paramonov ◽  
Lyudmila N. Shingarova ◽  
Vladimir V. Chupin ◽  
...  

2009 ◽  
Vol 74 (7) ◽  
pp. 756-765 ◽  
Author(s):  
Z. O. Shenkarev ◽  
E. N. Lyukmanova ◽  
O. I. Solozhenkin ◽  
I. E. Gagnidze ◽  
O. V. Nekrasova ◽  
...  

2004 ◽  
Vol 126 (47) ◽  
pp. 15340-15341 ◽  
Author(s):  
Anna A. De Angelis ◽  
Alexander A. Nevzorov ◽  
Sang Ho Park ◽  
Stanley C. Howell ◽  
Anthony A. Mrse ◽  
...  

1969 ◽  
Vol 52 (5) ◽  
pp. 1074-1092 ◽  
Author(s):  
L H Keith ◽  
A L Alford ◽  
A W Garrison

Abstract The high resolution nuclear magnetic resonance spectra of the DDT class of pesticides and related compounds are discussed, including a study of the resonances of the aromatic protons as they are affected by various substiluents. The CCl3 moiety on the α-carbon strongly deshields the ortho protons on the aromatic rings, and this deshielding effect is greatly enhanced by substitution of a chlorine ortho rather than para on the aromatic ring. These deshielding effects are explained by a consideration of the electronegativity of the substituents and the stereochemistry of the molecule. The chemical shifts and coupling constants are tabulated.


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