I’m not aware of a wide study on NAD carboxamide conformation. Lacking atomic 
resolution, optimizing the hydrogen bonding can be used to determine the 
orientation of the carboxamide, as you wrote. You may have to consider 
intramolecular hydrogen bonding within NAD+ as well as intermolecular hydrogen 
bonding with the protein. For example, Fig. 5 from below shows a case in which 
the carboxamide of NADPH donates a hydrogen bond to a backbone carbonyl, while 
accepting a hydrogen bond from the NADPH pyrophosphate.

https://www.ncbi.nlm.nih.gov/pubmed/28258219


John J. Tanner
Professor of Biochemistry and Chemistry
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Department of Biochemistry
University of Missouri-Columbia
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On May 17, 2017, at 2:46 PM, Jorge Iulek 
<[email protected]<mailto:[email protected]>> wrote:

Dear all,

    I came across some difficulty to refine a NAD molecule in a structure, 
specially its amide of the nicotinamide moiety.
    A (very) brief search in deposited structures seems to point that not so 
ever the C2N-C3N-C7N-N7N dihedral is close to either 0 or 180 degrees, but in 
most cases it is to one of these, with a preference towards 0 degrees. Another 
search in the literature, and I could not find any study on either NAD or even 
the nicotinamide alone to calculate the energy barrier to rotate around this 
bond (in vacuum, eg).
    My data quality and resolution do not put much confidence on B-factor 
differences, but they seem to indicate that the cited dihedral angle should be 
close to 180 degrees, id est, O7N is "closer" to C2N (and, consequently, to 
N1N) than N7N is. In fact, I have a glutamine nearby whose terminal amide is 
interacting with the nicotinamide amide, so my idea is to make one's nitrogen 
to interact with other's oxygen. Concerning b-factor differences for this 
glutamine, they favor its NE2 to point to nicotinamide amide, what would imply 
that the C2N-C3N-C7N-N7N dihedral to would be close to 180 degrees rather than 
0 degree.
    Is there any wide study on NAD nicotinamide amide conformation? Specially, 
bound to protein structures?
    Thanks,

Jorge


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