## Abstract ^13^C chemical shifts and coupling constants of phosphoserine in aqueous solutions were studied as a function of pH values. Carboxyl and α‐amino titration shifts agree with those observed in amino acids. The analysis of the coupling constants indicates that for rotation about the (C)C
Conformational study of phosphoserine in aqueous solutions. II—1H n.m.r. results
✍ Scribed by L. Pogliani; D. Ziessow; Ch. Krüger
- Publisher
- John Wiley and Sons
- Year
- 1977
- Tongue
- English
- Weight
- 486 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The 270 MHz n.m.r. spectra of phosphoserine (PSer) have been measured and completely analysed for seven pD values. The resulting vicinal coupling constants ^3^J(HαHβ) and ^3^J(PHβ) are used to discuss the conformations of PSer with respect to the (Hα)CαCβ(O) and (Cα)CβO(P) bond axes. The all‐trans conformer predominates for all pD values, with its fractional population being minimal at pD values close to neutrality. The CβO bond rotamer populations agree reasonably well with those obtained from ^13^C investigations.
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