Conformational dependence of the intrinsic acidity of the aspartic acid residue sidechain in N-acetyl-L-aspartic acid-N '-methylamide
The sidechain conformational potential energy hypersurfaces (PEHS) for the gamma(L), beta(L), alpha(L), and alpha(D) backbone conformations of N-acetyl-L-aspartate-M-methylamide were generated. Of the 81 possible conformers initially expected for the aspartate residue, only seven were found after ge...
Elmentve itt :
| Szerzők: | |
|---|---|
| Dokumentumtípus: | Cikk |
| Megjelent: |
2003
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| Sorozat: | JOURNAL OF MOLECULAR STRUCTURE: THEOCHEM
620 No. 2-3 |
| Tárgyszavak: | |
| doi: | 10.1016/S0166-1280(02)00639-5 |
| mtmt: | 1132561 |
| Online Access: | http://publicatio.bibl.u-szeged.hu/28638 |