Peptide models XXV. Side-chain conformational potential energy surface, E=E(χ1,χ2) of N -formyl- l -aspartic acidamide and its conjugate base N -formyl- l -aspartatamide in their γ l backbone conformations
- 1 February 2000
- journal article
- Published by Elsevier in Journal of Molecular Structure: THEOCHEM
- Vol. 497 (1-3) , 39-63
- https://doi.org/10.1016/s0166-1280(99)00196-7
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- Peptide models XIX: Side-chain conformational energy surface and amide I vibrational frequencies of N-formyl-l-phenylalaninamide (For-Phe-NH2) in its γL or γinv or C7eq backbone conformationJournal of Molecular Structure: THEOCHEM, 1996
- Conformations of ethylbenzene (CH3CH2Ph). An ab initio studyJournal of Molecular Structure: THEOCHEM, 1996
- Peptide models XI. Substitution effects on peptide chains. The magnitude of side-chain–backbone interactions in oligopeptides HCO-(NHCHRCO)n-NH2 for R=CH3. An ab initio studyCanadian Journal of Chemistry, 1995
- Peptide models 4. Topological features of molecular mechanics and ab initio 2D-ramachandran mapsJournal of Molecular Structure: THEOCHEM, 1993
- New Perspectives in Cell Adhesion: RGD and IntegrinsScience, 1987