Abstract
The charge density of a hexapeptide was determined from high-resolution CCD area-detector experiments at 100 K. Two datasets, one from a rotating anode and a second one from synchrotron radiation, were measured and the results are compared. The data are interpreted in terms of the 'rigid pseudoatom' model. The topology of the experimental density is analyzed and compared with the topology of the constituting amino acids, and shows good agreement. All critical points of the electron density at the covalent and hydrogen bonds, as well as those of the Laplacian, were located. With respect to the transferability of electronic and bond topological properties the six peptide bonds were compared with values given in the literature.
Original language | English |
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Pages (from-to) | 721-727 |
Number of pages | 7 |
Journal | Acta Crystallographica Section B: Structural Science |
Volume | 58 |
Issue number | 4 |
DOIs | |
State | Published - Aug 2002 |