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Journal of Physical Chemistry B, Vol.101, No.16, 3304-3310, 1997
Variation of the Energy Landscape of a Small Peptide Under a Change from the Ecepp/2 Force-Field to Ecepp/3
The multicanonical ansatz is used to study variations in the energy landscape of a small peptide, Met-enkephalin, under a change from the ECEPP/2 force field to ECEPP/3. Local minima with energies up to 5 kcal/mol higher than the global minima are sampled and classified according to H-bridges and backbone angles. The distribution and relative weight fur various temperatures of the minima an calculated and compared for the two force fields. We demonstrate that while there are small differences in the energy landscape our results at relevant temperatures are robust under changes between ECEPP/2 to ECEPP/3.
Keywords:HYDROGEN-BOND INTERACTIONS;OCCURRING AMINO-ACIDS;ISING SPIN-GLASS;NONBONDED INTERACTIONS;MULTICANONICAL ALGORITHMS;GEOMETRICAL PARAMETERS;PHASE-TRANSITIONS;MET-ENKEPHALIN;POLYPEPTIDES;SIMULATIONS