AbstractThe inclusion of the presence and flexibility of the CH2CH2OH end chain in the computation of the energy profile for single occupancy by Na+ of the gramicidin A channel modifies substantially the profile obtained without that chain. The binding site (deepest minimum) in the profile is situated at 10.5 Å from the center of the channel, in satisfactory agreement with the conclusions based on 13C-NMR studies. The existence of an external minimum at the mouth is confirmed
The potential of mean force for Na+ and K+ ions as a function of position in the interior of a perio...
The structural and thermodynamic factors responsible for the singly and doubly occupied saturation s...
SummaryThe gating mechanism of the open state of the gramicidin A (gA) channel is studied by using a...
AbstractThe inclusion of the presence and flexibility of the CH2CH2OH end chain in the computation o...
AbstractThe energy profiles for single occupancy by Cs+ and Na+ in the gramicidin A channel assumed ...
AbstractThe effect of the conformational freedom of the ethanolamine tail of gramicidin A on the ene...
AbstractThe energy profile for Na+ in the channel formed by the gramicidin A β-helical dimer backbon...
A 6-12-1 atom-atom pair potential for the interaction of a Na+ion with gramicidin A (GA) has been de...
The valence selectivity of the gramicidin channel is examined using computer simulations based on at...
The location of the main binding site for sodium in the gramicidin A (GA) channel was investigated w...
The reaction path and free energy profile of Na+ were computed in the interior of the channel protei...
The relation between chemical structure and permeability characteristics of transmembrane channels h...
The free energy profiles for four organic cations in right-handed single-helix gramicidin A dimers w...
The modulation of gramicidin A single-channel characteristics by the amino acid side chains was inve...
Empirical energy function calculations were used to evaluate the effects of minimization on the stru...
The potential of mean force for Na+ and K+ ions as a function of position in the interior of a perio...
The structural and thermodynamic factors responsible for the singly and doubly occupied saturation s...
SummaryThe gating mechanism of the open state of the gramicidin A (gA) channel is studied by using a...
AbstractThe inclusion of the presence and flexibility of the CH2CH2OH end chain in the computation o...
AbstractThe energy profiles for single occupancy by Cs+ and Na+ in the gramicidin A channel assumed ...
AbstractThe effect of the conformational freedom of the ethanolamine tail of gramicidin A on the ene...
AbstractThe energy profile for Na+ in the channel formed by the gramicidin A β-helical dimer backbon...
A 6-12-1 atom-atom pair potential for the interaction of a Na+ion with gramicidin A (GA) has been de...
The valence selectivity of the gramicidin channel is examined using computer simulations based on at...
The location of the main binding site for sodium in the gramicidin A (GA) channel was investigated w...
The reaction path and free energy profile of Na+ were computed in the interior of the channel protei...
The relation between chemical structure and permeability characteristics of transmembrane channels h...
The free energy profiles for four organic cations in right-handed single-helix gramicidin A dimers w...
The modulation of gramicidin A single-channel characteristics by the amino acid side chains was inve...
Empirical energy function calculations were used to evaluate the effects of minimization on the stru...
The potential of mean force for Na+ and K+ ions as a function of position in the interior of a perio...
The structural and thermodynamic factors responsible for the singly and doubly occupied saturation s...
SummaryThe gating mechanism of the open state of the gramicidin A (gA) channel is studied by using a...