Topic: Communicating your research results using PyMOL Presenter: Daniel Cappel, Senior Applications Scientist, Schrödinger, Inc. Host: Jason Key Recorded on September 13, 2016
I entered a string of amino acids which I was expecting to be a beta sheet. Then I entered four amino acids which I was expecting to be a beta turn. Next I entered a string of amino acids which I was expecting to be an alpha helix. Then I entered another four amino acids which I was expecting to be a beta turn. Finally, I entered another string of residues with a high propensity to form a beta sheet. All secondary structures, except for the beta turn, were composed of 23 amino acids. Yet, what appears is not what I expected. There doesn't seem to be any secondary structure at all. Is there a way to make the peptide fold into the correct secondary structures?
THX a lot
please Dear all, I would like to learn more bout CHARMM-GUI, Autodock and Autodock vina.
Great, thanks.
Awesome!!!
I entered a string of amino acids which I was expecting to be a beta sheet. Then I entered four amino acids which I was expecting to be a beta turn. Next I entered a string of amino acids which I was expecting to be an alpha helix. Then I entered another four amino acids which I was expecting to be a beta turn. Finally, I entered another string of residues with a high propensity to form a beta sheet. All secondary structures, except for the beta turn, were composed of 23 amino acids.
Yet, what appears is not what I expected. There doesn't seem to be any secondary structure at all. Is there a way to make the peptide fold into the correct secondary structures?
thx
where are this program pleace
thanks video.
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