Dear amber users,
I did a 5ns MD run on a protein using AMBER9. The analysis of the run
showed that, overall, the structure averaged over the last 500 frames is
pretty similar to the crystal structure after the run, apart from meaningful
dynamics at some parts. However, while investigating the structure in Pymol,
I noticed that there is a change in some secondary structure elements. More
specific: a couple of B-strands changed to loops, two short parts of long
loops turned to B-strands and finally, a short helix turned into a loop. I
know I do need to investigate this further by calculating the secondary
structure following DSSP. But, visually I can feel the changes mentioned
above.
I understand that, in principle, a change in secondary structure could
happen during MD, as a non-folded structure can be folded during simulation.
But, I want to be sure that what I see is not an artifact of the simulation.
I remember I came across some comment about the sensitivity of AMBER to
B-strands stability compared to helices. Of course, this comment could be
true for the previous versions of the program (I'd love to hear the
developers' comments on that) which might be not the case for the current
version.
I'd appreciate if people with more experience could give me their opinions,
and point me to publications where secondary structure change is reported.
Thanks in advance of your help and your valuable comments.
Regards,
Ibrahim
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Received on Sun Mar 02 2008 - 06:07:17 PST
