To all Amber users,
I have just recently started using Leap with Amber6 and would like
to know if there is a way to load a coordinate (or restart) file
directly into XLEaP, e.g. to visualize a molecule where minimization
or MD has just been carried out, and to proceed further on that structure.
Some solvated molecules are too big for pdbgen to handle (max. 12000
atoms).
I would appreciate any suggestions--I looked in the manual but didn't
find any such command.
Thank you very much,
Sincerely,
Michael G. Cooney
Department of Biochemistry and Molecular Biology
The University of Georgia
Athens, GA 30602, USA
Received on Wed Sep 20 2000 - 08:55:17 PDT
