Robert,
Great point! My original script had selections from protein A to a
ligand in any other protein B. I just left it in there.
I agree that creating a named selection for each object is
unnecessary. If he really wanted a clean namespace, he could dump all
of those into a group(s) or a mult
Hi Jason,
On Sun, 29 Nov 2009 12:29:08 -0500, Jason Vertrees
wrote:
> You can automate the task. Load your 100 proteins. Use a wildcard
> from the command line or a script like loadDir
> (http://pymolwiki.org/index.php/LoadDir). Align them. Then, run:
>
> python
> for n in cmd.get_names("ob
Chimed,
You can automate the task. Load your 100 proteins. Use a wildcard
from the command line or a script like loadDir
(http://pymolwiki.org/index.php/LoadDir). Align them. Then, run:
python
for n in cmd.get_names("objects"):
selName = "s" + n
cmd.select(selName, n)
cmd.distance("dist
