Thanks!
I download the executable probe and reduce and add them to .coot. Now it
works well. Thank you very much!
2010/2/8 William G. Scott
> On Feb 8, 2010, at 2:07 PM, Nathaniel Echols wrote:
>
> > On Mon, Feb 8, 2010 at 1:51 PM, William G. Scott <
> wgsc...@chemistry.ucsc.edu
> >> wrote:
> >
Xavier, can't help you with the HIV protease movie, but most movies (all of the
HIV protease movies that I tried anyway!) can be downloaded from YouTube with
this Firefox add-on:
http://www.downloadhelper.net
HTH!
Cheers
-- Ian
> -Original Message-
> From: owner-ccp...@jiscmail.ac.uk
Paul,
It seems the distance criteria apply to protein atoms only, not including
bound water. Is there a way to include atoms from water molecules in the
distance constraint?
Yong
Paul Emsley
Sent by: CCP4 bulletin board
02/01/2010 09:02 AM
Please respond to
Paul Emsley
To
CCP4BB@JISC
A postdoctoral position is available immediately for a highly motivated
candidate at the University of Maryland, School of Medicine and the
Institute of Human Virology, in Baltimore, Maryland. Successful
candidate will join an ongoing research project focused on structural
characterization of b
> You can build any 3D molecule easily in Discovery Studio Visualizer - It
is free but > not for Mac OS
I have been pretty impressed with Discovery Studio Visualizer and feel that
it can serve as a nice compliment to Pymol.
I wrote up a brief overview and comparison between the two programs her
On Feb 7, 2010, at 11:13 PM, Wataru Kagawa wrote:
> Hi all,
>
> I would like to create a pdb file for a chemical compound (FW ~600) that was
> created in our chemistry department. ChemDraw 3D appears capable of doing
> this, but I would like to know if there are free alternatives that work grea
Hi, Dear All,
I have a mac 10.4 with 4GB memory, I thought it should be pretty fast.
However when I run coot, it's kind of slow. Even when I push the space key
to go to next residue, I can feel it is really walking to the next residue.
Is this normal or something maybe not set up correct? I wonde
Dear all,
Apologies for a off topic question. I could not think of a better
place to ask this.
Suppose, we have four enzymes turning over five molecules, either in
the living cell, or in fresh mammalian cell lyset. The molecules could
be as simple as ATP, GTP, NADP, GSH etc. Now, one can add a in
