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Dear Wenhe,
what you name 'general' may in fact be quite specific and hence running
a single program without any options provided is rather unlikely to give
the answers you seek.
moleman2 and other USF utilities (not a ccp4 program) come closest to
w
Hi board,
Although i do not want to endorse anything personally
earlier mail to Yuris response reflects my personal reflection of what i like.
Here is a plate from Molecualr dimensions that i found
may be an alternate where you can chose the sandwich thickness
good idea but do not know what advant
DEADLINE APPROACHING!
Our group has been involved in structural studies of several novel enzymes
interesting from the point of view of biotechnologies,
such as Laccase from *S. coeliocolor, *beta-galactosidase from Arthrobacter
(660 kDa) or recently plant metal-dependent bifunctional nuclease or
b
Dear Raj,
please follow exactly what is written in the FAQ
http://www.ysbl.york.ac.uk/~lohkamp/coot/wincoot-faq.html#mozTocId860510. I
just updated it slightly to hopefully make things even clearer (*). You
seem to be mixing different possible setups. Either you move the files
to WinCoot\bin
Check with Daniel which one he recommends.
Mark Saper
3040 & 3250 Chemistry Building
Dept of Biological Chemistry
sa...@umich.edu
734 764 3353 office 734 276 6505 mobile
On Feb 26, 2012, at 7:00 PM, CCP4BB automatic digest system
wrote:
> There are 8 messages totaling 1732 lines in this iss
Hi all
I have collected 2 datasets; one for the native proteins (2.3Å resolution)
while other is for a protein-protein complex (3.5Å resolution). The unit
cell parameters for the native are a=120, b=196, c=109, a=g=90, b=114,
while for the complex data it is a=122, b=197, c=300, a=g=90, b=93. I hav
