Too many peaks, all with similar Z scores isnt a very good sign - one
prefers high contrast but it is hard to make a rule - it depends on many
factors; number of molecules in asymmetric unit, similarity of model and
new structure, data quality, etc etc..
The automated procedures, MrBump or Bal
Post-doctoral positions (x2) in Protein Crystallography Research Complex at
Harwell (RCaH)
We have two postdoctoral positions available for protein crystallographers at
the Research Complex at Harwell (RCaH), a new laboratory currently nearing
completion adjacent to the UK Diamond synchrotr
Dear All:
Sorry for this off-topic subject. This maybe an old topic, but I could not find
the previous discussion about it.
There are some sugars, i.e.,NAD and NDG that form covalent bonds with ASN in my
protein.I tried to load the NAG by "Got Monomer" in COOT, but I couldn't build
the co
JXQI wrote:
> Dear All:
>
> Sorry for this off-topic subject.
It's not off topic. CCP4BB is for protein crystallography. Discussions
of crystallographic programs are particularly ON TOPIC! But so are
media, viruses, vectors and buffers...
Having said that, you might like to consider the Coot mail
Hi
yes, it will. If you go to the ftp site. ftp.ccp4.ac.uk you will find the
beta of 6.1.3 under ccp4/6.1.3-beta (or similar). It will actually be 6.1.3 we
are pretty happy with it
Charles Ballard
CCP4
-Original Message-
From: CCP4 bulletin board on behalf of Jürgen Bosch
Sent: Wed
Okay, I got the problem resolved in the following way (thanks go to Clint
Leysath):
1. removed the tcltk++ directory that came with my ccp4 download
2. installed Activestate's tcltk 8.4.19.2 from
https://www.activestate.com/activetcl/downloads/
3. downloaded blt2.4z.tar.gz and the blt2.4z-patch-2
