Hi,
I have a java program named Switch.java, I want to run it under fedora5
core, I donnot know any compiler
I need to install? I installed a package named jre-1_5_0_11-
linux-i586-rpm.bin, when I use command
java Switch.java
wrong information came out:
Exception in thread "main" java.lang.NoCl
Message from Eleanor Dodson
I am chairing a session at the ECM 24 to be held in Morocco at the end of
August on
*Advances in crystallographic phasing and refinement*
I am interpreting this as mostly to be about Macromoolecular studies.
There are 6 slots for speakers, 2
Hi,
l have a crystal grow at condition screen l 40:
0.1M tri-sodium citrate dihydrate pH5.6 isoproponal 20%PEG4k 20%
and the crystal need a cryoprotectant, we have used the 30% glycerol but it
is not good, the mosaicity of
the diffraction pattern is a little high, so anyone knows which is the be
The file you need to run should end .class or .jar. If you don't have
such a file, you'll need to compile it first. You probably need a java
sdk rather than jre, although gcj might do the trick.
Then:
javac Switch.java
should make the .class file. (You may need to include the path to your
jav
Kevin Cowtan schrieb:
The file you need to run should end .class or .jar. If you don't have
such a file, you'll need to compile it first. You probably need a java
sdk rather than jre, although gcj might do the trick.
Then:
javac Switch.java
should make the .class file. (You may need to includ
Dear Yang Li,
Cryoprotection of crystals is not an exact predictive science - you have
to try a number of things, and in the worst case scenario, none of the
stuff you try may work out.
Assuming that your crystals are OK to start with (capillary mounted room
temp. pattern would confirm that), you
Dear All,
Please pass the following advertisement on to anyone you think might be
interested in this position.
Thank you.
With best regards,
Dirk
-
-
Hi all,
I'm refining the structure of a complex at low resolution (4.5).
Certainly refinement at low resolution will become more common, but
there isn't a whole lot out there now to use as a guide. I've
incorporated most of the suggestions from DeLaBarre and Brunger, but I'm
looking for any o
Sounds like a pretty successful refinement, given the resolution!
The fact that releasing NCS improves R-free suggests there are
real ncs violations (otherwise releasing ncs increases R-free).
But they may be confined to a few residues in contact areas.
You can locate these violations by comparin
I would recommend any one of these things:
1. Increase the concentration of the chemicals present, i.e. add more
iso-propanol OR add more PEG, but use a low molecular weight, like PEG400.
Either one or both. You will need 5% glycerol to get a good (ice-free)
cryo-condition or 10% PEG400 or 10
We are using a combination of X-ray crystallography and cryo-EM to determine
the structures of eukaryotic ribosomes undergoing translation initiation and
during elongation (refs 1,2). To help us further develop our programme, we are
seeking to appoint a Post-Doctoral Research Assistant, initiall
By the way, I'll extend that question: the validation
software Verify3D assigns not only buried state but
also polar fraction and secondary structure, using the
probability of finding given residues in the different
"environment" defined when combining all this
information to calculate a "score" of
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