The keyboard combo to get the settings is control+option+0
Sincerely,
Scott
> On Sep 18, 2013, at 19:14, Scott Classen wrote:
>
> I think if you press option + command + 0 a menu will pop up in the middle of
> the screen. There should be a display settings icon there. You can choose
> full s
I think if you press option + command + 0 a menu will pop up in the middle of
the screen. There should be a display settings icon there. You can choose full
screen or 1:1 pixel ratio etc. Just explore the various options and something
should work for you hopefully.
Sincerely,
Scott
> On S
check out the hidden .nx folder in your home directory.
You should have a folder named config.
You may have a .nxs file or .cfg file there just edit the file with a text
editor.
You probably need to change this value:
If you have a retina MacBook I guess you need to double that value perhaps.
J
I've got a question to people using a remote access to synchrotron computers.
I've got Macbook pro with Mac OSX 10.7.4, which requires the use of nxplayer
instead of commonly used nxclient. It works, but the size of emulated screen
gets twice bigger than the size of my computer's screen. As a r
Hi all,
Can anyone recommend software to dock previously solved domains into a (very)
low-resolution experimentally phased map?
I am working on a rather marginal case where this would be useful - very large
assembly (500kDA per ASU), native goes to 6.9A, and the best derivative goes to
8A with
On Wed, Sep 18, 2013 at 03:41:34PM +0100, Peter Keller wrote:
> I hope that this isn't quite what you meant There are already
> mutually-incompatible CIF dialects out there that have been created
> by developers coding to their own understanding and interpretations
> of the CIF/STAR format. I
Dear Colleagues,
There are two major issues that tend to trip up CIF programmers:
1. Dealing with the order independence of CIF. Unlike PDB format,
tags in CIF can validly
be presented in any order. This means you cannot simply scan a CIF for
a tag you want and
start processing from th
I didn't mean that, though reflection loop data shouldn't be problematic I
think (and may be very long). As you say tokenization is necessary but not
sufficient
I'm sure you have faced lots of corner cases, and naive approaches (that I
would have gone for) like "divide at spaces, then strip quo
Hi Phil,
I agree that the issue that you raise (about the need to define the data
items and categories propery) is an important one that needs proper
consideration. However, your mail could be read to suggest that correct
parsing of CIF-format data is a secondary issue that doesn't deserve the
The current version of scalepack already calculates CC1/2 and reports it in the
log file.
From: CCP4 bulletin board [CCP4BB@JISCMAIL.AC.UK] on behalf of Francesco
Angelucci [francesco.angelu...@uniroma1.it]
Sent: Wednesday, September 18, 2013 5:21 AM
To: CCP4BB@
Hi Phil,
When I wrote cif2cif to deal with reflection files from the PDB I opted for
good-enough parsing to provide input for cif2mtz. This was a while ago,
reflection files were still a mess at the time and my programming skills
never tested in practice. I just added support for anything that cou
As a novice looking at mmCIF from a developers point of view, for reflection
data, the complication is not so much tokenising (parsing), but what items to
write or to expect to read. For example as far as I can see an observed
intensity may be encoded in a reflection loop (merged or unmerged) as
As long as the .sca file is scaled but unmerged, then one way is
pointless -copy scain denzo.sca hklout denzo.mtz
aimless hklin denzo.mtz << EOF
scales constant
onlymerge
EOF
Phil
On 18 Sep 2013, at 11:21, Francesco Angelucci
wrote:
> Dear All,
>
> I am wondering if is possible to calculate
Dear All,
I am wondering if is possible to calculate the CC1/2 factor from the denzo
.sca file.
Thank you in advance
Francesco Angelucci
Hi Xiang.
If you are doing in vitro experiments like binding studies then try BODIPY
Fluorophores.
It conjugates the protein. Advantage is molecular weight of these BODIPY
Fluorophores is few hundreds Da.
Also, these dyes have well separable absorption and emission spectrums.
Good luck
Raj
On M
Dear All,
My name is Ryo Mizuta, I am a placement student working at the Institut
Laue-Langevin in Grenoble, France in the Life Sciences department. I am
currently designing/developing a prototype crystallization module for
proteins (based on batch crystallization) which enables automated
temper
*Postdoc position in Structural Biology at University of Bayreuth*
We are currently looking for a highly motivated postdoc for our
laboratory at the Dept. of Biochemistry at University Bayreuth, Germany.
Our work involves biochemical and structural studies on cellular
signalling systems with relev
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