Hello Klaus,
I think you should give Gerard some "Hofnarrenfreiheit". (That's a fine
German word for you to figure out, Gerard.) He is certainly not an evil
racist at heart.
Andreas
Klaus Piontek wrote:
Greetings (or in "correct" Swiss German "Grüezi wohl", with Umlaut=vowel
mutation) t
ROTECTED]>
Sender: CCP4 bulletin board
From: Gerard DVD Kleywegt <[EMAIL PROTECTED]>
Subject: [ccp4bb] Swiss humour - no laughing
matter? (Re: [ccp4bb] process SeMet labelled
data)
Comments: To: Dirk Kostrewa <[EMAIL PROTECTED]>
To: CCP4BB@JISCMAIL.AC.UK
L
We all begin at some point, and should help ourselves before we ask others
for help. Shivesh's question shows he has not even tried looking at
programs, initiate things on his own. I think such e mails should be
discouraged. I found what Mark said quite funny. All my labmates were
laughing..
Ar
shivesh kumar wrote:
Dear all,
I have a data set at 2.2A, of the selenomethionene labelled
protein.How should I process the data.Thanx for the help.
Shivesh
I think you should ask your local crystallographer for help. There are
several programs ( MOSFLM in CCP4, DENZO, XDS, D*TREK ) but you
On 1 Mar 2007, at 10:46, James Whisstock wrote:
Once you have integrated (run in ccp4 for MOSFLM), then you need to
scale the data using, for example, SCALA.
Have a look at the following tutorial for running scala.
http://www.ccp4.ac.uk/courses/ECM2004/runningscala.pdf
An updated versi
Dear Shivesh
Below I've tried to give you some broad ideas about where to look / read and
some packages / approaches to try.
For a start there is a very comprehensive tutorial on the ccp4 site together
with the experiemental phasing roadmaps.
http://www.ccp4.ac.uk/dist/examples/tutorial/html/h
I have found in my usenet adventures that usenet mavens often point
to this link before trying to sort out among themselves exactly what
level of humor to take with dubious posts:
http://www.catb.org/~esr/faqs/smart-questions.html
Of course usenet mavens also complain a little too m
Goede dag Gerard,
interesting that you think my last e-mail was addressed to you ;-)!
Yes, this was my first moralizing posting on this board after some 16
years. A bit sense of humor is fine, but the last posting was simply too
much. We shouldn't attack people personally or discriminate agains
gruzi dirk,
come on - lighten up a little! your reply wasn't funny or helpful either -
just moralising. (by the way - 't is a strange fact that whenever i get any
negative reactions to my own postings they stem *exclusively* from any or all
of these three countries: the us, germany and switzer
Dear all,
I wholeheartedly agree with Dirk. I was quite speechless yesterday when
seeing one sarcastic reply after another being sent to this correspondent,
who has probably been put off using this BB ever again. Its purpose is to
help people who need to ask such questions, rather than to ser
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Dear ccp4bbers,
I agree with Dirk. I have also noticed that much due to the way X-ray
crystallography is evolving, a lot of students/early-postdocs find
themselves "doing crystallography" in labs without a tradition in
crystallography, even without "r
Hi Mark,
although Shivesh's question was not very specific, and he should have
clearly given some more informations about what he would like to know,
he is probably a beginner in crystallography and simply asked for help
on this board. Not everyone has always time or is always in the mood to
why don't you just send all your images to the ccp4bb, then we'll
process them, solve the structure and publish it for you.
And we might put you in the acknowledgements, if you are lucky.
Mark
On 28 Feb 2007, at 16:35, Jonathan Grimes wrote:
Anastassis Perrakis wrote:
On Feb 28, 2007, at 14:3
>On Feb 28, 2007, at 14:37, shivesh kumar wrote:
>
>Dear all,
>I have a data set at 2.2A, of the selenomethionene labelled
>protein.How should I process the data.
Some hopefully useful remarks (fairly random and not complete and
exhaustive):
1. make sure to mask out the backstop and beamstop hol
Anastassis Perrakis wrote:
On Feb 28, 2007, at 14:37, shivesh kumar wrote:
Dear all,
I have a data set at 2.2A, of the selenomethionene labelled
protein.How should I process the data.
Carefully !
Thanx for the help.
Shivesh
Tassos
i am sure what tassos really meant was "Very Careful
> Dear all,
> I have a data set at 2.2A, of the selenomethionene labelled
> protein.How should I process the
> data.
Properly
On Feb 28, 2007, at 14:37, shivesh kumar wrote:
Dear all,
I have a data set at 2.2A, of the selenomethionene labelled
protein.How should I process the data.
Carefully !
Thanx for the help.
Shivesh
Tassos
Dear all,
I have a data set at 2.2A, of the selenomethionene labelled
protein.Howshould I process the
data.Thanx for the help.
Shivesh
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