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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
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
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
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.
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
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
board CCP4BB@JISCMAIL.AC.UK
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
List-Help: http://www.jiscmail.ac.uk
Dear all,
I have a data set at 2.2A, of the selenomethionene labelled
protein.How should I process the
data.
Properly
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
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 holder
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
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