Dear Supratim,
In my experience, as long as you do not run into an overlap problem, a
large mosaicity is not a problem. If the statistics look good, you can
safely use the data. However, if the completeness of the data is much
lower than what was predicted, many spots may have been thrown out
bec
Hi friends
what is the maximum mosaicity value to work with. When i am doing Heavy metal
replacement my mosaicity value is around 1 - 1.2 after processing through HKL.
I don't know is it acceptable data. I have used mercuric chloride for my
protein and it has shown good results .However in case
Hi friends
what is the maximum mosaicity value to work with. When i am doing Heavy
metal replacement my mosaicity value is around 1 - 1.2 after processing
through HKL. I don't know is it acceptable data. I have used mercuric
chloride for my protein and it has shown good results .However in case of
Hi,
A post-doctoral opening in protein crystallography in the laboratory of
Prof. Chris Dealwis at the Cleveland Center for Membrane and Structural
biology. The project involves structure determination of protein-protein
complexes and protein drug interactions. We are seeking for an individual
tha
Hi Rob,
thank you, your comments helped a lot.
From the Refmac5 paper I did not get the fact that d is set to d_current
after each step. In that case you are right, jelly-body corresponds rather to
DEN with gamma=1 than to gamma=0.
And of course, a very important difference is, as you said,
Dear all,
Thank you for your help and suggestions. Actually I need to consult the
book in order to analyze some of our experimental results and I was in a
bit hurry. Honestly my intention was not however, to violate the copyright
issues but I thought scientific problems demands much than the mere
*Microlytic is excited to announce the following opportunity: Applications
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The qualified applicant will possess a Ph.D. in Biochemistry and/or
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The correct URL for the MSc in Structural Molecular Biology via the web at
Birkbeck is: http://www.bbk.ac.uk/study/pg/science/TMSBISCL.html.
Dr Tracey Barrett,
Crystallography,
Institute for Structural and Molecular Biology,
Birkbeck College,
Malet Street,
London WC1E 7HX
Tel: 020 7
*CALL FOR PROPOSALS FOR ESRF BEAM TIME WITH ONLINE MICROSPEC*Proposal
Deadline *4th September 2012*
There will be beam time available at the ESRF for MX data collection
with a setup that allows online monitoring of UV/VIS absorbance or
fluorescence spectral changes of the crystal during the X-
Dear all,
registration is currently open for the postgraduate certificate
course in Protein Crystallography via the web at Birkbeck that starts on
Monday October the 1st. It is for the duration of 1 year during which all
aspects of protein crystallography will be covered from the fundame
Hi All,
May I ask opinion of those who currently have standalone UV microscope whether
or not they are happy with their choice? Few that I know are from Formulatrix,
JanScientific and Corima. Pros and cons of your instument are greatly
appreciated.
I'll send the summary to the list.
Regards,
-BEGIN PGP SIGNED MESSAGE-
Hash: SHA1
Dear Sudipta,
wouldn't distributing such a soft copy ("the unprinted digital
document file", wikipedia) be pretty illegal, at least in most
countries? If this is the case, your email does not follow this list's
etiquette.
I appreciate being corrected
There is a web site
used.addall.com
that searches through many used booksellers. It appears that
there are copies available for under $3.00 (plus postage, obviously).
Frances
=
Bernstein + So
Dear All,
I am collecting one data set (resolution around 2.4) for a protein SG P21.
After collecting few frames (42 frames) the completeness is showing 49%, R
merge 11%, mosaicity is 1.08, intensity 9.7. but the chi square value is
showing very high, around 3.061. I tried changing error scale
The CCP-EM project aims to provide computational support for scientists and
software developers using electron cryo-microscopy for structural biology, by
analogy with similar successful projects in macromolecular crystallography
(CCP4) and biological nuclear magnetic resonance spectroscopy (CCPN
Hi Teresa,
An additonal disadvantage of using plastic plates would be the
polarisation of the plastic. Many users use cross-polarisation to image
LCP plates.
Flip
Op 8/29/2012 21:24, Theresa Hsu schreef:
Dear all
Is there any pros and cons of using plastic plates for LCP crystallization? T
Also, plastic plates are suitable for in-situ diffraction tests where glass
ones cannot be used due to the high absorption of X-rays by glass.
Best wishes,
Tadeusz
From: CCP4 bulletin board [mailto:CCP4BB@JISCMAIL.AC.UK] On Behalf Of Jim
Fairman
Sent: 29 August 2012 21:19
To: CCP4BB@JISCMAIL
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