Hi all,
I have my home source X-ray equipment up for grab. I used all the equipment one
month ago and collected a beautiful 1.9Å data on a nuclear receptor LBD so
everything is in working order, but I give no garantees.
It is yours if you come and pack and ship it yourselves. If anyone wants
Dear Colleagues,
I do not think it is highly inappropriate that a crucial episode in the
history of crystallography is described/commmented on in this thread, and I am
not sure by whom its removal will be highly appreciated, other than by Prof.
Berger. I do not know any of the protagonists of
Dear Colleagues,
The Structural and Computational Biology Unit at EMBL Heidelberg,
Germany is looking to recruit an Engineer for Scientific Computing in
Structural Biology to handle the following responsibilities:
- Development and support of the scientific computing environment of the
Hi all,
I am trying to calculate accessible surface area between 2 helices from 2
different domains of protein. PISA gives me either total interface of the
protein or per residue. Can anyone please suggest me what would be the best
possible way to get it?
Thanks and regards
Atul
How about cutting up the pdb file into the desired sections and using pisa on
them?
JPK
From: CCP4 bulletin board [mailto:CCP4BB@JISCMAIL.AC.UK] On Behalf Of Atul Kumar
Sent: Monday, May 04, 2015 1:56 PM
To: CCP4BB@JISCMAIL.AC.UK
Subject: [ccp4bb] calculation of ASA between two helices
Hi all,
Hello everyone
Can anybody suggest me a cryo condition for a crystal obtained in
MIDAS screen of Molecular Dimension:
G1 0.1MTris8.0G10.1Mpotassium chloride25% v/vSOKALAN®CP7 0.1MHEPES7.0
G20.3Mammonium formate20% v/vSOKALAN® CP 5 0.1MHEPES7.0
Crystals are in beautiful cuboid shaped but all
How long are you cryoprotecting for?
You don't really need more than a few seconds. If I have sensitive crystals i
tend to just swipe them slowly through the final CP solution and often that
works. If I would leave them in the CP solution for more than say 30 seconds
the crystals would behave
High concentration of ammonium formate is a cryosolvent
On Mon, May 4, 2015 at 5:20 PM, Tristan Croll tristan.cr...@qut.edu.au
wrote:
What about nature's favourite cryoprotectant, trehalose?
From: CCP4 bulletin board CCP4BB@JISCMAIL.AC.UK on behalf of
What about nature's favourite cryoprotectant, trehalose?
From: CCP4 bulletin board CCP4BB@JISCMAIL.AC.UK on behalf of Roger Rowlett
rrowl...@colgate.edu
Sent: Tuesday, 5 May 2015 7:22 AM
To: CCP4BB@JISCMAIL.AC.UK
Subject: Re: [ccp4bb] cryo condition
We
Dear All,
when starting CCP4i via the icon, AutoSharp remains greyed out, suggesting it
is not installed. However, when I start CCP4i in an XQuartz window (i.e. “ccp4i
”), AutoSharp can be run.
I guess this may be because in first way my “.profile” file is not read, any
ideas how to fix this?
We rarely use glycerol anymore, because it seems to fail so often for
many of our current proteins. Try glucose, 25-30%. This is most
conveniently done by weighing 125-150 mg of glucose in a microcentrifuge
tube, then addding well solution to the 0.5 mL mark and mixing until
completely
If in doubt, try dragging the crystal through a 1:1 mix of Paratone-N and
Mineral oil until most or all the mother liquor from surrounding the
crystal has been removed.
There are more tips here:
http://hamptonresearch.com/tip_detail.aspx?id=99
Good luck!
D
On Mon, 4 May 2015 19:45 Faisal
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