You need to say what the cell dimensions are for these 2 options..
Eleanor
On 29 May 2012 15:59, Andrey Lebedev andrey.lebe...@stfc.ac.uk wrote:
Hi Mike.
I would be more careful about incorrect space group. Yes, sometimes
auto-indexing gives strange results.
However, in your case two sets
Well - I am not familiar with the PHENIX dictionary but you are right; if
you restrain metal bond distances the structure will reflect the restraints
but if you don't restrain the distances then the respective gradients for a
light atom and a heavy one can produce some very odd and unrealistic
Space groups F23 and P4132 are not subgroups of each other (without
invoking pseudotranslational symmetry) so they cannot be related by
twinning. The end of theoretical analysis.
Zbyszek Otwinowski
You need to say what the cell dimensions are for these 2 options..
Eleanor
On 29 May 2012
Post-Doctoral Research Assistant in Biochemistry
Molecular Diagnostics and Thereputics
*University of Southampton*
*Location: *Highfield Campus
*Salary: * £27,578 to £33,884
Full Time Fixed Term
*Closing Date: * Tuesday 12 June 2012
*Interview Date: * To be confirmed
Hi Eleanor,
was there recently an update to beverage ? Could you send me a link to version
2.0 perhaps ?
And more importantly it hopefully was compiled with EtOH and some vitamins :-)
Jürgen
On May 31, 2012, at 7:02 AM, Eleanor Dodson wrote:
Or do something like beverage, and again you will
Hi all,
E3 ubiquitin ligase is responsible for flagging proteins for degradation by
transferring ubiquitin from a donor protein onto the molecule to be degraded.
It is activated by phosphorylation of a tyrosine which promotes a huge
conformational change, swinging its RING domain 180 degrees
Dear All,
I am looking for a way to calculate the size of a protein cavity which is
occupied by a loop from a ligand protein. The goal is to see what's the maximum
length of peptide allowed in this cavity.
Thanks,
Tongqing
Tongqing Zhou, Ph.D.
Staff Scientist
Structural Biology Section
Hi,
You could try CASTp (http://sts.bioengr.uic.edu/castp/). If your protein is in the pdb it may well be in their database, if not, just upload it.
Cheers,
Boaz
Boaz Shaanan, Ph.D.
Dept. of Life Sciences
Ben-Gurion University of the Negev
Beer-Sheva 84105
Israel
E-mail:
Meant to include the following link in the previous message:
http://www.youtube.com/watch?v=9Jn8K8EA7-Q
JPK
On Thu, May 31, 2012 at 1:20 PM, Jacob Keller
j-kell...@fsm.northwestern.edu wrote:
Dear Crystallographers,
in case you have not heard, it would appear that the Rmerge statistic
has
It wasn't doing well lately. So, it was expected.
From: CCP4 bulletin board [CCP4BB@JISCMAIL.AC.UK] on behalf of Jacob Keller
[j-kell...@fsm.northwestern.edu]
Sent: Thursday, May 31, 2012 2:20 PM
To: CCP4BB@JISCMAIL.AC.UK
Subject: [ccp4bb] Death of Rmerge
Rpim (from the East) just told me You don't need to be helped any longer.
You've always had the power to go back to Kansas.
-Original Message-
From: CCP4 bulletin board [mailto:CCP4BB@JISCMAIL.AC.UK] On Behalf Of
Oganesyan, Vaheh
Sent: Thursday, May 31, 2012 2:27 PM
To:
We used VOIDOO recently and it worked well
Kleywegt, G. J. Jones, T. A. (1994). Detection, delineation,
measurement and display of cavities in macromolecular structures. Acta
Crystallogr. D Biol. Crystallogr. 50, 178-185.
On Thu, May 31, 2012 at 12:41 PM, Zhou, Tongqing (NIH/VRC) [E]
A list that you might want to check if it is useful for you.
http://www.caver.cz/index.php?sid=133
Enjoy.
Allan
Quoting Zhou, Tongqing (NIH/VRC) [E] tz...@mail.nih.gov:
Dear All,
I am looking for a way to calculate the size of a protein cavity
which is occupied by a loop from a ligand
Yes! I want a copy of this program RESCUT.
REMARK 200 R SYM FOR SHELL(I) : 1.21700
I noticed structure 3RKO reported Rmerge in the last shell greater
than 1, suggesting the police who were defending R-merge were fighting
a losing battle. And this provides a lot of ammunition to
Alas, how many lines like the following from a recent Science paper
(PMID: 22605777), probably reviewer-incited, could have been avoided!
Here, we present three high-resolution crystal structures of the
Thermus thermophilus (Tth) 70S ribosome in complex withRMF, HPF, or
YfiA that were refined by
On 05/31/12 12:07, Jacob Keller wrote:
Alas, how many lines like the following from a recent Science paper
(PMID: 22605777), probably reviewer-incited, could have been avoided!
Here, we present three high-resolution crystal structures of the
Thermus thermophilus (Tth) 70S ribosome in complex
Good idea, but how to get it to catch on without publishing in Science?
JPK
On Thu, May 31, 2012 at 4:21 PM, Dale Tronrud det...@uoxray.uoregon.edu wrote:
On 05/31/12 12:07, Jacob Keller wrote:
Alas, how many lines like the following from a recent Science paper
(PMID: 22605777), probably
On Thursday, May 31, 2012 02:21:45 pm Dale Tronrud wrote:
The resolution limit of the data set has been such an important
indicator of the quality of the resulting model (rightly or wrongly)
that it often is included in the title of the paper itself. Despite
the fact that we now want to
There are things you can expect to learn from a
2Å structure that you are unlikely to learn from a 5Å structure, even
if equal care has been given to both experiments, so it makes sense
for the title to give the potential reader an idea which of the two
cases is presented. But for this
In the meantime we could follow Phoebe Rice's example and put
the resolution at I/sigma=2 in REMARK 2 resolution of structure
but put the actual bleeding-edge resolution we used in the
reduction and refinement statistics (At least if the PDB
will allow us to have different values in these three
I am little curious about the anisotropically truncated data for 3RKO:
Percent Possible(All)96.0
Mean I Over Sigma(Observed) 0.8
In the supplementary table of the nature paper it was made clear that this
3.16-3.0A, I/sigmaI=0.8 and Rmerge=1.216 shell was the outer shell of the
Leo will probably answer better than I can, but I would say I/SigI counts only
the present reflection, so eliminating noise by anisotropic truncation should
improve it, raising the average I/SigI in the last shell.
F/sigF is expected to be better than I/sigI because dx^2 = 2Xdx,
dx^2/x^2 =
xdrawchem is free and will do this.
On May 31, 2012, at 8:01 PM, Appu kumar wrote:
Dear ccp4 user,
Sorry for offset question, Anyone please tell me
the name of programme which can be used to draw enzyme reaction mechanism (
like Sn1 and Sn2). Your kind help
Hi,
Anyone please tell me
the name of programme which can be used to draw enzyme reaction
mechanism (
like Sn1 and Sn2). Your kind help will be much appreciated
BKChem is also free software.
http://bkchem.zirael.org/
Takanori Nakane
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