support (as attached PDF format letters with your letter
head addressed to me), "Jim Naismith, Chair of CCP4". Please email these to
[EMAIL PROTECTED], marked CCP4.
If the letter is to be useful, you should explain who you are, what your lab
does and what it comprises, please
To clear up a few things.
International support is extremely welcome.
Commercial organization support is extremely welcome.
In fact both of these are essential and will count for more than UK
academics.
ANY letter of support from ANYONE is welcome.
Step change, paradigm shifting are anglosaxo
you feel (and only if) you can support CCP4, it would greatly help to
have letters of support (as attached PDF format letters with your letter
head addressed to me), "Jim Naismith, Chair of CCP4". Please email these to
[EMAIL PROTECTED], marked CCP4.
If the letter is to be useful,
g the case. Commercial organization support is extremely
welcome.
If you feel (and only if) you can support CCP4, it would greatly help to
have letters of support (as attached PDF format letters with your letter
head addressed to me), "Jim Naismith, Chair of CCP4". Please email these to
[
If memory serves correctly Ramachandran based his plot on VDW.
Therefore all programs which use VDW will tend to put residues in the right
place.
Certainly in phenix.refine adding H's to one of my problematic structures
(twinning) not only improved the clash score but pushed a further 4% into
th
I have a multidomain multimeric protein. I would be interested to see if the
TLS parameters correlate with some functional data.
TLSANAL tanks with overlap error (no overlap that I am aware of). I fed it
tls file and final pdb.
Does anyone know any other way to interpret TLS parameters? (preferabl
/ccp4license.php for further details.
Best
Jim Naismith
Chair of CCP4
The University of St Andrews is a charity registered in Scotland : No
SC013532
Dear All,
I have an interesting problem, we have a 3.45A structure of
a membrane protein. We have just been told that the structure is "too low
resolution to be considered as the uncertainty is too high". We use the
structure to identify helices which have moved.
Is there a blanke
I have a metal centre and I have constructed my dictionary. What I cannot do
is restrain the metal to water distance. All my amino acid links are
working. However even though I have created the dictionary and put the link
in PDB header REFMAC ignores it and pushes the water back to 2.45A (rather
th
I don't know how many of you are frustrated with AO5* in NADP NAP (and in
NAD). I trolled the web looking for a solution but did not find it.
I think I have converted the current NAP nomenclature from the EBI in REFMAC
and COOT to use the new agreed nomenclature for this residue. Simply replace
yo
Dear All,
Thanks to many of you who posted comments and suggestions.
The review process concluded on our paper.
I will try to distil the suggestions I found useful with some comments from
my own experience.
1 Do not be put off by editor, argue for a technical review in advance of
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