.*
To unsubscribe from the CCP4BB list, click the following link:
https://www.jiscmail.ac.uk/cgi-bin/WA-JISC.exe?SUBED1=CCP4BB&A=1
<https://www.jiscmail.ac.uk/cgi-bin/WA-JISC.exe?SUBED1=CCP4BB&A=1>
--
Dr.
missing in the structure
and interestingly, the Coot version coming with CCPEM (0.9.8.5) is also
not able to refine my sugar...
However, If I use CCPEM with the older CCP4-7.1, the refinement works fine.
Any idea ?
With many thanks,
Gia
--
Dr. Gianluca CIOCI
Toulouse Biotechnology
ooper. jon.b.coo...@protonmail.com
Sent from Proton Mail mobile
Original Message
On 21 Mar 2023, 16:43, Gianluca Cioci <
8d6e5314cb4c-dmarc-requ...@jiscmail.ac.uk> wrote:
Dear All,
I have collected a datase
nks in advance for any advice on how to rescue these data !
Cheers,
GIA
Click to zoom the image
--
Dr. Gianluca CIOCI
Toulouse Biotechnology Institute (TBI)
http://www.toulouse-biotechnology-institute.fr/en/research/enzyme-molecular-engineering-and-catalysis/cimes.html
PICT - Plateforme Intég
possible, I would prefer monomeric proteins (although not
really mandatory).
Is anybody able to give me some suggestions ?
Thank you,
GIA
--
1st French Congress on Integrative Structural Biology
Please check: http://bsi-2019.ipbs.fr
Dr. Gianluca CIOCI
Toulouse Biotechnology Institute (TBI
).
Is anybody able to give me some suggestions ?
Thank you,
GIA
--
1st French Congress on Integrative Structural Biology
Please check: http://bsi-2019.ipbs.fr
Dr. Gianluca CIOCI
Toulouse Biotechnology Institute (TBI)
BioCatalysis Team
http://www.toulouse-biotechnology-institute.fr/en/research
To unsubscribe from the CCP4BB list, click the following link:
https://www.jiscmail.ac.uk/cgi-bin/webadmin?SUBED1=CCP4BB&A=1
--
1st French Congress on Integrative Structural Biology
Please check: http://bsi-2019.ipbs.fr
Dr. Gianluca CIOCI
BioCatalysis
Dear All,
Is anybody using the HifliQ columns Ni/Co from Generon ? How well they
compare with the other brands ?
Thank you,
Gianluca
Hi,
Pure dextrans are linear alpha16 linked.
Branched or not depends on the enzyme (dextransucrase) that has been used
to synthesize it. If branching occurs this will be mostly on the alpha13.
Sulfation can occur on some or all the free hydroxyls groups.
Best regards
Gia
Il 28 Feb 2018 16:47,
Dear All
The ion exchange has the great advantage ,over other tecniques, to
concentrate the protein.
Histrap+sec is a big classic in protein purification but times it is worth
considering other schemes. Why doing a SEC? It is for removing aggregates
or a contaminant ? It the latter case probably
t would be interesting to know from an expert in anisotropy e.g. the
> creators of UCLA anisotropy server or Startaniso whether anisotropy can
> cause this problem and whether there is any way around it.
> >>
> >> Cheers, Paul
> >>
> >> Paul Steven Miller (PhD)
>
Dear All,
I am trying to refine a structure at 3.3A. Model has 60% identity to the
target. Maps look OK (for 3.3A) and rebuilding in Coot is relatively
straightforward. However, after some rebuilding cycles the R factors are
stuck at 0.37/0.39 (REFMAC).
XTRIAGE tells me that everything is normal (
Dear Narayanan
Which kind of resin are you using ?
In my lab we work with proteins that bind dextran which is often used as
crosslinker in chromatography resins.
Crosslinked resins have a highly reticulated structure made of sugars that
can be quite similar to peptidoglycan...
As a test, you could
Dear All,
I think this topics has been already treated many times but, knowing that
the majority of structures in the pdb have a DPI around ~0.15
I would like to know what is the consensus value that is commonly defined
as "acceptable", especially for low resolution structures (3.5A which
could s
14 matches
Mail list logo