Could it be a formate ion (HCO2−)? _Gang
-Original Message-
From: CCP4 bulletin board [mailto:CCP4BB@JISCMAIL.AC.UK] On Behalf Of Stephen
Cusack
Sent: Monday, October 09, 2017 5:40 PM
To: CCP4BB@JISCMAIL.AC.UK
Subject: [ccp4bb] help identifying unknown density
Dear All,
I am
Lysine-methylation has proved to be helpful to change the molecular packing
in protein crystals (i.e. you might obtain a completely different crystal
form). _Gang
From: CCP4 bulletin board [mailto:CCP4BB@JISCMAIL.AC.UK] On Behalf Of
Prerana G.
Sent: Friday, April 24, 2015 5:01 AM
To:
of the MBP lattice and was completely disordered. Therefore, I am
personally not very optimistic about the method.
Best wishes,
Gang DONG
On Fri, May 16, 2014 17:57, Randy Read wrote:
Dear Niu,
When it works, crystallising a fusion protein can be great, with the big
advantage that placing a model
Dear all,
Could anyone tell me your experience with Biacore (any models) or a similar
SPR-based technology for measuring interaction kinetics? I also want to know
the price ranges to discuss with our department/facility managers.
Thanks,
Gang
We mainly measure protein-protein interactions (sometimes protein-small
molecules). Thanks! _Gang
From: Bosch, Juergen [mailto:jubo...@jhsph.edu]
Sent: Monday, October 28, 2013 3:17 PM
To: Gang Dong
Cc: CCP4BB@JISCMAIL.AC.UK
Subject: Re: [ccp4bb] Biacore/SPR
Protein-protein interaction
Dear Kostas,
MBP by itself is a monomer. In most of our cases using it as a fusion tag,
the yield of a target protein increases drastically (i.e. 5 to 20 folds
more). However, we have seen in a couple of cases that the target proteins
strongly interact with the MBP tag, which causes
Try FTsite: http://ftsite.bu.edu/.
Gang
On Wed, May 29, 2013 09:17, Karsten Niefind wrote:
Dear colleagues,
please allow me to ask crystallography experts for advice in a
bioinformatics issue:
Which methods (programs, servers) would you use and recommend to search
computationally on the
