Job opportunity:
Eternity Bioscience is hiring a structure biologist. Details please see :
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Best regards,
Joe
Hi All,
I am trying to write a shell script to streamline a few steps, one of which
is Unique, see below. As you can see, this program requires symmetry and
cell parameters. In CCP4 GUI Scalepack2mtz, these info are automatically
extracted from .sca file (first two lines). But I don't know if
I guess you may have to decide whether you want to modify your current
conditions or just start over to find new conditions, to get around this
ultra-fast crystallization. I don't know if you have played around all
parameters of current condition, such as lower temperature, protein
concentration,
Could you identify the cleavage sites by protein sequencing and design new
constructs (truncated versions) accordingly? It might improve your crystal
quality to get better resolution.
Joe
On Wed, Jan 16, 2013 at 9:22 AM, Tom Murray-Rust
tom.murray.r...@gmail.comwrote:
Just to add to
Dear all,
Is there a simple way to determine whether ligand is bound or not by
comparing the diffraction patterns between ligand-free (structure known) and
ligand-soaked protein crystals? I would like to solve the ligand bound
protein structure, but before I do so, I have to find out if the