The Max Planck Institute of Molecular Physiology seeks to fill a
Postdoctoral Position in X-ray crystallography
The position is available immediately in the newly established Department of
Structural Biochemistry (Director: Stefan Raunser). It is initially limited to
3 years.
Job description:
Ou
Hello all,
I am currently running a Wyatt DynaPro Titan DLS using Dynamics 6.7.7.1. Ten
days ago, the hard drive on the XP computer running the instrument totally
failed and can no longer be accessed. I replaced it with a clone and tried to
reconnect the Titan, but the two drivers needed by t
Dear all,
I would like to remove two phospholipids bound to (actually into) a cytoplasmic
protein. The protein was expressed in E. coli and the crystal structure
revealed the presence of two co-purified phospholipids (most probably DPPE).
A web search gave me three methods to remove bound lipi
Hi Lionel,
A few musings/suggestions
If they are bound *inside* the protein, this suggests that the
phospholipids might be very tightly bound.
Do you have an affinity tag on your protein (e.g. His tag)? Perhaps you
might immobilise the protein on a suitable resin and wash with copious
amounts of
Dear CCP4BBers:
I'e got a problem about data processing when running SCALEPACK2mtz. Hope
you can give me some advice on that.
Here's my problem:
I have an .sca file processed by HKL2000 about 4 years ago, I just ran the
Scalepack2mtz program in order to transform it into .mtz file. However, the
Hi Jeff,
You can compare volume of binding cavities of two proteins. You can quickly
check cavity size in your structure using PDBsum or you can use a program
called viodoo to calculate volume of the cavity.
Following paer can be helpful
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2683046/
Rega
