* The successful candidate will join the Groton Structural and
Molecular Sciences group which has extensive expertise in the gene to structure
pipeline, in addition to biophysics and chemical biology. Our mission is to
provide integrated molecular insights into drug targets and
Yes, I agree! This (“Please look at my structure, and here are my files from
the last cycle of refinement") happens to me almost every week. :)
Diana
**
Diana R. Tomchick
Professor
Departments of Biophysics and Biochemistry
University of Texas
As someone who uses those "superfluous" columns all the time, I would
like to chime in in favor of keeping the default output columns of
refmac. If only I had a nickle for every time someone asked me to "look
at" a structure and only gave me the output files of refinement. Kind
of ties your
Hi
I wanted to draw a peptide interaction in the catalytic site together with
side chain of the enzyme. What is a good program to do that, or web based
service. I see the LIGPLOT and I am wondering if there are some other
alternatives of that.
best
Jiri
Hello Tang,
1) For MR, you might want to try a range of homologs, or even a stack of
overlapping homologs. A normal modes server like elNemo might also help
if it can predict the "bend" your molecule undergoes upon binding. A
long shot perhaps, but stranger things have happened. You also
HelloI have two questions if anyone can help:1. Does anyone know how PDBe Pisa
calculate if the residues interact? I can't find an explanation for this.
2. Also, I want to do SAXS on a liquid sample using a rigaku smartlab x-ray
diffractometer. It is set up for powder and the software they use
