Hello,
I am learning how to use PanDDA and would appreciate some clarifications on the
modeling and refining steps.
I realize that maybe some questions will be too obvious, but I would appreciate
the confirmation of my guesses so I might learn to do it the correct way.
I managed to get to step
Dear Community,
There is this nice web server, ZipperDB
(https://services.mbi.ucla.edu/zipperdb/intro), that predicts the fibrillogenic
propensity of a given peptide segment. However, it seems to have been down for
a couple of months now. I have emailed them a few times but have not received a
Thank you all for your thoughtful answers.
I'll stick to the crystallographic data and model as much as I can with
reasonable occupancy and B factors, even if the result is a truncated model.
I don't believe in the zero occupancy trick either. I just thought the PDB
was more flexible these days,
Dear All
The University of California, Irvine is currently accepting applications for a
specialist position to manage the day-to-day operations of the biological side
of the electron microscopy facilities and services to users at the UC Irvine
Materials Research Institute (IMRI) see https://im
