If you’re sure about your refinement parameters and results, I would check
PDBredo just in case. I’d go for better Rs, but maybe it’s not possible with
your data.
Best,
Lorenzo
domingo, 24 de março de 2019 01:17 -0300 de biophysics.w...@gmail.com
:
ALL.
I have data at 2.4 A in P21 sp gr, he
Good morning all,
I need to identify my dimer and tetramer interfaces, and point them out in
Pymol. Any website/program/script suggestions? I tried PISA, but it only shows
me some residues from some interfaces, I need something more "complete".
Thank you very much,
Lorenzo
Hello Maria!
I would recommend these 2 links:
https://strucbio.biologie.uni-konstanz.de/xdswiki/index.php/Tutorial(First_Steps)
and for difficult datasets:
https://strucbio.biologie.uni-konstanz.de/xdswiki/index.php/Difficult_datasets
Are you having problems with the “generate XDS.inp?” Maybe
Dear Phenixbb and CCP4bb members,
I'm currently refining a structure and facing some problems. It's originally a
tetramer in solution, but I could only solve it in P1 group, with 8 molecules
in the asymmetric unit (two tetramers). One of my chains is complete, but the
others present some signi
