Hi,John,
I faced the similar situation before even the resolution about 2.4. At
that region the residues are all hydrophobic ones and should be very
flexible . Arp/warp and phenix do not work well and resolve does not
improve the density either. At the end I just try to build the model
as I
Hi all !!
I am working with two data sets of same protein (130a/a) with resolutions
2.8 and 3.2 A. In both the cases the density for 100-130 aa is not very
clear.. it forms couple of helices.. i can see a long tube going but it is
feature less.. It is a MR solution.. i have tried TLS refinement
