You may want to check your geometry weighting (3 Angstroms isn't that
low; but I think the default matrix-weight is meant for higher resolutions).
Pete
vincent Chaptal wrote:
Hi,
we are refining a low resolution (3A) membrane protein using coot
0.6_pre2228.
In alpha helical regions, coot in doing a very good job but we have more
trouble in loops or kinks in helices.
Typically, in those regions, we just have density for the main chain
carbonyls and the CB of the side chains.
My question is how to use real space refinement in those regions?
very often, the side chain of large residue (Lys, Arg, Glu, Trp...) is
moving either in the main chain density, or in a neighboring density and
the refinement is impossible. My way around is to mutate those large
residues to Ala and back to the original when i'm happy with the
refinement, but that doesn't seem optimum.
What i would like is to have coot only take care of the main chain,
trying to fit carbonyls and CB in the blobs of the main chain.
will *set-refinement-move-atoms-with-zero-occupancy 0* do the trick?
is it possible to have a button saying "perform real space refinement
only on the main chain + CB" ? (say in the R/RC control box?)
thanks very much
vincent
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