Not easy to do that in the abstract! Look for obvious errors - is there a CISpeptide near by which has been labelled wrongly in the PDB? Is there a genuine error - too many residues, lost residues etc? Or is it just that the density is poor, and it is hard to fit any coordinates and equally hard to refine them sensibly.
If you are sure there are no obvious errors to correct the is a rEFINE option to improve the Ramachandran plot - or you can restrain the ramachandran angles.. But if there is an error the plot is correctly trying to alert you and the error needs creating.... Eleanor On 11 January 2015 at 12:06, Dialing Pretty < [email protected]> wrote: > Dear All, > > Will you please introduce me the ways to correct Ramachandran outlier by > Coot? > > Dialing >
