Dear all,
I am trying to crystallize a small soluble protein. I have collected few
diffraction data sets for the same. Every time I collect a data set I find that
the crystal is diffracting at different angles only in one particular
direction, the z direction. These are few examples for the native data sets I
have collected.
Native crystal: space group P 31 2 1 48.52 48.52 161.90 90 90 120
P 31 2 1 48.94 48.94 169.89
90 90 120
P 3 2 1 48.40 48.40 154.48
90 90 120
We see similar pattern in SeMet crystals too. Thus, it becomes difficult to
merge the native and SeMet data sets. Is there a way to get around this
problem? I am looking forward to suggestions.
Megha
