be nice if
these two refinement programs (my standard 2) could understand each other.
I have been hesitant to use a phenix.refine output with ANSIOU
information as a MR model through phaser, but I suspect that my hesitation
is unfounded.
Kevin P Madauss V-161a
US
Jim is making from the 3.45A structure that is properly restrained and
refined.
Kevin P Madauss V-161a
US Structural Biology GlaxoSmithKline
Office: 919.483.3759 5 Moore Drive
Cell: 919.924.6436 RTP, NC 27709
I would suspect radiation damage for the S density . I have not seen
radiation damage of only COO carbons, but then again, I do not routinely
get such good diffraction.
Kevin P Madauss V-161a
US Structural Biology GlaxoSmithKline
Office
I would start looking at the buffer conditions for the protein. One place
to start is to reduce the salt. I would half, quarter, and then try no
salt at all. I
Kevin P Madauss V-161a
US Structural Biology GlaxoSmithKline
Office: 919.483.3759
would cut 15-20 residues of the N and C terminus and try in phaser and
Molrep again.
Kevin P Madauss V-161a
US Structural Biology GlaxoSmithKline
Office: 919.483.3759 5 Moore Drive
Cell: 919.924.6436 RTP, NC