[phenixbb] histidine flip in refinement
smith_liu123 at 163.com
Tue Jul 21 20:10:36 PDT 2015
Related to Joel's question, suppose the resolution is about 2-3 A, and I have added H (should be modelled "H"）for the refinement. If I want to measure the H-bond length between the NE2 and H of OH of Tyr, I need to measure the distance between NE2 and the "modelled H" of OH of Tyr. Is this "modelled H" position reliable for the length measurement of the H-bond?
At 2015-07-22 10:04:39, "Pavel Afonine" <pafonine at lbl.gov> wrote:
as was suggested main.nqh_flips=False should disable this.
However I'm puzzled about this. NQH flips functionality is designed to flip these residues such that the clashes are minimized and plausible H-bonding is achieved. So I wonder why it is not working in your case?
Would it be possible to send me input files (off list) so that I can reproduce this and investigate. Also please indicate HIS in question.
On 7/21/15 02:07, Joel Tyndall wrote:
We are trying to optimise a histidine interaction where NE2 would ideally make a hydrogen bond with an adjacent tyrosine hydroxyl. The starting point contains the hydrogen bond. However upon refinement the ring flips (chi2 x 180 degrees) to place the CE1 adjacent to the tyrosine hydroxyl.
Is it possible to stop this as I see no reason why phenix.refine would want to do this
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