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<p>Dear Oleg,</p>
<p>sorry for the log.</p>
<p>The strange thing is that the input structure (output from NAMD MDFF where we also apply SS restraints to NA has a correct and better SS than the one at the end of the RealSpace refine.</p>
<p>I also checked the restraints in the .geo file and it seems correct. I only found in previ<span style="font-size: 12pt;">ious calculations that the atom identity of some atoms (in the charmm 36 topology) must be changed for the NA restraints to be correctly
set by phenix (C3M of THY must be changed for C7). </span></p>
<p>My only hypothesis at the moment is that the occupancy refinement (currently at a value of 1.00 for all atoms) tends to distort strongly the extremities of the duplex because the electron density is weak in these regions with a bad shape and that this (presumlably)
distorts the NA structure to fit the poor density that does not ressemble the one for a B-DNA in these regions. This could be solved if we have a way to increase the harmonic constants for the SS restraints, but i dont see this possibility.</p>
<p>Your advice on this hypothesis is welcome.</p>
<p>Best regards.</p>
<p>Philippe.</p>
<p><br>
</p>
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<div id="divRplyFwdMsg" dir="ltr"><font face="Calibri, sans-serif" color="#000000" style="font-size:11pt"><b>De :</b> Oleg Sobolev <osobolev@lbl.gov><br>
<b>Envoyé :</b> mardi 30 janvier 2024 18:21:02<br>
<b>À :</b> CUNIASSE Philippe<br>
<b>Cc :</b> phenixbb@phenix-online.org<br>
<b>Objet :</b> Re: [phenixbb] RealSpaceRefine Nucleic acid SS restraints ?</font>
<div> </div>
</div>
<div>
<div dir="ltr">Dear Philippe,
<div><br>
</div>
<div>Most often the problem is that the geometry of the input model is so distorted that the procedure fails to find base pairs and therefore restrain them. </div>
<div><br>
</div>
<div>Couple of ways to check for this are: </div>
<div>1. Look in the .log into </div>
<div> Finding SS restraints...<br>
Secondary structure from input PDB file:<br>
0 helices and 0 sheets defined<br>
0.0% alpha, 0.0% beta<br>
12 base pairs and 21 stacking pairs defined.<br>
Time for finding SS restraints: 0.04<br>
Creating SS restraints...<br>
<br>
No hydrogen bonds defined for protein.<br>
Restraints generated for nucleic acids:<br>
32 hydrogen bonds<br>
64 hydrogen bond angles<br>
0 basepair planarities<br>
12 basepair parallelities<br>
21 stacking parallelities<br>
</div>
<div><br>
</div>
<div>This part would give a general idea if anything worked at all.</div>
<div><br>
</div>
<div>2. Inspect .geo file after refinement and look for "Basepair parallelity restraints" and "Bond-like restraints" (secondary structure H-bonds) sections. Here you can see exactly what restraints were applied and if the basepairs in question were in fact
restrained.</div>
<div><br>
</div>
<div>If you supply the restraints in the .parameter file, check the nucleic_acid.hbond_distance_cutoff parameter. The default is 3.4, you may need to increase it so your annotations are not filtered out.</div>
<div><br>
</div>
<div>I'm happy to look at your files (model and parameter, if any) to figure out what is happening. Please send them off-list indicating problematic residues. Files will be treated confidentially.</div>
<div><br>
</div>
<div>Best regards,</div>
<div>Oleg Sobolev.</div>
</div>
<br>
<div class="gmail_quote">
<div dir="ltr" class="gmail_attr">On Tue, Jan 30, 2024 at 7:20 AM CUNIASSE Philippe <<a href="mailto:Philippe.CUNIASSE@cea.fr">Philippe.CUNIASSE@cea.fr</a>> wrote:<br>
</div>
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<p>Dear all,</p>
<p>I am currently refining a protein-nucleic acid structure obtained by MDFF (NAMD) with a 2.9 Å cryo-EM map.</p>
<p>Dues to the poor density of the map at the end of the DNA duplex (likely due to breathing at the ends of the duplex), the structure of the DNA tends to be distorted.</p>
<p>I tried to set up a set of nucleic acid restraints (Base pairing and base stacking for the full sequence), h<span style="font-size:12pt">owever, despite the fact that the syntax was checked and no error message is present in the log file, it seems that the
restraints are not taken into account as if the constant restraints were two weak. And indeed when examining the refined structure, the pairing and stacking restraints for the base pairs at the extremities of the DNA duplex are not fulfilled.</span></p>
<p>Have you a suggestion to solve this problem ?</p>
<p>Thanks in advance for your help.</p>
<p>Best regards.</p>
<p>Philippe.</p>
<p><br>
</p>
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<span lang="EN-US" style="font-family:Courier">Philippe Cuniasse, PhD/HDR.<u></u><u></u></span></p>
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