<html><head></head><body style="word-wrap: break-word; -webkit-nbsp-mode: space; -webkit-line-break: after-white-space; ">Hello,<div><br></div><div><span class="Apple-tab-span" style="white-space:pre"> </span>I was wondering if there is a way to place in a molecule into a DNA and then minimize that structure either with chimera or in combination with other programs using chimera. For example, on page "1928" of the paper I attached they discuss posing a small molecule in between bases of the DNA. Here's the paragraph and the underlined sentences are of interest to me. </div><div><br></div><div>If you are wondering why I don't use DeepView for this, my answer is that it is very unstable and crashes more often then producing useful results.</div><div><br></div><div>Thanks for your help in advance. </div><div><span class="Apple-style-span" style="color: rgb(26, 26, 24); font-family: Times; font-size: 10px; "><br></span></div><div><font class="Apple-style-span" color="#1a1a18" face="Times" size="2"><br></font></div><div><span class="Apple-style-span" style="color: rgb(26, 26, 24); font-family: Times; font-size: 10px; "><br></span></div><div><span class="Apple-style-span" style="color: rgb(26, 26, 24); font-family: Times; font-size: 10px; "><br></span></div><div><span class="Apple-style-span" style="font-size: 14px;"><span class="Apple-style-span" style="color: rgb(26, 26, 24); font-family: Times; ">In a second stage, the crystallographic receptors were replaced by canonical B-DNA with similar sequences, generated with X3DNA.</span><span class="Apple-style-span" style="color: rgb(26, 26, 24); font-family: Times; "><span style="font: 7.0px Times">49 </span></span><span class="Apple-style-span" style="color: rgb(26, 26, 24); font-family: Times; ">Since structural changes in the macromolecule are not allowed during docking, one canoni- cal oligomer was previously modified to include an “inter- calation gap”. <b><u>In this way, Swiss PDB Viewer</u></b></span><span class="Apple-style-span" style="color: rgb(26, 26, 24); font-family: Times; "><span style="font: 7.0px Times"><b><u> </u></b></span></span><span class="Apple-style-span" style="color: rgb(26, 26, 24); font-family: Times; "><b><u>was used to pose an ellipticine molecule between two base pairs of canonical DNA, parallel to the base rings. After that, the complex was minimized by the steepest descent method, using the GROMACS package with the GROMOS 53A6 force field. </u></b>The result was a modified B-DNA in which the base pairs flanking ellipticine were separated by 6.50 Ĺ. Ellipticine was removed from the complex, and the modified B-DNA (see Figure 6B/F) was used as a target for docking with ellipticine. The sequences of the X3DNA generated oligomers are d(CGCAATTGCG)</span><span class="Apple-style-span" style="color: rgb(26, 26, 24); font-family: Times; "><span style="font: 6.5px Times">2 </span></span><span class="Apple-style-span" style="color: rgb(26, 26, 24); font-family: Times; ">(without gap) and d(CG- </span><span class="Apple-style-span" style="color: rgb(26, 26, 24); font-family: Times; "><b>GC</b></span><span class="Apple-style-span" style="color: rgb(26, 26, 24); font-family: Times; ">ATGCCG)</span><span class="Apple-style-span" style="color: rgb(26, 26, 24); font-family: Times; "><span style="font: 6.5px Times">2 </span></span><span class="Apple-style-span" style="color: rgb(26, 26, 24); font-family: Times; ">(with gap, indicated in bold)</span></span></div><div><span class="Apple-style-span" style="color: rgb(26, 26, 24); font-family: Times; font-size: 10px; "><br></span></div><div><span class="Apple-style-span" style="color: rgb(26, 26, 24); font-family: Times; font-size: 10px; "><br></span></div><div><span class="Apple-style-span" style="color: rgb(26, 26, 24); font-family: Times; font-size: 10px; "><br></span></div><div><span class="Apple-style-span" style="color: rgb(26, 26, 24); font-family: Times; font-size: 10px; ">.</span></div></body></html>