<div>Thank you Emanuel. I will try what you have suggested and I think I will try to confirm it exeprimentally to be sure about my initial structure. This is terminal which is highly flexible and beta loops are very common for this sequence. </div>
<div>Thanks a lot!</div>
<div> </div>
<div>Steven<br><br></div>
<div class="gmail_quote">On Mon, Jan 9, 2012 at 9:19 AM, Emanuel Peter <span dir="ltr"><<a href="mailto:Emanuel.Peter@chemie.uni-regensburg.de">Emanuel.Peter@chemie.uni-regensburg.de</a>></span> wrote:<br>
<blockquote style="BORDER-LEFT:#ccc 1px solid;MARGIN:0px 0px 0px 0.8ex;PADDING-LEFT:1ex" class="gmail_quote">
<div style="FONT-FAMILY:Helvetica,Arial,sans-serif;FONT-SIZE:13px">Hi Steven,<br><br>There is a difference between homology modelling and ab-initio modelling.<br>With SWISS-modeller or ITASSER you have a lot of templates, which are searched<br>
automatically. In case, if this part of the sequence does not have any homology,<br>then your model contains loops and has no secondary-structure as alpha-helices<br>or beta-sheets.<br>As one possibility you could model these parts by ab-initio modelling (ROBETTA).<br>
Another possibility could be the MODELLER.<br>From the bunch of models you should decide yourself, what's the most<br>reasonable one. <br>[ Radius of gyration (SAXS). Secondary structure prediction (SSPRED) ]<br><br>I am not sure if this could help you further and of course I am not an expert in<br>
this field. I do not want to open a huge discussion with personal attacks as it <br>is usually done in this list. <br><br>Bests,<br><br>Emanuel<br><br>>>> Steven Neumann <<a href="mailto:s.neumann08@gmail.com" target="_blank">s.neumann08@gmail.com</a>> 09.01.12 9.51 Uhr >>>
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<div class="h5"><br>
<div>Dear Gmx Users,</div>
<div> </div>
<div>I am wondering whether any of you faced a problem of predicting terminal of the protein. I submitted my sequence to the software like ITASSER or LOMETS and obtined some models forming loops which are expected. The confidence of those models (as this is terminal) are not so high and I am wondering whether I will confirm sencondary structure of my protein exeprimentally (CD exepriment) I can trust and choose one of models formed by the server? Please, let me know if you had similar problem in your past. </div>
<div>I am writing this message on this forum as many people are studiyng proteins in Gromacs. If you can suggest other mailing list I would be grateful.</div>
<div> </div>
<div>Thank you,</div>
<div> </div>
<div>Steven</div></div></div></div></blockquote></div><br>