- modeller_usage - salilab.org

exploding GTP
by Jonathan Winger 09 Oct '07

09 Oct '07

When modeling GTP and metal ions into my protein, using a template with 2 metal ions and an ATP analog, the GTP atoms end up disconnected from each other and scattered around the active site, and one of the two metals is launched out of the protein. What can I do to fix this? Thanks much, Jon

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qsub and cis restraints
by Gordon Wells 08 Oct '07

08 Oct '07

Do classes inheriting from automodel get propagated when using the sge_qsub parallel job? I can get a parallel run to work with automodel, but not with a new class including a cis-peptide restraint defined in special_restraints (which I can get to run in single proc mode). I get the following error: # Traceback (most recent call last): File "psamdc.py", line 77, in ? a.make() File "/home/namd/lib/modeller9v2/modlib/modeller/automodel/automodel.py", line 110, in make self.multiple_models(atmsel) File "/home/namd/lib/modeller9v2/modlib/modeller/automodel/automodel.py", line 214, in multiple_models self.parallel_multiple_models(atmsel) File "/home/namd/lib/modeller9v2/modlib/modeller/automodel/automodel.py", line 234, in parallel_multiple_models self.outputs.extend(job.run_all_tasks()) File "/home/namd/lib/modeller9v2/modlib/modeller/parallel/job.py", line 110, in run_all_tasks self.finish_next_task() File "/home/namd/lib/modeller9v2/modlib/modeller/parallel/job.py", line 127, in finish_next_task self.process_event(obj, s) File "/home/namd/lib/modeller9v2/modlib/modeller/parallel/job.py", line 141, in process_event task = obj.task_results() File "/home/namd/lib/modeller9v2/modlib/modeller/parallel/slave.py", line 54, in task_results r = self.get_data(allow_heartbeat=True) File "/home/namd/lib/modeller9v2/modlib/modeller/parallel/communicator.py", line 78, in get_data (cmdtype, obj) = self._recv() File "/home/namd/lib/modeller9v2/modlib/modeller/parallel/communicator.py", line 116, in _recv raise RemoteError(obj, self) modeller.parallel.communicator.RemoteError: AttributeError: 'module' object has no attribute 'cismodel' from <SGE qsub slave, ID 107.1> Is there a convenient way around this? Thanks in advance Regards -- I think perhaps the most important problem is that we are trying to understand the fundamental workings of the universe via a language devised for telling one another when the best fruit is. -- Terry Pratchett, alt.fan.pratchett -- Gordon Wells Bioinformatics and Computational Biology Unit Department of Biochemistry University of Pretoria

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Re: [modeller_usage] Mutations
by laura.buttazzo＠email.it 04 Oct '07

04 Oct '07

Hi, I tried the example in http://salilab.org/modeller/wiki/Mutate_model, but my model hasn't chains. It has been calculated with Modeller and the residue that I would like to change is the 27: ATOM 203 N ASP 27 16.536 9.555 15.986 1.00 91.26 1SG 204 ATOM 204 CA ASP 27 16.891 10.947 16.025 1.00 91.26 1SG 205 ATOM 205 CB ASP 27 18.072 11.218 16.974 1.00 91.26 1SG 206 ATOM 206 CG ASP 27 18.307 12.718 17.052 1.00 91.26 1SG 207 ATOM 207 OD1 ASP 27 17.470 13.485 16.504 1.00 91.26 1SG 208 ATOM 208 OD2 ASP 27 19.335 13.117 17.662 1.00 91.26 1SG 209 ATOM 209 C ASP 27 17.319 11.354 14.653 1.00 91.26 1SG 210 ATOM 210 O ASP 27 17.069 12.473 14.212 1.00 91.26 1SG 211 However I tried to change the following parts in the script: >#first argument >modelname, respos, restyp, chain, = sys.argv[1:] I put: modelname, respos, restyp, = sys.argv[1:] >s = selection(mdl1.chains[chain].residues[respos]) I put s = selection(mdl1.residues[respos]) >s = selection(mdl1.chains[chain].residues[respos]) s = selection(mdl1.residues[respos]) But I have obtained a model very similar as that in input. Should I try to change some parameter in the script? Thank you in advance. Laura --------- Original Message -------- Da: Modeller Caretaker <modeller-care(a)salilab.org> To: Cc: modeller_usage(a)salilab.org Oggetto: Re: [modeller_usage] Mutations Data: 25/09/07 19:46 > > > > laura.buttazzo(a)email.it wrote: > > I'm a new user of Modeller and I have a question about the model computing. > > If I take one/or more models with a given alignment and I change just one or > > more amino acids maintaning the same alignment, should I obtain a different > > model? > > In other words, Can Modeller be used for calculating mutations? > > Certainly - there has been some work done for SNPs using Modeller; see > http://salilab.org/modeller/wiki/Mutate_model for an example script. > > Ben Webb, Modeller Caretaker > -- > modeller-care(a)salilab.org http://www.salilab.org/modeller/ > Modeller mail list: http://salilab.org/mailman/listinfo/modeller_usage > > > -- Email.it, the professional e-mail, gratis per te: http://www.email.it/f Sponsor: In REGALO 'Meravigliosa Creatura' la super hit di GIANNA NANNINI Clicca qui: http://adv.email.it/cgi-bin/foclick.cgi?mid=6615&d=20071004

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entangled domains
by Russell Green 03 Oct '07

03 Oct '07

Hello, I'm new to Modeller. I have a protein segment I'm trying to model that consists of 2 domains. This protein has 4 very similar domains; 2 have been resolved and the other 2 have not (the ones I want to model). I go through the motions of aligning the sequences and building the model; however, the 2 domains I modelled are basically entangled. Thus, my question is, how can I keep this from happening (such as specifying a straight link between the domains instead of the current one that loops back, if this is even plausible)? Any suggestions are greatly appreciated. Thank you, Russell Green

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Models from secondary structure and distance constraints alone?
by Andrew D. Fant 28 Sep '07

28 Sep '07

[it appears that I accidentally sent this to the listowner rather than the list. oops. sorry Ben] This may seem like a rather strange question, but is it possible to get Modeller to output a PDB structure based only on secondary structure information and a few distance constraints (primarily dicystene relationships). I realize that without an alignment to a known structure, anything that is generated probably bears little resemblance to reality, but I have a relatively short fragment that isn't significantly related to anything in the PDB, and between the disulfide linkages and a couple other known constraints, there aren't that many ways that it could bend together. Basically, I'm trying to generate a consistent structure that is in a possible conformation that doesn't violate steric boundaries and such, without having to manually generate the coordinates from the helix and sheet parameters. Can anyone make any suggestions? Thanks, Andy

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Modeling of a C-terminal segment
by Bo Yang 28 Sep '07

28 Sep '07

Hello, Modeller: I have a question of modelling the C-terminal region of my target. The protein matches with the crystal structure templates except the C-terminal region (named as C-tail here). I did BLAST search using this segment to against the proteins with known structures at Protein Data Band. It returns a match with a short region of an antibody at 56% sequence identity with the inclusion of 4 gaps. The function of my target protein has nothing to do with antibody. I am not sure if it is reasonable to use the BLAST match results as templates to model the conformation of the C-tail. I have thought to model this C-tail region using the Loop Model in Modeller. There are some concerns here. First, the C-tail contains 24 amino acids. Will this be too long for the loop-model in Modeller? If the length is not the problem, how reliable are the conformations of the segment? Second, the segment is at the C-terminal of the protein. For my understanding, the Loop Model in Modeller requires the N and C terminus of the segment to be fixed. The position of the last residues of the segment will have significant influence on the Loop conformation. Which one is more reasonable, to model this segment based on the sequence homology, or use a loop modelling algorithm? Your help and inputs will be much appreciated! Bo --------------------------------- Check out the hottest 2008 models today at Yahoo! Autos.

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September 70% OFF
by VIAGRA � Official Site 26 Sep '07

26 Sep '07

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_modeller.error: read_al_373E> Protein specified in ALIGN_CODES(i) was not found in the alignment file; ALIGN_CODES( 1) = 1CPG
by DANIEL TAYLOR 25 Sep '07

25 Sep '07

Hello People I know this has been raised before but when looking through the archieves I could'nt find an answer to this problem, I've redone all the tutorials and out of ideas, so please can somebody help with this error message I'm getting? 'import site' failed; use -v for traceback Traceback (most recent call last): File "modeller.top.py", line 18, in ? a.make() # do the actual homology modeling File "/home/fraizerangus/bin/modeller9v2/modlib/modeller/automodel/automodel.py", line 99, in make self.homcsr(exit_stage) File "/home/fraizerangus/bin/modeller9v2/modlib/modeller/automodel/automodel.py", line 399, in homcsr aln = self.read_alignment() File "/home/fraizerangus/bin/modeller9v2/modlib/modeller/automodel/automodel.py", line 389, in read_alignment aln.append(file=self.alnfile, align_codes=self.knowns+[self.sequence]) File "/home/fraizerangus/bin/modeller9v2/modlib/modeller/alignment.py", line 74, in append rewind_file, close_file) _modeller.error: read_al_373E> Protein specified in ALIGN_CODES(i) was not found in the alignment file; ALIGN_CODES( 1) = 1CPG Many Thanks Dan

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Mutations
by laura.buttazzo＠email.it 25 Sep '07

25 Sep '07

Dear all, I'm a new user of Modeller and I have a question about the model computing. If I take one/or more models with a given alignment and I change just one or more amino acids maintaning the same alignment, should I obtain a different model? In other words, Can Modeller be used for calculating mutations? Thank you so much, Laury -- Email.it, the professional e-mail, gratis per te: http://www.email.it/f Sponsor: Cerchi unauto usata, vuoi vendere il camper o il cellulare? Prova Email.it Annunci, pochi click per pubblicare e trovare ciò che vuoi! Clicca qui: http://adv.email.it/cgi-bin/foclick.cgi?mid=6893&d=20070925

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regarding loop refinement
by simran jeet 25 Sep '07

25 Sep '07

After loop refinement, we get files with .IL and .BL extensions. Which one should be used as the final model out of these? And after refinement through modeler there are some bad contacts and disallowed regions. How can we assess the models accuracy?

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