- modeller_usage - salilab.org

Inserting Chain ID Into Model
by David Johnson 07 Jan '13

07 Jan '13

Hello, I am doing a model of a single chain protein. My target model comes out as I expect save for one thing, it is missing a chain ID. How do I get modeller to insert a chain ID into the model, even for single chain proteins. Thank you. DJ

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how to get pdb_95.bin file
by BALA SUBRAMANI G L 07 Jan '13

07 Jan '13

hai friends, can any tell me how to get pdb_95.bin file from modeller website. I need this file to run modeller scripts. please assist me in this regard. -- Thanks & Regards, G.L.Balasubramani (Project Assistant), c/o.Dr.S.Kumaran, Structural & Quatitative Biology Lab, GNRPC, Institute of Microbial Technology (CSIR), Sector 39-A, Chandigarh, India-160036. ph : +91-9041280408/8284860166 off : 0172-6665475 ______________________________________________________________________ सूक्ष्मजीव प्रौद्योगिकी संस्थान (वैज्ञानिक औद्योगिक अनुसंधान परिषद) Institute of Microbial Technology (A CONSTITUENT ESTABLISHMENT OF CSIR) सैक्टर 39 ए, चण्डीगढ़ / Sector 39-A, Chandigarh पिन कोड/PIN CODE :160036 दूरभाष/EPABX :0172 6665 201-202

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Syntax errors in defining model atoms
by doranhen＠post.tau.ac.il 07 Jan '13

07 Jan '13

Dear all, I am trying to create distance restraints in a model based on an example script from the modeller manual named model-addrsr.py . I am following the exact same syntax of this script, yet I need to change the numbering of my residues (since my restraints are for a model that starts at residue 2 and not 1) so I add another restraint to renumber it (self.rename_segments), however, when I try to use my new script (listed at the bottom of this mail), I get an error message that the atom I listed OG1:132A:A does not exist: 'No such atom: OG1:132A:A', does anyone know what am I doing wrong here? Thank you, Doran My script: # Homology modeling by the automodel class from modeller import * # Load standard Modeller classes from modeller.automodel import * # Load the automodel class log.verbose() # request verbose output env = environ(rand_seed = -500) # create a new MODELLER environment to build this model in env.io.atom_files_directory = './:' # directories for input atom files env.io.hetatm = True # read HETATM records (for Na ions) ################################ # define the modeling parameters class mymodel(automodel): def special_restraints(self, aln): self.rename_segments (segment_ids=('A'),renumber_residues=(2)) rsr = self.restraints at = self.atoms rsr.add(forms.gaussian(group=physical.xy_distance,feature=features.distance(at['OG1:132A:A'],at['NA:310A:A']),mean=2.4, stdev=0.1)) def user_after_single_model(self): self.rename_segments (segment_ids=('A'),renumber_residues=(2)) a = mymodel(env, alnfile = 'file.pir', # alignment filename knowns = ('No_anis'), # codes of the templates sequence = ('target')) # code of the target in the pir file a.starting_model= 1 # index of the first model a.ending_model = 1 # index of the last model # (determines how many models to calculate) a.deviation = 2.0 # Deviation in models #a.md_level = refine.very_slow a.make() # do the actual homology modeling

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Modeller error, 631E
by si yang 07 Jan '13

07 Jan '13

Hi, Modeller caretakers... Recently, i am trying to introduce HETATM into my built model, however i have encountered a problem, which is 631E: "No aligned template residues for BLK residue; number of templates: @I1 Make sure that each BLK residue in your target sequence is aligned with your templates. (This can also be caused by a lack of structural information. Make sure you are using a PIR, not FASTA, alignment file, and that the template headers use 'structureX' not 'sequence'.)" and this is my alignment: >P1;2ZWRA structureX:2ZWR.pdb: 1 :A:+202 :A:MOL_ID 1; MOLECULE METALLO-BETA-LACTAMASE SUPERFAMILY PROTEIN; CHAIN A, B; ENGINEERED YES:MOL_ID 1; ORGANISM_SCIENTIFIC THERMUS THERMOPHILUS; ORGANISM_TAXID 300852; STRAIN HB8; GENE TTHA1623; EXPRESSION_SYSTEM ESCHERICHIA COLI; EXPRESSION_SYSTEM_TAXID 562; EXPRESSION_SYSTEM_VECTOR_TYPE PLASMID; EXPRESSION_SYSTEM_PLASMID PET11A: 2.20: 0.19 MRVFPVTLGPLQENAYLVETG-EGPVLIDPGDEPEKLLALFQTTGLIPLAILLTHAHFDHVGAVAPLVEALDLPV YLHP-----L-DLPLYEGADLAARAWGLAIPKPPLPVRPLEEGMRLFGFQVLHLPGHSPGHVAFYDPEGAQVFSG DLLFRGSVGRYDLPGADPKALFASLK-RLLSLPPETRVHPGHGPGTTLGLEARTNPFL..* >P1;Metallo-beta-lactamase sequence:Metallo-beta-lactamase: :212 : : ::: 0.00: 0.00 M-FKQIPLGPIQTNAYVLYNDDKEAVIFDPGGDAEALITWLKREQLTPLAILLTHAHFDHIGAVDAVRDTFSIPV YLHTKERHWLEDPALNGSSRLTGRPITTAKPADHLLTNEKSLTIGTFTFSVFHTPGHSPGSVSYYYQKEAVLFSG DVLFQQSIGRTDLRGGDHTLLLASIHNKILPLPERTIVASGHGPLTTIGQEMDHNPFLTGY--..* Your suggestion is much more appreciated... Thank you -- Zhao Yang

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Re: [modeller_usage] Fwd: Modelling of Chimeric protein
by flavio seixas 12 Dec '12

12 Dec '12

Hi James. Thanks for the return. Have fun! Flavio --- On Wed, 12/12/12, James Starlight <jmsstarlight(a)gmail.com> wrote: > From: James Starlight <jmsstarlight(a)gmail.com> > Subject: Re: [modeller_usage] Fwd: Modelling of Chimeric protein > To: "flavio seixas" <oivalf_nix(a)yahoo.com> > Date: Wednesday, December 12, 2012, 1:58 PM > Thanks Flavio! It works perfect! > > James > > 2012/12/10, flavio seixas <oivalf_nix(a)yahoo.com>: > > Hi James! > > > > I am glad to help. > > > > The easier way to include hetatoms to model is to treat > them as BLK, with > > the single letter code "."(dot) > > > > In the alignment file, put "." at the position of your > hetatms, eg: > > > > aaaaaaaa---------.- (dot refers to > hetatm of the first template) > > --------bbbbbbbbb-. (dot refers to > hetatm of the second template) > > ccccccccccccccccc.. (model with hetatm > of both templates) > > > > To make your life easier, renumber the templates > sequentially. E.g., > > renumber the first template from 1 to 200 (hetatm is > 401) and the second > > from 201 to 400 (hetatm is 402). > > > > The hetatm of the first and second templates must be > renumbered as they will > > appear in the final model (as alignment above). > > > > Do not forget to put in your script file: > > > > # Read in HETATM records from template PDBs > > env.io.hetatm = True > > > > See http://salilab.org/modeller/manual/node18.html > for details. > > > > Regards, > > > > Flavio > > > > > > > > > > > > --- On Mon, 12/10/12, James Starlight <jmsstarlight(a)gmail.com> > wrote: > > > >> From: James Starlight <jmsstarlight(a)gmail.com> > >> Subject: Re: [modeller_usage] Fwd: Modelling of > Chimeric protein > >> To: "flavio seixas" <oivalf_nix(a)yahoo.com> > >> Date: Monday, December 10, 2012, 6:33 PM > >> Hi, Flavio! > >> > >> Thanks for advises! I've used Nedit and exactly the > problem > >> was in the > >> incorrect alignment of y input data. With the > corrections > >> the modeler > >> produced very good models. > >> > >> Could you also tell me about possible options to > include > >> HETATM groups > >> from templates to the model? > >> > >> E.g both of my templates have two HETATM groups; > from GFP > >> protein its > >> chromophore group which is covalently bonded to > the > >> polypeptide chain > >> (like retinal in rhodopsin or HEM in globins) of > that > >> protein. > >> from the second globular domain- its small cyclic > GMP > >> molecule which > >> is the diffusive ligand of that protein. > >> > >> In the final model I'd like to include both of the > groups > >> from both of > >> the templates (chromophore to the GFP part as well > as cGMP > >> to the > >> interior of the second protein). > >> > >> By the way should I define chromophore group as the > part of > >> the first > >> (gfp) as well as 3rd (output fussed chimera) > sequence or > >> there is > >> another way to its inclusion ? > >> > >> Thanks for help again, > >> > >> James > >> > >> 2012/12/10, flavio seixas <oivalf_nix(a)yahoo.com>: > >> > Hi James, > >> > > >> > Modeller results are reproducible. I see you > are > >> producing just one model. > >> > Each time you run your script, it will produce > the same > >> model with the same > >> > error. > >> > > >> > Try to run more models and compare them. Try > at least > >> 100. I usually > >> > produces 1000 and select the best by modeller > dope > >> score and procheck > >> > evaluation. > >> > > >> > First of all, try to correct your alignment > file. > >> > > >> > Your alignment file still incorrect (see > attached). I > >> see that in your file, > >> > the sequences are: > >> > > >> > > >> > aaaaaa------* > >> > ----bbbbbbb* > >> > ccccccccccccccc* > >> > > >> > > >> > All sequences must have the same length! > >> > > >> > Maybe this is a problem with your text editor. > Try to > >> use Nedit (for linux). > >> > This editor does not have limits for number of > columns > >> and does not break > >> > the lines. > >> > > >> > I suggest you use Uniprot tab for alignment > >> (www.uniprot.org) > >> > > >> > You can display the alignment in fasta or pir > format. > >> > > >> > regards, > >> > > >> > Flavio > >> > > >> > > >> > > >> > > >> > --- On Mon, 12/10/12, James Starlight <jmsstarlight(a)gmail.com> > >> wrote: > >> > > >> >> From: James Starlight <jmsstarlight(a)gmail.com> > >> >> Subject: Re: [modeller_usage] Fwd: > Modelling of > >> Chimeric protein > >> >> To: "flavio seixas" <oivalf_nix(a)yahoo.com> > >> >> Date: Monday, December 10, 2012, 7:26 AM > >> >> Flavio, > >> >> > >> >> below you could find my script as well as > new > >> alignment > >> >> file. That > >> >> inpud data produces still wrong result in > the > >> conformation > >> >> of second > >> >> template > >> >> > >> >> # Homology modeling with multiple > templates > >> >> from modeller import * > >> >> # Load standard Modeller classes > >> >> from modeller.automodel import * # > Load the > >> >> automodel class > >> >> > >> >> log.verbose() # request verbose > output > >> >> env = environ() # create a new MODELLER > >> environment to > >> >> build this model in > >> >> > >> >> # directories for input atom files > >> >> env.io.atom_files_directory = ['.', > >> '../atom_files'] > >> >> > >> >> a = automodel(env, > >> >> > >> >> alnfile = 'align-multiple.ali', # > alignment > >> filename > >> >> > >> >> knowns = ('1gfl', '3u10'), > >> >> # codes of the templates > >> >> sequence = > >> >> 'seq') > >> >> # code of the target > >> >> automodel.initial_malign3d= True > >> >> a.starting_model= 1 > >> >> # index of the first model > >> >> a.ending_model = 1 > >> >> # index of the last model > >> >> > >> >> > >> >> # (determines how many models to > calculate) > >> >> a.make() > >> >> # do the > >> >> actual homology modeling > >> >> > >> >> > >> >> >P1;1gfl > >> >> structureX:1gfl:1 ::238 : > :::-1.00:-1.00 > >> >> > >> > ASKGEELFTGVVPILVELDGDVNGHKFSVSGEGEGDATYGKLTLKFICTTGKLPVPWPTLVTTFSYGVQCFSRYPDHMKRHDFFKSAMPEGYVQERTIFFKDDGNYKTRAEVKFEGDTLVNRIELKGIDFKEDGNILGHKLEYNYNSHNVYIMADKQKNGIKVNFKIRHNIEDGSVQLADHYQQNTPIGDGPVLLPDNHYLSTQSALSKDPNEKRDHMVLLEFVTAAGITHGMDELYK---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------* > >> >> > >> >> >P1;3u10 > >> >> structureN:3u10:470 :A:671 : > :A::-1.00:-1.00 > >> >> > >> > --------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------DSSRRQYQEKYKQVEQYMSFHKLPADFRQKIHDYYEHRYQGKMFDEDSILGELNGPLREEIVNFNCRKLVASM > >> >> > >> > PLFANADPNFVTAMLTKLKFEVFQPGDYIIREGTIGKKMYFIQHGVVSVLTKGNKEMKLSDGSYFGEICLLTRGRRTASV > >> >> > RADTYCRLYSLSVDNFNEVLEEYPMMRRAFETVAIDRLDRIGKKNSILL* > >> >> > >> >> >P1;seq > >> >> sequence:seq: : : > >> >> : ::: 0.00: 0.00 > >> >> > >> > ASKGEELFTGVVPILVELDGDVNGHKFSVSGEGEGDATYGKLTLKFICTTGKLPVPWPTLVTTFSYGVQCFSRYPDHMKRHDFFKSAMPEGYVQERTIFFKDDGNYKTRAEVKFEGDTLVNRIELKGIDFKEDGNILGHKLEYNYNSHNVYIMADKQKNGIKVNFKIRHNIEDGSVQLADHYQQNTPIGDGPVLLPDNHYLSTQSALSKDPNEKRDHMVLLEFVTAAGITHGMDELYKDSSRRQYQEKYKQVEQYMSFHKLPADFRQKIHDYYEHRYQGKMFDEDSILGELNGPLREEIVNFNCRKLVASMPLFANADPNFVTAMLTKLKFEVFQPGDYIIREGTIGKKMYFIQHGVVSVLTKGNKEMKLSDGSYFGEICLLTRGRRTASVRADTYCRLYSLSVDNFNEVLEEYPMMRRAFETVAIDRLDRIGKKNSILLH* > >> >> > >> >> > >> >> by the way do you know any web servers > for > >> produccing such > >> >> multiple > >> >> ali files for modeller input like > >> >> aaaa---- > >> >> ----bbbb > >> >> > >> >> for protein aaaabbbb > >> >> ? > >> >> > >> >> ( the above file I've done manually) > >> >> > >> >> James > >> >> > >> >> > >> >> 2012/12/9, flavio seixas <oivalf_nix(a)yahoo.com>: > >> >> > Hi James. > >> >> > > >> >> > Maybe if you post your script, it > becomes more > >> easier > >> >> to help. > >> >> > > >> >> > But, from your post I can see that > the lenght > >> of your > >> >> target and sequence > >> >> > alignment are not equal. > >> >> > > >> >> > See from http://salilab.org/modeller/9.10/manual/node21.html > >> >> > > >> >> > that the differences in the lenght > are filled > >> with "-" > >> >> > > >> >> > Maybe you should check this. > >> >> > > >> >> > Regards, > >> >> > > >> >> > Flavio > >> >> > > >> >> > > >> >> > --- On Sun, 12/9/12, James Starlight > <jmsstarlight(a)gmail.com> > >> >> wrote: > >> >> > > >> >> >> From: James Starlight <jmsstarlight(a)gmail.com> > >> >> >> Subject: Re: [modeller_usage] > Fwd: > >> Modelling of > >> >> Chimeric protein > >> >> >> To: "flavio seixas" <oivalf_nix(a)yahoo.com> > >> >> >> Date: Sunday, December 9, 2012, > 6:23 PM > >> >> >> Hi Flavio! > >> >> >> > >> >> >> In the align-multiple.ali file > >> >> >> structureN:3u10:470 ::203 : > >> :::-1.00:-1.00 > >> >> >> 470 is the number of first > residue (in pdb > >> file) > >> >> and 203 is > >> >> >> the length > >> >> >> of the sequence of that protein > >> >> >> > >> >> >> I have superimpose both of the > templates > >> and locate > >> >> them in > >> >> >> the > >> >> >> desired location in the initial > pdb's > >> templates. > >> >> >> > >> >> >> > >> >> >> Is there any string that I should > add to > >> my script > >> >> ? > >> >> >> ( that example I have used > >> >> >> http://salilab.org/modeller/9.10/manual/node21.html ) > >> >> >> > >> >> >> Also I've added the string > >> >> automodel.initial_malign3d= True > >> >> >> but there were no difference in > the output > >> modell > >> >> >> > >> >> >> James > >> >> >> > >> >> >> 2012/12/9, flavio seixas <oivalf_nix(a)yahoo.com>: > >> >> >> > Hi James, > >> >> >> > > >> >> >> > I have 2 suggestions. > >> >> >> > > >> >> >> > 1) The alignment file of > your second > >> template > >> >> is set: > >> >> >> >> >P1;3u10 > >> >> >> >> structureN:3u10:470 > ::203 : > >> >> :::-1.00:-1.00 > >> >> >> > > >> >> >> > I think the correct must be > (first > >> residie to > >> >> last > >> >> >> residue): > >> >> >> >> >P1;3u10 > >> >> >> >> structureN:3u10:203 > ::470 : > >> >> :::-1.00:-1.00 > >> >> >> > > >> >> >> > > >> >> >> > 2) Did you put both > templates in the > >> same > >> >> coordinated > >> >> >> system? I mean, did > >> >> >> > you superpose (Secondary > Strucuture > >> Match > >> >> supermpose) > >> >> >> both the templates in > >> >> >> > a way that generated models > will > >> reflect the > >> >> template > >> >> >> structure? > >> >> >> > > >> >> >> > Regards > >> >> >> > > >> >> >> > Flavio > >> >> >> > > >> >> >> > --- On Sun, 12/9/12, James > Starlight > >> <jmsstarlight(a)gmail.com> > >> >> >> wrote: > >> >> >> > > >> >> >> >> From: James Starlight > <jmsstarlight(a)gmail.com> > >> >> >> >> Subject: > [modeller_usage] Fwd: > >> Modelling > >> >> of > >> >> >> Chimeric protein > >> >> >> >> To: "modeller_usage" > <modeller_usage(a)salilab.org>, > >> >> >> "Modeller Caretaker" > >> >> >> >> <modeller-care(a)salilab.org> > >> >> >> >> Date: Sunday, December > 9, 2012, > >> 11:25 AM > >> >> >> >> Dear Modeler Users! > >> >> >> >> > >> >> >> >> > >> >> >> >> Recently I've done my > chimeric > >> protein > >> >> based on > >> >> >> two > >> >> >> >> different > >> >> >> >> templates in accordance > to the > >> >> >> >> http://salilab.org/modeller/9.10/FAQ.html#1 > >> >> >> >> > >> >> >> >> using that script > >> >> >> >> http://salilab.org/modeller/9.10/manual/node21.html > >> >> >> >> > >> >> >> >> below the alignment of > my > >> templates as > >> >> well as > >> >> >> sequence > >> >> >> >> > >> >> >> >> >P1;1gfl > >> >> >> >> structureX:1gfl:1 > ::238 : > >> >> :::-1.00:-1.00 > >> >> >> >> > >> >> >> > >> >> > >> > ASKGEELFTGVVPILVELDGDVNGHKFSVSGEGEGDATYGKLTLKFICTTGKLPVPWPTLVTTFSYGVQCFSRYPDHMKRHDFFKSAMPEGYVQERTIFFKDDGNYKTRAEVKFEGDTLVNRIELKGIDFKEDGNILGHKLEYNYNSHNVYIMADKQKNGIKVNFKIRHNIEDGSVQLADHYQQNTPIGDGPVLLPDNHYLSTQSALSKDPNEKRDHMVLLEFVTAAGITHGMDELYK---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------* > >> >> >> >> > >> >> >> >> >P1;3u10 > >> >> >> >> structureN:3u10:470 > ::203 : > >> >> :::-1.00:-1.00 > >> >> >> >> > >> >> >> > >> >> > >> > --------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------DSSRRQYQEKYKQVEQYMSFHKLPADFRQKIHDYYEHRYQGKMFDEDSILGELNGPLREEIVNFNCRKLVASMPLFANADPNFVTAMLTKLKFEVFQPGDYIIREGTIGKKMYFIQHGVVSVLTKGNKEMKLSDGSYFGEICLLTRGRRTASVRADTYCRLYSLSVDNFNEVLEEYPMMRRAFETVAIDRLDRIGKKNSILL.* > >> >> >> >> > >> >> >> >> >P1;seq > >> >> >> >> sequence:seq: : > : > >> >> >> >> : ::: 0.00: 0.00 > >> >> >> >> > >> >> >> > >> >> > >> > ASKGEELFTGVVPILVELDGDVNGHKFSVSGEGEGDATYGKLTLKFICTTGKLPVPWPTLVTTFSYGVQCFSRYPDHMKRHDFFKSAMPEGYVQERTIFFKDDGNYKTRAEVKFEGDTLVNRIELKGIDFKEDGNILGHKLEYNYNSHNVYIMADKQKNGIKVNFKIRHNIEDGSVQLADHYQQNTPIGDGPVLLPDNHYLSTQSALSKDPNEKRDHMVLLEFVTAAGITHGMDELYKDSSRRQYQEKYKQVEQYMSFHKLPADFRQKIHDYYEHRYQGKMFDEDSILGELNGPLREEIVNFNCRKLVASMPLFANADPNFVTAMLTKLKFEVFQPGDYIIREGTIGKKMYFIQHGVVSVLTKGNKEMKLSDGSYFGEICLLTRGRRTASVRADTYCRLYSLSVDNFNEVLEEYPMMRRAFETVAIDRLDRIGKKNSILLH* > >> >> >> >> > >> >> >> >> > >> >> >> >> As the result I've > obtain model > >> where > >> >> first > >> >> >> template ( > >> >> >> >> beta-can GFP) > >> >> >> >> was in correct form but > the > >> conformation > >> >> of the > >> >> >> second > >> >> >> >> protein was > >> >> >> >> differ from the used > template ( > >> pdb id > >> >> 3u10). > >> >> >> >> > >> >> >> >> > >> >> >> >> Could you tell me why my > model > >> was so > >> >> distorted and > >> >> >> how I > >> >> >> >> can improve > >> >> >> >> it further? > >> >> >> >> > >> >> >> >> Thanks for help > >> >> >> >> > >> >> >> >> James > >> >> >> >> > >> >> >> >> 2012/8/8, Modeller > Caretaker > >> <modeller-care(a)salilab.org>: > >> >> >> >> > On 8/8/12 6:27 AM, > James > >> Starlight > >> >> wrote: > >> >> >> >> >> I want to model > chimeric > >> protein > >> >> which > >> >> >> consist of > >> >> >> >> two fussed proteins > >> >> >> >> >> ( tail to head > fussion C > >> to N > >> >> termi). > >> >> >> It's > >> >> >> >> important that both of > that > >> >> >> >> >> proteins have > known > >> spatial > >> >> structures > >> >> >> which could > >> >> >> >> be used as the > >> >> >> >> >> templates. > >> >> >> >> > > >> >> >> >> > http://salilab.org/modeller/9.10/FAQ.html#1 > >> >> >> >> > > >> >> >> >> >> Is there any > way to use > >> both of > >> >> the > >> >> >> templates to > >> >> >> >> guide such modelling > >> >> >> >> >> ? In the input > option > >> I've found > >> >> only > >> >> >> possibility > >> >> >> >> to use one template. > >> >> >> >> > > >> >> >> >> > 'knowns' can be a > list of > >> multiple > >> >> templates. > >> >> >> See > >> >> >> >> > http://salilab.org/modeller/9.10/manual/node21.html > >> >> >> >> > > >> >> >> >> > Ben Webb, > Modeller > >> Caretaker > >> >> >> >> > -- > >> >> >> >> > modeller-care(a)salilab.org > >> >> >> >> http://www.salilab.org/modeller/ > >> >> >> >> > Modeller mail > list: > >> >> >> >> > http://salilab.org/mailman/listinfo/modeller_usage > >> >> >> >> > > >> >> >> >> > >> >> >> >> > >> >> > _______________________________________________ > >> >> >> >> modeller_usage mailing > list > >> >> >> >> modeller_usage(a)salilab.org > >> >> >> >> https://salilab.org/mailman/listinfo/modeller_usage > >> >> >> >> > >> >> >> > > >> >> >> > >> >> > > >> >> > >> > > >

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modeller on windows 7
by Krupal Jethava 12 Dec '12

12 Dec '12

Hi, Please help me in this regard. I was working on windows XP with Modeller 9v5 and python v 2.5.1. Now I have another PC with Windows 7 Ultimate. I tried to run modeller 9v5 and python 2.5.1. on windows7. There was no error and no files generated in folder. What should I do? Is it because of wrong combination of modeller and python. If yes then which versions I should use. script I used. # Homology modeling with multiple templates from modeller import * # Load standard Modeller classes from modeller.automodel import * # Load the automodel class log.verbose() # request verbose output env = environ() # create a new MODELLER environment to build this model in # directories for input atom files env.io.atom_files_directory = ['.', '../atom_files'] a = automodel(env, alnfile = 'alignment.ali', # alignment filename knowns = ('tseq.pdb'), # codes of the templates sequence = 'qseq') # code of the target a.starting_model= 1 # index of the first model a.ending_model = 1 # index of the last model # (determines how many models to calculate) a.make() # do the actual homology modeling Thanks in advance.

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(no subject)
by mario rossi 12 Dec '12

12 Dec '12

http://tummyfitindia.com/wp-content/plugins/google.html

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Protein-ligand simulate annealing
by flavio seixas 11 Dec '12

11 Dec '12

Hi Ben I successfully generate charmm force fields (parameter and topology files) using swissparam server, for the ligand that is bonded to my protein template. Now I want to built models bonded to this ligand and also optimize them using Modeller protocol for MD and SA. My questions are: 1) How can I make modeller reads the parameter and topology files for the ligand? Is there a command for it? 2) Or should I copy and paste the ligand topology data to top_heav.lib file? 3) If the second option is the choice, where to paste the information regarding the parameters? 4) In the alignment file, how to set the symbol for the ligand? I think if I set it as BLK "." no changes will be made. Is that right? Best regards, Flavio

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mutate protion dimer
by Sangita Kachhap 11 Dec '12

11 Dec '12

hello All I have a protein dimer and I have to insert amino acid rsidues in both monomer at same palce. Is it possible to do with Modller without affecting interaction between protein in crystal structure? With regards Sangita Kachhap SRF BIC,IMTECH CHANDIGARH ______________________________________________________________________ सूक्ष्मजीव प्रौद्योगिकी संस्थान (वैज्ञानिक औद्योगिक अनुसंधान परिषद) Institute of Microbial Technology (A CONSTITUENT ESTABLISHMENT OF CSIR) सैक्टर 39 ए, चण्डीगढ़ / Sector 39-A, Chandigarh पिन कोड/PIN CODE :160036 दूरभाष/EPABX :0172 6665 201-202

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scoring function and optimization
by sdimicco 11 Dec '12

11 Dec '12

Dear Modellers, I have three points to discuss. 1) As I changed the optimization protocol, I woul dlike to check if my set up has been done. Where could I check it? 2) I am building a multimeric protein. The DOPE and GA341 scores are developed for single chain models. How can I asses the quality of my models? The sole molpdf is sufficient? 3) I found thie messagge in the log file: Treating residue type GSH as a BLK (rigid body) even though topology information appears to be at least partially available. To treat this residue flexibly instead, remove the corresponding 'MODELLER BLK RESIDUE' REMARK from the input PDB file. I have understood that the input PDB file is the .ini, which is written during the calculation. Thus, how can I "remove the corresponding 'MODELLER BLK RESIDUE" to treat the residue flexible? Have I to define it as my own residue? Thank you in advance All the best Simone

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