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question about protein docking results

I am using the docking_protocol.linux for high resolution complex. I found there are many parameters in *.fasc file such as:

fa_atr fa_dun fa_rep fa_sol hack_elec hbond_bb_sc hbond_lr_bb hbond_sc hbond_sr_bb interchain_contact interchain_env interchain_pair interchain_vdw.

So, I am wondering which one would be a measurement for final model selection?

BTW, could this protocol support MPI multiple CPU running?


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packing option "explicit_h2o" and "solvate"

Hi everyone,
Does anyone know whether the packing option "packing::explicit_h2o" and "packing::solvate" work out in Rosetta3.1?
This paper "A 'Solvated Rotamer' Approach to Modeling Water-Mediated Hydrogen Bonds at Protein–Protein Interfaces" said that Rosetta could recover water-mediated h-bond using a rotamer library called Solvated Rotamer. How to use it, add "explicit_h2o" or "solvate" flag ? But I read the code of Rosetta3.1 and couldn't find the source code implemented these two option.


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Abinitio Calculations - typical parameters

Dear all,
I am using rosetta for abintio calculations for a while now. I am curious to know what are other parameter other than mentioned in the documentation, to play with to simulate protein size of 150 aminoacids. I am not really satisfied with the results obtained with typical parameters and wondering my laptop took only like one hour to complete the job ( but heard previously it is computationally intensive process)

Here is my flag file
-database /home/vamsi/Programs/Rosetta31/rosetta_database/
-in:file:fasta inputs/t000_.fasta

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relax with restraints

Hi there,

Is it possible to use the relax app to relax an structure while restraining the C-alpha coordinates to their initial positions in order to stop things blowing up? There seems to be an option -constrain_relax_to_start_coords but it doesn't appear to have much effect when I tried using it.

thanks for your help!

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