Difference between revisions of "DOCK GA Tutorials"
| Stonybrook (talk | contribs)  (Created page with "For this experiment required files will include 2NNQ.lig.mol2 =='''I. Fragment Library Generation for 2NNQ'''==  ===Fragment Libraries=== For this experiment a general fragmen...") | Stonybrook (talk | contribs)  | ||
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|       num_scored_conformers                                        1 |       num_scored_conformers                                        1 | ||
|       rank_ligands                                                 no |       rank_ligands                                                 no | ||
| + | |||
| + | The only aspect that is relevant of this fragment library generated is the torsion environment that should be titled 2NNQ.fraglib_torenv.dat | ||
| + | Following this step the torsion environments of this molecule will be combined with the file titled full_sorted_fraglib.dat using the python software combine_torenv.py  | ||
| + |      py /gpfs/projects/rizzo/zzz.programs/torsion_env_combination/combine_torenv.py 2NNQ.fraglib_torenv.dat /gpfs/projects/rizzo/zzz.programs/dock6.10_2019.06.18/parameters/fraglib_torenv.dat | ||
| + | |||
| + | This should generate a new list of torsion environments titled unique_full_sorted_fraglib.dat | ||
| + | =='''II. Performing a GA using 2NNQ'''== | ||
| + | |||
| + | For this part a new directory will be created in the 2NNQ_GA. This will just be 2NNQ_GA_results. cd into that directory and create a new file titled 2NNQ_GA.in. | ||
| + |      mkdir 2NNQ_GA_results | ||
| + |      cd 2NNQ_GA_results | ||
| + |      touch 2NNQ_GA.in | ||
| + | Following this dock6 will be performed on the molecule | ||
| + |      dock6 -i 2NNQ_GA.in -o 2NNQ_GA.out | ||
| + | Input the following in order to get the GA working properly | ||
Revision as of 15:34, 24 June 2019
For this experiment required files will include 2NNQ.lig.mol2
I. Fragment Library Generation for 2NNQ
Fragment Libraries
For this experiment a general fragment library to account for all the possible ligands the GA can produce. A focused Fragment library will not be enough to account for all the possibilities since it is too small of a set of data.
The first step for this experiment is to generate a directory to perform the work in
mkdir 2NNQ_GA
Go into this new directory and then create another directory that will store all the fragment molecules
mkdir fraglib
Enter the file directory fraglib
cd fraglib
Create a new file called 2NNQ.fraglib
     touch 2NNQ.fraglib
     dock6 -i 2NNQ.fraglib
Answer the following prompts using these responses
    conformer_search_type                                        flex
    write_fragment_libraries                                     yes
    fragment_library_prefix                                      2NNQ.fraglib
    fragment_library_freq_cutoff                                 1
    fragment_library_sort_method                                 freq
    fragment_library_trans_origin                                no
    use_internal_energy                                          no
    ligand_atom_file                                             ../../2NNQ_Tutorial/1.dockprep/2nnq_lig_withH.mol2
    limit_max_ligands                                            no
    skip_molecule                                                no
    read_mol_solvation                                           no
    calculate_rmsd                                               no
    use_database_filter                                          no
    orient_ligand                                                no
    bump_filter                                                  no
    score_molecules                                              no
    atom_model                                                   all
    vdw_defn_file                                                /gpfs/projects/AMS536/zzz.programs/dock6/parameters/vdw_AMBER_parm99.defn 
    flex_defn_file                                               /gpfs/projects/AMS536/zzz.programs/dock6/parameters/flex.defn
    flex_drive_file                                              /gpfs/projects/AMS536/zzz.programs/dock6/parameters/flex_drive.tbl
    ligand_outfile_prefix                                        2NNQ_frag_output
    write_orientations                                           no
    num_scored_conformers                                        1
    rank_ligands                                                 no
The only aspect that is relevant of this fragment library generated is the torsion environment that should be titled 2NNQ.fraglib_torenv.dat Following this step the torsion environments of this molecule will be combined with the file titled full_sorted_fraglib.dat using the python software combine_torenv.py
py /gpfs/projects/rizzo/zzz.programs/torsion_env_combination/combine_torenv.py 2NNQ.fraglib_torenv.dat /gpfs/projects/rizzo/zzz.programs/dock6.10_2019.06.18/parameters/fraglib_torenv.dat
This should generate a new list of torsion environments titled unique_full_sorted_fraglib.dat
II. Performing a GA using 2NNQ
For this part a new directory will be created in the 2NNQ_GA. This will just be 2NNQ_GA_results. cd into that directory and create a new file titled 2NNQ_GA.in.
    mkdir 2NNQ_GA_results
    cd 2NNQ_GA_results
    touch 2NNQ_GA.in
Following this dock6 will be performed on the molecule
dock6 -i 2NNQ_GA.in -o 2NNQ_GA.out
Input the following in order to get the GA working properly
