Difference between revisions of "2013 DOCK tutorial with Orotodine Monophosphate Decarboxylase"

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For additional Rizzo Lab tutorials see [[DOCK Tutorials]]. Use this link [http://www.mediawiki.org/wiki/Help:Formatting Wiki Formatting] as a reference for editing the wiki. This tutorial was developed collaboratively by the AMS 536 class of 2013, using DOCK v6.6.
+
For additional Rizzo Lab tutorials see [[DOCK Tutorials]]. Use this link [http://www.mediawiki.org/wiki/Help:Formatting Wiki Formatting] as a reference for editing the wiki. This tutorial was developed collaboratively by the AMS 536 class of 2013, using DOCK v6.6. It is assumed that users of this tutorial have a basic understanding of the command line and are able to navigate a Unix operating system.
  
 
==I. Introduction==
 
==I. Introduction==
Line 12: Line 12:
 
# Non-rigid segments added in layers; energy minimized.
 
# Non-rigid segments added in layers; energy minimized.
 
# The resulting configurations are 'pruned' and energy re-minimized, yielding the docked configurations.
 
# The resulting configurations are 'pruned' and energy re-minimized, yielding the docked configurations.
−
 
  
 
===Orotodine Monophosphate Decarboxylase===
 
===Orotodine Monophosphate Decarboxylase===
 
The protein receptor which is the subject of this tutorial is orotodine monophosphate decarboxylase (OMP), a homodimeric protein from the organism ''Methanobacterium thermoautotrophicum''. OMP is involved in the biosynthesis of several pyrimidines including uridine monophosphate (UMP), the ligand used in this tutorial. UMP is a pyrimidine-based nucleotide monomer of RNA. The structure used for this tutorial can be found at the Protein Data Bank under accenssion number [http://www.pdb.org/pdb/explore/explore.do?structureId=1LOQ 1LOQ].
 
The protein receptor which is the subject of this tutorial is orotodine monophosphate decarboxylase (OMP), a homodimeric protein from the organism ''Methanobacterium thermoautotrophicum''. OMP is involved in the biosynthesis of several pyrimidines including uridine monophosphate (UMP), the ligand used in this tutorial. UMP is a pyrimidine-based nucleotide monomer of RNA. The structure used for this tutorial can be found at the Protein Data Bank under accenssion number [http://www.pdb.org/pdb/explore/explore.do?structureId=1LOQ 1LOQ].
−
 
  
 
===Organizing Directories===
 
===Organizing Directories===
  
−
While performing docking, it is convenient to adopt a standard directory structure / naming scheme, so that files are easy to find / identify. For this tutorial, we will use something similar to the following:
+
While performing docking, it is convenient to create a project directory (here we call it ~AMS536/dock-tutorial/), and adopt a standard directory structure / naming scheme, so that files are easy to find and identify. For this tutorial, we will use something similar to the following:
  
 
  ~username/AMS536/dock-tutorial/00.files/
 
  ~username/AMS536/dock-tutorial/00.files/
Line 31: Line 29:
 
                               /07.virtual-screen/
 
                               /07.virtual-screen/
 
                                
 
                                
−
In addition, most of the important files that are derived from the original crystal structure will be given a prefix that is the same as the PDB code, '1LOQ'. The following sections in this tutorial will adhere to this directory structure / naming scheme.
+
Before beginning the tutorial, it may be easiest to make all of the sub-directories at the same time. From here on in, these subdirectories will be referred to as ~00.files/, ~01.dockprep/ etc. In addition, most of the important files that are derived from the original crystal structure will be given a prefix that is the same as the PDB code, '1LOQ'.
  
 
==II. Preparing the Receptor and Ligand==
 
==II. Preparing the Receptor and Ligand==
Line 37: Line 35:
 
===Downloading the PDB file (1LOQ)===
 
===Downloading the PDB file (1LOQ)===
  
−
Go to PDB homepage (http://www.rcsb.org/pdb/home/home.do ) enter the protein ID (1LOQ) in the search bar, click Download Files in the top-right of the webpage, then select PDB File (text). In the new window, save the file in Downloads.
+
Go to PDB homepage (http://www.rcsb.org/pdb/home/home.do ) enter the protein ID (1LOQ) in the search bar, click Download Files in the top-right of the webpage, then select PDB File (text). In the new window, save the file in your ~00.files/ folder.
  
 
===Preparing the ligand and receptor in Chimera===
 
===Preparing the ligand and receptor in Chimera===
  
−
In this section, we will create four new files and save them in the 00.files/ folder:
+
NOTE: If you are accessing files remotely (i.e. through a terminal) and want to use a visualization program such as Chimera, first transfer the files to your local computer, run Chimera, and transfer the files back.
 +
 
 +
In this section, we will create four new files and save them in the ~01.dockprep/ folder:
  
 
   1LOQ.dockprep.mol2      (complete system with hydrogens and charges)
 
   1LOQ.dockprep.mol2      (complete system with hydrogens and charges)
 
   1LOQ.receptor.mol2      (the receptor alone)
 
   1LOQ.receptor.mol2      (the receptor alone)
−
   1LOQ.receptor.noH.mol2  (the receptor alone, without hydrogens)
+
   1LOQ.receptor.noH.pdb  (the receptor alone, without hydrogens)
 
   1LOQ.ligand.mol2        (the ligand alone)
 
   1LOQ.ligand.mol2        (the ligand alone)
  
−
To prepare these files, first copy the original PDB file into the 00.files/ folder and open it with VIM ($ vim 1LOQ.pdb). Because the residue name of the ligand (U) will give us some problems when assigning charges, change the residue name "U" to "LIG" starting at line 2082. Here is an example command that will change all instances of "  U" into "LIG", while preserving the correct spacing:
+
To prepare these files, first make a copy of the original PDB file in the ~00.files/ folder (named, for example, 1LOQ.copy.pdb) and open it with VIM ($ vim 1LOQ.copy.pdb). Because the residue name of the ligand (U) will give us some problems when assigning charges, change the residue name "U" to "LIG" starting at line 2082. Here is an example command that will change all instances of "  U" into "LIG", while preserving the correct spacing.  Note there are two blank spaces before U in the following expression:
  
 
   %s/  U/LIG/gc
 
   %s/  U/LIG/gc
Line 54: Line 54:
 
For this command, '''g'''  is short for global and '''c''' is short for check with the user before making the change.
 
For this command, '''g'''  is short for global and '''c''' is short for check with the user before making the change.
  
−
Next, open up the PDB file (1LOQ.pdb) in Chimera. To delete water molecules and other ligands, click ''Tools'' -> ''Structure Editing'' -> ''Dock Prep''. Check all boxes and click ''Okay'' to the end. Alternatively, the waters can be deleted manually by choosing ''Select'' -> ''Residue'' -> ''HOH'', then go to ''Actions'' -> ''Atoms/Bonds'' -> ''Delete''. Hydrogen atoms can be added manually by choosing ''Tools'' -> ''Structure Editing'' -> ''Add H''.
+
Next, open up the PDB file (1LOQ.copy.pdb) in Chimera. To delete water molecules and other ligands, click ''Tools'' -> ''Structure Editing'' -> ''Dock Prep''. Check all boxes and click ''Okay'' to the end. Alternatively, the waters can be deleted manually by choosing ''Select'' -> ''Residue'' -> ''HOH'', then go to ''Actions'' -> ''Atoms/Bonds'' -> ''Delete''. Hydrogen atoms can be added manually by choosing ''Tools'' -> ''Structure Editing'' -> ''Add H''.
  
 
Next, to add charges to the ligand and receptor,  go to ''Select'' -> ''Residue'' -> ''LIG'', then go to ''Tools'' -> ''Structure Editing'' -> ''Add Charge''. Choose ''AMBER ff99SB'' as the charge model, click ''Okay'', and when prompted chose AM1-BCC charges for the ligand, and make sure the ''Net Charge'' is set to ''-1''. (You must consider the chemistry of the ligand when assigning a charge state).
 
Next, to add charges to the ligand and receptor,  go to ''Select'' -> ''Residue'' -> ''LIG'', then go to ''Tools'' -> ''Structure Editing'' -> ''Add Charge''. Choose ''AMBER ff99SB'' as the charge model, click ''Okay'', and when prompted chose AM1-BCC charges for the ligand, and make sure the ''Net Charge'' is set to ''-1''. (You must consider the chemistry of the ligand when assigning a charge state).
  
−
Finally, save this file as '''1LOQ.dockprep.mol2'''.
+
Finally, save this file as '''1LOQ.dockprep.mol2''' into your ~01.dockprep/ folder.
  
 
===Generating the final files===
 
===Generating the final files===
Line 64: Line 64:
 
To create the receptor file: Open 1LOQ.dockprep.mol2, click ''Select'' -> ''Residue'' -> ''LIG''. Then click ''Actions'' -> ''Atoms/Bonds'' -> ''Delete''. Save the file as '''1LOQ.receptor.mol2'''.
 
To create the receptor file: Open 1LOQ.dockprep.mol2, click ''Select'' -> ''Residue'' -> ''LIG''. Then click ''Actions'' -> ''Atoms/Bonds'' -> ''Delete''. Save the file as '''1LOQ.receptor.mol2'''.
  
−
To create the receptor file with no hydrogen atoms: Open 1LOQ.dockprep.mol2, click ''Select'' -> ''Chemistry'' -> ''Element'' -> ''H'', then chose ''Actions'' -> ''Atoms/Bonds'' -> ''Delete''. Save the file as '''1LOQ.receptor.noH.mol2'''.
+
To create the receptor file with no hydrogen atoms: Open 1LOQ.receptor.mol2, click ''Select'' -> ''Chemistry'' -> ''Element'' -> ''H'', then chose ''Actions'' -> ''Atoms/Bonds'' -> ''Delete''. Save the file as '''1LOQ.receptor.noH.pdb'''.
  
 
To create the ligand file: Open 1LOQ.dockprep.mol2, click ''Select'' -> ''Residue'' -> ''LIG'', then click ''Select'' -> ''Invert'', then chose ''Actions'' -> ''Atoms/Bonds'' -> ''Delete''. Save the file as '''1LOQ.ligand.mol2'''.
 
To create the ligand file: Open 1LOQ.dockprep.mol2, click ''Select'' -> ''Residue'' -> ''LIG'', then click ''Select'' -> ''Invert'', then chose ''Actions'' -> ''Atoms/Bonds'' -> ''Delete''. Save the file as '''1LOQ.ligand.mol2'''.
Line 71: Line 71:
  
 
=== Receptor Surface ===
 
=== Receptor Surface ===
 +
 +
The next section of this tutorial will be performed in your ~02.surface-sphgen/ folder.
  
 
In order to generate the receptor surface one can perform the following steps (working in Chimera):
 
In order to generate the receptor surface one can perform the following steps (working in Chimera):
−
# Go ''File -> Open'' and choose the PDB file of the protein containing no hydrogens (1LOQ.receptor.noH.pdb)
+
# Go ''File -> Open'' and choose the PDB file of the protein containing no hydrogens (1LOQ.receptor.noH.pdb) from '''01.dockprep'''
 
# Further, ''Actions'' -> ''Surface'' -> ''Show''
 
# Further, ''Actions'' -> ''Surface'' -> ''Show''
 
# Go ''Tools'' -> ''Structure Editing'' -> ''Write DMS'' in order to obtain a ''dms'' file, which we will need while placing spheres
 
# Go ''Tools'' -> ''Structure Editing'' -> ''Write DMS'' in order to obtain a ''dms'' file, which we will need while placing spheres
Line 82: Line 84:
  
 
=== Placing Spheres ===
 
=== Placing Spheres ===
 +
 +
For more information SPHGEN, please consult the DOCK online owners manual at:
 +
 +
http://dock.compbio.ucsf.edu/DOCK_6/dock6_manual.htm
  
 
In order to place the spheres on the receptor surface, the following steps are required:
 
In order to place the spheres on the receptor surface, the following steps are required:
Line 87: Line 93:
 
'''1.''' Create a file called '''INSPH''' (an input file we will need later) and fill it out as follows (parameter descriptions included to the right), then save it.
 
'''1.''' Create a file called '''INSPH''' (an input file we will need later) and fill it out as follows (parameter descriptions included to the right), then save it.
  
−
  1LOQ.receptor.dms           #molecular surface file that we got from previous step
+
  1LOQ.receptor.dms
−
  R                           #sphere outside of surface (R) or inside surface (L)
+
  R
−
  X                           #specifies subset of surface points to be used (X=all points)
+
  X
−
  0.0                         #prevents generation of large spheres with close surface contacts(defalut=0.0)                       
+
  0.0
−
  4.0                         #maximum sphere radius in angstroms (default=4.0)
+
  4.0
−
  1.4                         #minimum sphere radius in angstroms (default=radius of probe)
+
  1.4
−
  1LOQ.receptor.sph           #clustered spheres file that we want to generate
+
  1LOQ.receptor.sph
 +
 
 +
Here is a line-by-line break down on what each line does:
  
−
''Make sure that your file doesn't contain any blank lines or the comments (denoted by #) from above, otherwise it won't work.''
+
*1LOQ.receptor.dms - molecular surface file that we got from previous step
 +
*R - sphere outside of surface (R) or inside surface (L)
 +
*X - specifies subset of surface points to be used (X=all points)
 +
*0.0 - prevents generation of large spheres with close surface contacts(defalut=0.0)
 +
*4.0 - maximum sphere radius in angstroms (default=4.0)
 +
*1.4 - minimum sphere radius in angstroms (default=radius of probe)
 +
*1LOQ.receptor.sph - clustered spheres file that we want to generate
  
 
'''2.''' Run the sphgen program from the command line:
 
'''2.''' Run the sphgen program from the command line:
Line 119: Line 133:
 
'''4.''' Run the '''sphere_selector''' program from the command line as follows:
 
'''4.''' Run the '''sphere_selector''' program from the command line as follows:
  
−
  sphere_selector 1LOQ.receptor.sph ../01-dockprep/1LOQ.ligand.mol2 8.0
+
  sphere_selector 1LOQ.receptor.sph ../01.dockprep/1LOQ.ligand.mol2 8.0
  
 
This program selects the spheres within a user-defined radius (8.0 here) of a target molecule from the previously obtained file '''1LOQ.receptor.sph'''. As a result a new file '''selected_spheres.sph''' will be generated. Again, the spheres can and should be visualized by using '''showsphere''' and '''Chimera'''.
 
This program selects the spheres within a user-defined radius (8.0 here) of a target molecule from the previously obtained file '''1LOQ.receptor.sph'''. As a result a new file '''selected_spheres.sph''' will be generated. Again, the spheres can and should be visualized by using '''showsphere''' and '''Chimera'''.
Line 146: Line 160:
 
==IV. Generating Box and Grid==
 
==IV. Generating Box and Grid==
  
−
===Box===
+
This section of the tutorial will be performed in your ~03.box-grid/ folder. For more information GRID, please consult the DOCK online owners manual at:
−
 
 
−
We will create a box around the binding site to define the boundaries of ligand sampling and aid in energy calculations. As a general rule, we will create a box around the spheres (from the previous step) with margins of at least 8.0 Angstroms on all sides.
 
  
−
First create a directory where you put all your grid and box files:
+
http://dock.compbio.ucsf.edu/DOCK_6/dock6_manual.htm
  
−
mkdir 03.box-grid
+
===Box===
−
cd 03.box-grid
 
  
−
Then you need to create a '''showbox.in''' file to generate the box:
+
We will create a box around the binding site to define the boundaries of ligand sampling and aid in energy calculations. As a general rule, we will create a box around the spheres (from the previous step) with margins of at least 8.0 Angstroms on all sides. You first need to create a '''showbox.in''' file to generate the box:
  
 
  vim showbox.in
 
  vim showbox.in
Line 176: Line 187:
 
===Grid===
 
===Grid===
  
−
Grids are used as a method to speed up evaluation of the energy scoring function by pre-computing electrostatic and VDW potential energies on the receptor at defined grid points within the box.  
+
Grids are used as a method to speed up evaluation of the energy scoring function by pre-computing electrostatic and VDW potential energies on the receptor at defined grid points within the box. VDW parameters are stored in a file that was installed with DOCK, and we will find it convenient to copy it and two other files to our ~00.files/ folder. In this class, DOCK was installed in the following location:
 +
 
 +
/home/wjallen/AMS536/local/dock6/
 +
 
 +
You can determine the path to your DOCK installation by typing:
 +
 
 +
which dock6
 +
 
 +
From that location, copy the following three files to your local ~00.files/ folder:
 +
 
 +
/home/wjallen/AMS536/local/dock6/parameters/vdw_AMBER_parm99.def
 +
/home/wjallen/AMS536/local/dock6/parameters/flex.defn
 +
/home/wjallen/AMS536/local/dock6/parameters/flex_drive.tbl
  
 
Use grid program to generate the grid and answer the questions as following:
 
Use grid program to generate the grid and answer the questions as following:
Line 197: Line 220:
 
  bump_overlap                  0.75
 
  bump_overlap                  0.75
 
  receptor_file                  ../01.dockprep/1LOQ.receptor.mol2
 
  receptor_file                  ../01.dockprep/1LOQ.receptor.mol2
−
  box_file                      ../03.box.grid/1LOQ.box.pdb
+
  box_file                      ../03.box-grid/1LOQ.box.pdb
 
  vdw_definition_file            ../00.files/vdw_AMBER_parm99.defn
 
  vdw_definition_file            ../00.files/vdw_AMBER_parm99.defn
 
  score_grid_prefix              1LOQ.grid
 
  score_grid_prefix              1LOQ.grid
Line 205: Line 228:
  
 
==V. Docking a Single Molecule for Pose Reproduction==
 
==V. Docking a Single Molecule for Pose Reproduction==
 +
 +
This part of the tutorial will be performed in your ~04.dock/ folder. For more information DOCK, please consult the DOCK online owners manual at:
 +
 +
http://dock.compbio.ucsf.edu/DOCK_6/dock6_manual.htm
  
 
===Rigid Docking===
 
===Rigid Docking===
  
−
When docking a molecule ''rigidly'' in DOCK, no conformations or rotamers will be sampled other than the input configuration which, in our case, was dervied from the crystal structure. This will be much faster that ''flexible'' docking, but it is not appropriate for virtual screening because the docked conformation of compounds from a library is generally not known. First create and empty input file for docking:
+
When docking a molecule ''rigidly'' in DOCK, no conformations or rotamers will be sampled other than the input configuration which, in our case, was derived from the crystal structure. This will be much faster that ''flexible'' docking, but it is not appropriate for virtual screening because the docked conformation of compounds from a library is generally not known. First create an empty input file for docking:
 
  touch dock.in
 
  touch dock.in
 
Then execute DOCK6:
 
Then execute DOCK6:
Line 219: Line 246:
 
  calculate_rmsd                                              no  
 
  calculate_rmsd                                              no  
 
  use_database_filter                                          no
 
  use_database_filter                                          no
−
  orient_ligand                                                no
+
  orient_ligand                                                yes
 +
automated_matching                                          yes
 +
receptor_site_file                                          ../02.surface-sphgen/selected_spheres.sph
 
  use_internal_energy                                          no
 
  use_internal_energy                                          no
 
  flexible_ligand                                              no
 
  flexible_ligand                                              no
Line 252: Line 281:
 
With these input parameters, the rigid docking experiment will result in a single scored ligand pose. Open Chimera to visualize the docking result. After opening the receptor file in surface view, open the ligand file (named "output_scored.mol2") by going under ''Tools'' -> ''Surface/Binding Analysis'' -> ''ViewDock''.
 
With these input parameters, the rigid docking experiment will result in a single scored ligand pose. Open Chimera to visualize the docking result. After opening the receptor file in surface view, open the ligand file (named "output_scored.mol2") by going under ''Tools'' -> ''Surface/Binding Analysis'' -> ''ViewDock''.
  
−
 
+
[[Image:dock_original ligand.png|thumb|375px|center|Rigid docking result]]
−
[[file:dock_original ligand.png|500px|Rigid docking result]]
 
  
 
===Flexible Docking===
 
===Flexible Docking===
  
−
For flexible docking, change input parameters. These changes will generate additional questions. Some changes to parameters are shown below:
+
Flexible docking will take longer, but is necessary for virtual screening. For flexible docking, several input parameters need to be changed, and these changes will generate additional questions prompted to the user. Some changes to parameters are shown below:
 
  calculate_rmsd                                              yes
 
  calculate_rmsd                                              yes
−
orient_ligand                                                yes
 
 
  flexible_ligand                                              yes
 
  flexible_ligand                                              yes
 
  use_internal_energy                                          yes
 
  use_internal_energy                                          yes
Line 265: Line 292:
 
  num_scored_conformers                                        10
 
  num_scored_conformers                                        10
  
−
This flexible ligand protocol can be used with multiple ligand input files.  
+
Once these changes have been made to the input file, execute DOCK6 again:
 +
dock6 -i dock.in
  
 +
This flexible ligand protocol can be used with multiple ligand input files. The docked ligand poses can be compared using RMSD (Root Mean Squared Deviation). RMSD is a measurement of the distance between atoms on the original crystal structure ligand with the newly generated ligand conformation. An RMSD under 2 Angstroms would indicate a good conformation. Below are two examples of a final docked ligand in the receptor binding site pocket. The worst and best energy scored ligands are shown below. The original ligand is in cyan and the docked ligand is colored in heteroatom.
  
 +
[[Image:dock_bestligand_and original.png|thumb|375px|center|Best scored ligand result (-78.3 kcal/mol)]]
  
−
The docked ligand poses can be compared using RMSD (Root mean squared Deviation). RMSD is a measurement of the distance between atoms on the original crystal structure ligand with the newly generated ligand conformation. An RMSD under 2 Angstroms would indicate a good conformation.
+
[[Image:dock_worstligand_and original.png|thumb|375px|center|Worst scored ligand result (-67.4 kcal/mol)]]
−
 
 
−
 
 
−
Below are two examples of a final docked ligand in the receptor active site pocket. The worst and best energy scored ligands are shown below. The original ligand is in cyan and the docked ligand is colored in heteroatom.
 
−
 
 
−
[[file:dock_bestligand_and original.png|500px|Best scored ligand result]]
 
−
Best scored ligand result
 
−
 
 
−
 
 
−
[[file:dock_worstligand_and original.png|500px|Worst scored ligand result]]
 
−
Worst scored ligand result
 
  
 
==VI. Virtual Screening==
 
==VI. Virtual Screening==
  
−
'''Virtual Screening Introduction'''
+
===Virtual Screening Introduction===
  
 
A virtual screen of various ligand allows for the comparison of both qualitative (e.g. position in binding site) and quantitative (e.g. energy scores) data pertaining to the each screened ligand with an originally docked molecule.  Virtual screening is often used as a method to cut the cost of experimentation by narrowing down the ligands within a database and predicting which will exhibit the most favorable binding to a specific protein (with a pre-determined .grid file).
 
A virtual screen of various ligand allows for the comparison of both qualitative (e.g. position in binding site) and quantitative (e.g. energy scores) data pertaining to the each screened ligand with an originally docked molecule.  Virtual screening is often used as a method to cut the cost of experimentation by narrowing down the ligands within a database and predicting which will exhibit the most favorable binding to a specific protein (with a pre-determined .grid file).
  
 +
===Running the Database Filter===
  
−
'''Creating a Filter for the Virtual Screen'''
+
When first beginning the virtual screen, a filter should be specified in order save computational power by only screening potentially effective ligands within the directory ~06.database-filter/.  This involves limiting several variables of ligands specified in a .mol2 file.  To limit the ligands from the original database, a file "dock_filter.in" is created and executed using DOCK.  Note that in this example the file "cdiv_p0.0.mol2" is a multi mol2 file containing thousands of ligands from the CHEMDIV vendor which was previously downloaded from the UCSF ZINC database (https://zinc.docking.org/about/ucsf).  ZINC is a great resource of purchasable compounds for virtual screening. Here are the contents of the file:
−
 
 
−
When first beginning the virtual screen, a filter should be specified in order save computational power by only screening potentially effective ligands within the directory 06.database-filter/.  This involves limiting several variables of ligands specified in a .mol2 file.  To limit the ligands from the original database, a file dock_filter.in is created.  Here are the contents of the file:
 
  
 
  ligand_atom_file                                            /home/wjallen/AMS536/multi-mol2-files/cdiv_p0.0.mol2
 
  ligand_atom_file                                            /home/wjallen/AMS536/multi-mol2-files/cdiv_p0.0.mol2
Line 320: Line 339:
 
  rank_ligands                                                no
 
  rank_ligands                                                no
  
−
In this file some important characteristics of the ligands that are limited are '''dbfilter_max_heavy_atoms''', '''dbfilter_max_rot_bonds''', '''dbfilter_max_molwt''', and both '''dbfilter_max_formal_charge''' and '''dbfilter_min_formal_charge'''.  As show in the text of the file, a file called filtered_scored.mol2 will be created with all of the ligands from the original database that fit into the specified limits of number of heavy atoms, number of rotatable bonds, molecular weight, and formal charge.
+
In this file some important characteristics of the ligands that are limited are ''dbfilter_max_heavy_atoms'', ''dbfilter_max_rot_bonds'', ''dbfilter_max_molwt'', and both ''dbfilter_max_formal_charge'' and ''dbfilter_min_formal_charge''.  As show in the text of the file, a file called filtered_scored.mol2 will be created with all of the ligands from the original database that fit into the specified limits of number of heavy atoms, number of rotatable bonds, molecular weight, and formal charge. '''''Note:''''' ''The max and min formal charge specified in this file (-1 to -2) are an extremely limited range, and are only used in this tutorial as an illustration.''
  
 +
===Running the Virtual Screen===
  
−
'''Proceeding to the Virtual Screen'''
+
After creating a new directory, ~07.virtual-screen/, a dock.in file must be created.  So as not to confuse the virtual screen file with the original dock.in of the docked ligand, the new file created is called dock_vs.in.  Running this file in dock6 allows us to fill in the important details of the file that terminate in a virtual screening of the input ligand.
−
 
 
−
After creating a new directory, 07.virtual-screen/, a dock.in file must be created.  So as not to confuse the virtual screen file with the original dock.in of the docked ligand, the new file created is called dock_vs.in.  Running this file in dock6 allows us to fill in the important details of the file that terminate in a virtual screening of the input ligand.
 
  
 
  ligand_atom_file                                            ../06.database-filter/filtered_scored.mol2
 
  ligand_atom_file                                            ../06.database-filter/filtered_scored.mol2
Line 399: Line 417:
 
'''ligand_atom_file''' - here we have specified the new file created after filtering the initial ligand database file
 
'''ligand_atom_file''' - here we have specified the new file created after filtering the initial ligand database file
  
−
'''calculate_rmsd''' - we select the default <no> because calculating the rmsd for roughly 1000 molecules would be a huge computational cost and it would be better to wait until we have selected a handful of strongly bound ligands to calculate the rmsd for
+
'''calculate_rmsd''' - we select the default <no> because since we are screening a library of compounds, there will be no reference position to compare them to
  
 
'''orient_ligand''' - here we would like to the have the ligand oriented in the binding pocket
 
'''orient_ligand''' - here we would like to the have the ligand oriented in the binding pocket
Line 415: Line 433:
 
'''grid_score_primary''' - we want the grid score to be the primary method of scoring the screened ligands
 
'''grid_score_primary''' - we want the grid score to be the primary method of scoring the screened ligands
  
−
'''grid_score_grid_prefix''' - the input step for the .grid file created earlier
+
'''grid_score_grid_prefix''' - the input for the .grid file created earlier
  
 
'''atom_model''' - we select the all atom model
 
'''atom_model''' - we select the all atom model
Line 421: Line 439:
 
'''num_scored_conformers''' - we only want to produce one scored conformer from each screened ligand because we only want the best conformations
 
'''num_scored_conformers''' - we only want to produce one scored conformer from each screened ligand because we only want the best conformations
  
−
Note that if you are performing a small sample virtual screening it is possible to run it in Mathlab; however, if you are running the virtual screening to a very large scale (i.e. hundreds or thousands of ligands) you will need to use several nodes in Seawulf to produce results in a timely fashion.
+
Note that if you are performing a small sample virtual screening it is possible to run it on a local computer in a reasonable amount of time; however, if you are running the virtual screening to a very large scale (i.e. hundreds or thousands of ligands) you will need to use several nodes in Seawulf to produce results in a timely fashion.
−
 
 
  
−
'''Virtual Screen Results'''
+
===Analyzing the Results===
  
−
When your virtual screening has run completely and you are ready to analyze the results, open Chimera.  In Chimera you can prepare your protein by opening 1LOQ.receptor.noH.pdb and choosing "'''Actions''' --> '''Surface''' --> '''show'''".  You may also wish to open up the original ligand file 1LOQ.ligand.mol2 in order to show the position of the original ligand/substrate in the receptor's active site.
+
When your virtual screening has run completely and you are ready to analyze the results, open Chimera.  In Chimera you can prepare your protein by opening 1LOQ.receptor.noH.pdb and choosing ''Actions'' -> ''Surface'' -> ''show''.  You may also wish to open up the original ligand file 1LOQ.ligand.mol2 in order to show the position of the original ligand/substrate in the receptor's active site.
  
−
To view the results of your virtual screening go to '''Tools''' --> '''Surface/Binding Analysis''' --> '''ViewDock''' and from their you can select your virtual screen output file.  In the "ViewDock" pop-up window you can then select '''Column''' --> '''Show''' --> '''Grid Score''' which will add a column to the ViewDock window with the grid score of each ligand.  You can double-click on the column heading '''Grid Score''' to sort the ligands based on their grid scores.
+
To view the results of your virtual screening go to ''Tools'' -> ''Surface/Binding Analysis'' -> ''ViewDock'' and from their you can select your virtual screen output file.  In the "ViewDock" pop-up window you can then select ''Column'' --> ''Show'' --> ''Grid Score'' which will add a column to the ViewDock window with the grid score of each ligand.  You can double-click on the column heading ''Grid Score'' to sort the ligands based on their grid scores.
  
 
[Chimera image1] [Chimera image2]
 
[Chimera image1] [Chimera image2]
Line 435: Line 452:
 
The [http://www.stonybrook.edu/seawulfcluster/ Seawulf] Cluster is a 470-processor Linux Cluster capable of highly parallel processing. This parallel processing allows dock virtual screens to be completed in a fraction of the time as a single processor.
 
The [http://www.stonybrook.edu/seawulfcluster/ Seawulf] Cluster is a 470-processor Linux Cluster capable of highly parallel processing. This parallel processing allows dock virtual screens to be completed in a fraction of the time as a single processor.
  
−
If you are docking multiple ligands, you can use more than one processor in parallel mode, but you should never use more processors than you have ligands.  
+
If you are docking multiple ligands, you can use more than one processor in parallel mode, but you should never use more processors than you have ligands. Before we can run DOCK on Seawulf, we need to copy the proper files from Herbie to Seawulf. If we CD into the AMS536 folder we can use the following command from the mathlab computer to copy all of the dock-tutorial files
−
Before we can run DOCK on Seawulf, we need to copy the proper files from Herbie to Seawulf.
 
−
If we CD into the AMS536 folder we can use the following command from the mathlab computer to copy all of the dock-tutorial files
 
  
−
  $scp -r /dock-tutorial/  username@herbie.mathlab.sunysb.edu:~/AMS536/
+
  scp -r /dock-tutorial/  username@herbie.mathlab.sunysb.edu:~/AMS536/
  
 
Now we have all of our DOCK preparation files and folders on the seawulf cluster.
 
Now we have all of our DOCK preparation files and folders on the seawulf cluster.
  
−
'''Running DOCK in Serial on a Single Processor'''
+
===Running DOCK in Serial on a Single Processor===
  
−
Running on a single processor is very similar to running dock on the mathlab comptuer.
+
Running on a single processor is very similar to running dock on the mathlab computer.
  
 
If you make a file called qsub.csh with the text:
 
If you make a file called qsub.csh with the text:
Line 481: Line 496:
 
See also [http://ringo.ams.sunysb.edu/index.php/PBS_Queue PBS] commands.
 
See also [http://ringo.ams.sunysb.edu/index.php/PBS_Queue PBS] commands.
  
−
'''Running DOCK in Parallel using MPI'''
+
===Running DOCK in Parallel using MPI===
  
 
In order to run DOCK in parallel you have to use a slightly different build of DOCK6 called dock6.mpi.
 
In order to run DOCK in parallel you have to use a slightly different build of DOCK6 called dock6.mpi.

Latest revision as of 16:26, 14 January 2015

For additional Rizzo Lab tutorials see DOCK Tutorials. Use this link Wiki Formatting as a reference for editing the wiki. This tutorial was developed collaboratively by the AMS 536 class of 2013, using DOCK v6.6. It is assumed that users of this tutorial have a basic understanding of the command line and are able to navigate a Unix operating system.

I. Introduction

DOCK

DOCK is a molecular docking program used in drug discovery. It was developed by Irwin D. Kuntz, Jr. and colleagues at UCSF (see UCSF DOCK). This program, given a protein binding site and a small molecule, tries to predict the correct binding mode of the small molecule in the binding site, and the associated binding energy. Small molecules with highly favorable binding energies could be new drug leads. This makes DOCK a valuable drug discovery tool. DOCK is typically used to screen massive libraries of millions of compounds against a protein to isolate potential drug leads. These leads are then further studied, and could eventually result in a new, marketable drug. DOCK works well as a screening procedure for generating leads, but is not currently as useful for optimization of those leads.

DOCK 6 uses an incremental construction algorithm called anchor and grow. It is described by a three-step process:

  1. Rigid portion of ligand (anchor) is docked by geometric methods.
  2. Non-rigid segments added in layers; energy minimized.
  3. The resulting configurations are 'pruned' and energy re-minimized, yielding the docked configurations.

Orotodine Monophosphate Decarboxylase

The protein receptor which is the subject of this tutorial is orotodine monophosphate decarboxylase (OMP), a homodimeric protein from the organism Methanobacterium thermoautotrophicum. OMP is involved in the biosynthesis of several pyrimidines including uridine monophosphate (UMP), the ligand used in this tutorial. UMP is a pyrimidine-based nucleotide monomer of RNA. The structure used for this tutorial can be found at the Protein Data Bank under accenssion number 1LOQ.

Organizing Directories

While performing docking, it is convenient to create a project directory (here we call it ~AMS536/dock-tutorial/), and adopt a standard directory structure / naming scheme, so that files are easy to find and identify. For this tutorial, we will use something similar to the following: 

~username/AMS536/dock-tutorial/00.files/
                              /01.dockprep/
                              /02.surface-sphgen/
                              /03.box-grid/
                              /04.dock/
                              /05.mini-virtual-screen/
                              /06.database-filter/
                              /07.virtual-screen/

Before beginning the tutorial, it may be easiest to make all of the sub-directories at the same time. From here on in, these subdirectories will be referred to as ~00.files/, ~01.dockprep/ etc. In addition, most of the important files that are derived from the original crystal structure will be given a prefix that is the same as the PDB code, '1LOQ'.

II. Preparing the Receptor and Ligand

Downloading the PDB file (1LOQ)

Go to PDB homepage (http://www.rcsb.org/pdb/home/home.do ) enter the protein ID (1LOQ) in the search bar, click Download Files in the top-right of the webpage, then select PDB File (text). In the new window, save the file in your ~00.files/ folder.

Preparing the ligand and receptor in Chimera

NOTE: If you are accessing files remotely (i.e. through a terminal) and want to use a visualization program such as Chimera, first transfer the files to your local computer, run Chimera, and transfer the files back.

In this section, we will create four new files and save them in the ~01.dockprep/ folder: 

 1LOQ.dockprep.mol2      (complete system with hydrogens and charges)
 1LOQ.receptor.mol2      (the receptor alone)
 1LOQ.receptor.noH.pdb   (the receptor alone, without hydrogens)
 1LOQ.ligand.mol2        (the ligand alone)

To prepare these files, first make a copy of the original PDB file in the ~00.files/ folder (named, for example, 1LOQ.copy.pdb) and open it with VIM ($ vim 1LOQ.copy.pdb). Because the residue name of the ligand (U) will give us some problems when assigning charges, change the residue name "U" to "LIG" starting at line 2082. Here is an example command that will change all instances of " U" into "LIG", while preserving the correct spacing. Note there are two blank spaces before U in the following expression: 

 %s/  U/LIG/gc

For this command, g is short for global and c is short for check with the user before making the change.

Next, open up the PDB file (1LOQ.copy.pdb) in Chimera. To delete water molecules and other ligands, click Tools -> Structure Editing -> Dock Prep. Check all boxes and click Okay to the end. Alternatively, the waters can be deleted manually by choosing Select -> Residue -> HOH, then go to Actions -> Atoms/Bonds -> Delete. Hydrogen atoms can be added manually by choosing Tools -> Structure Editing -> Add H.

Next, to add charges to the ligand and receptor, go to Select -> Residue -> LIG, then go to Tools -> Structure Editing -> Add Charge. Choose AMBER ff99SB as the charge model, click Okay, and when prompted chose AM1-BCC charges for the ligand, and make sure the Net Charge is set to -1. (You must consider the chemistry of the ligand when assigning a charge state).

Finally, save this file as 1LOQ.dockprep.mol2 into your ~01.dockprep/ folder.

Generating the final files

To create the receptor file: Open 1LOQ.dockprep.mol2, click Select -> Residue -> LIG. Then click Actions -> Atoms/Bonds -> Delete. Save the file as 1LOQ.receptor.mol2.

To create the receptor file with no hydrogen atoms: Open 1LOQ.receptor.mol2, click Select -> Chemistry -> Element -> H, then chose Actions -> Atoms/Bonds -> Delete. Save the file as 1LOQ.receptor.noH.pdb.

To create the ligand file: Open 1LOQ.dockprep.mol2, click Select -> Residue -> LIG, then click Select -> Invert, then chose Actions -> Atoms/Bonds -> Delete. Save the file as 1LOQ.ligand.mol2.

III. Generating Receptor Surface and Spheres

Receptor Surface

The next section of this tutorial will be performed in your ~02.surface-sphgen/ folder.

In order to generate the receptor surface one can perform the following steps (working in Chimera):

  1. Go File -> Open and choose the PDB file of the protein containing no hydrogens (1LOQ.receptor.noH.pdb) from 01.dockprep
  2. Further, Actions -> Surface -> Show
  3. Go Tools -> Structure Editing -> Write DMS in order to obtain a dms file, which we will need while placing spheres
  4. In the new window save the surface as 1LOQ.receptor.dms


Receptor surface

Placing Spheres

For more information SPHGEN, please consult the DOCK online owners manual at:

http://dock.compbio.ucsf.edu/DOCK_6/dock6_manual.htm

In order to place the spheres on the receptor surface, the following steps are required:

1. Create a file called INSPH (an input file we will need later) and fill it out as follows (parameter descriptions included to the right), then save it. 

1LOQ.receptor.dms
R
X
0.0
4.0
1.4
1LOQ.receptor.sph

Here is a line-by-line break down on what each line does:

  • 1LOQ.receptor.dms - molecular surface file that we got from previous step
  • R - sphere outside of surface (R) or inside surface (L)
  • X - specifies subset of surface points to be used (X=all points)
  • 0.0 - prevents generation of large spheres with close surface contacts(defalut=0.0)
  • 4.0 - maximum sphere radius in angstroms (default=4.0)
  • 1.4 - minimum sphere radius in angstroms (default=radius of probe)
  • 1LOQ.receptor.sph - clustered spheres file that we want to generate

2. Run the sphgen program from the command line: 

sphgen -i INSPH -o OUTSPH

OUTSPH is the output file containing the information on the sphgen run, while 1LOQ.receptor.sph is the file which contains the spheres.

3. (optional) If one wants to have a look at the spheres received as an outcome of sphgen, one should run showsphere, by typing in the command line: 

showsphere

The following questions will be prompted on the command line: 

Enter name of sphere cluster file:
Enter cluster number to process (<0 = all):
Generate surfaces as well as pdb files (<N>/Y)?
Enter name for output file prefix:
Process cluster 0 (contains ALL spheres) (<N>/Y)?

As the questions have been answered the program will generate the spheres, writing the data in a PDB file, afterwards the spheres may be observed by opening this file in Chimera.

4. Run the sphere_selector program from the command line as follows: 

sphere_selector 1LOQ.receptor.sph ../01.dockprep/1LOQ.ligand.mol2 8.0

This program selects the spheres within a user-defined radius (8.0 here) of a target molecule from the previously obtained file 1LOQ.receptor.sph. As a result a new file selected_spheres.sph will be generated. Again, the spheres can and should be visualized by using showsphere and Chimera.

5. Run showsphere in order to visualize the spheres: 

showsphere

When prompted on the command line, answering the questions as follows: 

selected_spheres.sph
-1
N
output_spheres_selected
N
  • Launch Chimera, choose File -> Open, choose 1LOQ.receptor.noH.pdb
  • Go File -> Open, choosing output_spheres_selected.pdb
  • Go Select -> Residue -> SPH
  • Finally, Actions -> Atoms/Bonds -> sphere

The picture like one placed below will be obtained afterwards.

Selected spheres

IV. Generating Box and Grid

This section of the tutorial will be performed in your ~03.box-grid/ folder. For more information GRID, please consult the DOCK online owners manual at:

http://dock.compbio.ucsf.edu/DOCK_6/dock6_manual.htm

Box

We will create a box around the binding site to define the boundaries of ligand sampling and aid in energy calculations. As a general rule, we will create a box around the spheres (from the previous step) with margins of at least 8.0 Angstroms on all sides. You first need to create a showbox.in file to generate the box: 

vim showbox.in

Edit this file as following: 

Y                                           # Yes, generate a box
8.0                                         # box margin
../02.surface-sphgen/selected_spheres.sph   # input sphere files
1                                           # which sphere cluster to use
1LOQ.box.pdb                                # output file name

Note: Do not include the comments in the showbox.in file. To run the program showbox, give the name of the program on the command line and provide the showbox.in file: 

showbox < showbox.in
Box Image


Grid

Grids are used as a method to speed up evaluation of the energy scoring function by pre-computing electrostatic and VDW potential energies on the receptor at defined grid points within the box. VDW parameters are stored in a file that was installed with DOCK, and we will find it convenient to copy it and two other files to our ~00.files/ folder. In this class, DOCK was installed in the following location: 

/home/wjallen/AMS536/local/dock6/

You can determine the path to your DOCK installation by typing: 

which dock6

From that location, copy the following three files to your local ~00.files/ folder: 

/home/wjallen/AMS536/local/dock6/parameters/vdw_AMBER_parm99.def
/home/wjallen/AMS536/local/dock6/parameters/flex.defn
/home/wjallen/AMS536/local/dock6/parameters/flex_drive.tbl

Use grid program to generate the grid and answer the questions as following: 

touch grid.in
grid -i grid.in

compute_grids                  yes
grid_spacing                   0.4
output_molecule                no
contact_score                  no
energy_score                   yes
energy_cutoff_distance         9999
atom_model                     a
attractive_exponent            6
repulsive_exponent             9
distance_dielectric            yes
dielectric_factor              4
bump_filter                    yes
bump_overlap                   0.75
receptor_file                  ../01.dockprep/1LOQ.receptor.mol2
box_file                       ../03.box-grid/1LOQ.box.pdb
vdw_definition_file            ../00.files/vdw_AMBER_parm99.defn
score_grid_prefix              1LOQ.grid


Grid Image

V. Docking a Single Molecule for Pose Reproduction

This part of the tutorial will be performed in your ~04.dock/ folder. For more information DOCK, please consult the DOCK online owners manual at:

http://dock.compbio.ucsf.edu/DOCK_6/dock6_manual.htm

Rigid Docking

When docking a molecule rigidly in DOCK, no conformations or rotamers will be sampled other than the input configuration which, in our case, was derived from the crystal structure. This will be much faster that flexible docking, but it is not appropriate for virtual screening because the docked conformation of compounds from a library is generally not known. First create an empty input file for docking: 

touch dock.in

Then execute DOCK6: 

dock6 -i dock.in

You will be prompted for answers to many questions. For the rigid docking experiments, suggested parameters are as follows: 

ligand_atom_file                                             ../01.dockprep/1LOQ.ligand.mol2
limit_max_ligands                                            no
skip_molecule                                                no
read_mol_solvation                                           no
calculate_rmsd                                               no 
use_database_filter                                          no
orient_ligand                                                yes 
automated_matching                                           yes
receptor_site_file                                           ../02.surface-sphgen/selected_spheres.sph
use_internal_energy                                          no
flexible_ligand                                              no
bump_filter                                                  no
score_molecules                                              yes
contact_score_primary                                        no
contact_score_secondary                                      no
grid_score_primary                                           yes
grid_score_secondary                                         no
grid_score_rep_rad_scale                                     1
grid_score_vdw_scale                                         1
grid_score_es_scale                                          1
grid_score_grid_prefix                                       ../03.box-grid/1LOQ.grid
multigrid_score_secondary                                    no 
dock3.5_score_secondary                                      no
continuous_score_secondary                                   no
descriptor_score_secondary                                   no
gbsa_zou_score_secondary                                     no
gbsa_hawkins_score_secondary                                 no
SASA_descriptor_score_secondary                              no
amber_score_secondary                                        no
minimize_ligand                                              no
atom_model                                                   all
vdw_defn_file                                                ../00.files/vdw_AMBER_parm99.defn
flex_defn_file                                               ../00.files/flex.defn
flex_drive_file                                              ../00.files/flex_drive.tbl
ligand_outfile_prefix                                        output
write_orientations                                           no
num_scored_conformers                                        1
rank_ligands                                                 no

With these input parameters, the rigid docking experiment will result in a single scored ligand pose. Open Chimera to visualize the docking result. After opening the receptor file in surface view, open the ligand file (named "output_scored.mol2") by going under Tools -> Surface/Binding Analysis -> ViewDock.

Rigid docking result

Flexible Docking

Flexible docking will take longer, but is necessary for virtual screening. For flexible docking, several input parameters need to be changed, and these changes will generate additional questions prompted to the user. Some changes to parameters are shown below: 

calculate_rmsd                                               yes
flexible_ligand                                              yes
use_internal_energy                                          yes
minimize_ligand                                              yes
num_scored_conformers                                        10

Once these changes have been made to the input file, execute DOCK6 again: 

dock6 -i dock.in

This flexible ligand protocol can be used with multiple ligand input files. The docked ligand poses can be compared using RMSD (Root Mean Squared Deviation). RMSD is a measurement of the distance between atoms on the original crystal structure ligand with the newly generated ligand conformation. An RMSD under 2 Angstroms would indicate a good conformation. Below are two examples of a final docked ligand in the receptor binding site pocket. The worst and best energy scored ligands are shown below. The original ligand is in cyan and the docked ligand is colored in heteroatom.

Best scored ligand result (-78.3 kcal/mol)
Worst scored ligand result (-67.4 kcal/mol)

VI. Virtual Screening

Virtual Screening Introduction

A virtual screen of various ligand allows for the comparison of both qualitative (e.g. position in binding site) and quantitative (e.g. energy scores) data pertaining to the each screened ligand with an originally docked molecule. Virtual screening is often used as a method to cut the cost of experimentation by narrowing down the ligands within a database and predicting which will exhibit the most favorable binding to a specific protein (with a pre-determined .grid file).

Running the Database Filter

When first beginning the virtual screen, a filter should be specified in order save computational power by only screening potentially effective ligands within the directory ~06.database-filter/. This involves limiting several variables of ligands specified in a .mol2 file. To limit the ligands from the original database, a file "dock_filter.in" is created and executed using DOCK. Note that in this example the file "cdiv_p0.0.mol2" is a multi mol2 file containing thousands of ligands from the CHEMDIV vendor which was previously downloaded from the UCSF ZINC database (https://zinc.docking.org/about/ucsf). ZINC is a great resource of purchasable compounds for virtual screening. Here are the contents of the file: 

ligand_atom_file                                             /home/wjallen/AMS536/multi-mol2-files/cdiv_p0.0.mol2
limit_max_ligands                                            no
skip_molecule                                                no
read_mol_solvation                                           no
calculate_rmsd                                               no
use_database_filter                                          yes
dbfilter_max_heavy_atoms                                     50
dbfilter_min_heavy_atoms                                     0
dbfilter_max_rot_bonds                                       10
dbfilter_min_rot_bonds                                       0
dbfilter_max_molwt                                           9999.0
dbfilter_min_molwt                                           0.0
dbfilter_max_formal_charge                                   -1.0
dbfilter_min_formal_charge                                   -2.0
orient_ligand                                                no
use_internal_energy                                          no
flexible_ligand                                              no
bump_filter                                                  no
score_molecules                                              no
atom_model                                                   all
vdw_defn_file                                                ../00.files/vdw_AMBER_parm99.defn
flex_defn_file                                               ../00.files/flex.defn
flex_drive_file                                              ../00.files/flex_drive.tbl
ligand_outfile_prefix                                        filtered
write_orientations                                           no
num_scored_conformers                                        1
rank_ligands                                                 no

In this file some important characteristics of the ligands that are limited are dbfilter_max_heavy_atoms, dbfilter_max_rot_bonds, dbfilter_max_molwt, and both dbfilter_max_formal_charge and dbfilter_min_formal_charge. As show in the text of the file, a file called filtered_scored.mol2 will be created with all of the ligands from the original database that fit into the specified limits of number of heavy atoms, number of rotatable bonds, molecular weight, and formal charge. Note: The max and min formal charge specified in this file (-1 to -2) are an extremely limited range, and are only used in this tutorial as an illustration.

Running the Virtual Screen

After creating a new directory, ~07.virtual-screen/, a dock.in file must be created. So as not to confuse the virtual screen file with the original dock.in of the docked ligand, the new file created is called dock_vs.in. Running this file in dock6 allows us to fill in the important details of the file that terminate in a virtual screening of the input ligand. 

ligand_atom_file                                             ../06.database-filter/filtered_scored.mol2
limit_max_ligands                                            no
skip_molecule                                                no
read_mol_solvation                                           no
calculate_rmsd                                               no
use_database_filter                                          no
orient_ligand                                                yes
automated_matching                                           yes
receptor_site_file                                           ../02.surface-sphgen/selected_spheres.sph
max_orientations                                             1000
critical_points                                              no
chemical_matching                                            no
use_ligand_spheres                                           no
use_internal_energy                                          yes
internal_energy_rep_exp                                      12
flexible_ligand                                              yes
user_specified_anchor                                        no
limit_max_anchors                                            no
min_anchor_size                                              5
pruning_use_clustering                                       yes
pruning_max_orients                                          1000
pruning_clustering_cutoff                                    100
pruning_conformer_score_cutoff                               100
use_clash_overlap                                            no
write_growth_tree                                            no
bump_filter                                                  no
score_molecules                                              yes
contact_score_primary                                        no
contact_score_secondary                                      no
grid_score_primary                                           yes
grid_score_secondary                                         no
grid_score_rep_rad_scale                                     1
grid_score_vdw_scale                                         1
grid_score_es_scale                                          1
grid_score_grid_prefix                                       ../03.box-grid/1LOQ.grid
multigrid_score_secondary                                    no
dock3.5_score_secondary                                      no
continuous_score_secondary                                   no
descriptor_score_secondary                                   no
gbsa_zou_score_secondary                                     no
gbsa_hawkins_score_secondary                                 no
SASA_descriptor_score_secondary                              no
amber_score_secondary                                        no
minimize_ligand                                              yes
minimize_anchor                                              yes
minimize_flexible_growth                                     yes
use_advanced_simplex_parameters                              no
simplex_max_cycles                                           1
simplex_score_converge                                       0.1
simplex_cycle_converge                                       1.0
simplex_trans_step                                           1.0
simplex_rot_step                                             0.1
simplex_tors_step                                            10.0
simplex_anchor_max_iterations                                500
simplex_grow_max_iterations                                  500
simplex_grow_tors_premin_iterations                          0
simplex_random_seed                                          0
simplex_restraint_min                                        no
atom_model                                                   all
vdw_defn_file                                                ../00.files/vdw_AMBER_parm99.defn
flex_defn_file                                               ../00.files/flex.defn
flex_drive_file                                              ../00.files/flex_drive.tbl
ligand_outfile_prefix                                        output
write_orientations                                           no
num_scored_conformers                                        1
rank_ligands                                                 no


A few of the questions addressed in the terminal window while running a virtual screen are as follows:

ligand_atom_file - here we have specified the new file created after filtering the initial ligand database file

calculate_rmsd - we select the default <no> because since we are screening a library of compounds, there will be no reference position to compare them to

orient_ligand - here we would like to the have the ligand oriented in the binding pocket

receptor_site_file - this is our selected_spheres.sph file from earlier

internal_energy_rep_exp - here we select 12 rather than 9 because using a repulsive exponent of 12 gives us a slightly steeper rising potential as radius between the atoms falls below the optimal distance (sigma)

flexible_ligand - when performing a virtual screen of a random database it is always advisable to set the ligands to flexible

min_anchor_size - ensures that major features on the molecules are used as anchors and not just simple small groups

score_molecules - we always want to score the molecules of a virtual screen in order to determine which are the best fit for the binding pocket

grid_score_primary - we want the grid score to be the primary method of scoring the screened ligands

grid_score_grid_prefix - the input for the .grid file created earlier

atom_model - we select the all atom model

num_scored_conformers - we only want to produce one scored conformer from each screened ligand because we only want the best conformations

Note that if you are performing a small sample virtual screening it is possible to run it on a local computer in a reasonable amount of time; however, if you are running the virtual screening to a very large scale (i.e. hundreds or thousands of ligands) you will need to use several nodes in Seawulf to produce results in a timely fashion.

Analyzing the Results

When your virtual screening has run completely and you are ready to analyze the results, open Chimera. In Chimera you can prepare your protein by opening 1LOQ.receptor.noH.pdb and choosing Actions -> Surface -> show. You may also wish to open up the original ligand file 1LOQ.ligand.mol2 in order to show the position of the original ligand/substrate in the receptor's active site.

To view the results of your virtual screening go to Tools -> Surface/Binding Analysis -> ViewDock and from their you can select your virtual screen output file. In the "ViewDock" pop-up window you can then select Column --> Show --> Grid Score which will add a column to the ViewDock window with the grid score of each ligand. You can double-click on the column heading Grid Score to sort the ligands based on their grid scores.

[Chimera image1] [Chimera image2]

VII. Running DOCK in Serial and in Parallel on Seawulf

The Seawulf Cluster is a 470-processor Linux Cluster capable of highly parallel processing. This parallel processing allows dock virtual screens to be completed in a fraction of the time as a single processor.

If you are docking multiple ligands, you can use more than one processor in parallel mode, but you should never use more processors than you have ligands. Before we can run DOCK on Seawulf, we need to copy the proper files from Herbie to Seawulf. If we CD into the AMS536 folder we can use the following command from the mathlab computer to copy all of the dock-tutorial files 

scp -r /dock-tutorial/  username@herbie.mathlab.sunysb.edu:~/AMS536/

Now we have all of our DOCK preparation files and folders on the seawulf cluster.

Running DOCK in Serial on a Single Processor

Running on a single processor is very similar to running dock on the mathlab computer.

If you make a file called qsub.csh with the text: 

#!/bin/tcsh                 
#PBS -l nodes=1:ppn=1        
#PBS -l walltime=01:00:00   
#PBS -N dock6           
#PBS -M user@ic.sunysb.edu 
#PBS -j oe                   
#PBS -o pbs.out            

cd /nfs/user03/zfoda/AMS536/dock-tutorial/07.virtscreen
/nfs/user03/wjallen/local/dock6/bin/dock6 -i dock.in -o dock.out

An explanation of the commands: 

#!/bin/tcsh                                                 #Execute script with tcsh
#PBS -l nodes=1:ppn=1                                       #Use one node, and one processor per node, so one single processor 
#PBS -l walltime=01:00:00                                   #Allow 1 hour for your job run 
#PBS -N dock6                                               #Name of your job
#PBS -M user@ic.sunysb.edu                                  #Get an email notifying you when your job is completed
#PBS -j oe                                                  #Combine the output and error streams into a single output file
#PBS -o pbs.out                                             #Name of your output file

cd /nfs/user03/zfoda/AMS536/dock-tutorial/07.virtscreen       #Change to your home directory and folder with dock files           
/nfs/user03/wjallen/local/dock6/bin/dock6 -i dock.in -o dock.out #Specifies path to dock executable and provide input and output filenames

To submit the experiment use the command: 

qsub qsub.csh

You will have submitted a DOCK experiment to the seawulf queue.

See also PBS commands.

Running DOCK in Parallel using MPI

In order to run DOCK in parallel you have to use a slightly different build of DOCK6 called dock6.mpi. Message passing interface (MPI) is basically a program that allows programs like DOCK to run in parallel.

So, make another file called qsub.vs.csh with the contents: 

#!/bin/tcsh
#PBS -l nodes=4:ppn=2 
#PBS -l walltime=24:00:00
#PBS -N screen
#PBS -o qsub.log
#PBS -j oe
#PBS -V

cd /nfs/user03/username/AMS536/dock-tutorial/07.virtscreen
mpirun -np 8 /nfs/user03/wjallen/local/dock6/bin/dock6.mpi -i dockvs.in -o dockvs.out

As you can see there are two major changes: 

#PBS -l nodes=4:ppn=2 #Use 4 nodes, and 2 processors per node, so 8 processors

Note: since one processor is used to distribute the processes, this will run DOCK as 7 (n-1) parallel processes. 

mpirun -np 8 /nfs/user03/wjallen/local/dock6/bin/dock6.mpi -i dockvs.in -o dockvs.out #this line uses mpi to run dock.mpi on multiple processors

And then we can run: 

 qsub qsub.vs.csh
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