AutoDock4 Pose Reproduction Tutorial

From Rizzo_Lab
Jump to: navigation, search

The purpose of this tutorial is to provide members of the Rizzo lab a way to benchmark the AutoDock4 software to compare the Pose Reproduction success rates against the DOCK6 software. (Note: The program version used for this experiment was AutoDock4.2.6 and DOCK6.9

I. Introduction

AutoDock4 is a commonly used docking program which assess the affinity of a ligand, a drug candidate to a target site (Protein, Enzyme, RNA). To evaluate a software's ability to accurately reproduce experimental results, an experiment called Pose Reproduction was developed

Pose Reproduction used an experimental known ligand and protein complex from the PDB database and attempts to dock this ligand back into it's original location. If the lowest energy ligand(most energetically favorable) is within 2.0 RMSDh of the original target site, this is referred to as a docking success. If any of the ligands, but not the lowest energy ligand is within 2.0 RMSDh of the original target site, this is referred to as a scoring failure. If none of the ligands are within 2.0 RMSDh of the original target site this is referred to as a sampling failure.

Pose Reproduction Intro.JPG

II.Prepping Directories

First step is prepare a file with a list of systems within it. For this docking experiment this file was called


Second step run the script to prepare a directory for each system in the file. The 1st arguement is the list of systems file made in the previous step. The 2nd Arguement is the new directory that will be made where all the AutoDock4 experiments will be performed

bash ./ ../ AutoDock4_Tutorial

The directory where all the directories will be formed is


Each System will have it's own directory in this file


III.Preparing Receptors and Ligands

For this part of the experiment, the receptors and ligands were prepared into pdbqt format. To accomplish this part of the experiment the original mol2 files were used from the testset to convert these systems. The ligands will be assigned gasteiger charges and am1bcc charges will be assigned to the receptor, which produced the highest success rates in previous experiments and was performed in previous papers. Scripts were developed to process these systems from mol2 to pdbqt.

Command to convert these files

Step 1) Make sure you are in the correct directory

cd AutoDock4_Tutorial/

Step 2) Run the correct bash script to run these molecules

bash ./../ /gpfs/projects/rizzo/yuchzhou/RCR/DOCK_testset/ ../AutoDock4_Tutorial

This script will create a ligand and pdbqt receptor in each system directory

cd 121P/

Further Processing may be needed to prepare these systems, will explain later

IV.Preparing Grids

For this part of the experiment the grids will be generated for each ligand and receptor

Step 1) Enter the correct directory

cd AutoDock4_Tutorial

Step 2) Run the bash script that creates the grids, recommending submitting to the qsub

bash ./../ /gpfs/projects/rizzo/yuchzhou/RCR/DOCK_testset/ ../AutoDock4_Tutorial > AutoDock4_grid_output

This will generate all of the grids by using the ligand and receptor previously generated

Following this cd into the 121P system directory

cd AutoDock4_Tutorial/121P/


This will always generate the grids, .fld, .xyz, a variety of .map files will be generated for each chemical type present within the systems, and a log file of the results a .glg file


Trouble Shooting

Some of these systems may present issues such as zero charge atom types or non-integral charge systems(ex. is a ligand with a charge of 2.48) This should only occur with ligands because the receptors are maintaining their am1bcc charges.

To trouble shoot this a script was developed to put all these problematic systems into a folder. These systems had then been prepared manually using Chimera to add gasteiger charges to all these systems.

Following all this the grids were regenerated for all these systems. Once these ligands, receptors, and grids have been generated once. You'll be able to reuse these systems and not need to repeat all the previous steps again.

V.Docking Ligands