Difference between revisions of "2014 DOCK tutorial with HIV Protease"
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=== Joe ===
=== Joe ===
Revision as of 15:06, 3 March 2014
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.
- 1 I. Introduction
- 2 II. Preparing the Receptor and Ligand
- 3 III. Generating Receptor Surface and Spheres
- 4 IV. Generating Box and Grid
- 5 V. Docking a Single Molecule for Pose Reproduction
- 6 VI. Virtual Screening
- 7 VII. Running DOCK in Parallel on Seawulf
- 8 VIII. Frequently Encountered Problems
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:
- Rigid portion of ligand (anchor) is docked by geometric methods.
- Non-rigid segments added in layers; energy minimized.
- The resulting configurations are 'pruned' and energy re-minimized, yielding the docked configurations.
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:
~username/AMS536/dock-tutorial/00.files/ /01.dockprep/ /02.surface-spheres/ /03.box-grid/ /04.dock/ /05.mini-virtual-screen/ /06.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, '1HVR'. The following sections in this tutorial will adhere to this directory structure / naming scheme.
II. Preparing the Receptor and Ligand
III. Generating Receptor Surface and Spheres
Generating the Receptor Surface
Check to make sure 02.surface-spheres directory exists under dock-tutorial. If not then make the following directory:
mkdir 02.surface-sphgen cd 02.surface-sphgen
The following steps will be carried out to generate the receptor surface using Chimera:
Open Chimera by simply typing chimera into the terminal window
| Go File -> Open and choose the PDB file of the protein containing no hydrogens (1HVR.receptor.noH.pdb) from 01.dockprep
| Further, Actions -> Surface -> Show
| Go Tools -> Structure Editing -> Write DMS in order to obtain a dms file, which we will need to place spheres
| In the new window save the surface as 1HVR.receptor.dms
IV. Generating Box and Grid
1.) Make a new directory and name it: 03.box-grid/
V. Docking a Single Molecule for Pose Reproduction
Jess Junjie Kai
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).
VII. Running DOCK in Parallel on Seawulf
VIII. Frequently Encountered Problems
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command or input file