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

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===Streptavidin & Biotin===
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===Orotodine Monophosphate Decarboxylase & Uridine Monophostphate===
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'''Streptavidin'''
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'''Orotodine Monophosphate Decarboxylase (OMP)'''
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is a tetrameric prokaryote protein that binds the co-enzyme biotin with an extremely high affinity. The streptavidin monomer is composed of eight antiparallel beta-strands which folds to give a beta barrel tertiary structure. A biotin binding-site is located at one end of each β-barrel, which has a high affinity as well as a high avidity for biotin. Four identical streptavidin monomers  associate to give streptavidin’s tetrameric quaternary structure. The biotin binding-site in each barrel consists of residues from the interior of the barrel, together with a conserved Trp120 from neighboring subunit. In this way, each subunit contributes to the binding site on the neighboring subunit, and so the tetramer can also be considered a dimer of functional dimers.
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is a homodimeric protein from the organism '''Methanobacterium thermoautotrophicum''' that is involved in biosynthesis of pyrimidines including uridine monophosphate, a component of RNA.  
  
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'''Biotin'''
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is a water soluble B-vitamin complex which is composed of an ureido (tetrahydroimidizalone) ring fused with a tetrahydrothiophene ring. It is a co-enzyme that is required in the metabolism of fatty acids and leucine. It is also involved in gluconeogenesis.
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'''Uridine Monophosphate'''
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is a pyrimidine-based nucleotide monomer of RNA.
  
  
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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 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:
  
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  ~username/AMS536/DOCK-Tutorial/00-original-files/
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  ~username/AMS536/DOCK-Tutorial/00.original-files/
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                               /01-dockprep/
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                               /01.dockprep/
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                               /02-surface-spheres/
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                               /02.surface-spheres/
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                               /03-box-grid/
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                               /03.box-grid/
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                               /04-dock/
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                               /04.dock/
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                               /05-virtual-screen/
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                               /05.virtual-screen/
  
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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, '1DF8'. The following sections in this tutorial will adhere to this directory structure / naming scheme.
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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.
  
 
==II. Preparing the Receptor and Ligand==
 
==II. Preparing the Receptor and Ligand==

Revision as of 13:55, 25 February 2013

For additional Rizzo Lab tutorials see DOCK Tutorials. Use this link Wiki Markup as a reference for editing the wiki. This tutorial was developed collaboratively by the AMS 536 class of 2012.

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 & Uridine Monophostphate

Orotodine Monophosphate Decarboxylase (OMP) is a homodimeric protein from the organism Methanobacterium thermoautotrophicum that is involved in biosynthesis of pyrimidines including uridine monophosphate, a component of RNA.


Uridine Monophosphate is a pyrimidine-based nucleotide monomer of RNA.


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: 

~username/AMS536/DOCK-Tutorial/00.original-files/
                              /01.dockprep/
                              /02.surface-spheres/
                              /03.box-grid/
                              /04.dock/
                              /05.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.

II. Preparing the Receptor and Ligand

III. Generating Receptor Surface and Spheres

IV. Generating Box and Grid

V. Docking a Single Molecule for Pose Reproduction

Results

VI. Virtual Screening

VII. Running DOCK in Serial and in Parallel on Seawulf

VII. Frequently Encountered Problems

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