2010 DOCK tutorial with Streptavidin
- 1 About DOCK
- 2 About Streptavidin & Biotin
- 3 Downloading the PDB complex (1DF8)
- 4 Manipulating the PDB file using vi for DOCK
- 5 Preparing the Enzyme and Ligand in Chimera
- 6 Generation of Enzyme Surface, Spheres, and Grid for DOCK
- 7 Running DOCK
- 8 Docking Results
DOCK was developed by Irwin D. "Tack" Kuntz, Jr., PhD and colleagues at UCSF. Please see the webpage at UCSF DOCK.
DOCK is a molecular docking program used in drug discovery. This program, given a protein active site and a small molecule, tries to predict the correct binding mode of the small molecule in the active 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.
About Streptavidin & Biotin
Downloading the PDB complex (1DF8)
Download the neuraminidase file from here into your working directory. To get the monomer, download using the blue file arrow icon. Choose biological unit gz under download files folder at the left side. In that way you can downlad a biological gz file. If you download it by using "fetch by ID" in Chimera, you can only download a pdb gz file.
If the pdb gz file is downloaded the monomeric structure of neuraminidase with the bound ligand is seen.
However if the biological gz file is downloaded a tetramer complex of neuraminidase is seen.
When docking, we will only choose a monomer of the whole protein and its ligands instead of the whole tetramer. And it will be painful if you follow the procedure below, use vi to prepare the enzyme and ligand. Because you need to make sure the ligand you extract from the whole pdb files is right the one that match the monomer you've chosen.