Rizzo Lab Downloads
SB2010 Docking Database [2010.05.19 Initial Release]
The base version of the database is presented as Receptors, Ligands and Spheres, which is applicable to any docking program. The spheres and grids are meant to be used with any version of the DOCK program. SB2010 is an on-going project; more structures and related resources will be added in the future.
|Receptors, Ligands and Spheres||SB2010.05.19_rec.lig.sph.tar.gz|
|Energy and Bump Grids||To be released|
DOCK Input Files
These are the DOCK input files used to evaluate the database.
|Fixed Anchor (FAD)||FAD|
|Flexible Ligand (FLX)||FLX|
SB2010 Ligand Flexibility Subsets
The Flexibility Subset Lists divide the database into three subsets to allow benchmarking of docking programs across three ligand flexibility ranges.
|7 or less||7orless|
|8 to 15||8to15|
SB2010 Protein Families [2010.05.19 Initial Release]
The 25 large protein families in the database are presented as subsets below. Another 25 smaller families (i.e less than 7 members) are also present in the database.
|HMG COA Reductase||20|
Alignment for 5 protein families are presented. Each receptor was aligned to the first PDB code in the corresponding family list above. The same transformation was then applied to the ligand.
Sample Docking Results
Sample docking results with the top scored pose for each pdb code. These results were produced with DOCK 6.4, using the dock input files shown above. Please note that you will get slightly different results, depending on the environment you use to compile the dock binaries.
Alternative Ligand Starting Geometries
XXXX.lig.mmff94x_gasmin.mol2 are alternative initial ligand coordinates obtained from gas-phase minimization (in absence of the receptor) with the MMFF94x forcefield with the MOE 2009.10 program. MMFF94x charges are assigned to the ligands before minimization.
This database is derived from structures originally downloaded from the Protein Data Bank. This resource is meant to be freely useably by the docking community, both academic and commercial institutions. The manuscript for this work has been submitted and is currently under review.