2 research outputs found
CRDOCK: An Ultrafast Multipurpose ProteināLigand Docking Tool
An ultrafast docking and virtual screening program, CRDOCK,
is
presented that contains (1) a search engine that can use a variety
of sampling methods and an initial energy evaluation function, (2)
several energy minimization algorithms for fine tuning the binding
poses, and (3) different scoring functions. This modularity ensures
the easy configuration of custom-made protocols that can be optimized
depending on the problem in hand. CRDOCK employs a precomputed library
of ligand conformations that are initially generated from one-dimensional
SMILES strings. Testing CRDOCK on two widely used benchmarks, the
ASTEX diverse set and the Directory of Useful Decoys, yielded a success
rate of ā¼75% in pose prediction and an average AUC of 0.66.
A typical ligand can be docked, on average, in just ā¼13 s.
Extension to a representative group of pharmacologically relevant
G protein-coupled receptors that have been recently cocrystallized
with some selective ligands allowed us to demonstrate the utility
of this tool and also highlight some current limitations. CRDOCK
is now included within VSDMIP, our integrated platform for drug discovery
Interactions of Bacterial Cell Division Protein FtsZ with C8-Substituted Guanine Nucleotide Inhibitors. A Combined NMR, Biochemical and Molecular Modeling Perspective
FtsZ
is the key protein of bacterial cell-division and target for
new antibiotics. Selective inhibition of FtsZ polymerization without
impairing the assembly of the eukaryotic homologue tubulin was demonstrated
with C8-substituted guanine nucleotides. By combining NMR techniques
with biochemical and molecular modeling procedures, we have investigated
the molecular recognition of C8-substituted-nucleotides by FtsZ from <i>Methanococcus jannaschii</i> (Mj-FtsZ) and <i>Bacillus
subtilis</i> (Bs-FtsZ). STD epitope mapping and trNOESY bioactive
conformation analysis of each nucleotide were employed to deduce differences
in their recognition mode by each FtsZ species. GMP binds in the same
anti conformation as GTP, whereas 8-pyrrolidino-GMP binds in the syn
conformation. However, the anti conformation of 8-morpholino-GMP is
selected by Bs-FtsZ, while Mj-FtsZ binds both anti- and syn-geometries.
The inhibitory potencies of the C8-modified-nucleotides on the assembly
of Bs-FtsZ, but not of Mj-FtsZ, correlate with their binding affinities.
Thus, MorphGTP behaves as a nonhydrolyzable analog whose binding induces
formation of Mj-FtsZ curved filaments, resembling polymers formed
by the inactive forms of this protein. NMR data, combined with molecular
modeling protocols, permit explanation of the mechanism of FtsZ assembly
impairment by C8-substituted GTP analogs. The presence of the C8-substituent
induces electrostatic remodeling and small structural displacements
at the association interface between FtsZ monomers to form filaments,
leading to complete assembly inhibition or to formation of abnormal
FtsZ polymers. The inhibition of bacterial Bs-FtsZ assembly may be
simply explained by steric clashes of the C8-GTP-analogs with the
incoming FtsZ monomer. This information may facilitate the design
of antibacterial FtsZ inhibitors replacing GTP