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A bright future for fragment-based drug discovery: what does it hold?
Modeling the allosteric modulation of CCR5 function by Maraviroc
α-helix mimicry of a β-turn
Similar interactions of natural products with biosynthetic enzymes and therapeutic targets could explain why nature produces such a large proportion of existing drugs
 Dual Function for U2AF 35 in AG-Dependent Pre-mRNA Splicing
Solution structure of a conformationally constrained Arg-Gly-Asp-like motif inserted into the alpha/beta scaffold of leiurotoxin I
Comparative evaluation of eight docking tools for docking and virtual screening accuracy
sc-PDB: a database for identifying variations and multiplicity of 'druggable' binding sites in proteins
Multi-target Fragments Display Versatile Binding Modes
Ranking Targets in Structure-Based Virtual Screening of Three-Dimensional Protein Libraries: Methods and Problems
Structural Searching of Biosynthetic Enzymes to Predict Protein Targets of Natural Products
Binding mode information improves fragment docking
Do Fragments and Crystallization Additives Bind Similarly to Drug-like Ligands?
Comparing atom-based with residue-based descriptors in predicting binding site similarity: do backbone atoms matter?
Comparison and Druggability Prediction of Protein–Ligand Binding Sites from Pharmacophore-Annotated Cavity Shapes
A chemogenomic analysis of the transmembrane binding cavity of human G-protein-coupled receptors
Is it time for artificial intelligence to predict the function of natural products based on 2D-structure
Modeling of CCR5 Recognition by HIV-1 gp120: How the Viral Protein Exploits the Conformational Plasticity of the Coreceptor
sc-PDB: a 3D-database of ligandable binding sites—10 years on
New Insights into the Mechanisms whereby Low Molecular Weight CCR5 Ligands Inhibit HIV-1 Infection

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