Fragment-based drug design tools, practical approaches, and examples / edited by Lawrence C. Kuo.

Other author Kuo, Lawrence C.
Format Electronic
Edition1st ed.
Publication InfoSan Diego, Calif. : Elsevier/Academic Press,
Descriptionli, 591 p., [16] p. of plates : ill. (some col.) ; 24 cm.
Supplemental ContentFull text available from ScienceDirect Enzymology Book Series
Supplemental ContentFull text available from Methods in Enzymology
Subjects

Other title Fragment based drug design
SeriesMethods in enzymology, 0076-6879 ; vol. 493
Methods in enzymology ; v. 493. 0076-6879 ^A497553
Contents Designing a diverse high-quality library for crystallography-based FBDD screening -- Preparation of protein samples for NMR structure, function, and small-molecule screening studies -- Key factors for successful generation of protein-fragment structures requirement on protein, crystals, and technology -- Predicting the success of fragment screening by X-ray crystallography -- Fragment screening of stabilized G-protein-coupled receptors using biophysical methods -- Using computational techniques in fragment-based drug discovery -- How to avoid rediscovering the known -- From experimental design to validated hits a comprehensive walk-through of fragment lead identification using surface plasmon resonance -- Practical aspects of NMR-based fragment screening -- Binding site identification and structure determination of protein-ligand complexes by NMR a semiautomated approach -- Protein thermal shifts to identify low molecular weight fragments -- HTS reporter displacement assay for fragment screening and fragment evolution toward leads with optimized binding kinetics, binding selectivity, and thermodynamic signature -- Fragment screening purely with protein crystallography -- Computational approach to de novo discovery of fragment binding for novel protein states -- Lead generation and examples opinion regarding how to follow up hits -- Medicinal chemistry inspired fragment-based drug discovery -- Effective progression of nuclear magnetic resonance-detected fragment hits -- Advancing fragment binders to lead-like compounds using ligand and protein-based NMR spectroscopy -- Electron density guided fragment-based drug design--a lead generation example -- Experiences in fragment-based lead discovery -- Fragment screening of infectious disease targets in a structural genomics environment.
Bibliography noteIncludes bibliographical references and indexes.
Access restrictionAvailable only to authorized users.
Technical detailsMode of access: World Wide Web
Genre/formElectronic books.
ISBN9780123812742
ISBN0123812747