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Docking Screens for Drug Discovery / edited by Walter Filgueira de Azevedo Jr.

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Holman Biotech Commons QH506 .M45 v.1 (1984)-v.20 (1993),v.22 (1994),v.24 (1994)-v.53 (1996), v.42 (1995) and v.51 (1995) reported missing 3-13-2000 v.55 (1995),v.58 (1996)-v.63 (1997), v.65 (1996)-v.154 (2001), v.156 (2001)-190 (2002), v.192 (2002)-v.407 (2007) v.409 (2007)-v.416 (2008),v.418 (2008)-v.466 v.468-v.490,v.492,v.494,v.496-499 501-506,508,510-512,514,516-517,519-536 538,540-569,571 573-589,591-608,610-615,617,620-627,630-633,636,638,642
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Format:
Book
Contributor:
de Azevedo Jr., Walter Filgueira, editor.
SpringerLink (Online service)
Series:
Springer Protocols (Springer-12345)
Methods in molecular biology 1064-3745 ; 2053.
Methods in Molecular Biology, 1064-3745 ; 2053
Language:
English
Subjects (All):
Pharmacology.
Proteins.
Bioinformatics.
Computational biology.
Pharmacology/Toxicology.
Protein-Ligand Interactions.
Computer Appl. in Life Sciences.
Local Subjects:
Pharmacology/Toxicology.
Protein-Ligand Interactions.
Computer Appl. in Life Sciences.
Physical Description:
1 online resource (XVII, 286 pages) : 163 illustrations, 10 illustrations in color.
Edition:
First edition 2019.
Contained In:
Springer eBooks
Place of Publication:
New York, NY : Springer New York : Imprint: Humana, 2019.
System Details:
text file PDF
Summary:
This book focuses on recent developments in docking simulations for target proteins with chapters on specific techniques or applications for docking simulations, including the major docking programs. Additionally, the volume explores the scoring functions developed for the analysis of docking results and to predict ligand-binding affinity as well as the importance of docking simulations for the initial stages of drug discovery. Written for the highly successful Methods in Molecular Biology series, this collection presents the kind of detail and key implementation advice to ensure successful results. Authoritative and practical, Docking Screens for Drug Discovery aims to serve those interested in molecular docking simulation and also in the application of these methodologies for drug discovery.
Contents:
Building Machine-Learning Scoring Functions for Structure-Based Prediction of Intermolecular Binding Affinity
Integrating Molecular Docking and Molecular Dynamics Simulations
How Docking Programs Work
SAnDReS: A Computational Tool for Docking
Electrostatic Energy in Protein-Ligand Complexes
Van der Waals Potential in Protein Complexes
Hydrogen-Bonds in Protein-Ligand Complexes
Molecular Dynamics Simulations with NAMD2
Docking with AutoDock4
Molegro Virtual Docker for Docking
Docking with GemDock
Docking with SwissDock
Molecular Docking Simulations with ArgusLab
Web Services for Molecular Docking Simulations
Homology Modeling of Protein Targets with MODELLER
Machine Learning to Predict Binding Affinity
Exploring the Scoring Function Space.
Other Format:
Printed edition:
ISBN:
978-1-4939-9752-7
9781493997527
Access Restriction:
Restricted for use by site license.

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