DOVIS 2.0: an efficient and easy to use parallel virtual screening tool based on AutoDock 4.0 (original) (raw)

Computational protein-ligand docking and virtual drug screening with the AutoDock suite

Arthur Olson

Nature protocols, 2016

View PDFchevron_right

Dockomatic - automated ligand creation and docking

Greg Hampikian

BMC Research Notes, 2010

View PDFchevron_right

MS-DOCK: Accurate multiple conformation generator and rigid docking protocol for multi-step virtual ligand screening

David Lagorce

BMC Bioinformatics, 2008

View PDFchevron_right

Comparative Study of the Efficiency of Three Protein-Ligand Docking Programs

Abderrahmane Bensegueni

Journal of Proteomics & Bioinformatics, 2008

View PDFchevron_right

Fast Structure-Based Virtual Ligand Screening Combining FRED, DOCK, and Surflex

Maria Hwa

Journal of Medicinal Chemistry, 2005

View PDFchevron_right

High Throughput Computing Validation for Drug Discovery Using the DOCK Program on a Massively Parallel System

carlos sosa

2008

View PDFchevron_right

Docking, virtual high throughput screening and in silico fragment-based drug design

Aurélien Grosdidier

Journal of Cellular and Molecular Medicine, 2009

View PDFchevron_right

DOVIS: an implementation for high-throughput virtual screening using AutoDock

Kamal Kumar

BMC Bioinformatics, 2008

View PDFchevron_right

MetaDOCK: A Combinatorial Molecular Docking Approach

Izaz Monir Kamal

ACS Omega, 2023

View PDFchevron_right

Molecular Docking: Challenges, Advances and its Use in Drug Discovery Perspective

Manobjyoti Bordoloi

Current Drug Targets, 2019

View PDFchevron_right

rDock: A Fast, Versatile and Open Source Program for Docking Ligands to Proteins and Nucleic Acids

Szilveszter Juhos

PLoS Computational Biology, 2014

View PDFchevron_right

Docking-based virtual screening: recent developments

Tiziano Tuccinardi

… Chemistry &# 38; High Throughput Screening, 2009

View PDFchevron_right

Protein-Based Virtual Screening of Chemical Databases. 1. Evaluation of Different Docking/Scoring Combinations

Gerd Folkers

Journal of Medicinal Chemistry, 2000

View PDFchevron_right

PharmDock: a pharmacophore-based docking program

Markus Lill

Journal of Cheminformatics, 2014

View PDFchevron_right

Outstanding challenges in protein-ligand docking and structure-based virtual screening

Bohdan Waszkowycz

Wiley Interdisciplinary Reviews: Computational Molecular Science, 2011

View PDFchevron_right

Binding Estimation after Refinement, a New Automated Procedure for the Refinement and Rescoring of Docked Ligands in Virtual Screening

Alberto Del Rio

Chemical Biology & Drug Design, 2009

View PDFchevron_right

AMIDE v2: High-Throughput Screening Based on AutoDock-GPU and Improved Workflow Leading to Better Performance and Reliability

Laurence Voutquenne

International Journal of Molecular Sciences

View PDFchevron_right

AMDock: a versatile graphical tool for assisting molecular docking with Autodock Vina and Autodock4

Pedro Valiente

Biology Direct

View PDFchevron_right

A Handbook on Protein-Ligand Docking Tool: AutoDock 4

Lokesh Ravi

Journal of the Medical Sciences, 2016

View PDFchevron_right

Comparative study of several algorithms for flexible ligand docking

Badry Bursulaya

Journal of Computer-Aided Molecular Design, 2003

View PDFchevron_right

Surrogate docking: structure-based virtual screening at high throughput speed

David Hartsough

Journal of Computer-Aided Molecular Design, 2005

View PDFchevron_right

Fast, accurate, and reliable molecular docking with QuickVina 2

Yuguang Mu

Bioinformatics, 2015

View PDFchevron_right

Ph4Dock: pharmacophore-based protein-ligand docking

Ryoichi Kataoka

Journal of medicinal chemistry, 2004

View PDFchevron_right

Computational Molecular Docking Methods in Drug Discovery: Recent Advances and Software

Rutuja Sonawane

European Chemical Bulletin, 2023

View PDFchevron_right

Docking and scoring in virtual screening for drug discovery: methods and applications

Douglas Kitchen

Nature Reviews Drug Discovery, 2004

View PDFchevron_right

Docking and chemoinformatic screens for new ligands and targets

Rafaela Ferreira

Current Opinion in Biotechnology, 2009

View PDFchevron_right

VoteDock: Consensus docking method for prediction of protein-ligand interactions

Dariusz Plewczynski

Journal of Computational Chemistry, 2011

View PDFchevron_right

Molecular Docking: An Explanatory Approach in Structure-Based Drug Designing and Discovery

Neha Chauhan

International Journal of Pharmacy and Pharmaceutical Sciences, 2021

View PDFchevron_right

Insights into molecular docking: A comprehensive view

Innovative Publication

International Journal of Pharmaceutical Chemistry and Analysis, 2023

View PDFchevron_right

AutoDockFR: Advances in Protein-Ligand Docking with Explicitly Specified Binding Site Flexibility

Arthur Olson

PLOS Computational Biology, 2015

View PDFchevron_right

GlamDock: Development and Validation of a New Docking Tool on Several Thousand Protein−Ligand Complexes

Simon Tietze

Journal of Chemical Information and Modeling, 2007

View PDFchevron_right

Task-parallel message passing interface implementation of Autodock4 for docking of very large databases of compounds using high-performance super-computers

Roland Schultz

Journal of Computational Chemistry, 2011

View PDFchevron_right

Knowing when to give up: early-rejection stratagems in ligand docking

Irina Voiculescu

Journal of Computer-Aided Molecular Design, 2009

View PDFchevron_right