Molegro Virtual Docker
Molegro Virtual Docker is a protein-ligand docking simulation program that allows us to carry out docking simulations in a fully integrated computational package. MVD has been successfully applied to hundreds of different proteins, with docking performance similar to other docking programs such as A.
It is easy to import and prepare molecules.
Molecular structure files are parsed into relevant components (ligands, cofactors, water molecules and proteins) and can be automatically prepared.
Parsing warnings and errors are shown in a convenient hierarchy.
- Molegro Virtual Docker is a good software for predicting protein ligand interactions. In a simple graphical environment, the program enables the preparation of molecules, the prediction and investigation of potential junctions with different ligands. Connections are displayed in a high quality 3D graphics environment.
- Molekular Docking dengan Metode Molegro Virtual Docker. (Ayik Rosita P) 43 Sisi aktif bakteri Bacillus subtilis terdiri dari residu asam amino seperti dengan Lys 411, Ser 299, Ser 52, dan Thr 412. Sisi aktif bakteri Escherichia coli terdiri dari residu asam amino Tyr 136 dan Tyr 52. Hal ini terlihat pada.
Molegro Virtual Docker Free Download
The built-in cavity detector identifies promising binding locations, making it possible to restrict the search space to the most interesting regions.
A protonation wizard allows you to quickly identify potential protonation targets (e.g. histidine residues) and change their protonation state quickly using a context menu.
The Docking process is managed via the Docking Wizard. The wizard allows you to:
- Select which structures to include in the simulation.
- Choose the potential binding region (MVD will automatically display potential binding pockets).
- Configure search algorithm properties and set up clustering and data logging.
- Manage additional constraints.
- Inspect warnings about unlikely preparations and missing structural information (e.g. unknown residues).
The Pose Organizer allows you to browse the poses returned by the docking engine. It is capable of loading poses from a docking run dynamically, making it possible to browse thousands of ligands.
It is possible to inspect the various energy terms and interactions and it is also possible to calculate the more advanced reranking and binding affinity measures. Hydrogen bonds and electrostatic interactions are updated dynamically when switching between poses.
The Sequence Viewer allows you to quickly identify and select residues in a protein.
The cartoon visualization highlights the different regions of secondary structure.
Various constraints makes it possible to alter the energy landscape (e.g. by rewarding certain regions of the search space) or to force or prevent certain interactions from occurring.
Constraints can be defined based on chemical properties (e.g. hydrogen bond acceptors or ring atoms) or individual atoms can be specified for each ligand.
The ‘Molegro Data Modeller’ product bundled with MVD makes it possible to create regression and classification models, extract statistical measures, and visualize data.
- Predict numerical properties of docked compounds from MVD docking runs. User-created models can be applied directly in the Pose Organizer.
- Create regression models using imported numerical descriptors (e.g. from third-party software).
- Feature selection for finding the relevant descriptors.
- Algebraic data transformation plugin for manipulating descriptors or creating derived descriptors.
- 1D plots (histograms), 2D plots (X-Y plots), and 3D plots.
- Various statistical measures.
In MVD, sidechain flexibility is implemented by softening the potential during the docking (by increasing the tolerance of the PLP-potentials or by weakening selected sidechains interactions), docking a diverse set of poses, and finally optimizing the sidechain configurations. It is also possible to manually minimize a receptor structure.
After the docking simulation has completed, the found poses can be inspected simultaneously with their matching receptor conformation directly in the pose organizer.
MVD makes it possible to dock ligands against docking templates. Similar to pharmacophores, templates are build from relevant chemical properties (like charge and hydrogen bonding capabilities) and can be auto-generated from one or more ligand conformations. Templates can be used in several ways:
- To flexibly align a number of ligands (and determine a score for their similarity).
- To focus or guide the docking simulation by combining the template similarity score with a receptor-based docking scoring function.
- To extract a fine-grained similarity score from each template point and create a regression model using Molegro Data Modeller (3D QSAR).
Molegro Virtual Docker Manual
- KNIME workflow support.
- Customizable molecular surfaces and backbone representation.
- Biomolecule generator for PDB files containing symmetry transformation information.
- Advanced text labelling for various molecular properties.
- Extensive help in PDF user manuals and automatic check for updates.
- MVD can be scripted using either its own scripting language or by external scripting languages.
- Pose Modifier for manually modifying poses.
- Extensible and customizable macro system with built-in editor.
Molegro Virtual Docker Ppt
Please see the user manual for a more thorough explanation of Molegro Virtual Docker features.