mutadock 1.8

MUTADOCK is a comprehensive library designed for mutation studies and multiple receptor-ligand docking. Refer to README for more information.

MUTADOCK

Introduction

MUTADOCK is a comprehensive library designed for mutation studies and multiple receptor-ligand docking. It provides tools and methods to analyze and predict the effects of mutations on receptor-ligand interactions, enabling researchers to study protein function and drug binding affinity in a detailed manner.

Description

Our software is designed to facilitate protein mutation analysis and molecular docking. It integrates automated protein mutation using PyRosetta and a docking library capable of docking multiple proteins with multiple ligands.

Key Features

Automated Protein Mutation:

• Utilizes PyRosetta for systematic protein mutations.
• Supports various mutation strategies (e.g., single-point mutations, double-point mutations and triple-point mutations).
• Allows customization of mutation and docking parameters.

Docking Library:

• Capable of docking a list of proteins against a list of ligands.
• Employs AutoDock Vina to predict binding affinities and best poses.
• Provides detailed output files with docking scores and poses.

User Interface:

• Command-Line Interface: Simple CLI for both beginner and expert users.
• Python Bindings: The library can be imported in other codes for increased customizability by expert users

Try it Now

The basic codes to perform mutation studies as used by us for our project can be found in a Jupyter Notebook here. The same notebook can be found on collab here.

How To Guide

Installation

MutaDock has been deployed on PyPi, making installation quick and simple

pip install mutadock

The Pyrosetta Installer will be automatically installed but Pyrosetta should be installed using

python3 -c 'import pyrosetta_installer; pyrosetta_installer.install_pyrosetta()'

• Currently there is a problem with the vina on PyPi, so vina needs to be installed separately, the installation guide can be found at https://autodock-vina.readthedocs.io/en/latest/installation.html

Mutation Studies

Mutation Studies for a protein is a very fast process with just a PDB file of the protein as the input. (We assume for the tutorial that the name of the PDB file is “protein.pdb”)

md_mutate -i protein.pdb

Other optional arguments can be changed as required, to check the usage run

md_mutate -h

The md_mutate will output CSV files and one text file, their description is in the table below:

No.	File Name	Description
1.	protein_modified_mutations_all.csv	Contains all possible mutations for the given protein
2.	protein_modified_mutations.csv	Contains mutations that are possible according to the PAM matrix for the given protein
3.	protein_modified_mutations_ddG.csv	The single mutation ddG values for the mutation in the File-2
4.	protein_modified_mutations_ddG_sorted.csv	Sorted File-3 from lowest to highest ddG values
5.	protein_modified_double_ddg.csv	The ddG values of the double mutation for all the combinations of the most negative single ddG compounds
6.	protein_modified_double_ddg_sorted.csv	Sorted File-5 from lowest to highest ddG values
7.	protein_modified_triple_ddg.csv	The ddG values of the triple mutation for all the combinations of the most negative double ddG compounds
8.	protein_modified_triple_ddg_sorted.csv	Sorted File-7 from lowest to highest ddG values
9.	protein_modified_mutants.txt	Generates a list of all the mutated PDB files created. Can be directly used as input for the md_dock command in our mutadock library

Docking Studies

Docking for multiple receptors and ligands is made simple and efficient by mutadock. The text files containing the names of the receptors and ligands need to be given as input, after that everything is automated. (If md_mutate is used, the text file for receptor is generated automatically) Every receptor in the receptor file will be docked with every ligand in the ligand file. A standard Vina configuration file or an AutoSIte prediction output is required. Example:

md_dock -r receptors.txt -l ligands.txt -c config.txt

Other optional arguments can be changed as required, to check the usage run

md_dock -h

The output of md_dock with their description is in the table below:

No.	Output	Description
1.	PDBQT files	The receptors and ligands will be converted to PDBQT files for AutoDock Vina.
2.	Output Log	The output of AutoDock Vina with the docking scores will be stored in a log file for each combination.
3.	Output PDB	The output of AutoDock Vina with the 5 best docking poses will be stored in a PDB file for each combination.
4.	Output PDBQT	The output of AutoDock Vina Split with the best pose will be stored in a PDBQT file for each combination.
5.	Output SDF	The best pose after docking will be stored in a SDF file for visualization and better usability.
6.	Docking Results CSV	All the docking affinities are tabulated in a CSV to make analysis trivial.

All CLI Scripts

No.	Command	Description
1.	md_mutate	Predicts the best mutation of the given protein
2.	md_dock	Docked all combinations from a list of receptors and ligands
3.	md_vina_dock	CLI for AutoDock Vina
4.	md_csv_generator	Generates all possible mutations for a protein and also the mutations possible according to PAM Matrix
5.	md_csv_sort	Can sort any CSV file according to the column name or number chosen
6.	md_ddg_single	Calculates single ddG values for a given CSV of mutations
7.	md_ddg_double	Calculates double ddG values for all combinations using a given CSV of mutations
8.	md_ddg_triple	Calculates triple ddG values for all combinations using a given CSV of mutations

Applications

• Protein Engineering: Designing mutated proteins with enhanced stability or new functionalities.
• Drug Discovery: Screening potential drug candidates by predicting binding affinities.
• Biochemical Research: Studying protein-ligand interactions to understand biological processes.

Documentation

• README is included in the repository to serve as a comprehensive guide
• ReadtheDocs Page for updated documentation can be found here

Future Developments

• Developing a Graphical User Interface (GUI): Enhancing user experience by providing a user-friendly interface for easier interaction with the software.
• Creating a Web Server: Allowing remote access and usage of the software through a web-based platform, making it accessible from anywhere.
• Increasing Parameter Customizability: Offering more options for users to fine-tune mutation and docking parameters to suit specific research needs and conditions.

Acknowledgements

• Open-source tools and libraries used in the development.

Contact

• For questions, suggestions, or collaboration, please contact Naisarg Patel.