tutorial.md

layout	title	zenodo_link	level	questions	objectives	requirements	time_estimation	key_points	follow_up_training	contributors
tutorial_hands_on	Setting up molecular systems	https://zenodo.org/record/2600690	Intermediate	How to get started modelling a protein and a ligand?	learn about the Protein Data Bank learn how to set up up a model protein and ligand system (with CHARMM-GUI) learn how to upload the system to Galaxy	type topic_name tutorials internal computational-chemistry setting-up-molecular-systems	2H	The PDB is a key resource for finding protein structures. Using CHARMM-GUI is one way to prepare a protein and ligand system. To get data into Galaxy you can upload a file from your computer or paste in a web address.	type topic_name tutorials internal computational-chemistry md-simulation-namd	chrisbarnettster simonbray

{% icon comment %} Audience

This tutorial is intended for those who are new to the computational chemistry tools in Galaxy. {: .comment}

Introduction

{:.no_toc}

In this tutorial, we'll cover the basics of molecular modelling by setting up a protein in complex with a ligand and uploading the structure to Galaxy. This tutorial will make use of CHARMM-GUI. Please note that the follow-up to this tutorial (located [here]({% link topics/computational-chemistry/tutorials/md-simulation-namd/tutorial.md %})) requires access to NAMD Galaxy tools, which can be accessed using the Docker container but are currently not available on any public Galaxy server.

Agenda

In this tutorial, we will cover:

1. TOC {:toc}

{: .agenda}

Cellulase and cellulose

To start we'll look at the PDB and find the entry for a fungal enzyme that cleaves cellulose. The enzyme is 7CEL, a hydrolase as seen in the figure.


In this section we'll access the PDB, download the correct structure, import it and view in Galaxy.

{% icon details %} Background: What is the PDB (Protein Data Bank) and format?

The Protein Data Bank (PDB) format contains atomic coordinates of biomolecules and provides a standard representation for macromolecular structure data derived from X-ray diffraction and NMR studies. Each structure is stored under a four-letter accession code. For example, the PDB file we will use is assigned the code 7CEL).

More resources:

• Multiple structures are stored and can be queried at https://www.rcsb.org/
• Documentation describing the PDB file format is available from the wwPDB at http://www.wwpdb.org/documentation/file-format.php. {: .details}

{% icon details %} Background: Why choose a cellulase?

Using enzymes to break down abundant cellulose into disaccharide units (cellobiose) is a method to optimise the biofuel process. {% cite barnett11 %}

More resources:

• https://en.wikipedia.org/wiki/Cellulase
• https://en.wikipedia.org/wiki/Biofuel
• Fungal Cellulases
• Cellobiohydrolase I Induced Conformational Stability and Glycosidic Bond Polarization {: .details}

Get data

The 7CEL PDB does not include a complete 8 unit substrate and some modelling is required. The correctly modelled substrate is provided for this tutorial.

{% icon details %} More details about the modelling done

• VMD (visualisation software) was used for atomic placement and CHARMM was used for energy minimisation.
• The PDB structure contains a mutation at position 217 (glumatate to glutamine). Our structure reverses this.
• The ligand was modelled separately and inserted into the binding site.

{: .details}

{% icon hands_on %} Hands-on: Data upload

1. Create a new history for this tutorial.

   {% snippet faqs/galaxy/histories_create_new.md %}

2. Import the files from the Zenodo link provided.

   https://zenodo.org/record/2600690
   

   {% snippet faqs/galaxy/datasets_import_via_link.md %} {% snippet faqs/galaxy/datasets_import_from_data_library.md %}

3. Rename the datasets.

4. Check that the datatype is correct. The file should have the PDB datatype.

   {% snippet faqs/galaxy/datasets_change_datatype.md datatype="datatypes" %}

{: .hands_on}

Modelling with CHARMM-GUI

It is convenient to set up the molecular system outside Galaxy using a tool such as CHARMM-GUI. Alternative methods are possible - see the [GROMACS tutorial]({% link topics/computational-chemistry/tutorials/md-simulation-gromacs/tutorial.md %}) for an example. {% cite jo17 %}

{% icon tip %} Tip: Viewing figures

• Some of the figures are screenshots and it may be difficult to make out details
• Right-click on the image and choose 'Open image in new tab' to view
• Zoom in and out as needed to see the content {: .tip}


Go to the correct section depending on which MD engine you will be using.

CHARMM

Upload the PDB to CHARMM-GUI

Navigate to CHARMM-GUI and use the Input Generator, specifically the PDB Reader tool and upload the Cellulase PDB file. Press 'Next Step: Select Model/Chain' in the bottom right corner.

{% icon hands_on %} Hands-on: Upload the PDB to CHARMM-GUI

1. Retrieve the modelled PDB structure from Zenodo.
2. Upload the PDB and choose CHARMM format.  {: .hands_on}

Select both protein and ligand models

{% icon hands_on %} Hands-on: Generate PDB file

Two model chains are presented for selection: the protein (PROA) and the hetero residue, which is the ligand or glycan in this case (HETA). Select both, and press 'Next Step: Generate PDB' in the bottom right corner.  {: .hands_on}

Manipulate the system

{% icon hands_on %} Hands-on: Make necessary modifications

Rename the hetero chain to BGLC and add ten disulfide bonds to the protein, as shown in the figure. Then press 'Next Step: Manipulate PDB' in the bottom right corner.  {: .hands_on}

Download the output

{% icon hands_on %} Hands-on: Download CHARMM output

The output is a .tgz file (a tarball or zipped tarball). Inside the archive you will see all inputs and outputs from CHARMM-GUI.  {: .hands_on}

{% icon tip %} What is a .tgz file?

This is a compressed file which contains all the output files created by the CHARMM-GUI. To access them, the .tgz file needs to be decompressed. There should be a tool available on your operating system for this. If you prefer to use the command line, tar will work fine on Linux or Mac tar -zxvf example.tgz. On Windows use 7zip, or download Git for windows and use Git Bash. {: .tip}

Upload to Galaxy

{% icon hands_on %} Hands-on: Upload files to Galaxy

Upload the step1_pdbreader.psf and step1_pdbreader.crd files to your BRIDGE instance and run the system setup tool. {: .hands_on}

NAMD

Upload the PDB to CHARMM-GUI

{% icon hands_on %} Hands-on: Upload the PDB to CHARMM-GUI

Retrieve the modelled PDB structure from Zenodo. Navigate to CHARMM-GUI and use the Input Generator, specifically the Quick MD Simulator tool. Upload the PDB file, selecting 'CHARMM' as the file format. Press 'Next Step: Select Model/Chain' in the bottom right corner.  {: .hands_on}

Select both protein and ligand models

{% icon hands_on %} Hands-on: Generate PDB file

Two model chains are presented for selection: the protein (PROA) and the hetero residue, which is the ligand or glycan in this case (HETA). Select both, and press 'Next Step: Generate PDB' in the bottom right corner.  {: .hands_on}

Manipulate the system

{% icon hands_on %} Hands-on: Make necessary modifications

Rename the hetero chain to BGLC and add disulfide bonds.  {: .hands_on}

Set up the waterbox and add ions

{% icon hands_on %} Hands-on: Solvate the protein

Set up a waterbox. Use a size of 10 angstroms and choose a cubic box ('rectangular' option).  {: .hands_on}

{% icon question %} Question

Why is 10 angstrom a fair choice for the buffer? Why choose 0.15M NaCl?

{% icon solution %} Solution

Under periodic boundary conditions, we need to ensure the protein can never interact with its periodic image, otherwise artefacts are introduced. Allowing 10 angstroms between the protein and the box edge ensures the two images will always be at minimum 20 angstroms apart, which is sufficient.

Some of the residues on the protein surface are charged and counter-ions need to be present nearby to neutralise them. Failure to explicitly model salt ions may destabilise the protein. {: .solution} {: .question}

Generate the FFT automatically

{% icon hands_on %} Hands-on: Generate the FFT

Particle Mesh Ewald (PME) summation is the method being used to calculate long-range interactions in this system. To improve the computational time a Fast Fourier Transform (FFT) is used. A detailed discussion of FFT will not be presented here; there are many articles on the subject. Try Wikipedia and Ewald summation techniques in perspective: a survey.  {: .hands_on}

Download the output

{% icon hands_on %} Hands-on: Solvate the protein

The output is a .tgz file (a tarball or zipped tarball). Inside the archive you will see all inputs and outputs from CHARMM-GUI.  {: .hands_on}

{% icon tip %} What is a .tgz file?

This is a compressed file and needs to be uncompressed using the correct tool. On Linux or Mac: tar will work fine tar -zxvf example.tgz. On Windows use 7zip or download Git for windows and use Git Bash. {: .tip}

Upload to Galaxy

{% icon hands_on %} Hands-on: Upload files to Galaxy

Upload the following files to your BRIDGE instance and ensure the correct datatype is selected:

• step3_pbcsetup.xplor.ext.psf -> xplor psf input (psf format)
• step3_pbcsetup.pdb -> pdb input (pdb format)
• Checkfft.str -> PME grid specs (txt format)
• step2.1_waterbox.prm -> waterbox prm input (txt format) {: .hands_on}

You are now ready to run the NAMD workflow, which is discussed in another [tutorial]({% link topics/computational-chemistry/tutorials/md-simulation-namd/tutorial.md %}).

Conclusion

{:.no_toc}

{% icon trophy %} Well done! You have started modelling a cellulase protein and uploaded it into Galaxy. The next step is running molecular dynamics simulations ([tutorial]({% link topics/computational-chemistry/tutorials/md-simulation-namd/tutorial.md %}))