Difference between revisions of "Test Set Construction SB2024 V1 DOCK6.10 A"

Revision as of 19:12, 16 February 2024

!!!!!!Under Construction!!!!!!

The purpose of this tutorial is to develop a uniform method for adding systems to the Rizzo Lab test set, and rebuilding the set from initial files. This is the protocol to be used by all lab members. If the protocol is changed, a new tutorial should be made, preserving this tutorial.

I.Introduction

A key development for this tutorial is bookkeeping scripts to manage the count of heavy atoms during processing and indicate unaccounted changes (II.G). Test cases are also included which should be visually inspected for indicated elements to be sure that processing occurred as expected (III). It is critical these steps are completed.

II.Scripts for System Preparation

Each script should process the system in a fully automated manner. These scripts are located at (https://github.com/rizzolab/Testset_Protocols.git). There are key elements to check after each script before proceeding to the next. The output to be checked from each step is written to a folder "zzz.outfiles" with a unique file for each system, at each step. At the top of this file is the netid of the user who ran each process.

These scripts are designed to run in parallel on an HPC. Each step below has approximate timing indicated. If running 100 structures on a step with a timing of 10 minutes, at least 1000 cpu-minutes should be requested. There are averages and individual systems may take much less or more time.

A. Preliminary File Preparation

The receptor and ligand should be prepared from the initial PDB file as outlined in student provided VS tutorials (https://ringo.ams.stonybrook.edu/index.php/Tutorials). Briefly:

(1) The ligand should have hydrogens added with careful attention to protonation state and gasteiger charges added. The extracted ligand is saved as "${pdb_id}.lig.moe.mol2" .

(2) The receptor is saved in isolation. Generally any water molecules are deleted, except specialized experiments. Any atomic ions within 8 angstroms of the ligand are retained as part of the receptor. The protocols have prep and frcmod files integrated for Heme cofactors, so these should be retained as part of the receptor. Once the receptor, metal ions, and heme cofactor are extracted they are saved together as "${pdb_id}.rec.foramber.pdb"

(3) Any biologically relevant organic small molecule cofactor (such as NADH / NADPH) other than Heme should be treated as a ligand (1) and saved as "${pdb_id}.cof.moe.mol2".

(4) Files from (1) (2) and (3) should be moved to the folder zzz.master in the upper folder Testset_Protocols from the github repo.

For further clarification, review the student tutorials as indicated.

B. Ligand Preparation

    Timing=10 minutes

This step will assign am1bcc charges based on the charge in the preliminary file ${pdb_id}.lig.moe.mol2 and be saved as ${pdb_id}.lig.am1bcc.mol2

In the script submit.run.001.sh, if using a list of PDB codes other than "zzz.lists/clean.systems.all", change this in the script first.

    sbatch submit.run.001.sh

After the job has completed check to see if any of the ligands did not process successfully.

    bash run.001b.check.sh 

Any ligands or cofactors which did not pass will be listed in:

    zyy.01.lig_missing.dat / zyy.01.cof_missing.dat

The output for each system is written to file with the netid of the user at the top:

    vi zzz.outfiles/${pdb_id}.001.lig.out

These files should be checked for the phrase Fatal. This may mean the ligand failed or may have another issue. It does not mean with certainty the molecule is wrong, but should be inspected.

    grep "Fatal" zzz.outfiles/*001.lig.out

Output with Fatal Error (yellow) and user netid (top)

Some cofactors require unexpected bond orders to pass antechamber. If there is a correct version of the cofactor with the same res id such as "NAP" in zzz.master which passes antechamber, use this as a template.

    python zzz.scripts/bond_order_diff.py ${pdb_id_1}.cof.moe.mol2 ${pdb_id_2}.cof.moe.mol2 

This assumes atom names are equivalent for the mol2 (Hydrogen can be disregarded). Any bonds with different orders are printed, preserving the order input at command line (first argument prints on left, second argument prints on right). The script does not fix the bond orders for you, but helps quickly assigns how to match template.

Output from bond_order_diff.py shows difference in bond order

Other common problems are with carboxylic acid and nitro functional groups. It is best to assign these functional groups "ar" bond types.

C. Receptor Preparation

    Timing=1 minute

    sbatch submit.run.002.sh

After completion check for missing systems:

    bash run.002b.check.sh

Any complexes which did not pass will be listed in:

    zyy.02.rec_missing.dat 

Check the output file for any large RMSD from amber minimization. Restraints in this step are set high so any RMSD > 0.5 Angstroms should be considered dubious. Any structure RMSD > 2.0 Angstroms should be rejected from the test set.

RMSD of Protein, Ligand and Complex for single system

Due to an error in an Amber translation table P.3 atoms are converted to C.3 atoms in cofactors when written to ${pdb_id}.rec.clean.mol2. At this point it is currently corrected manually, but is to be corrected in Amber23. This includes but not restricted to cofactors "NAP","NAD","NDP". If not using Amber23, please check "COF" ${pdb_id}.rec.clean.mol2 to fix these cases.

Atom type of P1 is C.3 when should be P.3

D. Sphere Generation

    Timing=1 minute

    sbatch submit.run.003.sh

After completion check for missing systems:

    bash run.003b.check.sh

Any systems which did not pass will be listed in:

    zyy.03.sph_missing.dat 

E. Single Grid Generation

    Timing=15 minutes

    sbatch submit.run.004.sh

After completion check for missing systems:

    bash run.004b.check.sh

Any systems which did not pass will be listed in:

    zyy.04.grd_missing.dat

It should be checked that monoatomic ions were successfully integrated into the grid. Changes in naming could cause issues.

    vi ${pdb_id}/004.grid/grid.out

F. Multi Grid Generation

    Timing=15 minutes

    sbatch submit.run.005.sh

After completion check for missing systems:

    bash run.005b.check.sh

Any systems which did not pass will be listed in:

    zyy.05.mgr_missing.dat 

G. Bookkeeping of Heavy Atoms

Bookkeeping scripts are to account the count of heavy atoms in the initial files compared to final processed files. There are changes to the receptor during processing which are accounted for. This includes: (I) Heavy atoms added to incomplete residues (II) Dual Occupancy atoms deleted (III) Defined mutation from non-standard residue to standard residue. If all atoms are accounted for, the Overall Balance should be 0. Any system that is unbalanced should be inspected.

There are a minority of false positives that have an Overall Balance not equal to 0: (I) Monoatomic ions other than Zn, Mg, Ca come up unbalanced (II) Some pdb have merged columns (ie residue number and x-coordinates do not have space in between).

    UCSF Chimera must be loadable as a module to run bookkeeping scripts!

III.Test Cases for Preparation Integrity

These are cases which that need to be visually inspected to ensure key operations during preparation were executed. This step is crucial after building the test set in batch mode.

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2GQG with Phosphotyrosine

2Y03 Disulfide Bond

5UPG Histidine Correct Protonation

3D94 MHO to MET mutation

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IV.To Do

1. Integrate prep and frcmod files for cofactors available at http://amber.manchester.ac.uk/
2. Fix false positives in bookkeeping scripts
3. Add bookkeeping of receptor heavy atoms processed in grid.out 

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Tutorial Written By: Christopher Corbo, Rizzo Lab, Stony Brook University (2024)

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