Difference between revisions of "2020 AMBER tutorial with PDBID 3VJK"
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In this tutorial, we will be modeling the dynamics of the ligand with the receptor using AMBER 16. Amber is a molecular dynamics simulation software package. | In this tutorial, we will be modeling the dynamics of the ligand with the receptor using AMBER 16. Amber is a molecular dynamics simulation software package. | ||
| − | + | =Generating Parameters for the simulation= | |
In order to utilize Amber for molecular dynamic, parameters for the bio molecules will be needed. Luckily, there have been years of parameter development so parameters for the protein do not have to worried about. However, the small ligand does not have parameters in the standard protein force field. Consequently, we will need to generate a fcmod file specific for the ligand. | In order to utilize Amber for molecular dynamic, parameters for the bio molecules will be needed. Luckily, there have been years of parameter development so parameters for the protein do not have to worried about. However, the small ligand does not have parameters in the standard protein force field. Consequently, we will need to generate a fcmod file specific for the ligand. | ||
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The output shows that the parameters that were generated were sufficient to continue. | The output shows that the parameters that were generated were sufficient to continue. | ||
| − | + | =Build system with TLeap= | |
Before we can simulate the protein and ligand complex, we must build the whole system together. This involves adding solvent and solvent ions to the protein and ligand complex. In order to accomplish this we will be using tleap. | Before we can simulate the protein and ligand complex, we must build the whole system together. This involves adding solvent and solvent ions to the protein and ligand complex. In order to accomplish this we will be using tleap. | ||
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[[File:3vjk_solvated_wet8.jpg|thumb|center|800px|The image shows the solvated complex without waters. The gray colored object is the ligand in the active site and the green spheres are the Na+ ions]] | [[File:3vjk_solvated_wet8.jpg|thumb|center|800px|The image shows the solvated complex without waters. The gray colored object is the ligand in the active site and the green spheres are the Na+ ions]] | ||
| − | + | =Minimization and Equilibration= | |
Before we can make production runs, we must minimize and equilibrate the system. This is required because the structure was taken from a crystal. This means that there could be unenergetnyicall favored angles, bonds, clash, ect. We will seek to reduce these un-energetically favored states by relaxing the structure. Additionally, this process is important because new atoms were added to the structure--in particular hydrogens. These hydrogens were added using chimera and may not be in the optimal position. | Before we can make production runs, we must minimize and equilibrate the system. This is required because the structure was taken from a crystal. This means that there could be unenergetnyicall favored angles, bonds, clash, ect. We will seek to reduce these un-energetically favored states by relaxing the structure. Additionally, this process is important because new atoms were added to the structure--in particular hydrogens. These hydrogens were added using chimera and may not be in the optimal position. | ||
Revision as of 00:34, 4 April 2020
In this tutorial, we will be modeling the dynamics of the ligand with the receptor using AMBER 16. Amber is a molecular dynamics simulation software package.
Generating Parameters for the simulation
In order to utilize Amber for molecular dynamic, parameters for the bio molecules will be needed. Luckily, there have been years of parameter development so parameters for the protein do not have to worried about. However, the small ligand does not have parameters in the standard protein force field. Consequently, we will need to generate a fcmod file specific for the ligand.
We will need to have some structures for running the simulation. This can be all stored in a directory called zzz.master. In this directory we will have the following files:
3vjkFH.pdb 3VJK_hydrogen_protein.mol2 3VJK_ligand_hydrogens.mol2
Please note that 3VJK_hydrogen_protein.mol2 had to be converted to a pdb using tleap because there were incapability issues that arose in a later step. To convert you do the following:
tleap rec= loadmol2 3VJK_hydrogen_protein.mol2 savepdb rec 3vjkFH.pdb quit
First we will make a specific directory dedicated for the generation of the parameters for the ligand:
mkdir 000.parameters
In this directory we will run the following command:
antechamber -i ./../zzz.master/3VJK_ligand_hydrogens.mol2 -fi mol2 -o 3vjk_ligand_antechamber.mol2 -fo mol2 -at gaff2 -c bcc -rn LIG -nc 2
notice that will be using gaff2. This stands for general amber force field 2. This will allow us to parameterize ligands for simulations. Additionally, the ligand has a charge of +2 and that was noted with the -nc flag. Once this command has run, it is beneficial to check to find if any parameters are missing:
parmchk2 -i 3vjk_ligand_antechamber.mol2 -f mol2 -o 3vjk_ligand.am1bcc.frcmod
The output shows that the parameters that were generated were sufficient to continue.
Build system with TLeap
Before we can simulate the protein and ligand complex, we must build the whole system together. This involves adding solvent and solvent ions to the protein and ligand complex. In order to accomplish this we will be using tleap.
We will make a new directory for the system:
mkdir 001.tleap_build
now, we will make a tleap.in file--which will contain information about building the system: vim tleap.in
#!/usr/bin/sh
###load protein force field
source leaprc.protein.ff14SB
###load GAFF force field (for our ligand)
source leaprc.gaff
###load TIP3P (water) force field
source leaprc.water.tip3p
###load ions frcmod for the tip3p model
loadamberparams frcmod.ionsjc_tip3p
###needed so we can use igb=8 model
set default PBradii mbondi3
###load protein pdb file
rec=loadpdb ./../zzz.master/3vjkFH.pdb
##@make disulfide bonds
bond rec.328.SG rec.339.SG
bond rec.385.SG rec.394.SG
bond rec.444.SG rec.447.SG
bond rec.454.SG rec.472.SG
bond rec.649.SG rec.762.SG
###load ligand frcmod/mol2
loadamberparams ./../000.parameters/3vjk_ligand.am1bcc.frcmod
lig=loadmol2 ./../000.parameters/3vjk_ligand_antechamber.mol2
###create gase-phase complex
gascomplex= combine {rec lig}
###write gas-phase pdb
savepdb gascomplex 3vjk.gas.complex.pdb
###write gase-phase toplogy and coord files for MMGBSA calc
saveamberparm gascomplex 3vjk.complex.parm7 3vjk.gas.complex.rst7
saveamberparm rec 3vjk.gas.receptor.parm7 3vjk.gas.receptor.rst7
saveamberparm lig 3vjk.gas.ligand.parm7 3vjk.gas.ligand.rst7
###create solvated complex (albeit redundant)
solvcomplex= combine {rec lig}
###solvate the system
solvateoct solvcomplex TIP3PBOX 12.0
###Neutralize system
addions solvcomplex Cl- 0
addions solvcomplex Na+ 0
#write solvated pdb file
savepdb solvcomplex 3vjk.wet.complex.pdb
###check the system
charge solvcomplex
check solvcomplex
###write solvated toplogy and coordinate file
saveamberparm solvcomplex 3vjk.wet.complex.parm7 3vjk.wet.complex.rst7
quit
Note that the number of ions of Cl- and Na+ was set to zero. In this situation, we allowed tleap to use a grid to calculate the ions that are needed to neutralize the system. Later on, we will see that amber correctly added the about of ions to set the system equal to zero. This is an important condition to look at. The system can crash if charges are not resolved. The following files should have been created:
3vjk.complex.parm7 3vjk.gas.complex.pdb 3vjk.gas.complex.rst7 3vjk.gas.ligand.parm7 3vjk.gas.ligand.rst7 3vjk.gas.receptor.parm7 3vjk.gas.receptor.rst7 3vjk.wet.complex.parm7 3vjk.wet.complex.pdb 3vjk.wet.complex.rst7
Now that the system is built, it is important to visualize the system to make sure that everything was generated correctly. You may do this using chimera or VMD. Please note that chimera has a special way of loading parm7 and rst7 files. You must go to trajectory and select the two files in order to visualize. Below are the images that were generated using VMD
Minimization and Equilibration
Before we can make production runs, we must minimize and equilibrate the system. This is required because the structure was taken from a crystal. This means that there could be unenergetnyicall favored angles, bonds, clash, ect. We will seek to reduce these un-energetically favored states by relaxing the structure. Additionally, this process is important because new atoms were added to the structure--in particular hydrogens. These hydrogens were added using chimera and may not be in the optimal position.
In order to start this process, we must generate the input files for pmemd
01.min.mdin
Minmize all the hydrogens &cntrl
imin=1, ! Minimize the initial structure ntmin=2, ! Use steepest descent Ryota Added maxcyc=5000, ! Maximum number of cycles for minimization ntb=1, ! Constant volume ntp=0, ! No pressure scaling ntf=1, ! Complete force evaluation ntwx= 1000, ! Write to trajectory file every ntwx steps ntpr= 1000, ! Print to mdout every ntpr steps ntwr= 1000, ! Write a restart file every ntwr steps cut= 8.0, ! Nonbonded cutoff in Angstroms ntr=1, ! Turn on restraints restraintmask="!@H=", ! atoms to be restrained restraint_wt=5.0, ! force constant for restraint ntxo=1, ! Write coordinate file in ASCII format ioutfm=0, ! Write trajectory file in ASCII format
/ 02.equil.mdin MD simualation &cntrl
imin=0, ! Perform MD nstlim=50000 ! Number of MD steps ntb=2, ! Constant Pressure ntc=1, ! No SHAKE on bonds between hydrogens dt=0.001, ! Timestep (ps) ntp=1, ! Isotropic pressure scaling barostat=1 ! Berendsen taup=0.5 ! Pressure relaxtion time (ps) ntf=1, ! Complete force evaluation ntt=3, ! Langevin thermostat gamma_ln=2.0 ! Collision Frequency for thermostat ig=-1, ! Random seed for thermostat temp0=298.15 ! Simulation temperature (K) ntwx= 1000, ! Write to trajectory file every ntwx steps ntpr= 1000, ! Print to mdout every ntpr steps ntwr= 1000, ! Write a restart file every ntwr steps cut= 8.0, ! Nonbonded cutoff in Angstroms ntr=1, ! Turn on restraints restraintmask=":!@H=", ! atoms to be restrained restraint_wt=5.0, ! force constant for restraint ntxo=1, ! Write coordinate file in ASCII format ioutfm=0, ! Write trajectory file in ASCII format iwrap=1, ! iwrap is turned on
/ 03.min.mdin Minmize all the hydrogens &cntrl
imin=1, ! Minimize the initial structure maxcyc=1000, ! Maximum number of cycles for minimization ntb=1, ! Constant volume ntp=0, ! No pressure scaling ntf=1, ! Complete force evaluation ntwx= 1000, ! Write to trajectory file every ntwx steps ntpr= 1000, ! Print to mdout every ntpr steps ntwr= 1000, ! Write a restart file every ntwr steps cut= 8.0, ! Nonbonded cutoff in Angstroms ntr=1, ! Turn on restraints restraintmask="!@H=", ! atoms to be restrained restraint_wt=2.0, ! force constant for restraint ntxo=1, ! Write coordinate file in ASCII format ioutfm=0, ! Write trajectory file in ASCII format
/ 04.min.mdin
Minmize all the hydrogens
&cntrl
imin=1, ! Minimize the initial structure maxcyc=1000, ! Maximum number of cycles for minimization ntb=1, ! Constant volume ntp=0, ! No pressure scaling ntf=1, ! Complete force evaluation ntwx= 1000, ! Write to trajectory file every ntwx steps ntpr= 1000, ! Print to mdout every ntpr steps ntwr= 1000, ! Write a restart file every ntwr steps cut= 8.0, ! Nonbonded cutoff in Angstroms ntr=1, ! Turn on restraints restraintmask="!@H=", ! atoms to be restrained restraint_wt=0.1, ! force constant for restraint ntxo=1, ! Write coordinate file in ASCII format ioutfm=0, ! Write trajectory file in ASCII format
/ 05.min.mdin
Minmize all the hydrogens
&cntrl
imin=1, ! Minimize the initial structure maxcyc=1000, ! Maximum number of cycles for minimization ntb=1, ! Constant volume ntp=0, ! No pressure scaling ntf=1, ! Complete force evaluation ntwx= 1000, ! Write to trajectory file every ntwx steps ntpr= 1000, ! Print to mdout every ntpr steps ntwr= 1000, ! Write a restart file every ntwr steps cut= 8.0, ! Nonbonded cutoff in Angstroms ntr=1, ! Turn on restraints restraintmask="!@H=", ! atoms to be restrained restraint_wt=0.05, ! force constant for restraint ntxo=1, ! Write coordinate file in ASCII format ioutfm=0, ! Write trajectory file in ASCII format
/
06.equil.mdin
MD simualation &cntrl
imin=0, ! Perform MD nstlim=50000 ! Number of MD steps ntb=2, ! Constant Pressure ntc=1, ! No SHAKE on bonds between hydrogens dt=0.001, ! Timestep (ps) ntp=1, ! Isotropic pressure scaling barostat=1 ! Berendsen taup=0.5 ! Pressure relaxtion time (ps) ntf=1, ! Complete force evaluation ntt=3, ! Langevin thermostat gamma_ln=2.0 ! Collision Frequency for thermostat ig=-1, ! Random seed for thermostat temp0=298.15 ! Simulation temperature (K) ntwx= 1000, ! Write to trajectory file every ntwx steps ntpr= 1000, ! Print to mdout every ntpr steps ntwr= 1000, ! Write a restart file every ntwr steps cut= 8.0, ! Nonbonded cutoff in Angstroms ntr=1, ! Turn on restraints restraintmask="!@H=", ! atoms to be restrained restraint_wt=1.0, ! force constant for restraint ntxo=1, ! Write coordinate file in ASCII format ioutfm=0, ! Write trajectory file in ASCII format iwrap=1, ! iwrap is turned on
/ 07.equil.mdin MD simulation &cntrl
imin=0, ! Perform MD nstlim=50000 ! Number of MD steps ntx=5, ! Positions and velocities read formatted irest=1, ! Restart calculation ntc=1, ! No SHAKE on for bonds with hydrogen dt=0.001, ! Timestep (ps) ntb=2, ! Constant Pressure ntp=1, ! Isotropic pressure scaling barostat=1 ! Berendsen taup=0.5 ! Pressure relaxtion time (ps) ntf=1, ! Complete force evaluation ntt=3, ! Langevin thermostat gamma_ln=2.0 ! Collision Frequency for thermostat ig=-1, ! Random seed for thermostat temp0=298.15 ! Simulation temperature (K) ntwx= 1000, ! Write to trajectory file every ntwx steps ntpr= 1000, ! Print to mdout every ntpr steps ntwr= 1000, ! Write a restart file every ntwr steps cut= 8.0, ! Nonbonded cutoff in Angstroms ntr=1, ! Turn on restraints restraintmask="!@H=", ! atoms to be restrained restraint_wt=0.5, ! force constant for restraint ntxo=1, ! Write coordinate file in ASCII format ioutfm=0, ! Write trajectory file in ASCII format iwrap=1, ! iwrap is turned on
/ 08.equil.mdin MD simulations &cntrl
imin=0, ! Perform MD nstlim=50000 ! Number of MD steps ntx=5, ! Positions and velocities read formatted irest=1, ! Restart calculation ntc=1, ! No SHAKE on for bonds with hydrogen dt=0.001, ! Timestep (ps) ntb=2, ! Constant Pressure ntp=1, ! Isotropic pressure scaling barostat=1 ! Berendsen taup=0.5 ! Pressure relaxtion time (ps) ntf=1, ! Complete force evaluation ntt=3, ! Langevin thermostat gamma_ln=2.0 ! Collision Frequency for thermostat ig=-1, ! Random seed for thermostat temp0=298.15 ! Simulation temperature (K) ntwx= 1000, ! Write to trajectory file every ntwx steps ntpr= 1000, ! Print to mdout every ntpr steps ntwr= 1000, ! Write a restart file every ntwr steps cut= 8.0, ! Nonbonded cutoff in Angstroms ntr=1, ! Turn on restraints restraintmask=":1-730@CA,C,N", ! atoms to be restrained restraint_wt=0.1, ! force constant for restraint ntxo=1, ! Write coordinate file in ASCII format ioutfm=0, ! Write trajectory file in ASCII format iwrap=1, ! iwrap is turned on
/
09.equil.mdin
MD simulations &cntrl
imin=0, ! Perform MD nstlim=50000 ! Number of MD steps ntx=5, ! Positions and velocities read formatted irest=1, ! Restart calculation ntc=1, ! No SHAKE on for bonds with hydrogen dt=0.001, ! Timestep (ps) ntb=2, ! Constant Pressure ntp=1, ! Isotropic pressure scaling barostat=1 ! Berendsen taup=0.5 ! Pressure relaxtion time (ps) ntf=1, ! Complete force evaluation ntt=3, ! Langevin thermostat gamma_ln=2.0 ! Collision Frequency for thermostat ig=-1, ! Random seed for thermostat temp0=298.15 ! Simulation temperature (K) ntwx= 1000, ! Write to trajectory file every ntwx steps ntpr= 1000, ! Print to mdout every ntpr steps ntwr= 1000, ! Write a restart file every ntwr steps cut= 8.0, ! Nonbonded cutoff in Angstroms ntr=1, ! Turn on restraints restraintmask=":1-730@CA,C,N", ! atoms to be restrained restraint_wt=0.1, ! force constant for restraint ntxo=1, ! Write coordinate file in ASCII format ioutfm=0, ! Write trajectory file in ASCII format iwrap=1, ! iwrap is turned on
/
