Theory

The .pdb is generated from X-ray diffraction crystallography. This process requires a crystal of the protein, which occurs only at low temperature (~5°K). Taking this in consideration, we have to go through different steps to bring our protein to lab conditions. Please refer to the page on .conf parameters to see how to perform these steps in namd.

Initial minimization

We start with a few minimization rounds, to reach a minimum in the sense of potential energy.

Heating

When the protein is stable, we have to add heat (kinetic energy) to reach a higher temperature (~300°K). We have to take a special care not to add heat too fast, which would result in protein burst and explosion of our system.

First NPT

This is a relaxation step, with the number of atoms N, the pressure P and the temperature T all kept constant (NPT step). This is a kind of homogenization of the distribution of atoms inside our box.

NVT

This is also a relaxation step, with atom number, volume and temperature constant.

Second NPT

Now we perform another relaxation NPT to reach lab conditions.

Final NPT

This is the final NPT, which last much longer and gives us the ouput of the simulation.

Launch the simulation

On a single processor

Here is a safe command. It will send the output (> outpu...) to a file and be run in the background (&).

namd2 CONFIG_FILE.conf > output/namd_log &

On a cluster

This is performed using a library that will split the process between nodes.

updalpe1pc9 .epfl.ch (UPDALPE1PC9)

The path to the binary has to be localized using: which namd2. The option +p4 specifies how many procs we are using (don't ue more than 4 on this cluster!). The rest is similar to single processor launch. We use this computer to visualize or perform small stabilization. charmrun /usr/local/bin/namd2 +p4 ++local 2v0w_hydr_wb_eq_try.conf > ./output_eq2/namd_log &

updalpe1linuxsrv1 .epfl.ch (master.cluster)

This is the real cluster.