Category:Modeling and Editing Structures
- 1 Modeling in PyMOL
- 1.1 Saving with transformed coordinates
- 1.2 Translate or rotate individual objects
- 1.3 Moving one segment relative to the rest
- 1.4 Split states to objects
- 1.5 Altering secondary structures
- 1.6 Altering van der Waals radii
- 1.7 Altering atom coordinates
- 1.8 Deleting bonds
- 1.9 Converting D- to L- amino acids
- 1.10 Adding disulfide bonds
- 1.11 Adding hydrogen bonds
- 1.12 Protonating ligands
- 1.13 Superposition of two molecules
- 1.14 Manual superposition of two molecules
- 1.15 Adding and using your own fragments
Modeling in PyMOL
Saving with transformed coordinates
Here is a simple script that saves the molecule with coordinates from the current orientation. (invoke it with 'run save_transformed.py' and type the new save_transformed.py command thereafter).
# Adds the command save_transformed # Usage: save_transformed object, file def save_transformed(object,file): m = cmd.get_view(0) ttt = [m, m, m, 0.0, m, m, m, 0.0, m, m, m, 0.0, 0.0, 0.0, 0.0, 1.0] cmd.transform_object(object,ttt) cmd.save(file,object) cmd.extend('save_transformed',save_transformed)
Translate or rotate individual objects
There is a "translate" function similar to "rotate", the docs for these don't exist yet, because the implementation isn't finished. However, feel free to use them in the following forms:
translate vector,object-name,state (vector needs to be something like [x,y,z]) translate [1,0,0],pept rotate axis,angle,object-name,state (axis can be either the letter x,y,z or a 3D vector [x,y,z]) rotate x,90,pept rotate [1,1,1],10,pept
Moving one segment relative to the rest
This means moving two parts of one object into different directions. The easiest way to do this is to split the objects and then use the rotate command.
load 1FJ1.pdb # split PDB file create anti=(chain F) create fab=(chain A,B) # delete original object delete 1FJ1 # color objects color green,fab color pink,anti # color interface select inter = (byres ((fab within 5 of anti)\ or (anti within 5 of fab))) color yellow,inter # splay apart orient origin fab rotate y,60,fab origin anti rotate y,-60, anti # zoom interface region zoom inter show sph,inter disable inter
Split states to objects
There is also a new command in the 0.95 series:
which will spread a PDB "biological unit" (or any multi-state object -- including SD files) over a series of independent objects. This makes it possible to interact with such objects more naturally than with "all_states = 1".
Altering secondary structures
alter A/10:34/, ss='H' alter A/35:40/, ss='L' alter A/41:60/, ss='S'
Altering van der Waals radii
alter (elem Fe),vdw=1.8 rebuild
(The value for Fe is wrecked in PyMOL at the moment, so running the above line might be a good idea).
Altering atom coordinates
The latter section can contain formulae involving at least the xyz coordinates, lots of constants and the (+-*/) operators.
Select the bond using Ctrl-right-click, then either
or hit Ctrl-D.
Converting D- to L- amino acids
The inversion function was changed in version 0.95 to take advantage of multiple picked atoms. To invert a center, Ctrl-middle-click to pick the center atom as pk1 and two stationary atoms as pk2 and pk3. Then type Ctrl-E to invert.
Adding disulfide bonds
You can use the Cmd bond command to attach them:
bond 24/sg,26/sg bond 56/sg,99/sg unpick
(unpick will hide the bond baton which gets displayed.) Additionally, the residue names can be changed for bonded cysteines:
or for specific residues
Adding hydrogen bonds
See 'displaying biochemical properties'.
If your ligands come in with valid valencies and formal charges, PyMOL's h_add command can protonate ligands. (NOTE that there is a minor technical hiccup with SD-files which are loaded by default as immutable "discrete" objects.) Suffice it to say that in order to make changes to the chemical structure, an object must be loaded with the "discrete" flag set to zero. Unfortunately, much of the molecular editing stuff remains to be documented. Here's an example sequence, but I'm not sure it will help to much...as indicated in the manual, this is immature functionality with some major gaps. Attach in particular is very limited...
# show valences set valence=0.05 # load cysteine fragment fragment cys # remove hydrogens remove (hydro) # edit gamma S edit cys////sg # add hydrogen attach H,1,1 # add planer, trivalent nitrogen onto C terminus edit cys////C attach N,3,3 # edit that nitrogen edit (elem N and neighbor cys////C) # attach a tetrahedral methyl (note random position) attach C,4,4 # here's an example of adding a whole residue from the library edit cys////N editor.attach_amino_acid("pk1","ace") # now restore missing hydrogens (note that the names are off...) h_add
Superposition of two molecules
Using pair_fit requires that you specify a set of paired atoms in each structure. Fortunately, you no longer have to specify each pair separately, so long as the ordering is the same in each selection (almost always true).
pair_fit ( trna10 and resid 10:15 and name P ), ( ref4 and resid 10:15 and name P )
pair_fit prot1///11-26/CA, prot2///34-49/CA
would superimpose prot1 on prot2 using C-alphas from residues 11-26 in prot1 and 34-49 in prot2.
Manual superposition of two molecules
You can also align to structures using mouse rotation/translation. For this, you need to protect those molecules you don't want to move with (action menu -> movement -> protect) in the selection menu.
Protect one object, deprotect the other, grab the deprotected object and move with Shift-Mouse. Don't forget to switch to Mouse Editing mode.
Adding and using your own fragments
Pymol has some build-in fragments (amino acids and simple functional groups). You can add your own fragments, eg. sugars, in this way:
Create the molecule you want to use as a fragment. Save it as a .pkl file in <pymol_path>/data/chempy/fragments.
How to use the fragment:
Pick the atom (ctrl-middle) where you want to add the fragment. This will usually be a hydrogen atom (which will be removed). Then use the command:
where my_fragment_name is the name of the pkl-file (w/o .pkl extension) and 11 is the number of the connecting (hydrogen) atom in the fragment. To determine this number, press '[L]abel' -> 'atom identifiers' -> 'index' and choose the hydrogen atom you want.
If you want a hotkey for your fragment, you can probably put it in <pymol_path>/modules/pmg_tk/skins/normal/__init__.py, but I haven't tried this.