Re: [modeller_usage] Block Ligand stereo chemistry problem
To: Andre Fischer <>
Subject: Re: [modeller_usage] Block Ligand stereo chemistry problem
From: Modeller Caretaker <>
Date: Thu, 26 Jul 2007 09:50:53 -0700
Cc:
Andre Fischer wrote:
I am modelling a Protein with a ligand. The Ligand comes from the pdb
template as a blk. Modeller works fine and the protein model seems
reasonable, except that the modelled ligand is mirrored along its length
axis compared to the template ligand. Also BLK Residues are defined
rigid. some stereo operations seem to be allowed. How can i get rid of
those? I want the ligand only to act as a steric constraint.
The rigidity is maintained by imposing restraints on all atom-atom
distances within the BLK ligand. (See the nonstd_restraints function in
the automodel class, at modlib/modeller/automodel/automodel.py, for the
Python code that generates these restraints.) Therefore, it is possible
that if your starting structure is sufficiently distorted, these
restraints may result in an inverted structure rather than the original
(or in rare cases they may not be satisfied at all).
When Modeller builds a model, the starting structure is randomized a
little to ensure that each final structure is different. By default, the
BLK residues are also randomized. You can thus ensure that no inversion
or mirroring occurs by changing this randomization procedure to leave
BLK residues untouched. See the documentation of automodel.rand_method.
By default this is set to randomize.xyz, which from
modlib/modeller/automodel/refine.py you can see does:
def xyz(atmsel):
"""Randomize all coordinates"""
mdl = atmsel.get_model()
atmsel.randomize_xyz(deviation=mdl.deviation)
- i.e., randomizes all coordinates by automodel.deviation. One way to
prevent BLK residues being randomized is to do something like