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CCP4BB  July 2012

CCP4BB July 2012

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Subject:

Re: Chiral volume outliers SO4

From:

Robbie Joosten <[log in to unmask]>

Reply-To:

Robbie Joosten <[log in to unmask]>

Date:

Wed, 11 Jul 2012 14:16:20 +0200

Content-Type:

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text/plain (50 lines)

Hi Ian,

 
> > @Ian: You'd be surprised how well Refmac can flatten sulfates if you
> > have a chiral volume outlier (see Figure 1d in Acta Cryst. D68: 484-496
> (2012)).
> But this is only because the 'negative' volume sign was erroneously used
in
> the chiral restraint instead of 'both' (or better still IMO no chiral
restraint at
> all), right?  If so I don't find it surprising at all that Refmac tried to
flip the
> sulphate and ended up flattening it.
>  Seems to be a good illustration of the GIGO (garbage in - garbage
> out) principle.  Just because the garbage input in this case is in the
official
> CCP4 distribution and not (as is of course more commonly the
> case) perpetrated by the user doesn't make it any less garbage.
The problem is that in the creation of chiral volume targets chemically
equivalent (groups of) atoms are not recognized as such. So any new or
recreated restraint files will have either 'positiv' or 'negativ' and the
problem starts all over again. That is why it is better to stay consistent
and choose one chirality (the same one as in the 'ideal' coordinates in the
PDB ligand descriptions). This will also make it easier compare ligands
after aligning them (this applies to ligands more complex than sulfate).
Obviously, users should not be forced to deal with these things. Programs
like Refmac and COOT should fix chiral volume inversions for the user,
because it is only relevant inside the computer. That is the idea of chiron,
just fix these 'problems' automatically by swapping equivalent atoms
whenever Refmac gives a chiral volume inversion warning.  It should make
life a bit easier.
	

> The point I was making is that in this and similar cases you don't need a
chiral
> restraint at all: surely 4 bond lengths and 6 bond angles define the
chiral
> volume pretty well already?  Or are there cases where without a chiral
> restraint the refinement still tries to flip the chirality (I would fine
that hard to
> believe).
I agree with you for sulfate, and also for phosphate ;). I don't know what
happens in other compounds at poor resolution, when bond and angle targets
(and their SDs) are not equivalent. I guess that some angle might 'give way'
before others. That is something that should be tested. I have a growing
list of chiral centers that have this problem if you are interested.

Cheers,
Robbie

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