I can help if share ,, no problem.
Regards
Umer

On Fri, Jun 4, 2021, 7:39 PM Harry Powell - CCP4BB <
[email protected]> wrote:

> I’d have to say that Phil is possibly one of the small molecule
> crystallographers who could probably sort this out in a flash - hence my
> last suggestion…
>
> Harry
>
> > On 4 Jun 2021, at 14:40, Phil Jeffrey <[email protected]> wrote:
> >
> > Unlike macromolecular crystallography, small molecule crystallography is
> infrequently starved for data.  So it makes no sense at all to extend your
> data to e.g. I/sigI of 1.0 amd Rmeas > 80% unless you want your R1 to be
> >10% for no good reason or utility, which is what was behind my suggestion
> - test to see if the data cutoff is an issue.  Also about the fastest test
> you can do in SHELXL.
> >
> > > Yes, ANIS and adding hydrogens (in SHELXL) are good things to do -
> with 0.8Å data most small molecule crystallographers would do this as a
> first step after fitting all the non-H atoms.
> >
> > Actually, adding AnisoB's and hydrogens too soon will mess up your
> disorder modeling, so blanket statements like that work for well-behaved
> structures but not so much for more challenging ones.
> >
> > e.g. in one of the the four structures I've done this week, one had
> significant main-molecule disorder so that comes ahead of adding hydrogens,
> and refining unrestrained anisoB (as is the default) for disordered atoms
> is asking for trouble.  It's not as cookie-cutter as you represent, and I
> stick to all my suggestions.
> >
> > Phil Jeffrey
> > Princeton
> >
> > On 6/4/21 4:27 AM, Harry Powell - CCP4BB wrote:
> >> Hi
> >> Yes, ANIS and adding hydrogens (in SHELXL) are good things to do - with
> 0.8Å data most small molecule crystallographers would do this as a first
> step after fitting all the non-H atoms.
> >> One thing I can’t agree with is to cut the resolution of your data
> _unless_ you have a very, very good reason to do so. Normal small molecule
> refinements will use data to ~0.8Å and not use a cut-off based on
> resolution or I/sig(I). A good dataset will often go to higher resolution
> and small molecule crystallographers will be very happy to use these data
> (unless, as I say, they have a very good reason not to), and would
> certainly have to “explain to the referees” why they didn’t if they ignored
> a systematic chunk.
> >> Something else that you might not have thought of - have you actually
> told SHELXL what the reflection data are - i.e., are they F, F^2,
> intensity? It’s perfectly possible to solve a small molecule structure by
> e.g. telling the program you’re giving it F^2 but actually giving it F, but
> refinement would be somewhat less straightforward. SHELXL normally uses F^2
> in refinement, macromolecular programs still normally use F (AFAIK).
> >> What programs did you use for processing the diffraction data?
> >> Of course, lowering the R factor is not the objective of the exercise -
> a lower R-factor is a consequence of having a model that fits the data
> better.
> >> I would be strongly inclined to ask a small molecule crystallographer
> (or someone with a strong background in it) to have a look at your data &
> model - they could probably give you a definitive answer by return of
> e-mail.
> >> Just my two ha’porth
> >> Harry
> >>> On 4 Jun 2021, at 03:10, Jon Cooper <
> [email protected]> wrote:
> >>>
> >>> Agreed, ANIS is the command to try.
> >>>
> >>> Sent from ProtonMail mobile
> >>>
> >>>
> >>>
> >>> -------- Original Message --------
> >>> On 3 Jun 2021, 20:18, Philip D. Jeffrey < [email protected]>
> wrote:
> >>>
> >>> R1 of 17% is bad for small molecule.
> >>> 0.8 Å is in the eye of the beholder - if you're using macromolecular
> cutoffs then these might be too aggressive for small molecule-type
> refinement stats - try a more conservative cutoff lie 0.9 and see how that
> changes R1.  However I suspect it's more to do with how your model is
> fitting the data.
> >>>
> >>> Have you refined anisotropic Bfactors ?
> >>> Have you added hydrogens ?
> >>>
> >>> I would suggest non-CCP4 programs like Olex2 or SHELXLE as the
> interface for the refinements - I use the latter and it's somewhat Coot
> like with useful features that are particular to small molecule.  Also
> PLATON has some things (like expand-to-P1 and Squeeze) that, respectively,
> might be useful to explore space group issues and disordered solvent.
> PLATON also has a means to check for some forms of twinning.
> >>>
> >>> Phil Jeffrey
> >>> Princeton
> >>> From: CCP4 bulletin board <[email protected]> on behalf of Jacob
> Summers <[email protected]>
> >>> Sent: Thursday, June 3, 2021 2:49 PM
> >>> To: [email protected] <[email protected]>
> >>> Subject: [ccp4bb] Lowering R factor from small molecule structure
> >>>  Greetings!
> >>>
> >>> I am currently trying to reduce the R factor of a cyclic small
> molecule peptoid in ShelXle. The max resolution of the molecule is 0.8
> angstroms. The molecule itself fits the density very well, but there are a
> few unexplained densities around the molecule which do not seem to be
> anything in the crystallization conditions. The R1 factor of the refinement
> is 17.07% but I am unsure how to lower this value. Any ideas on how to
> better refine this molecule or fill densities to lower the R1 factor? I do
> not have much experience working with small molecule refinement or with
> ShelX.
> >>>
> >>> Thanks so much,
> >>> Jacob Summers
> >>>
> >>>
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