Hmm - is the refinement complete? Maybe the GLU on the right could be moved
to use some of that greenness?
I try to make all sensible corrections, then check blobs..
Eleanor

On 3 July 2018 at 04:22, zaigham mahmood khan <mahmood.zaig...@gmail.com>
wrote:

> Uma, that is not something that we see regularly in the crystal
> structures. But i never used PFPE either. So, you may try PFPE. If this
> is not PFPE, then you may read the biology of the protein.
>
> Also I can see green density, but these green blobs are devoid of blue
> density. So i will be cautious. May be just add water molecule in each
> blob, and re-run refinement. You will see a change in color of the blobs,
> that may indicate something.. If red blobs appear around the water
> molecules, i will consider it just a noise. Alternatively, you will see
> green density connecting the water molecules...
>
>
>
>
>
> Best wishes
>
> -Z
>
>
> Zaigham Mahmood Khan, PhD
>
> Icahn School of Medicine at Mount Sinai
> Department of Oncological Sciences
> 1470 Madison Avenue
> <https://maps.google.com/?q=1470+Madison+Avenue+New+York&entry=gmail&source=g>
> New York
> <https://maps.google.com/?q=1470+Madison+Avenue+New+York&entry=gmail&source=g>
>
> On Mon, Jul 2, 2018 at 10:23 PM, Uma Gabale <00000ebb5dcf3eaa-dmarc-
> requ...@jiscmail.ac.uk> wrote:
>
>> Dear all,
>>
>> We came across a blob of unidentified electron density in a shallow
>> cavity of a bacterial protein structure (pictures attached). It is
>> surrounded by residues Asp, Arg, Gln, His, Glu, Thr, and Trp.
>>
>> The protein was expressed in *E. coli* BL21(DE3) and purified on Ni-NTA
>> followed by gel filtration. The purification buffers included Tris,
>> crystallization condition had HEPES and PEG3350; perfluoropolyether was
>> used as a cryoprotectant.
>>
>> We would appreciate any help in identifying it.​
>>
>> Thanks and regards,
>>
>> Uma.
>> --
>> Uma Gabale, PhD
>> Research Associate
>> Molecular and Cellular Biochemistry
>> Indiana University Bloomington
>>
>>
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>
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