like others mentioned, looks like something in between a salt and a protein, 
perhaps TCEP, the ligand, a peptide cleaved from your protein by trace protease.
If possible, I would move the detector closer, collect an atomic resolution 
dataset and try to solve the structure by direct methods. You never know, it 
could be something interesting.

Mark J van Raaij
Dpto de Estructura de Macromoleculas, lab 20B
Centro Nacional de Biotecnologia - CSIC
calle Darwin 3
E-28049 Madrid, Spain
tel. +34 91 585 4616 (internal 432092)
Section Editor Acta Crystallographica F
https://journals.iucr.org/f/
https://namedrop.io/markvanraaij

> On 3 Feb 2023, at 09:22, kavyashreem <kavyashr...@instem.res.in> wrote:
> 
> Dear all,
> 
> We crystallized a protein (30kDa) + ligand (by cocrystallization), in the 
> condition 10%PEG3350, 50mM Zinc acetate.
> Protein was in the buffer 20mM HEPES, 150mM NaCl, 1uM ZnCl2, 4mM TCEP, pH 8. 
> Crystal:                             Crystal:                           
> crystal under UV m
> <b06fc576.png>     <e091c7fd.png>   <8ef9453e.png>
> When we collected the data at an in-house facility, it looked something like 
> this:
> <b903961d.png>
> The minimum resolution spot is around 9Ang and maximum ~2.2Ang. 
> I have not come across a protein diffraction like this, nor of a salt. When I 
> ran the gel for the incubated protein (protein+ligand), there was no 
> degradation.
> Although, I was sure there is some problem with this image I tried 
> processing, which could not be, But indexing showed a unit cell  of 11Ang, 
> 11Ang, 46Ang in P3. which was quite expected for two of the axes but not the 
> third.
> Can anyone please shed some light on this diffraction image?
> How can it happen?
>  
> Thank you
> Regards
> Kavya
>  
> 
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