What’s your spacegroup ? RWork / RFree?

Twinning by any chance?

Jürgen 

__________________________________________
Jürgen Bosch, Ph.D.
Division of Pediatric Pulmonology and Allergy/Immunology
Case Western Reserve University
2109 Adelbert Rd, BRB 835
Cleveland, OH 44106
Phone: 216.368.7565
Fax: 216.368.4223
https://www.linkedin.com/in/jubosch/

CEO & Co-Founder at InterRayBio, LLC

Johns Hopkins University
Bloomberg School of Public Health
Department of Biochemistry & Molecular Biology

> On Dec 16, 2019, at 1:50 PM, Jessica Besaw <[email protected]> wrote:
> 
> I am crystallizing this membrane protein in a medium (bicelles) that forms 
> lamella like sheets that stack on top of each other. 
> 
> The layer packing is shown below. Is this structure unreasonable?
> 
> <Screen Shot 2019-12-16 at 1.40.02 PM.png>
> 
> On Mon, 16 Dec 2019 at 13:38, Reza Khayat <[email protected] 
> <mailto:[email protected]>> wrote:
> ​​Hi Jessica,
> 
> 
> 
> The gap between the two proteins is a bit troubling. Perhaps it's the image, 
> but why would a crystal form if there is no crystal contact between the two 
> proteins?
> 
> 
> 
> Reza
> 
> 
> 
> Reza Khayat, PhD
> Assistant Professor 
> City College of New York
> Department of Chemistry
> New York, NY 10031
> From: CCP4 bulletin board <[email protected] 
> <mailto:[email protected]>> on behalf of Ashish Kumar 
> <[email protected] <mailto:[email protected]>>
> Sent: Monday, December 16, 2019 1:24 PM
> To: [email protected] <mailto:[email protected]>
> Subject: [EXTERNAL] Re: [ccp4bb] 1 out of 2 proteins in asymmetric unit does 
> not fit density
>  
> Hi Jessica,
> 
> It may be possible because of wrong MR solution as well. How were your stats 
> after MR. 
> Also it is correct that it could be possible because of wrong space group.
> Try changing the Space group and repeat MR.
> 
> Best Regards
> Ashish
> 
> On 16 Dec 2019 22:56, "Jessica Besaw" <[email protected] 
> <mailto:[email protected]>> wrote:
> Dear community, 
> 
> I am having a lot of trouble solving a protein structure. I think my problem 
> may caused by incorrectly placed proteins in molecular replacement. I have 
> two proteins in my asymmetric unit. It appears that one protein fits 
> perfectly, and the other one has many errors. (See snapshots below). I have 
> tried deleting the parts of the protein (and even the whole protein) to try 
> and rebuild it in COOT, but it was a bit too difficult for me to solve. 
> 
> I would appreciate any and all suggestions for potential strategies moving 
> forward. 
> 
> Other information: 
> (1) 2.4 Angstrom
> (2) 99% complete
> (3) "Translational NCS may be present at a level that may complicate 
> refinement"
> 
> Cheers!
> 
> Jessica 
> 
> <Screen Shot 2019-12-16 at 11.58.10 AM.png>
> <Screen Shot 2019-12-16 at 11.58.31 AM.png>
> 
> 
> 
> 
> 
> 
> 
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