Dear Pedro Matias,

Thanks for you advice. 


After I manually changed the side chain of the residues, I got a "artificial" 
primary structure. I did a blast by using this primary structure. 
Finally, I found the amino acid sequence of this protein. The electron density 
could perfectly match the sequence.
BTW, this protein is from a lovely weird bacteria which was cultured by a 
student.  


Best regards,


Jiyong




--
Yours Sincerely,


Jiyong Su


The School of Life Sciences
Northeast Normal University
Changchun 130024, China
Email: sujy...@nenu.edu.cn
Tele: + 0086 13244318851
 




在 2017-12-14 21:08:57,Pedro Matias <mat...@itqb.unl.pt> 写道:
>Hello,
>
>Welcome to the club of unexpected results!
>
>You don't provide a lot of background, but based on what you wrote you can:
>
>1. Do a BLAST search using a known part of your sequence to find whether
>this sequence has been deposited.
>
>2. Assign the different residues based on the chemical environment and
>electron density and refine the structure.
>
>I'm sure you can submit the refined structure to the PDB even from an
>unknown protein.
>
>Regards,
>
>Pedro Matias
>
>
>Às 12:08 de 14/12/2017, Jiyong Su escreveu:
>> Dear CCP4bb,
>>
>> In 2014, I collected a high quality data set from a crystal. But I
>> could not solve the structure of that crystal because this protein is
>> a contaminate. 
>> Recently, I used StruBE's Contaminer and fortunately got the solution.
>> Thanks ContaMiner!!!  This protein is a contaminate protein. 
>>
>> However, I found this protein is an unknown protein (about 180
>> residues) whose amino acid sequence is not totally same as E.coli.
>> There are about 20 point mutation sites comparing to the E.coli
>> protein. This means this protein may be from an unknown bacteria.  
>>
>> The space group of this crystal is new. There is also a new ligand in
>> this protein. 
>>
>> My question is how could I found the primary structure of this protein
>> and how to deposit this protein in PDB. 
>>
>> Best regards,
>>
>> Jiyong
>>
>
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