Hi,
One possible (formal, I should say) way around this would be to use one of the homology modeling servers (my favourite recently is phyre2 but go for any server you prefer) and feed it with the sequence of the protein in your structure as if you're trying to get its structure in the''apo'' form (a wrong term, as was pointed out on the bb recently). I'm quite certain that with the degree of conservation you mentioned it'll superpose extremely well on the other ''apo'' structure. This should satisfy the referee I would think (it's not me though).
Cheers,
Boaz


-------- Original message --------
From: Guillermo Montoya <guillermo.mont...@cpr.ku.dk>
Date: 01/02/2017 07:40 (GMT+02:00)
To: CCP4BB@JISCMAIL.AC.UK
Subject: [ccp4bb] comparison of different protein states


Dear all, 

first of all sorry for this off-topic question. I am requesting your help to 
find some papers  to convince one referee about the comparison
of two different protein states.

In our manuscript we show the crystal structure of an 
enzyme. This structure represents the enzyme after catalysis in complex with the product.
 In the discussion we have superimposed the enzyme in the apo conformation 
and the enzyme after catalysis in complex with the product 
and we have  commented the conformational changes observed
between these 2 states to propose a model.

The point of the referee is that this comparison is not valid because the 
enzymes that we used in the comparison belong to different species.
They are not the same protein.

However, and this is stated by us  in the figs and the manuscript, these two proteins are 
40% identical and 60% conserved, the polypeptide length is the same, and
the key amino acids and the domain structure are fully conserved. They are 
obviously orthologs.

I´d really appreciate if you can send me some literature/information
to support our approach 

Thanks a lot for your input


best 




Guillermo Montoya, Prof., Dr.
Research Director, Protein Structure and Function Programme 
Novo Nordisk Foundation Center for Protein Research
Faculty of Health and Medical Sciences, University of Copenhagen,
Blegdamsvej 3A, DK-2200 Copenhagen, Denmark




Reply via email to