This fact by itself is unusual to say the least (for me):
" we have NO rotational symmetry (2, 3, or 4-fold) whatsoever between 
interacting monomers in the ASU or relating those built up by the 
crystallographic symmetry"
There might be several ways of choosing molecules to represent the asymmetric 
unit. Is it possible to find ones that are related? Say something like 
non-crystallographic translation (or pseudo translation) + non-crystallographic 
rotation.

For long time I was thinking about such a possibility of having more than one 
molecule in au but no rotation or pst. May be I've missed but never found an 
evidence, nor can I explain why would that be impossible.


Vaheh Oganesyan
www.medimmune.com

From: CCP4 bulletin board [mailto:[email protected]] On Behalf Of Hay Dvir
Sent: Thursday, December 11, 2014 12:04 PM
To: [email protected]
Subject: Re: [ccp4bb] asymmetric homotrimer in the asu

Dear Michael,

Thank you very much for the useful comments.

Indeed, we are of course looking at it biochemically, which isn't a clear cut 
so far..
As you pointed out it could be a monomer in solution, but the interface between 
monomers within this asymmetric trimer seems too extensive (compared to those 
responsible for the lattice packing) not to suspect a trimer as a solution 
assembly. PISA suggested this asymmetric trimer as the most likely assembly but 
it falls into the grey region of their criteria (see attached pic.)

[cid:[email protected]]


Since it's rare, we are interested to know of other similar reports, if any, to 
learn how they were resolved/concluded. I believe the case you describe is not 
similar, as we have NO rotational symmetry (2, 3, or 4-fold) whatsoever between 
interacting monomers in the ASU or relating those built up by the 
crystallographic symmetry. Therefore I can't see how the space group 
information may help, but it is p212121 in case it helps boosting your morning 
coffee experience with symmetry pondering ... :).

Cheers,
Hay



On Dec 11, 2014, at 3:47 PM, R. M. Garavito wrote:


Dear Hay,

And your point is?  I am not trying to be snarky (although I am just starting 
my morning coffee), but to bring up the fact that CCP4BB readers need more info 
to comment on your case, like space group, local interactions, and how packed 
is "tightly packed."

I have had two cases of "trimers," as my students initially called them, that 
were actually a dimer and a half.  The "half" dimer had its mate in another 
ASU.   Can it be a biological monomer that just happened to crystallize 3 
monomers to an ASU?  Non-symmetric homo-oligomers are rare, but sadly cannot be 
absolutely confirmed by crystallography alone, but by good old biochemistry.  
The PISA website (http://www.ebi.ac.uk/msd-srv/prot_int/pistart.html) can give 
you estimations of the strengths of the interfacial interactions, but they are 
mere estimates.  What does gel filtration say or cross linking? Does it fit 
with the biology/biochemistry expected of this protein?

Anyway, have fun with your structure, but use a lot of skepticism in your 
interpretation.  That will help you convince the reviewers.

Cheers,

Michael

****************************************************************
R. Michael Garavito, Ph.D.
Professor of Biochemistry & Molecular Biology
603 Wilson Rd., Rm. 513
Michigan State University
East Lansing, MI 48824-1319
Office:  (517) 355-9724     Lab:  (517) 353-9125
FAX:  (517) 353-9334        Email:  
[email protected]<mailto:[email protected]>
****************************************************************



On Dec 11, 2014, at 7:27 AM, Hay Dvir 
<[email protected]<mailto:[email protected]>> wrote:


Dear all,


We have a structure of a rather tightly packed homotrimer protein in the ASU 
with no apparent crystallographic or non-crystallographic rotational symmetry 
between monomers.
Attempting to establish the biological assembly, we are very interested to hear 
about additional similar cases you might know of.

Thanks in advance,
Hay


---------------------------
Hay Dvir               Ph. D.
Head           Technion Center for Structural Biology
Technion    Haifa 3200003, Israel
Tel:                       +(972)-77-887-1901
Fax:                      +(972)-77-887-1935
E-mail                   [email protected]<mailto:[email protected]>
Website                http://tcsb.technion.ac.il<http://tcsb.technion.ac.il/>



To the extent this electronic communication or any of its attachments contain 
information that is not in the public domain, such information is considered by 
MedImmune to be confidential and proprietary. This communication is expected to 
be read and/or used only by the individual(s) for whom it is intended. If you 
have received this electronic communication in error, please reply to the 
sender advising of the error in transmission and delete the original message 
and any accompanying documents from your system immediately, without copying, 
reviewing or otherwise using them for any purpose. Thank you for your 
cooperation. To the extent this electronic communication or any of its 
attachments contain information that is not in the public domain, such 
information is considered by MedImmune to be confidential and proprietary. This 
communication is expected to be read and/or used only by the individual(s) for 
whom it is intended. If you have received this electronic communication in 
error, please reply to the sender advising of the error in transmission and 
delete the original message and any accompanying documents from your system 
immediately, without copying, reviewing or otherwise using them for any 
purpose. Thank you for your cooperation.

Reply via email to