Hello Harry,

I think this is the paper you mean:
https://scripts.iucr.org/cgi-bin/paper?S0365110X56002552

They gave depressingly low estimates of how much the cell dimensions could 
change in order for isomorphous replacement to still work. In reality, unit 
cells can shrink and swell, but the fractional atomic coordinates remain 
relatively unchanged (right?) so bigger unit cell differences still allow the 
method to work.

Best wishes, Jon Cooper. jon.b.coo...@protonmail.com

Sent from Proton Mail mobile

-------- Original Message --------
On 21 Dec 2023, 09:07, Harry Powell wrote:

> Hi Didn’t Francis Crick have something to say about this in the early 1950s? 
> I’m sure it was published but off the top of my mind I can’t think where (one 
> of the more “established” members of this community will be able to give 
> chapter and verse)! If you want to read something a little more detailed than 
> people have mentioned here, there’s a “Methods in Enzymology” chapter by 
> Charlie Carter (?) et al from the early part of this century on the subject - 
> again, I can’t remember exactly who or when. Have a good break (which reminds 
> me to register for the CCP4 Study Weekend)! Harry > On 21 Dec 2023, at 08:04, 
> Tim Gruene  wrote: > > Hi Doeke, > > you can take the coordinates of B and do 
> a rigid body refinement > against the data from A. If this map is sufficient 
> to reproduce model A > (including model building and more refinement cycles), 
> then B is > isomorphous to A. You can do this the other way round, and the 
> result > may not be the same - hence, the mathematical definition of 
> isomorphous > is not identical to the practical use of 'isomorphous' 
> structures when > it comes to phasing. You can repeat this for each side of 
> the triangle > (each in two directions) in order to label the semantic 
> triangle. > > Merry Christmas, more peace on earth and sanity for the 
> elections in > 2024! > > Tim > > On Wed, 20 Dec 2023 20:15:17 +0000 "Hekstra, 
> Doeke Romke" >  wrote: > >> Dear colleagues, >> >> Something to muse over 
> during the holidays: >> >> Let's say we have three crystal forms of the same 
> protein, for >> example crystallized with different ligands. Crystal forms A 
> and B >> have the same crystal packing, except that one unit cell dimension 
> >> differs by, for example, 3%. Crystal form C has a different crystal >> 
> packing arrangement altogether. What is the right nomenclature to >> describe 
> the relationship between these crystal forms? >> >> If A and B are 
> sufficiently different that their phases are >> essentially uncorrelated, 
> what do we call them? Near-isomorphous? >> Non-isomorphous? Do we need a 
> different term to distinguish them from >> C or do we call all three datasets 
> non-isomorphous? >> >> Thanks for helping us resolve our semantic tangle. >> 
> >> Happy holidays! >> Doeke >> >> ===== >> >> Doeke Hekstra >> Assistant 
> Professor of Molecular & Cellular Biology, and of Applied >> Physics (SEAS), 
> Director of Undergraduate Studies, Chemical and >> Physical Biology Center 
> for Systems Biology, Harvard University >> 52 Oxford Street, NW311 >> 
> Cambridge, MA 02138 >> Office: 617-496-4740 >> Admin: 617-495-5651 (Lin Song) 
> >> >> >> >> 
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> https://www.jiscmail.ac.uk/policyandsecurity/ > > > > -- > -- > Tim Gruene > 
> Head of the Centre for X-ray Structure Analysis > Faculty of Chemistry > 
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