Superimposing that molecule on all the others?

Bostjan

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Bostjan Kobe FAA
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From: CCP4 bulletin board <[email protected]> on behalf of Medhanjali 
DasGupta <[email protected]>
Reply to: Medhanjali DasGupta <[email protected]>
Date: Thursday, 10 November 2022 at 9:05 am
To: "[email protected]" <[email protected]>
Subject: Re: [ccp4bb] A challenging MR problem

The data resolution is 2A.
I have 16 chains in my model  out of which only one of the chains has the 
"missing" domain modeled. Is there a way to do MR to predict where the missing 
domains will go in the rest of the chains, based on my solved structure?

Thanks for all the helpful suggestions!!

M

On Wed, Nov 9, 2022 at 3:11 PM Eleanor Dodson 
<[email protected]<mailto:[email protected]>>
 wrote:
Well you could just try the buccaneer pipeline. It would use the phases from 
your solved domain and try to fit the missing sequence. What are your twin 
fractions? And what is the resolution?
Eleanor

On Wed, 9 Nov 2022 at 21:06, Tim Gruene 
<[email protected]<mailto:[email protected]>> wrote:
Dear Medhanjali DasGupta,
unless the resolution is really poor, the quickest try would be shelxe,
starting from what you already have. It might work at, say, 2.8A
resolution or better...

Best,
Tim

On Wed, 9 Nov 2022 14:34:28 -0600 Medhanjali
DasGupta <[email protected]<mailto:[email protected]>> 
wrote:

> Hello!
> My protein structure has a missing domain and I am trying to figure
> out the best way to model this missing domain using the solved
> (modeled) fixed core domain? My data is also imperfectly twinned,
> with 4 twin fractions according to refmac5.
>
>  Any help/ idea is appreciated!
>
>
>



--
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Tim Gruene
Head of the Centre for X-ray Structure Analysis
Faculty of Chemistry
University of Vienna

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Thanks,
Medhanjali Dasgupta
Postdoctoral Research Scientist
Lawrence Berkeley National Laboratory
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