Hi Robbie et al.,

I'm very sure on the crystallization conditions, but I'll check the 
purification for BME, although it seems unlikely, since the crystallized 
protein is a Fab.

What I would be less sure on is the age of the reagents used. Is anyone aware 
of significant breakdown products which might be more reactive, particularly 
the alcohols?

Thanks,

Dr Richard Cowan
Research Associate

HWLSB 1/05
Department of Biochemistry
University of Leicester
Lancaster Road
Leicester, LE1 9HN, U.K.

Phone +44 (0) 116 229 7077

________________________________
From: robbie_joos...@hotmail.com <robbie_joos...@hotmail.com>
Sent: 27 March 2020 20:57
To: Cowan, Richard H. (Dr.) <rc...@leicester.ac.uk>
Cc: CCP4BB@JISCMAIL.AC.UK <CCP4BB@JISCMAIL.AC.UK>
Subject: Re: [ccp4bb] Covalent Cysteine Aduct

Are you absolutely sure about the conditions? The blob next to the sulfur looks 
pretty fat so I would guess BME.

Cheers,
Robbie

On 27 Mar 2020 21:32, "Cowan, Richard H. (Dr.)" <rc...@leicester.ac.uk> wrote:
Hi All,

During the current enforced shutdown, I've been going back over some older data 
and spotted this in one of my structures:

[cid:ddddd2ff-a10c-4f19-9f47-4db92e7620ef]


It's what appears to be a covalent aduct onto a cysteine on the surface 
(originally modeled as 2 waters!). The condition was optimized from the 
Morpheus Screen condition D1, so MES/Imidazole pH 6.5, PEG 500MME, PEG20k and a 
mix of 1,6-Hexanediol, 1-Butanol, 1,2-Propanediol, 2-Propanol, 1,4-Butanediol 
and 1,3-Propanediol. The data has been cut at 1.7A, with good stats.

Has anyone seen anything like this before? what do you think my best bet for 
modeling this is? and aduct of 1,3-propanediol? It looks too short for 
1-butanol or 1,4-butandiol, and it's linear so 2-propanol and 1,2-propanediol 
seem unlikely.

Thanks,

Dr Richard Cowan
Research Associate

HWLSB 1/05
Department of Biochemistry
University of Leicester
Lancaster Road
Leicester, LE1 9HN, U.K.

Phone +44 (0) 116 229 7077


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