Dear Shanti

Looks like you’re looking down the symmetry axis - so this could simply be 
‘noise’, or a superposition of two bound ligands on top of each other… what’s 
your cryo-protectant?

With regards,

Tony.
- - - - - - - - - - - - - - - - - -
Dr Antony W Oliver
Senior Research Fellow
CR-UK DNA Repair Enzymes Group
Genome Damage and Stability Centre
Science Park Road
University of Sussex
Falmer, Brighton, BN1 9RQ
- - - - - - - - - - - - - - - - - -
email: [email protected]<mailto:[email protected]>

tel (office): +44 (0)1273 678349
tel (lab): +44 (0)1273 677512

http://www.sussex.ac.uk/lifesci/oliverlab
http://tinyurl.com/aw-oliver
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On 23 Jun 2014, at 13:17, Shanti Pal Gangwar 
<[email protected]<mailto:[email protected]>> wrote:

Dear All

I have solved a structure of my protein at 3.0 A. The crystallization condition 
is consisting of PEG400, NaCl, MgCl2 and Sodium citrate. The protein was 
purified in HEPES buffer.
I can see an unidentified electron density blob in coot and I am not able to 
figure out what it could be?

I have attached the snapshot of that blob with this mail. I request everyone to 
please help me in identification of this blob.

Thanking you in advance.







Shanti Pal


********************
Best regards
Shanti Pal Gangwar, Ph.D
School of Life Sciences
Jawaharlal Nehru University
New Delhi-110067
India
Email:[email protected]<mailto:email%[email protected]>


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