Looks like you're on the twofold axis, which will make interpretation challenging. Anything you put in may end up being too close to itself in the neighboring AU. What happens if you put in a water and display the symmetry?
On Mon, Jun 23, 2014 at 8:17 AM, Shanti Pal Gangwar <[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] > > > -- [This e-mail message may contain privileged, confidential and/or proprietary information of H3 Biomedicine. If you believe that it has been sent to you in error, please contact the sender immediately and delete the message including any attachments, without copying, using, or distributing any of the information contained therein. This e-mail message should not be interpreted to include a digital or electronic signature that can be used to authenticate an agreement, contract or other legal document, nor to reflect an intention to be bound to any legally-binding agreement or contract.]
