***  For details on how to be removed from this list visit the  ***
***          CCP4 home page http://www.ccp4.ac.uk         ***


Hi Steve,
Jamie Cate used molecular replacement with EM maps to phase the ribosome at 18-9 angstroms. He described his technique (as applied to a 7.8A case) in Cate JH, Construction of Low-Resolution X-ray Crystallographic Electron Density Maps of the Ribosome, 2002, Methods 25(3):303-8.

Notably, he found that having accurately measured extremely low resolution reflections (near the dimensions of the particle) was absolutely critical. In one figure he compares a map from an 80-8A and a map from 300-8A. The former was almost uninterpretable, due to ripples in the FT, while the latter looks fine.

Also, the pseudo-atom technique he uses with CNS may be obsolete, now that Phaser can perform searches with maps.

Jacob


Q. Steven Xu wrote:
***  For details on how to be removed from this list visit the  ***
***          CCP4 home page http://www.ccp4.ac.uk         ***


Hi, everyone,

I am just wondering if anybody has experience on the molecular replacement at very low resolution (say 20A or only 1000~2000 reflections). Was there any successful case at this resolution? or MR has limitations on resolution (or the number of total reflections)? Any reference?

Many thanks.

Steve Xu
LBL



--
Jacob Corn
The Berger Lab
UC Berkeley - Molecular and Cell Biology
[EMAIL PROTECTED]
phone: 510-643-8893
fax: 510-643-9290

Reply via email to