Dear CCP4 community,

I am building a structure model from ~3.0 Å resolution cryo-EM map. The
structure consists of seven chains, with each chain containing an N-,
middle, and C-terminal domain. Although I attempted to directly fit the
Alfa-fold model, it became evident that the protein exhibited some
movement, leading to poor fitting of N-terminal. To improve the fitting, I
segmented the alfa-fold model into two parts: i) the N-terminal and ii) the
middle and C-terminal domain. These fragments were then fitted into the
map. After a few rounds of refinement using coot and phenix, the model
effectively fitted all seven chains.

The refinement resulted in a model to map correlation (CC mask) of over 60%
for the N-terminus. *However, even though the model appeared to fit well
inside the map, particularly in the middle and C-terminus regions, the
refining consistently resulted in a map to model correlation of 0%.*

For your perusal, I have included the snapshot of the phenix refinement
results, the correlation graph, and the fitted model within the map
(displaying one chain out of seven).

I am not able to figure out why the correlation is so poor even after fine
fitting of model to map.

Any support in resolving this issue would be much appreciated.


Thank,

Ketul Saharan



-- 

Ketul Saharan

Senior Research Fellow (Ph.D. Scholar)

Laboratory of Macromolecular Crystallography (Lab-8)

Institute of Life Sciences

Nalco Square, Chandrasekharpur

Bhubaneswar – 751023

Odisha State, INDIA



Phone: +91 8708290889
 124.png
<https://drive.google.com/file/d/1qYE_ge1M99zbkUt_g4JF3bNfEyDUelkS/view?usp=drive_web>
 correlation.tif
<https://drive.google.com/file/d/1bogOk15bImYXSLCPcnrUfC9gRH0cGame/view?usp=drive_web>
 map to model.tif
<https://drive.google.com/file/d/1y-QXMOwWslOTg2PRjS91PFf-gh1obiEt/view?usp=drive_web>

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