2191: Electron Density Reconstruction 12

Closed since over 3 years ago

Summary

• Created: August 25, 2022
• Expires: September 01, 2022 at 18:00 UTC
• Max points: 100

Description

The structure of this protein has already been solved and published, but close inspection suggests that there are some problems with the published solution. We'd like to see if Foldit players can use the same electron density data to reconstruct a better model.



Sequence:

LSLMPWFHGKISGQEAVQQLQPPEDGLFLVRESARHPGDYVLCVSFGRDVIHYRVLHRDGHLTIDAVFFCNLMDMVEHYSKDKGAICTKLVRPKRK

Top groups

• 1. Gargleblasters 100 pts. 18,901
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• 3. Go Science 47 pts. 18,874
• 4. Void Crushers 30 pts. 18,828
• 5. L'Alliance Francophone 19 pts. 18,787
• 6. Contenders 11 pts. 18,758
• 7. Marvin's bunch 7 pts. 18,725
• 8. FamilyBarmettler 4 pts. 18,492
• 9. WISE 380 Spring 21 A 2 pts. 18,341
• 10. Australia 1 pt. 18,152

Top evolvers

• 11. MrZanav 2 pts. 18,810
• 12. maithra 1 pt. 18,741
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• 14. guineapig 1 pt. 18,718
• 15. MicElephant 1 pt. 18,715
• 16. Oransche 1 pt. 18,701
• 17. BootsMcGraw 1 pt. 18,699
• 18. CharaLilith 1 pt. 17,842

Comments

[jeff101]

<pre>When Tabbing on different segments in this puzzle, I noticed that asp65 says PDB# A181 while ala66 says PDB# A183. Does this mean that residue PDB# A182 is missing, perhaps due to a blurry section in the Electron Density Cloud? If so, what amino acid is PDB# A182? Should we treat asp65 and ala66 as if they are far enough apart for PDB# A182 to fit between them? Should we instead treat asp65 and ala66 as if they are directly covalently-bonded to each other via a peptide bond?

If we need to leave space for the missing
residue PDB# A182, perhaps this puzzle should
break up the protein into two chains (one for
segments 1-65 and another for segments 66-96).
Maybe the 2 chains could be connected to each
other with a cut band or some other constraint.
What do you think?

Thanks!</pre></code>

[jeff101]

This puzzle's protein contains 3 cysteines.
Should our solutions have any disulfide bonds?

[jeff101]

https://fold.it/portal/node/2013447

[bkoep]

Yes it looks like we are missing a residue in the starting structure. Good find!

I'm not exactly sure how this happened; I'll have to take a look. In the published structure this residue is modeled with "zero occupancy," which is kind of like modeling that residue as a placeholder even though there is no density to suggest how the residue is folded.

[jeff101]

If there is a region in the Electron Density Cloud 
with "no density to suggest how the residue is folded",
instead of giving us a protein that is missing a residue 
there, why not give us the entire protein and instead 
change the Electron Density Cloud some? 

Would replacing the bad region with a constant density 
help? Some ideas for the constant density could be zero, 
the average density in the cloud, or the maximum density 
in the cloud. Zero would work best for generally empty 
regions, and large positive values would work best for 
tightly-packed interior regions of the protein. 

Another idea would be to approximate the overall 
Electron Density D as a spherical Gaussian in 3D, like: 
D=density=A*exp(-k*((x-xo)^2 + (y-yo)^2 + (z-zo)^2))
where A and k are positive constants, and xo,yo,zo is 
the approximate center of the Electron Density Cloud. 
With a good enough approximation, one could then 
replace the bad region with the density D given by 
the formula above.