LociOiling Lv 1
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Closed since about 6 years ago
Advanced Overall Prediction Electron DensityFold the transposase protein into a density map! This is a followup to Puzzle 1784: CRISPR-Cas Transposase Part I, now with a cryo-EM density map! Players may load in previous work from Puzzle 1784.
CRISPR-Cas is a mixed complex of RNA and proteins, which work together to make a very precise cut in a cell's DNA. Scientists recently discovered a variant of CRISPR-Cas that coopts a new protein called a transposase. In addition to cutting DNA, the transposase also allows precise insertion of new material into a target DNA strand. This new variant could lead to more efficient gene editing with CRISPR-Cas! New cryoEM experiments have shed some light on the transposase structure, which was previously unknown.
We're asking Foldit players to help solve how this transposase protein folds! The transposase is a large 400-residue protein, so this puzzle only includes the first half of the protein, and we will post the second half of the protein in a follow-up puzzle. In this puzzle we've provided only the portion of density for this half of the transposase protein.
Sequence:
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Yes!!! Just like 1784, but don't hold you breath waiting for a response!
I wonder if these comments are actually monitored. Perhaps the powers
that be at Foldit just couldn't care less! Hmmm, a tricky one.
Merf.
More time is needed for such complex ED: total 2 weeks.
7 days would be just fine if the definition was just a tad better. Think of our eyesight FC! lol
Not sure why the scoreboards are having trouble with these CRISPR puzzles… Still haven't been able to track down the issue
We want to do a quick first pass on both parts of this protein in just a couple weeks. If it seems like there is more to be done after that, we can post follow-ups with more time (and with sharing enabled from previous puzzles).
So frustrating! All those large sidechains (tyrosine, phenylalanine, tryptophan) and I can hardly pick out a one!
We need a better density cloud!
can't see where the loops are going.
It's an issue with the underlying cryoEM data… this is the best that could be done in the experiment. When the data isn't great, it makes things hard.