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It has been speculated for quite some time, that the DNA in nucleosomes is over twisted (approx. 10 bp per turn instead of 10.5), so I want to show this using 3DNA analysis. An intuitive way to get the value of average helical pitch would be summing the values of twist returned by 3DNA along the DNA and dividing by the number of base pairs. However, I'm not quite sure if this approach is rigorous, and whether one should sum up the values of helical twist of dimer step twist. What do you think?I am aware of the paper "Helical repeat of DNA in solution (http://www.ncbi.nlm.nih.gov/pubmed/284332)" by Wang (PNAS 1979) where it was found that "Analysis of the set ... gives the DNA helix repeat in solution as 10.4 base pairs per turn under physiological conditions, with an estimated probable error of +/- 0.1." The "twist" measurement here is an average of covalently closed DNAs. In my understanding, it is related to linker number and writhe, but differs from the dinucleotide-step twist angles from 3DNA. See "Two perspectives on the twist of DNA (http://www.ncbi.nlm.nih.gov/pubmed/20059113)" by Tobias et al. However, why not pursue your "intuitive way" further to see what you can get. It won't take much time, and the result (whatever it could be) would be informative.
2) During MD simulations some base pairs might become distorted and they are not found by find_pairs. I can force the calculations on them by manually editing .inp file, however, I assume that the Twist, Roll, Tilt values reported for the base pair steps would be arbitrary.Two points here. Regarding the issues of 'local' vs 'overall' twist, see above. Distorted base-pairs do not have "arbitrary" step parameters: they are derived based on the geometry given in a PDB/mmCIF input file, and can be used to 'rigorously' rebuild the original base pairs. More generally, the default cutoffs in 3DNA are a good starting point. However, there are always boundary cases where the choice is sort of arbitrary. For example, the vertical separation (stagger) is 2.5 Å by default. So a dinucleotide step with a value of 2.49 Å would satisfy this criterion, whereas 2.51 Å won't.
Will the summation of all twist angles along the DNA helix be meaningful in this case in order to obtain overall twist of the DNA helix?
I wonder if there are plans to implement such a property for calculation in 3DNA?In principle, I'd be interested in implementing such a property in 3DNA. To that end, I need direct access to details: either a worked example, or a working program with sample input and output files. Pure text descriptions or mathematical formula as often seen in scientific publications help for general understanding, but they are certainly not enough from a programatic point of view.
Funded by the NIH R24GM153869 grant on X3DNA-DSSR, an NIGMS National Resource for Structural Bioinformatics of Nucleic Acids
Created and maintained by Dr. Xiang-Jun Lu, Department of Biological Sciences, Columbia University