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[1] To refer the orientation and position of one base-pair (bp) relative toPlease also refer to another post in this forum on "h-twist vs. twist" (http://http://3dna.rutgers.edu:8080/forum/viewtopic.php?f=1&t=10) and the link therein.
the other, 6 parameters (3 rotations and 3 translations) are required.
One set of such parameters is (Shift, Slide, Rise, Tilt, Roll and
Twist), and the other set is (X-displacement, Y-displacement, Helical
Rise, Inclination, Tip and Helical Twist).
Obviously these two sets should be completely reversible/dependent: from
any one set you can get the other, rigorously. You can verify this point
using "step_hel", a utility program in 3DNA. Graphically this is best
illustrated by the Calladine-Drew A to B transition model by introducing
uniform Roll and Slide values at each dinucleotide step. You could see
these images in 3DNA website, Examples/Calladine_Drew/ directory in 3DNA
distribution and 3DNA user's manual. The key point is that by
introducing Roll, you also get Inclination, and with Slide, you get
X-displacement.
The "rebuild" program in 3DNA can construct a DNA structure using either
set of these parameters. Examples of such input files (e.g.,
"bp_step.par" and "bp_helical.par") can be generated by
"analyze". Please have a look of the Examples/Analyze_Rebuild directory.
[2] The define a local helical axis, we need two base-pair reference
frames (i and i + 1). 3DNA finds the single-helical axis (which is
actually dx times dy) that brings i to coincide with i + 1 by a Helical
Twist angle. The position which this helix passes through is defined by
Chasles' theorem as detailed in Figures 12 & 13 of Backcok et al.
(J. Mol. Biol. 1994, 237, pp 125-156). The calculation of
X-displacement, Y-displacement, Tip and Inclination is then exactly as
described in SCHNAaP (J. Mol. Biol. 273, 668-680, i.e., 3DNA calculates
a set of local helical parameters instead of linear global ones as given
in SCHNAaP and NewHelix/FreeHelix.)
To make the above point clear, let's use A1-A2-A3 triplet as an example.
First, A1-A2 define a local helical axis and a set of local base-pair
helical parameters are calculated. In 3DNA, these parameters are defined
in a symmetric manner that bp A1:T1 and bp A2:T2 have exactly the same
values except for a sign reversal for Y-displacement and Tip.
Similarly, step A2-A3 define another set of local base-pair helical
parameters. Thus bp A2:T2 has two sets of helical parameters associated
with it depending on its context, i.e., either with bp A1:T1 or with bp
A3:T3. Moreover, the local helical rise and helical twist are directly
related to a dinucleotide step. These are the reasons that "Local
base-pair helical parameters" as given in 3DNA refer to base-pair steps.
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