Curves+ vs 3DNA

While browsing Nucleic Acids Research recently, I noticed the paper titled Conformational analysis of nucleic acids revisited: Curves+ by Dr. Lavery et al. I read it through carefully during the weekend and played around with the software. Overall, I was fairly impressed, and also happy to see that “It [Curves+] adopts the generally accepted reference frame for nucleic acid bases and no longer shows any significant difference with analysis programs such as 3DNA for intra- or inter-base pair parameters.”

Anyone who has ever worked on nucleic acid structures (especially DNA) should be familiar with Curves, an analysis program that has been widely used over the past twenty years. Only in recent years has 3DNA become popular. By and large, though, it is my opinion that 3DNA and Curves are constructive competitors in nucleic acid structure analysis with complementary functionality. As I put it six years ago, before the 13th Conversation at Albany: “Curves has special features that 3DNA does not want to repeat/compete (e.g. global parameters, groove dimension parameters). Nevertheless, we provide an option in a 3DNA utility program (find_pair) to generate input to Curves directly from a PDB data file” on June 6, 2003, and emphasized again on June 09, 2003: “We also see Curves unique in defining global parameters, bending analysis and groove dimensions.” 3DNA’s real strength, as demonstrated in our 2008 Nature Protocols paper, lies in its integrated approach that combines nucleic acid structure analysis, rebuilding, and visualization into a single software package (see image below).

3DNA v2 composite image

Now the nucleic acid structure community is blessed with the new Curves+, which “is algorithmically simpler and computationally much faster than the earlier Curves approach”, yet still provides its ‘hallmark’ curvilinear axis and “a full analysis of groove widths and depths”. When I read the text, I especially liked the INTRODUCTION section, which provides a nice summary of relevant background information on nucleic acid conformational analysis. An important feature of Curves+ is its integration of the analysis of molecular dynamics trajectories. In contrast, 3DNA lacks direct support in this area (even though I know of such applications from questions posted on the 3DNA forum), mostly due to the fact that I am not an ‘energetic’ person. Of special note is a policy-related advantage Curves+ has over 3DNA: Curves+ is distributed freely, and with source code available. On the other hand, due to Rutgers’ license constraints and various other (undocumented) reasons, 3DNA users are still having difficulty in accessing 3DNA v2.0 I compiled several months ago!

It is worth noting that the major differences in slide (+0.47 Å) and x-displacement (+0.77 Å) in Curves+ vs the old Curves (~0.5 Å and ~0.8 Å, respectively) are nearly exactly those uncovered a decade ago in Resolving the discrepancies among nucleic acid conformational analyses [Lu and Olson (1999), J. Mol. Biol., 285(4), 1563-75]:

Except for Curves, which defines the local frame in terms of the canonical B-DNA fiber structure (Leslie et al., 1980), the base origins are roughly coincident in the different schemes, but are significantly displaced (~0.8 Å along the positive x-axis) from the Curves reference. As illustrated below, this offset gives rise to systematic discrepancies of ~0.5 Å in slide and ~0.8 Å in global x-displacement in Curves compared with other programs, and also contributes to differences in rise at kinked steps. (p. 1566)

Please note that Curves+ has introduced new name list variables — most notably, lib= — and other subtle format changes, thus rendering the find_pair generated input files (with option ‘-c’) no longer valid. However, it would be easy to manually edit the input file to make it work for Curves+, since the most significant part — i.e., specifying paired nucleotides — does not change. Given time and upon user request, however, I would consider to write a new script to automate the process.

Overall, it is to the user community’s advantage to have both 3DNA and Curves+ or a choice between the two programs, and I am more than willing to build a bridge between them to make users’ lives easier.



1. How do I enter tetranucleotide sequences, like ACGT into Curves+?
2. How do I enter tetranucleotide sequences, like ACGT into 3DNA?

Which software package, Curves+ or 3DNA will give me deeper insights into the influence of the tetranucleotide sequence on the three dimensional structure of the double helix?

Thanks for listening-

— HenryB · 2019-11-30 19:26 · #



I am not sure I fully understand your questions. For the part I understand to some extent, I do not think I can give a straight answer. Please be specific with your questions, using concrete examples.

For any further 3DNA-related technical questions, please post them on the 3DNA Forum.


— Xiang-Jun · 2019-11-30 21:11 · #



Thank you for printing this article from Please do not forget to visit back for more 3DNA-related information. — Xiang-Jun Lu