Messages

26

General discussions (Q&As) / Re: Rebuilding Z-DNA

« on: April 22, 2025, 09:57:23 am »

Apologies for it took a while to reply. Thank you for your help with the structure! I used phenix to minimise like you suggested and I can use it for my analysis now.

Thanks for the confirmation that the DSSR modeled Z-DNA structure works for your case. It is through interactions with real-world users like you that makes DSSR relevant and useful.

Even though virtual, a forum thread is just like a conversation. I strive to respond to users' questions timely and concretely. Users who initiate a thread are expected to follow up with their progress and share their findings, or the lack thereof. It’s a two-way street, and I appreciate your engagement and contributions to the forum.

As a follow up, I am planing to write a blogpost to summarize the discussion and provide step-by-step details on how the extended Z-DNA structure was built using DSSR. This may take a couple of days, and I will provide a link here once it is ready.

I would also look forward to Z-DNA backbones being included in DSSR modeling functionalities.

I have split a new thread titled "Rebuilding circular Z-DNA". Please share your thoughts and suggestions on this topic over there.

Best regards.

Xiang-Jun

27

RNA structures (DSSR) / Re: Can x3dna-dssr correctly handle N1-methyl-pseudouridine?

« on: April 22, 2025, 09:08:26 am »

Hi Di,

Thanks for your well formulated question regarding x3dna-dssr’s support of N1-methyl-pseudouridine, B8H.

I understand that x3dna-dssr can handle pseudouridine (PDB Chem ID: PSU) correctly. I'm inquiring about its support for N1-methyl-pseudouridine (PDB Chem ID: B8H). Specifically,​ does x3dna-dssr recognize B8H based on its PDB chemical ID, or does it rely on atomic connectivity?

FYI, I've tested x3dna-dssr with PDB entries 8PFK and 8PFQ, both containing B8H, and the analysis proceeded without errors, with the results looking reasonable. However, given the unique C5-C1′ glycosidic bond for B8H, I want to confirm that x3dna-dssr interprets this modification accurately.

DSSR uses atomic connectivity to identify pseudouridine or its modified forms, including B8H. DSSR User Manual contains the following relevant information:

Note that pseudouridine, the most prevalently modified nt in RNA, is denoted P† in DSSR and the small case p is reserved for potential modified pseudouridines. ... footnote: †Not to be confused with the phosphorus atom in the backbone phosphate group. The distinction should be clear in context.

While anticipated, your reported case of B8H is the first time I see a modified pseudouridine. In DSSR output for 8PFK, you will see the following:

Code: Text

1. #x3dna-dssr -i=8PFK.pdb -o=8PFK.out
2.  
3. From 8PFK.out
4. ****************************************************************************
5. List of 1 type of 1 modified nucleotide
6.       nt    count  list
7.    1 B8H-p    1    A.B8H7
8.  
9. From dssr-torsions.txt
10. 7     p A.B8H7 ... chi -155.3(anti)

The chi for B8H is defined using O4'--C1'--C5--C4 instead of O4'--C1'--N1--C2, which would make no sense for pseudouridine. This is a little detail that DSSR pays attention to where other tools may not. See my blogpost Torsion angles from DSSR. You could easily verify this, using PyMOL for example, to measure the torsion angle by clicking four atoms in order.

The DSSR results for 8PFQ are also as expected with correct identification of B8H as a modified pseudouridine.

Further, is there a comprehensive list of modified nucleotides currently supported by x3dna-dssr?​ I came across these two pages (https://x3dna.org/highlights/automatic-identification-of-nucleotides ; https://x3dna.org/highlights/modified-nucleotides-in-the-pdb ), but could not find the exact answer.

To answer your question, here is an excerpt from my recent response to a similar inquiry:

Over the years, I've refined the heuristics of the mapping process. In the early days with 3DNA, I kept an ever increasing list of 'baselist.dat' with hundreds of entries like: MIA   a that maps MIA as a modified A, denoted as lowercase 'a'. In the current DSSR, I keep only the standard ones, with 48 entries total (see attached DSSR-baselist.txt). If a residue is not a standard one, the following function is called to do the mapping (DSSR performs filtering to decide if it is a nucleotide, and if so R or Y). DSSR also has a command-line option --nt-mapping as documented in the screenshot.

The DSSR-baselist.txt is attached for your reference. I am planning to write blogpost with details on this topic.

Best regards,

Xiang-Jun

28

General discussions (Q&As) / Re: Rebuilding Z-DNA

« on: April 21, 2025, 04:20:23 pm »

Hi,

Thanks for chiming in on the discussion. Currently, DSSR can build DNA circles with right-handed helices, but not Z-DNA forms. The backbone of Z-DNA is dramatically different from that of B-DNA or A-DNA, and needs to be modeled differently. I'll look into how we can incorporate Z-DNA backbones into DSSR modeling functionalities, given enough interest from the community, and with a proper collaborator to work on it. See the DSSR-Jmol and DSSR-PyMOL integration for two concrete examples of what I have in mind for such collaborations.

As for the current thread, I'm hoping @shr could respond to my question on March 15, 2025:

Does the attached PDB file (with base schematic image) fulfill your needs?

See my recent post On registration and posting which includes a copy of "Registration Agreement for the Forum" at the bottom.

Best regards,

Xiang-Jun

29

Site announcements / On registration and posting

« on: April 19, 2025, 11:20:25 pm »

It has been 14 years since the Forum was created in 2011. Despite a four-year gap in NIH funding, we managed to keep the Forum operational. Maintaining and nurturing our community wasn't easy, but the users' enthusiasm in using and citing 3DNA/DSSR has kept us going. With the dedicated R24GM153869 grant, I am now committed to making the Forum even better.

Keeping the Forum spam-free is our top priority. In recent months, we have seen a dramatic increase in spams, which account for the majority of new registrations. That is why we have implemented 'Admin Approval' as the method of registration for new members. I carefully review each new registration to ensure only legitimate users are approved to join the Forum. Once approved, new users need to activate their accounts by clicking the activation link sent to their registered email address. I have noticed that some users did not activate their accounts upon approval. I normally send reminders to those inactivated users, but if they still do not respond in a few days, their registrations will be removed from the Forum.

It could also be the other way around: for example, the activation email sent from the 3DNA Forum might have been filtered out as spam by the user’s email agent. I have recently helped a few users with their registrations. If you have any questions or concerns about your registration, feel free to reach out to me directly via email. In today's age of AI, a personal touch goes a long way. Getting assistance directly from the developer ensures issues are resolved quickly and effectively.

I am dedicated to continuously enhancing X3DNA-DSSR, aiming to build it as a reputable brand symbolizing quality and value. Due to its exceptional functionality, ease of use, and direct support from the developer, X3DNA-DSSR significantly reduces the time and effort required compared to alternative solutions. Your comments, suggestions, and bug reports are greatly appreciated; I carefully consider every piece of user feedback, and always respond promptly. Specifically, I encourage you to openly share any challenges or negative experiences you encounter during installation or usage. Asking your questions on the public 3DNA Forum benefits not only yourself but also the wider user community.

Enclosed below is the Registration Agreement for the Forum

This forum is dedicated to topics generally related to the X3DNA-DSSR resource for the analysis, rebuilding, and visualization of 3D nucleic acid structures. To make the Forum a pleasant virtual community for all of us to learn from and contribute to, please be considerate and practice good netiquette (http://www.albion.com/netiquette/). See also the FAQ entry "How to make the best use of the Forum".

I strive to make the Forum spam free. Private emails (gmail.com, yahoo.com, qq.com, rambler.ru etc.) are not accepted; such registrations will be removed. Approved registrations that are not activated via email will be deleted. Activated accounts that are not accessed (logins) will be erased. Posts that are not 3DNA/DSSR related in the broad sense are taken as spams and are strictly forbidden. All administrative actions are performed without notification.

DSSR has completely superseded 3DNA (which is still maintained, but no new features other than bug fixes). DSSR integrates the disparate programs of 3DNA under one umbrella, and offers new advanced features, through a convenient interface. DSSR requires no set up or configuration: it just works. See the Overview Video and User Manual.

When posting on the Forum, please abide by the following rules:

0.  Do your homework; read the FAQ and browse the Forum.
1.  Ask your questions on the *public* 3DNA Forum instead of sending
        xiangjun emails or personal messages. Additionally, please note
        that your posts on the 3DNA Forum are in the *public domain*.
2.  Be specific with your questions; provide a minimal, reproducible
        example if possible; use attachments where appropriate.
3.  Respond to requests for clarification. Failure to do so may result in
        delay or no answer to your questions.
4.  Summarize the solution to your problem from a user's perspective
        by providing step-by-step details, for the community's benefit.
5+ Contribute back to the 3DNA project:
        o Report bugs — including typos
        o Make constructive suggestions — anything that can make 3DNA better
        o Answer other users' questions
        o Share your use cases in the "Users' contributions" section

In a nutshell, you are welcome to participate and should not hesitate to ask questions, but remember to play nice and preferably share what you learned! Please note that we do *not* tolerate spamming or off-topic trolling of any form.

30

Site announcements / Re: Download instructions

« on: April 19, 2025, 10:06:06 pm »

Only 3DNA v2.4.8-2023nov10 is available for download. The ANSI C source code and Ruby scripts are included in the package, along with precompiled binaries for Linux and macOS. The Linux version should also work under Windows using WSL2. In any case, you can compile the source code easily as long as you have a C compiler installed on your system.

31

General discussions (Q&As) / Re: Rebuilding Z-DNA

« on: March 17, 2025, 09:18:59 am »

But I am unable to properly download the pdb file.

What do you mean? Just click on the link and it should download automatically. I've never heard of any issues with downloading files as long as you have an active internet connection. Please clarify your issue so I can assist you better.

32

General discussions (Q&As) / Re: Rebuilding Z-DNA

« on: March 15, 2025, 12:18:44 am »

Does the attached PDB file (with base schematic image) fulfill your needs? The backbone connection between the two segments are a bit longer than normal O--P covalent bond distance, which you can regulated with energy minimizations (e.g., using Phenix, as shown in "Web 3DNA 2.0 for the analysis, visualization, and modeling of 3D nucleic acid structures" (https://doi.org/10.1093/nar/gkz394).

33

General discussions (Q&As) / Re: Rebuilding Z-DNA

« on: March 14, 2025, 08:12:34 am »

Thanks for your follow-up questions and the details you provided. It is always helpful to to be specific when discussing research topics.

Yes, "rebuild -atomic" would have issues with backbone connectivity, since in Z-DNA, nucleotide G is in syn conformation instead of anti (for C). The building block must be adjusted accordingly. I'll look into this further to see what we can get.

Another approach is to take the whole Z-DNA structure as a unit, and perform some transformations to extend it. See the PyMOL thread a few years ago on "create a 26 bp RNA from a 13 bp system" (https://www.mail-archive.com/pymol-users@lists.sourceforge.net/msg16190.html). The idea is applicable to Z-DNA as well. Note that the features are now available in the free DSSR Academic license (previously in DSSR Pro Academic only). Check if that method makes sense to you.

Best regards,

Xiang-Jun

34

General discussions (Q&As) / Re: Rebuilding Z-DNA

« on: March 13, 2025, 03:56:04 pm »

Thanks for your quick follow-up.

As noted in the x3dna_utils cp_std -h help message, the utility covers the most common use cases:

Select the standard data files to be used with "analyze" and "rebuild".
Available sets include BDNA, ADNA, NDB96 and RNA, which have exactly
the same base geometry and orientation (in the standard base reference
frame) but different backbone conformations.

Z-DNA is different from the standard right-handed DNA/RNA double helix in that it has not only a left-handed twist but also a base flip, and it has a di-nucleotide (most commonly CpG) as a the building block. So the x3dna_utils cp_std does not cover Z-DNA. However, you can run analyze, modify the output parameters (and extend as needed), and then rebuild a Z-DNA structure according to the modified parameters.

What specific Z-DNA structure you’d like to extend? If you do not want share details, please use a sample Z-DNA structure that helps illustrate your point. Reproducibility is important.

Best regards,

Xiang-Jun

35

General discussions (Q&As) / Re: Rebuilding Z-DNA

« on: March 13, 2025, 02:14:06 pm »

Hi,

Thanks for using 3DNA and for posting your questions on the Forum. 3DNA rebuild should be able to build Z-DNA structures given a set of parameters. Please be specific with what you are trying to achieve, and we can start from there.

Best regards,

Xiang-Jun

36

General discussions (Q&As) / Re: Generation of ssDNA PDB with m3C modification using 3DNA webserver

« on: February 28, 2025, 08:47:06 am »

Welcome back.

But I do not have a PDB structure with the m3C modification, I was hoping that we would be able to generate the PDB (and PSF) using 3DNA/DSSR by specifying the residues.

Are you expecting 3DNA/DSSR to "generate the PDB" by specifying the residues, including unknown ones?  3DNA/DSSR can build DNA/RNA structures with standard bases (A,C,G,T,U), or modified ones with *known* building block as illustrated in 5-methylcytosine in the FAQ. It does not generate structures for ligands like m3C. It is up to the user to provide such building blocks for 3DNA/DSSR to proceed. CCP4 and Phenix may have utilities to generate new ligands.

By the way, what does PSF stand for?

As a side question, what would be a good force field that can allow us to perform a phase separation simulation with the methylated ssDNA and IDR sequence?

Sorry, I'm not familiar with this field, and I cannot offer any valuable suggestions. Overall, this question is out of the scope of the Forum.

Best regards,

Xiang-Jun

37

MD simulations / Re: Update of do_x3dna package

« on: February 22, 2025, 11:23:27 pm »

Hi Rajendra,

Thanks for the update to do_x3dna for GROMACS-2025. It is great that the "binary package can be used with files generated by any version of GROMACS". Over the years, I've received emails about applying 3DNA to MD simulations, and I know that your do_x3dna package is well received by the community.

Best regards,

Xiang-Jun

38

General discussions (Q&As) / Re: Opening values and the definition for base-pair parameters

« on: February 07, 2025, 10:22:26 am »

Hi Jing,

Please follow what I suggested in the previous response. As for the 3DNA source code, did you notice the download link at the top and the Download instructions post?

Best regards,

Xiang-Jun

39

General discussions (Q&As) / Re: Opening values and the definition for base-pair parameters

« on: February 06, 2025, 11:14:10 am »

Hi Jing,

I have attached several pictures here. They are G and G pairs. The first two are with the opening \~180, the third picture is with \~-180, and the last two are with \~90.

Thanks for your follow up, and for providing images that illustrate G.G pairs with opening around 180 and 90 degrees. It would have been more helpful if you attached the corresponding PDB files. When posting questions in the future, thinks about providing (mininal) examples so others can *reproduce* the cases.

Now I understand the question you're asking. Let's use a G+G pair in G-tetrad of G-quadruplexes as an example, which has an opening around 90 degrees. Assuming you have downloaded the coordinates file `5ua3.pdb` for PDB entry 5ua3 on "Crystal structure of a DNA G-quadruplex with a cytosine bulge". Please try the following DSSR commands:

Code: [Select]

# This extract DG1 and DG6 from chain A into file 5ua3-GG.pdb
x3dna-dssr -i=5ua3.pdb --select-residue='A 1+6' -o=5ua3-GG.pdb

# Set the pair into the base reference frame of A.DG1
x3dna-dssr -i=5ua3-GG.pdb --frame='A.1' -o=5ua3-GG-frame1.pdb

# Generate the schematic with base blocks
x3dna-dssr -i=5ua3-GG-frame1.pdb --cartoon-block=sticks-label --block-file=slim-outline -o=5ua3-GG-frame1.pml
Load `5ua3-GG-frame1.pml` into PyMOL to see the attached image where the (`slim`) base blocks are nearly perpendicular, corresponding to an opening angle of ~90 degrees.

Analyze `5ua3-GG.pdb` (or `5ua3-GG-frame1.pdb`) with `--more` option to see the six base-pair parameters, including opening.

Code: [Select]

x3dna-dssr -i=5ua3-GG.pdb --more

# With the following detailed information:
List of 1 base pair
     nt1            nt2            bp  name        Saenger   LW   DSSR
   1 A.DG1          A.DG6          G+G --          06-VI     cWH  cW+M
       [-131.0(anti) ~C2'-endo lambda=62.6] [-128.4(anti) ~C2'-endo lambda=28.0]
       d(C1'-C1')=11.59 d(N1-N9)=9.65 d(C6-C8)=9.30 tor(C1'-N1-N9-C1')=10.9
       H-bonds[2]: "N1(imino)-O6(carbonyl)[2.95],N2(amino)-N7[2.91]"
       interBase-angle=1  Simple-bpParams: Shear=-2.67 Stretch=2.83 Buckle=-0.8 Propeller=0.5
       bp-pars: [1.61    3.54    -0.15   0.14    0.94    -89.63]
Note that the opening is reported as `-89.63` --- if you try to align A.DG6 to A.DG1, you need to rotate ~`-90` degrees as can be seen in the attached images. If you swap the pair, the opening would be ~`+90` degrees. See the [2003 3DNA paper in NAR](https://doi.org/10.1093/nar/gkg680), specifically the section "Base pair parameters".

With a clear understand of the above example, you should have little difficult in understanding opening ~180 degrees. You are suggested to follow the above example on one of such cases, and report back your findings.

Note that 3DNA/DSSR report angular parameters in the range of [0, +-180] instead of [0, 360]. So opening of `-175` is not that much a difference from `+175` (vs `+185`). Also notice the opposite sign of opening for M+N vs N+M pairs.

Please read the [DSSR manual](http://docs.x3dna.org/dssr-manual.pdf) and the [practical guide for the DSSR-PyMOL](http://skmatic.x3dna.org/dssr-schematic-guide.pdf) article.

Best regards,

Xiang-Jun

40

General discussions (Q&As) / Re: Opening values and the definition for base-pair parameters

« on: February 03, 2025, 06:05:26 pm »

Hi Jing,

Thanks for using 3DNA, and for posting your questions on the Forum. Your confusions about the details are understandable, and can be clarified most effectively using concrete examples. Do you have examples with opening ~90 and 180?

Since 3DNA source code is available, you can dig into it to see exactly how the base reference frames are defined and how the various parameters are calculated.

Best regards,

Xiang-Jun

41

General discussions (Q&As) / Re: Generation of ssDNA PDB with m3C modification using 3DNA webserver

« on: January 31, 2025, 08:51:31 am »

Hi Sunera,

Thanks for your follow up. Is the idea in FAQ "How can I mutate cytosine to 5-methylcytosine?" relevant? Do you have a PDB structure with m3C modification?

Best regards,

Xiang-Jun

42

General discussions (Q&As) / Re: Generation of ssDNA PDB with m3C modification using 3DNA webserver

« on: January 30, 2025, 11:10:45 am »

Hi,

Thanks for your interesting in using 3DNA and for posting your questions on the Forum.

The http://web.x3dna.org has features to build regular fiber models or customized structures (including single-stranded structure as detailed in the supplemental PDF). However, the web-server does not allow you to generate  single-stranded DNA containing a 3-methylated cytosine. The web server simply does not have 'knowledge' of what a 3-methylated cytosine is. I know of no other tools that can do this automatically.

However, 3DNA/DSSR has features that would allow for such modeling from the command line. I need more details of exactly what you want to achieve to be of further help.

See the FAQ: How can I mutate cytosine to 5-methylcytosine?

Best regards,

Xiang-Jun

43

MD simulations / Re: overwritten output files

« on: January 13, 2025, 10:47:57 am »

Hi Mamta,

The output file name is derived from the input PDB filename, by deleting extension and add ".out". Since your PDB frame is named "output-filename.pdb.${i}", the output file will always be "output-filename.pdb.out" by replacing ".{i}" with ".out". You could name your PDB frame "output-${i}.pdb" and the corresponding output file will be "output-${i}.out".

Have a look of the C source code, and the x3dna_ensemble script (x3dna_ensemble analyze -h). Overall, the x3dna-v2.4 support for MD analysis is limited. There is also do_x3dna -- I'm not sure if it is still actively maintained.

I'm in the process of incorporating x3dna-v2.4 features into DSSR (Free academic license available from CTV). Further improvement for MD support will be implemented in DSSR.

Best regards,

Xiang-Jun

44

MD simulations / Re: overwritten output files

« on: January 13, 2025, 08:30:07 am »

Hi Mamta,

Thanks for using 3DNA/DSSR and for posting your question on the 3DNA Forum. Could you please be specific with the command you used? The x3dna-v2.4 suite comes with a Ruby script 'x3dna_ensemble' for analyzing MODEL/ENDMDL delineated ensemble of NMR or MD structures. The x3dna-dssr program has an --nmr (--md) option that streamline the analysis of such ensembles.

Best regards,

Xiang-Jun

45

RNA structures (DSSR) / Re: DNA bend angle

« on: December 30, 2024, 10:49:36 pm »

Hi Narendra,

Thanks for using DSSR and for posting your question on the 3DNA Forum. Regarding DNA bending angle in 3DNA/DSSR, please refer to the FAQ How to calculate DNA bending angle?. With DSSR, the helical axis info is available with the --more option. See the step-by-step procedures for reproducing Figure 2 -- analysis of the yeast phenylalanine tRNA (1ehz) of the 2015 DSSR paper in NAR.

For your specific example of 1fjl, DSSR readily identifies a helix (stem) with details on the helical axis. However, DSSR does not directly provide you a bending angle for reason given in the above mentioned FAQ.

Best regards,

Xiang-Jun

46

Site announcements / DSSR-PyMOL enabled schematics on the covers of the RNA Journal

« on: December 16, 2024, 04:11:24 pm »

Cover image provided by X3DNA-DSSR, an NIGMS National Resource for structural bioinformatics of nucleic acids (R24GM153869; skmatics.x3dna.org). Image generated using DSSR and PyMOL (Lu XJ. 2020. Nucleic Acids Res 48: e74).

See the 2020 paper titled "DSSR-enabled innovative schematics of 3D nucleic acid structures with PyMOL" in Nucleic Acids Research and the corresponding Supplemental PDF for details. Many thanks to Drs. Wilma Olson and Cathy Lawson for their help in the preparation of the illustrations.


June 2025 (link to the source)

Structure of a group II intron ribonucleoprotein in the pre-ligation state (PDB id: 8T2R; Xu L, Liu T, Chung K, Pyle AM. 2023. Structural insights into intron catalysis and dynamics during splicing. Nature 624: 682–688). The pre-ligation complex of the Agathobacter rectalis group II intron reverse transcriptase/maturase with intron and 5′-exon RNAs makes it possible to construct a picture of the splicing active site. The intron is depicted by a green ribbon, with bases and Watson-Crick base pairs represented as color-coded blocks: A/A-U in red, C/C-G in yellow, G/G-C in green, U/U-A in cyan; the 5′-exon is shown by white spheres and the protein by a gold ribbon. Cover image provided by X3DNA-DSSR, an NIGMS National Resource for structural bioinformatics of nucleic acids (R24GM153869; skmatics.x3dna.org). Image generated using DSSR and PyMOL (Lu XJ. 2020. Nucleic Acids Res 48: e74).

May 2025 (link to the source)

Complex of terminal uridylyltransferase 7 (TUT7) with pre-miRNA and Lin28A (PDB id: 8OPT; Yi G, Ye M, Carrique L, El-Sagheer A, Brown T, Norbury CJ, Zhang P, Gilbert RJ. 2024. Structural basis for activity switching in polymerases determining the fate of let-7 pre-miRNAs. Nat Struct Mol Biol 31: 1426–1438). The RNA-binding pluripotency factor LIN28A invades and melts the RNA and affects the mechanism of action of the TUT7 enzyme. The RNA backbone is depicted by a red ribbon, with bases and Watson-Crick base pairs represented as color-coded blocks: A/A-U in red, C/C-G in yellow, G/G-C in green, U/U-A in cyan; TUT7 is represented by a gold ribbon and LIN28A by a white ribbon. Cover image provided by X3DNA-DSSR, an NIGMS National Resource for structural bioinformatics of nucleic acids (R24GM153869; skmatics.x3dna.org). Image generated using DSSR and PyMOL (Lu XJ. 2020. Nucleic Acids Res 48: e74).

April 2025 (link to the source)

Cryo-EM structure of the pre-B complex (PDB id: 8QP8; Zhang Z, Kumar V, Dybkov O, Will CL, Zhong J, Ludwig SE, Urlaub H, Kastner B, Stark H, Lührmann R. 2024. Structural insights into the cross-exon to cross-intron spliceosome switch. Nature 630: 1012–1019). The pre-B complex is thought to be critical in the regulation of splicing reactions. Its structure suggests how the cross-exon and cross-intron spliceosome assembly pathways converge. The U4, U5, and U6 snRNA backbones are depicted respectively by blue, green, and red ribbons, with bases and Watson-Crick base pairs shown as color-coded blocks: A/A-U in red, C/C-G in yellow, G/G-C in green, U/U-A in cyan; the proteins are represented by gold ribbons. Cover image provided by X3DNA-DSSR, an NIGMS National Resource for structural bioinformatics of nucleic acids (R24GM153869; skmatics.x3dna.org). Image generated using DSSR and PyMOL (Lu XJ. 2020. Nucleic Acids Res 48: e74).

February 2025 (link to the source)

Structure of the Hendra henipavirus (HeV) nucleoprotein (N) protein-RNA double-ring assembly (PDB id: 8C4H; Passchier TC, White JB, Maskell DP, Byrne MJ, Ranson NA, Edwards TA, Barr JN. 2024. The cryoEM structure of the Hendra henipavirus nucleoprotein reveals insights into paramyxoviral nucleocapsid architectures. Sci Rep 14: 14099). The HeV N protein adopts a bi-lobed fold, where the N- and C-terminal globular domains are bisected by an RNA binding cleft. Neighboring N proteins assemble laterally and completely encapsidate the viral genomic and antigenomic RNAs. The two RNAs are depicted by green and red ribbons. The U bases of the poly(U) model are shown as cyan blocks. Proteins are represented as semitransparent gold ribbons. Cover image provided by X3DNA-DSSR, an NIGMS National Resource for structural bioinformatics of nucleic acids (R24GM153869; skmatics.x3dna.org). Image generated using DSSR and PyMOL (Lu XJ. 2020. Nucleic Acids Res 48: e74).

January 2025 (link to the source)

Structure of the helicase and C-terminal domains of Dicer-related helicase-1 (DRH-1) bound to dsRNA (PDB id: 8T5S; Consalvo CD, Aderounmu AM, Donelick HM, Aruscavage PJ, Eckert DM, Shen PS, Bass BL. 2024. Caenorhabditis elegans Dicer acts with the RIG-I-like helicase DRH-1 and RDE-4 to cleave dsRNA. eLife 13: RP93979). Cryo-EM structures of Dicer-1 in complex with DRH-1, RNAi deficient-4 (RDE-4), and dsRNA provide mechanistic insights into how these three proteins cooperate in antiviral defense. The dsRNA backbone is depicted by green and red ribbons. The U-A pairs of the poly(A)·poly(U) model are shown as long rectangular cyan blocks, with minor-groove edges colored white. The ADP ligand is represented by a red block and the protein by a gold ribbon. Cover image provided by X3DNA-DSSR, an NIGMS National Resource for structural bioinformatics of nucleic acids (R24GM153869; skmatics.x3dna.org). Image generated using DSSR and PyMOL (Lu XJ. 2020. Nucleic Acids Res 48: e74).

How are the detailed steps used to generate the above cover image, using DSSR v2.4.6-2024nov15:

Code: Bash

1. # Download the PDB structure in cif format from RCSB
2. wget https://files.rcsb.org/download/8t5s-assembly1.cif -O 8t5s.cif
3.  
4. # Run DSSR with the following settings. See below for file "8t5s-specific.pml"
5. x3dna-dssr -i=8t5s.cif \
6.            --blocview=png-session-black \
7.            --block-file=wc-g4 \
8.            --block-depth=1.0 \
9.            --pymol-ray-size=5000 \
10.            --pymol-aa-color=gold \
11.            --block_color="minor:white" \
12.            --cartoon-cmd-file=8t5s-specific.pml \
13.            -o=8t5s.pml
14.  
15. # Run PyMOL to render the image. Here it is from the command line.
16. # You can also load the 8t5s.pml into PyMOL interactively.
17. # Generate file "8t5s-pymol.png"
18. pymol -Qkc 8t5s.pml
19.  
20. # Use ImageMagick to trim extra margins
21. magick 8t5s-pymol.png -trim +repage -bordercolor black -border 120 8t5s.png

Note the setting of black background, and coloring of minor-groove edge in white. By default, DSSR-PyMOL renders with a white background and black minor-groove edges, as in 8t5s. Whenever feasible, I've integrated features into DSSR to automate routine tasks as much as possible.

Here are the related files:

• 8t5s-specific.pml -- specific settings
• 8t5s.pse -- PyMOL session file
• 8t5s.pml -- PyMOL script file
• -- ray-traced image

Moreover, the following 30 [12(2021) + 12(2022) + 6(2023)] cover images of the RNA Journal were generated by the NAKB (nakb.org).

Cover image provided by the Nucleic Acid Database (NDB)/Nucleic Acid Knowledgebase (NAKB; nakb.org). Image generated using DSSR and PyMOL (Lu XJ. 2020. Nucleic Acids Res 48: e74).

47

FAQs / Re: How to set up 3DNA on Windows with WSL2

« on: December 14, 2024, 08:41:59 am »

Hi Chian,

Thanks for using 3DNA. Working in native Windows command-line (cmd or PowerShell) has seen lots of troubles, as evidenced from this long thread. I've split the thread so it is easier to see the new posts.

Since you are on Windows 11, please install WSL2 (Window Subsystem for Windows). The default ubuntu system is good to get 3DNA up and running quickly. Please have a try and report back how it goes.

Xiang-Jun

48

FAQs / Re: Running DSSR on macOS

« on: November 08, 2024, 09:30:04 pm »

As a follow up, please note that:

The CTV distributes DSSR Basic and Pro versions in zip format for macOS, Linux, and Windows. Each zip file contains a DSSR binary executable as well as the associated user manual.

Assuming basic command-line knowledge, users should be able to follow the instructions in the manual and reproduce reported results.

49

FAQs / Re: Running DSSR on macOS

« on: November 08, 2024, 06:46:53 pm »

Thanks for your interest in using DSSR. Your screenshot provides information that explains why you're having problems using DSSR.

You're on a macOS, and you have double-clicked the x3dna-dssr executable to run it. I can reproduce your case by installing x3dna-dssr under the ~/Downloads folder and double-clicking it. The error message is quite informative, by showing that x3dna-dssr is run, and immediately exit. Running x3dna-dssr without any options gives the following message:

missing required option: must specify -i=PDBFile/mmCIF

type: 'x3dna-dssr -h (or --help)' for further help
      'x3dna-dssr --citation' for preferred citation(s)

Time used: 00:00:00:00

That means DSSR is already successfully installed on your macOS. It is just that DSSR is a command-line (CLI) program, and you need a terminal window to run it. There are many online tutorials on how to get started using terminal on macOS. Here is one: Absolute BEGINNER Guide to the Mac OS Terminal. Once you are familiar with the terminal, running DSSR should be straightforward, as detailed in the User Manual.

The DSSR executable (x3dna-dssr for macOS and Linux, and x3dna-dssr.exe for Windows) is self-contained and does not rely on any third-party libraries. There is no need for any setup or configurations: type x3dna-dssr -h to verify your installation. Note that DSSR is a command-line program: you need a terminal window to run it.

If you're GUI-driven and do not want to use CLI at all, then you may find the following two resources helpful:

• DSSR-enabled Innovative Schematics of 3D Nucleic Acid Structures with PyMOL
• Web 3DNA 2.0 for the analysis, visualization, and modeling of 3D nucleic acid structures

Best regards,

Xiang-Jun

50

RNA structures (DSSR) / Re: plotting the helical axis along curved helices

« on: October 25, 2024, 08:46:14 pm »

Hi Di,

Do you have any idea of how to easily find the axis of each 2-bp segment of a helix?

The info is within DSSR, but not exposed. I'm considering to add this feature in DSSR JSON output for easy parsing. For WC-like pairs, things are not that complicated. However, with there are subtitles with non-Watson-Crick pairs, e.g., Hoogsteen and reverse Hoogsteen base pairs.

Also, I think an easier solution for A-form helix is to do a shift of the origin in the plane of the reference frame so that the shifted origin is where the axis passes through the plane.

See "Worked examples on base-pair parameters" in the DSSR Pro User Manual. especially Session "6 Local helical parameters". The vectors o1_h and o2_h are what you need. They are not simple shifts of the origin in the reference frame.

This thread actually prompt me to refine the detailed algorithmic descritpion and get the content published. They are the real meat of 3DNA!

Best regards,

Xiang-Jun