Hi Charles-Alexandre, Unfortunately our “nucleotides” expert is away this week, so we may need to wait for a definitive answer. Your guess is probably right, but there is no user-interface way to set the slab-controlling atom names. The GUI just assumes they are pyrimidine or purine base types attached to C1’. I tried swapping C1’ and C2’ atom names (just using a text-editor) in the first 3 residues of PDB 481D (HNA duplex) and then could show them as slabs or ladder rungs seemingly attached to the ribbon. Some of the HNA atoms then had to behidden manually. However, I haven’t done the stuff you did with your own ribbon style, and it’s possible the name-swapping could cause some other problems. It may work, but admittedly it is inconvenient and inelegant! I hope this helps, Elaine ---------- Elaine C. Meng, Ph.D. UCSF Computer Graphics Lab (Chimera team) and Babbitt Lab Department of Pharmaceutical Chemistry University of California, San Francisco
On Apr 4, 2017, at 2:54 AM, Charles-Alexandre Mattelaer <charlesalexandre.mattelaer@kuleuven.be> wrote:
Dear Chimera-users
I'm currently doing modeling on hexitol nucleic acids and using Chimera to visualize the trajectories. Since the atoms in the hexitol-ring are numbered differently than in the standard ribose, Chimera has some difficulties displaying the correct ribbon (backbone) and slab (bases). I've been able to define my own ribbon style using the Ribbon Style Editor and creating a new ribbon style based on the standard 'nuleic acid' trace and replacing the existing backbone atoms with the corresponding atom names for the non-standard hexitol residues.
The main problem is setting a slab object to replace the base atoms. The 'nucleotide objects' settings are based on a glycosidic bond on the C1' of ribose. In HNA the glycosidic bonds are found on C2' of hexitol. I believe this is causing the problem. Additionally, I can add that using the 'ladder'-like objects, a gap between the 'steps' and the backbone occurs. (I've tried setting the base as anchor but to no avail.) I was wondering if there would be a way to redefine the anchor atom of the nucleotide objects? (I searched in the manual but haven't found any ways to redefine the anchor itself.) This would greatly improve visibility of larger oligonucleotides and would help me a lot.
Kind regards and thank you in advance
Charles-Alexandre Mattelaer