Hello, (A) yes you can use the ChimeraX tool Model Loops to model missing parts with Modeller as long as these parts are included in your sequence. See tool help for description and instructions: <https://rbvi.ucsf.edu/chimerax/docs/user/tools/modelloops.html> However, that may not produce a helical conformation. Alternatively there are other things you could try: (B) See if that protein is already in the AlphaFold Database or ESM Metagenomic Atlas of already-predicted structures. Often the prediction will be almost the same as the known part and additionally have the unknown part. See ChimeraX tools AlphaFold and ESMFold, and/or commands "alphafold match" "alphafold search" "esmfold match" "esmfold search" <https://rbvi.ucsf.edu/chimerax/docs/user/tools/alphafold.html> <https://rbvi.ucsf.edu/chimerax/docs/user/tools/esmfold.html> <https://rbvi.ucsf.edu/chimerax/docs/user/commands/alphafold.html> <https://rbvi.ucsf.edu/chimerax/docs/user/commands/esmfold.html> (C) If not in already-predicted structure databases, you could try running a new prediction with AlphaFold (if the sequence is not too long) or ESMFold. See links above for the tools, and/or commands "alphafold predict" "esmfold predict" These other approaches (B,C) might not produce a helix either, although my guess is that they are more likely than (A) to do so. If you absolutely want a helix there is yet another approach: (D) use Build Structure, Start Structure and build a helical peptide. Then just stick the peptide model onto your original protein model with the Join Models section of Build Structure. See tool help for description and instructions: <https://rbvi.ucsf.edu/chimerax/docs/user/tools/buildstructure.html> I hope this helps, Elaine ----- Elaine C. Meng, Ph.D. UCSF Chimera(X) team Resource for Biocomputing, Visualization, and Informatics Department of Pharmaceutical Chemistry University of California, San Francisco
On Aug 20, 2024, at 2:52 AM, Enrico Martinez via ChimeraX-users <chimerax-users@cgl.ucsf.edu> wrote:
Dear Chimera-X users !
Suppose I have a pdb structure with a missed C-terminal fragment corresponding to the transmembrane helical part that should anchor the protein in the membrane. Is it possible to use some built-in utilities (modeller?) to predict this missing fragment based on the full length sequence of the entire construct?
Many thanks in advance
Enrico