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Hi , I would like to know about the generation of stomotosyte structure in protein sorting tutorial and how can I visualize the sorted protein on the surface? Thank you.
The text was updated successfully, but these errors were encountered:
You can visualise inclusions using Glyph option in Paraview (using vtu files). Also, if you convert a tsi file to a gro file using CNV script, then you can use VMD, which already visualises inclusions. To get a stomotosyte, you need to have a reduced-volume of below 0.5.
Hi , I would like to know about the generation of stomotosyte structure in protein sorting tutorial and how can I visualize the sorted protein on the surface? Thank you.
The text was updated successfully, but these errors were encountered: