RosettaCommons / RosettaCommons/RFdiffusion
Picking Hotspot
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- Dominant language
- Python
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Description
Hello community, In the Design Binder feature of RFdiffusion, the authors have stated that “define an interface hotspot residues as any residue on the target chain that is within 10 Angstrom Cbeta-Cbeta distance of the binder chain.” As I understand, their “binder” here is protein/peptide. However, my target (I got it from PBD) is in a complex with a small molecule. So, in my case, how can I pick hotspots?
Contributor guide
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First steps
- Read the whole issue, then the project's contributing guide.
- Comment on the issue to say you are picking it up — it saves two people doing the same work.
- Fork the repository and make your change on a branch.
- Open a pull request that references the issue number.
Research direction
Start with the Design Binder hotspot definition quoted in the issue and the target complex obtained from PDB. Determine how hotspot selection should be handled when the target is bound to a small molecule, then document the applicable procedure and its completion criteria. No source file or test is named, so project structure and existing guidance will need to be located first.
Written by the indexing model from the issue text.
Assessment
- Tech stack
- python
- Domain
- machine-learning
- Issue type
- Documentation
- Difficulty
- 4/5
- Estimated time
- 3-5 days
- Activity status
- Stale
- Clarity
- Needs clarification
- Newbie friendliness
- 25/100