How to use
- Copy the installation command and review the source package before installing it in your own agent environment.
- Check the source document for required tools, credentials and supported hosts.
- Describe your input and desired deliverable; review the output against the source material.
npx skills add https://github.com/nvidia-bionemo/bionemo-agent-toolkit --skill protein-binder-designBefore you start
- Installation does not include a model subscription, API allowance or permission to access your files.
- Repository stars and installation counts describe activity, not an independent quality or security test.
Rendered from the source repository. Headings, examples, code, tables, links, and referenced images are preserved.
Protein Binder Design (workflow)
Run a de novo binder design campaign by composing atomic NIM skills. This skill owns orchestration, handoff contracts, filtering, validation, and the run manifest. It does NOT duplicate per-NIM API details — defer those to each atomic skill's SKILL.md.
Composed skills
| Step | Skill | Owns |
|---|---|---|
| Backbones | rfdiffusion-nim | binder backbone PDBs (contigs + hotspots) |
| Sequences | proteinmpnn-nim | sequences for each backbone |
| Co-fold / score | boltz2-nim or openfold3-nim | binder–target complex + confidence / ipTM |
| MSA (optional) | msa-search-nim | target A3M for higher-quality folding |
The atomic NIM skills are recommended companions (one per NIM, from the BioNeMo NIM skill set). They are not required: references/pipeline.md carries the concrete request shape for every NIM call, so an agent with NIM access can follow this skill standalone. For endpoints/auth see Configuration below.
Pipeline
- Target prep — get the target PDB + epitope; map epitope/hotspot author
residue numbers to RFdiffusion hotspot_res strings; optionally build a target MSA with msa-search-nim.
- Backbones (
rfdiffusion-nim) — binder contig +hotspot_res; N backbones. - Sequences (
proteinmpnn-nim) — k sequences per backbone; drop the
native/WT row from mfasta.
- Co-fold + score (
boltz2-nim/openfold3-nim) — co-fold binder+target;
collect interface confidence (ipTM) and binder pLDDT.
- Self-consistency — CA-RMSD between the RFdiffusion backbone and the
predicted binder (scripts/metrics.py).
- Filter + rank — apply thresholds; rank survivors; write manifest + CSV.
Full handoff contracts, branching, and the cost funnel: references/pipeline.md.
Handoff contracts (the fragile glue)
- RFdiffusion
output_pdb→ ProteinMPNNinput_pdb(inline PDB text). - ProteinMPNN
mfasta→ Boltz2 binder polymersequence(exclude the
native/WT row; pair scores only with designed rows).
- Epitope author residue numbers → 1-based sequence indices: remap with
scripts/pdb_utils.py:remap_to_seq_index. RFdiffusion hotspot_res uses chain+author strings like "A50"; Boltz2 pocket/contacts use 1-based indices.
- Boltz2 complex
.cif→ binder chain → self-consistency RMSD vs the backbone.
Run manifest (reproducibility backbone)
Every campaign writes manifest.json (+ candidates.csv) under a run dir via scripts/manifest.py. It records lineage, params, scores, artifacts, filter status, and controls — enabling ranking, resumability, validation, and the final report. Schema and usage: references/manifest.md.
Filters (defaults)
- ipTM ≥ 0.8, binder pLDDT ≥ 80, self-consistency RMSD ≤ 2.0 Å.
- Override per campaign and record overrides in the manifest
filters.
Validation
Always run controls and report a success rate, not just top scores. Negative controls via scripts/controls.py (scrambled sequences); positive controls = published binders re-scored through the same pipeline. Benchmark targets live in assets/targets.json (scripts/registry.py). Methodology and metric definitions: references/validation.md.
Human-in-the-loop + cost
- Confirm target, epitope/hotspots, binder length range, and hosted-vs-local
with the user before generating backbones (AskUserQuestion).
- Co-folding is the expensive stage: co-fold a capped shortlist, review, then
expand. State hosted vs local once and reuse it across all NIM calls.
Responsible use
De novo binder design is dual-use. Decline requests aimed at enhancing pathogen fitness, toxin potency, or bioweapon function; keep designs to legitimate research and therapeutic intent.
Configuration (NIM access)
Each composed NIM is reached over HTTP; choose hosted or local once and reuse it for every call:
- Hosted (managed): base URL
https://health.api.nvidia.com/v1/...per NIM at
build.nvidia.com; set NVIDIA_API_KEY (sent as Authorization: Bearer). Read keys from the env — never hardcode them.
- Local (self-hosted NGC containers): point each NIM at its local URL
(e.g. http://localhost:8000/...); local NIMs need no auth header. To launch the NIMs yourself (docker run per NIM, persistent caches, health checks, and the GPU profile‑selection gotcha — some NIMs (e.g. Boltz2) need NIM_MODEL_PROFILE pinned on GPUs that have no bundled profile, while others (RFdiffusion/ProteinMPNN) auto‑select by compute capability): see `references/local-nim-setup.md`.
Per-NIM paths, request/response schemas, and worked curl/Python examples live in references/pipeline.md.
Scripts
scripts/manifest.py— campaign manifest (create / load / score / filter / rank / CSV).scripts/pdb_utils.py— PDB parse, chain extract, sequence, residue remap, CA coords.scripts/metrics.py— Kabsch CA-RMSD for self-consistency.scripts/controls.py— scrambled negative controls.scripts/registry.py+assets/targets.json— example benchmark target
registry (illustrative epitopes — verify against the cited structure before a real campaign). Replace with your own targets.



