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Boltz Protein Design

OpenAIOfficialCreated by BoltzDistributed by OpenAI

  • Skill
  • Tool integration
  • Science and research
  • MIT
  • Low risk
  • Has scripts

From the author

Design new protein binders with Boltz. Use when generating protein, peptide, antibody, nanobody, or custom binder candidates for a target. Not for screening existing proteins or small molecules.
— the description by Boltz

AutoGineer summary

Written by AutoGineer from the skill’s own files, not by the author

This skill provides a structured workflow for designing new protein binders. It guides users through target normalization, binder specification selection, and campaign sizing. The process includes a mandatory cost estimation step and requires explicit user authorization before initiating any design run. It supports multiple design modalities, including curated antibody/nanobody scaffolds, structure-templated redesigns, and sequence-based generation.

What it does

  • Designs de novo protein, peptide, antibody, and nanobody candidates.
  • Supports target exploration for unknown or complex binding sites.
  • Provides cost estimation for design campaigns based on target and binder parameters.
  • Manages the submission and background download of generated design results.
  • Ranks generated binders based on binding confidence and interaction metrics.

When to use it

  • When you need to generate novel protein binders for a specific target.
  • When you require antibody or nanobody candidates.
  • When you have a well-characterized binding site and want to design directly.
  • When you need to explore potential binding sites on a new or large target.

Advantages

  • Integrates directly with the Boltz API for end-to-end design workflows.
  • Enforces a mandatory spending gate to prevent unauthorized costs.
  • Provides standardized ranking metrics for evaluating generated binder candidates.
  • Supports flexible design specifications from curated scaffolds to custom motifs.

Usage examples

“I need to design a nanobody for this target protein structure.”
The agent will initiate the target exploration or direct design workflow, confirm the use of curated nanobody scaffolds, and guide you through cost estimation before submission.
“Design a peptide binder for this specific epitope.”
The agent will normalize the target, configure the peptide design parameters, and prepare the payload for cost estimation.

Install

  1. Download the skill as a ZIP:

    https://mp-staging.autogineer.com/agent-skills/openai/boltz-protein-design/download
  2. Unzip it into the cross-client skills folder of your project:

    mkdir -p .agents/skills && unzip boltz-protein-design.zip -d .agents/skills

Documentation by Boltz

Workflow

If boltz-api is missing from PATH, use boltz-cli-setup for install/update guidance before retrying. If a command reports missing or expired authentication, use boltz-cli-setup to start boltz-api auth login --device-code before retrying; do not ask permission first. If the agent host sandbox blocks boltz-api install/auth/API calls, use boltz-cli-setup to request the host sandbox bypass/escalation needed for user-wide CLI install, browser login, credential storage, temp files, or API access before retrying.

Use this skill when the user wants de novo protein / peptide / antibody / nanobody binders.

  1. Decide on target exploration first (new targets). For a new target where the user hasn't already fixed the binding site and crop, your first action — before authoring a payload, normalizing the target, or running estimate-cost — is to raise the choice between a target-exploration pass and designing directly, with a recommendation for this target:

    • Unknown site, or a multi-domain / large target → recommend exploration (it scouts different input configurations for generation, ≈50 designs each, and finds the best before a full run).

    • A well-characterized site → it's fine to recommend going (mostly) direct, perhaps with a quick check of whether conditioning on the epitope beats letting the model find its own spot. State this plainly, as part of a conversation with the user about their target and goals, and let them choose.

    Phrase it as a question that works with the user (they may know their target's biology), e.g.:

    "This is a fresh target — I'd suggest a quick exploration pass that scouts a few framings and picks the best before a full run. Or, if you already know the site and crop, we can design directly. Which would you like?"

    Do not mention a campaign size or tier here — not even folded into this opening approach question. The full-run size is settled later, after the scouting runs pick a winner (its yield informs the tier), so don't ask it up front when exploration is on the table. If the user opts into exploration — or has already said they want to explore / let the design find its own epitope — read references/target-exploration.md, follow it, then resume at step 8 with the chosen framing and recommended num_proteins. If they want to design directly, continue below.

  2. Normalize the target (same shape as protein-screen): structure_template if a CIF/PDB is available, else no_template.

  3. Pick the binder_specification variant. Supported variants include:

    • boltz_curated — recommended default for antibody and nanobody design. Boltz selects from maintained scaffold/template lists (binder: boltz_antibody or boltz_nanobody).

    • structure_template — redesign motifs in an existing binder scaffold (CIF + design_motifs with replacement / insertion segments).

    • no_template — generate from the sequence DSL (fixed residues + designed segments like 5..10 or 8).

  4. For antibody or nanobody requests, ask before authoring the payload: "I recommend Boltz's curated antibody/nanobody scaffolds for this. Do you want the curated default, or do you have custom scaffold structures/CDR motifs to use?" If the user picks curated, use type: boltz_curated; if they want custom scaffold control, use type: structure_template.

  5. Pick modality: peptide, antibody, nanobody, or custom_protein for structure_template and no_template (use custom_protein for a "miniprotein" or generic "protein binder"). If the user already named the modality, take it as given — don't ask again. Do not include modality on boltz_curated; use binder instead.

  6. Pick num_proteins — see Run sizing. Valid range is 10 to 1,000,000 (server rejects outside it); 10 is the hard floor but it is a test size, not a campaign. When the user has not given a count, propose a campaign tier (default 50,000), not the floor.

  7. Supported optional features include rules such as excluded amino acids, excluded sequence motifs with X wildcards, and max hydrophobic fraction. Add rules only on request; read references/api.md for exact shapes and examples.

  8. Author the payload YAML or JSON, then run estimate-cost and apply the spending gate (Always Do This) before start. (Cost model — tiered by total complex length, estimate-cost is the only source: see ## Cost in api.md.)

  9. start to submit. Capture the ID.

  10. Launch download-results with the agent runtime's background/non-blocking command facility. In Claude Code, use Bash with run_in_background: true. In Codex, run download-results as a foreground shell command with yield_time_ms: 1000; if Codex returns a session_id, keep it for optional same-thread polling, but treat download-status plus the run directory as the durable source of truth. In Codex app/desktop runtimes that expose same-thread heartbeat automations, create a heartbeat that checks download-status periodically and posts a concise completion or failure update when the download reaches a terminal state. After launching the downloader, always report the job ID, run name, and output directory. Include the next check cadence if the heartbeat was created; otherwise include the download-status command.

  11. Rank from <output-root>/<run-name>/results/index.jsonl by binding_confidence descending. Use iptm and min_interaction_pae as tiebreakers. optimization_score is not emitted for this endpoint. Read references/results.md for output layout and metric details.

Run sizing

De novo design is a generate-and-filter campaign: you make many binders and keep the rare good ones, so a real run is large. Do not anchor on the num_proteins floor of 10 — that is only useful for a quick setup test. When the user names a count, honor it (≥10). When they do not, explain the tiers and propose one:

Tiernum_proteinsWhen
Small screen20,000Quick look / tight budget
Medium (recommended)50,000Default for a real campaign
Large100,000Hard target / maximal coverage

Present the tiers as design counts, not dollars: don't put a price next to a tier unless estimate-cost returned it — run estimate-cost on the tier the user leans toward and show that figure, and never extrapolate one estimate across the others. Then apply the spending gate (Always Do This) before submitting. If the setup is unproven, suggest a small test run (tens of designs) or the full target-exploration pass first.

Command Pattern

# Replace placeholders with concrete absolute paths before running.
# Use a short descriptive run name, for example: protein-design-<modality>-<target>-v1

boltz-api protein:design estimate-cost \
  --input @yaml:///absolute/path/payload.yaml

boltz-api protein:design start \
       --idempotency-key "<run-name>" \
       --input @yaml:///absolute/path/payload.yaml \
       --raw-output --transform id

# Copy the printed job ID into this command, then launch it in the agent
# runtime's background/non-blocking mode.
# Claude Code: Bash with run_in_background=true.
# Codex: foreground shell command with yield_time_ms=1000; keep the returned session_id if one is provided.
# Do not append "&" or use nohup in Codex.
boltz-api download-results \
  --id "<job-id-from-start>" --name "<run-name>" \
  --root-dir "/absolute/path/boltz-experiments" \
  --poll-interval-seconds 60

Payload keys are num_proteins, target, binder_specification — API body field names.

Always Do This

  • For a new target, your first move is the step-1 conversation — never jump straight to a payload. Establish what the binder is for and whether the user has already fixed the binding site/crop, then recommend a target-exploration pass vs. designing directly and let them choose (step 1). Only normalize the target and author a payload after that. If they've already fixed the site/crop or explicitly want to design directly, proceed.

  • Enforce 10 <= num_proteins <= 1,000,000 before calling estimate-cost (server rejects outside that range), but 10 is the floor, not a campaign — see Run sizing and propose a tier (default 50,000) when the user gives no count.

  • Spending gate — explicit go-ahead before every start. start spends real money. A plan you already described, an earlier phase's approval, or a cost that looks "trivial" are not authorization — even a cheap run needs a fresh yes. Run estimate-cost, show the estimated_cost_usd it returns (summed for a batch), and wait for the user to say go. This holds even when tool calls are pre-approved (accept-edits / auto-accept / bypass modes) — there you are the only cost gate. Never quote or assume a dollar figure you didn't get from estimate-cost (cost model: ## Cost in api.md).

  • For antibody or nanobody design, recommend binder_specification.type: boltz_curated and ask the user to confirm they do not want custom scaffold/CDR control before building the payload. Use binder: boltz_antibody for antibody/Fab requests and binder: boltz_nanobody for nanobody/VHH requests.

  • Residue indices are 0-based everywhere (design_motifs.start_index/end_index, after_residue_index, epitope_residues, flexible_residues, bonds, constraints).

  • For CIF/PDB bytes, use @data:///abs/path/file.cif inside structure.data. Don't use bare @path.

  • Sequence DSL for designed_protein.value: uppercase letters = fixed residues; integer N = exactly N designed residues; MIN..MAX = variable-length designed segment. Examples: "20", "5..10", "ACDE8GHI", "MKTAYI5..10VKSHFSRQ".

  • Keep payload field names exactly as the API body names shown in references/api.md.

  • Use absolute paths for the output root, payload files, and embedded target files. Do not cd into the run directory for follow-up commands; pass the same --root-dir and use absolute paths so later relative paths do not drift.

  • Prefer one merged top-level payload via --input @yaml:///absolute/path/payload.yaml or @json:///absolute/path/payload.json for estimate-cost and start. Keep --idempotency-key and --workspace-id top-level; if they also appear inside --input, the top-level flags win.

  • Direct object flags still work as overrides, such as --target @yaml:///absolute/path/target.yaml or --binder-specification @json:///absolute/path/binder.json. Piped YAML / JSON on stdin also works, but it must use API body field names. Use the same slug for both --idempotency-key and --name.

  • In permission-gated agents such as Claude Code, keep each Boltz call as a top-level command that starts with boltz-api. Prefer concrete arguments over sh -c, inline environment assignments, aliases, wrapper scripts, loops, or pipelines around the boltz-api invocation unless the user already allowed that exact command form. Use --raw-output --transform id, read the printed ID, then paste that literal ID into the next download-results command.

  • Prefer the agent runtime's background/non-blocking command mode for download-results. In Codex specifically, keep download-results in the foreground and set the shell tool yield to 1000 ms; Codex will return a session_id if the command is still running. Do not append & or use nohup in Codex because the tool runner may clean up shell-backgrounded descendants before .boltz-run.json is fully written.

  • After the background/session starts, do not manually wait on it or run ad hoc polling loops. Wall-clock time scales roughly with num_proteins: under 100 often finishes in a few minutes, 100-1,000 may take several minutes to tens of minutes, and larger runs can take longer or hours depending on inputs and system load. Don't quote a fixed duration. --poll-interval-seconds 60 is a sensible downloader default. download-results emits JSONL progress on stderr by default; add --progress-format text --verbose only when you explicitly want human-readable logs.

  • In Codex app/desktop runtimes with same-thread heartbeat automation support, schedule a heartbeat after launching download-results. The heartbeat should run boltz-api --format json download-status --name "<run-name>" --root-dir "/absolute/path/boltz-experiments" and stop once terminal. Choose cadence by num_proteins: under 100 -> every 1-2 minutes; 100-1,000 -> every 5 minutes; over 1,000 -> every 15 minutes. Post only material status changes or terminal completion/failure. Poll the saved session_id with an empty write_stdin only for interactive, user-requested progress checks. Never run a manual poll loop in the current turn.

  • If the current host has no heartbeat automation support, do not claim an automatic next check. Report the job ID, run name, output directory, and the command needed to check download-status.

  • If detached download needs to be restarted, re-run boltz-api download-results with the same --name "<run-name>" and the same --root-dir.

  • Only add rules on explicit user request.

Escape Hatch

Read references/api.md for all binder_specification variants, motif shapes, sequence DSL, rules, modalities, and target variants. Read references/results.md after download when ranking designed binders or explaining outputs.

Outputs

Rank from results/index.jsonl after download-results; use references/results.md for local file layout, metric meanings, and the designed-binder entity type gotcha.

Files

references/api.md

Protein Design — Payload Reference

Covers the protein:design endpoint. Prefer a single merged top-level --input payload. Field names are API body field names.

Minimal CLI pattern:

boltz-api protein:design estimate-cost --input @yaml:///absolute/path/payload.yaml
boltz-api protein:design start --idempotency-key "<run-name>" --input @yaml:///absolute/path/payload.yaml --raw-output --transform id

In permission-gated agents, keep the submit command as a top-level boltz-api ... start invocation. Read the printed job ID from stdout and paste it into the later download-results command.

Keep --idempotency-key and --workspace-id top-level; if they also appear inside --input, the top-level flags win. Direct object flags still work as overrides, such as --target @yaml:///absolute/path/target.yaml or --binder-specification @json:///absolute/path/binder.json. Piped YAML / JSON on stdin remains supported when you need it, but the body must use API field names.

Contents

  • Top-level request

  • num_proteins minimum

  • Cost

  • binder_specification — variant 1: boltz_curated

  • binder_specification — variant 2: structure_template

  • binder_specification — variant 3: no_template

  • Sequence DSL (designed_protein.value)

  • rules

  • target — variant 1: structure_template

  • target — variant 2: no_template

  • bonds and constraints shapes

  • Outputs (after download-results)

  • Escape hatch

Top-level request

# payload.yaml
num_proteins: 10
target:
  type: structure_template
  structure:
    type: base64
    media_type: chemical/x-cif
    data: "@data:///abs/path/target.cif"
  chain_selection:
    A:
      chain_type: polymer
      crop_residues: all
      epitope_residues: [42, 43, 44]
binder_specification:
  type: boltz_curated
  binder: boltz_nanobody
  rules:
    max_hydrophobic_fraction: 0.5

Top-level fields:

  • num_proteins (required) — number to generate. Must be between 10 and 1,000,000 (server rejects outside this range).

  • target (required) — discriminated union: structure_template or no_template. Identical shape to protein-screen.

  • binder_specification (required) — discriminated union: boltz_curated, structure_template, or no_template. See below.

Also passed as separate start flags:

  • --idempotency-key <slug>

  • --workspace-id <id> (admin keys only)

num_proteins minimum

Server rejects num_proteins < 10 or > 1000000 with VALIDATION_ERROR. Validate client-side before submitting.

Cost

Cost is tiered by total complex length (target crop + binder), not flat per design, and both the target crop and the designed binder count toward the length — so the tier is easy to misjudge. estimate-cost returns breakdown.{application, cost_per_unit_usd, num_units} — num_units equals num_proteins, and the complex-length effect rides in cost_per_unit_usd (small targets cost less per design, large ones materially more). It is the only source to use: quote estimated_cost_usd from it and never compute, estimate, or state a cost yourself.

binder_specification — variant 1: boltz_curated

Recommended default for antibody and nanobody design. Boltz chooses from maintained antibody/nanobody scaffold template lists during design. In the API docs this shape appears as BoltzCuratedBinderSpec on requests and BoltzCuratedBinderSpecResponse on retrieved run records. Before using it, ask the user to confirm they want the curated default rather than a custom scaffold with explicit CDR/motif control.

Use boltz_nanobody for nanobody/VHH requests and boltz_antibody for antibody/Fab requests. Do not include modality, entities, structure, or chain_selection in this variant.

binder_specification:
  type: boltz_curated
  binder: boltz_nanobody             # or boltz_antibody
  rules:
    excluded_sequence_motifs: [NXS]  # optional; only add rules on request

binder_specification — variant 2: structure_template

Use when redesigning regions of an existing binder scaffold.

binder_specification:
  type: structure_template
  modality: peptide                # or antibody | nanobody | custom_protein
  structure:
    type: url
    url: "https://example.com/binder.cif"
  chain_selection:
    B:
      chain_type: polymer
      crop_residues: all           # or [0, 1, 2, ...]
      design_motifs:
        - type: replacement
          start_index: 0           # 0-based, inclusive
          end_index: 5             # 0-based, **inclusive** — residues start_index..end_index are replaced
          design_length_range:
            min: 4
            max: 8
  rules:
    excluded_amino_acids: [C, P]
structure source variants

URL or base64 — same as target:

structure:
  type: base64
  media_type: chemical/x-cif
  data: "@data:///abs/path/binder.cif"   # prefer @data:// for local CIF/PDB bytes
chain_selection values

Polymer chain:

B:
  chain_type: polymer
  crop_residues: all               # or [int, ...]
  design_motifs:                    # see motif types below
    - ...

Ligand chain:

B:
  chain_type: ligand
Motif types
replacement
- type: replacement
  start_index: 0                    # 0-based, inclusive
  end_index: 5                      # 0-based, **inclusive**
  design_length_range:
    min: 4
    max: 8

Residues from start_index to end_index inclusive are replaced with a new designed segment. Example: on a 17-mer scaffold with start_index: 2, end_index: 15, residues 2..15 (14 residues) are redesigned and residues 0..1 + 16 stay fixed. Verify sequence length on a test output before committing to a template.

insertion
- type: insertion
  after_residue_index: 12           # 0-based; use -1 to insert before residue 0
  design_length_range:
    min: 3
    max: 6

All residue indices are 0-based.

binder_specification — variant 3: no_template

Use when generating from sequence components + the DSL. For antibody or nanobody requests, prefer boltz_curated unless the user confirms they want direct sequence/scaffold control.

binder_specification:
  type: no_template
  modality: custom_protein          # or peptide | antibody | nanobody
  entities:
    - type: designed_protein
      chain_ids: [B]
      value: "MKTAYI5..10VKSHFSRQ"
  bonds: []                          # optional
  rules:
    max_hydrophobic_fraction: 0.5

Constraints:

  • At least one entity must be type: designed_protein.

  • modifications on fixed protein/rna/dna entities is optional (defaults to []).

  • designed_protein does NOT take modifications.

  • If bonds references an atom in a designed protein chain, residue indices are counted against the minimum designed length for each DSL segment. Example: in 1..3C1..2, the fixed C is residue index 1 (0-based) because the first designed segment uses its minimum length of 1.

Allowed entity types in binder_specification.entities (for no_template):

  • designed_protein — the sequence DSL target

  • protein, rna, dna — fixed partners

  • ligand_smiles, ligand_ccd — fixed cofactors

Sequence DSL (designed_protein.value)

  • Uppercase amino acid letters stay fixed.

  • Bare integer N means a designed segment of exactly length N.

  • MIN..MAX means a designed segment with variable length from MIN to MAX.

Examples:

  • "20" — generate a 20-residue designed sequence

  • "5..10" — variable-length designed segment

  • "ACDE8GHI" — fixed ACDE, then 8 designed residues, then fixed GHI

  • "MKTAYI5..10VKSHFSRQ" — fixed prefix and suffix with a variable-length designed middle

rules

Optional, applies to all binder_specification variants. Any of:

  • excluded_amino_acids: [<one-letter codes>] — never emit these residues in designed positions.

  • excluded_sequence_motifs: [<motif strings>] — reject designs containing these patterns. Use X as a single-position wildcard (e.g. "XPX").

  • max_hydrophobic_fraction: <float> — cap hydrophobic content in designed regions.

target — variant 1: structure_template

target:
  type: structure_template
  structure:
    type: url
    url: "https://example.com/target.cif"
  chain_selection:
    A:
      chain_type: polymer
      crop_residues: all              # or [int, ...]
      epitope_residues: [42, 43, 44]  # optional; subset of crop_residues
      flexible_residues: [40, 41, 42] # optional; subset of crop_residues
      non_binding_residues: [50, 51]  # optional; subset of crop_residues, must NOT overlap epitope_residues

Same semantics as protein-screen: epitope_residues / flexible_residues must be subsets of crop_residues, all 0-based.

target — variant 2: no_template

target:
  type: no_template
  entities:
    - type: protein
      chain_ids: [A]
      value: "MKTAYIAKQRQISFVKSHFSRQ"
  epitope_residues:
    A: [42, 43, 44]                   # optional; 0-based
  non_binding_residues:
    A: [50, 51]                       # optional; 0-based; must NOT overlap epitope_residues
  epitope_ligand_chains: [L]          # optional
  bonds: []                           # optional
  constraints: []                     # optional

Optional fields: epitope_residues, non_binding_residues (residues where binder contact is discouraged — 0-based, within crop_residues, must not overlap epitope_residues), epitope_ligand_chains, bonds, constraints.

bonds and constraints shapes

Same as the structure-and-binding skill — see references/api.md of that skill for full detail. Only include when the user explicitly asks for geometry constraints.

Outputs (after download-results)

Under <output-root>/<run-name>/:

  • .boltz-run.json

  • run.json — sanitized remote run record

  • results/index.jsonl — one generated design per line, copied from list-results metadata plus local artifact paths

  • results/<pres_*>/metadata.json — per-result metadata copied from the list-results record

  • results/<pres_*>/archive.tar.gz — one dir per generated design

  • results/<pres_*>/files/result/{metrics.json, <result-id>_predicted.cif, pae.npz} (the CIF is named <pres_*>_predicted.cif — prefer the paths.structure field from index.jsonl over hard-coding the filename)

Per-result fields (available in results/index.jsonl, results/<pres_*>/metadata.json, and the list-results stream):

  • id — server-assigned pres_* ID

  • entities — generated designs. Type-flip gotcha: the binder entity comes back as type: "protein" (not "designed_protein"), with the DSL resolved to a real AA sequence in value. Select the binder by chain_ids (the ID assigned at submit time), not by type == "designed_protein" — the latter match returns zero results.

  • metrics.binding_confidence — primary ranking metric

  • metrics.structure_confidence

  • metrics.iptm (higher is better)

  • metrics.min_interaction_pae (lower is better)

  • metrics.helix_fraction, metrics.sheet_fraction, metrics.loop_fraction

  • artifacts.structure.url, artifacts.archive.url (presigned, short-lived)

  • warnings — optional array of {code, message} quality flags (e.g. low_confidence, unusual_geometry); empty or absent on clean results. Surface them when presenting top designs.

optimization_score is not emitted for protein:design. Sorting by it yields an empty list.

Rank from results/index.jsonl after download-results by binding_confidence descending. Use iptm (higher better) and min_interaction_pae (lower better) as tiebreakers.

Escape hatch

Requirements and compatibility

Written for: OpenAI Codex

Works with: Claude Code, Claude apps, OpenAI Codex, GitHub Copilot, Cursor, Gemini CLI, Kiro, OpenCode, Goose, Amp, Roo Code, JetBrains Junie, Factory Droid, Devin (ex-Windsurf), Mistral Vibe, OpenHands, Letta

“Works with” means the tool reads the open Agent Skills format; a skill written for one tool may use features others lack.

Needs: Needs Python

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Attribution and licence

Created by
Boltz
Publisher
OpenAI (Official)
Distributed by
OpenAI
Source
openai/plugins · plugins/boltz-api-cli/skills/boltz-protein-design · commit d420d13
Licence
MIT License (redistribution allowed)
  • LICENSE (added by AutoGineer from plugins/boltz-api-cli/LICENSE)
  • ATTRIBUTION.md (written by AutoGineer)
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