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View technical comparison →Boltz v0.1.1
Predict structures, screen molecules and proteins, and design binders
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Predict EGFR L858R binding to osimertinib
Developer declarations; not independently tested. Listing last checked Nov 6, 2026. Package observed Nov 6, 2026.
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Use Boltz from Codex for biomolecular modeling workflows: predict structure and binding for protein, RNA, DNA, and ligand complexes; rank small-molecule or protein libraries against targets; and design novel small molecules, peptides, antibodies, nanobodies, or custom protein binders with structures and confidence metrics.
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Interactive Write
Use Boltz from Codex for biomolecular modeling workflows: predict structure and binding for protein, RNA, DNA, and ligand complexes; rank small-molecule or protein libraries against targets; and design novel small molecules, peptides, antibodies, nanobodies, or custom protein binders with structures and confidence metrics.
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---
name: boltz-check-status
description: Boltz job status and result recovery. Use when listing jobs, checking progress, resuming downloads, recovering results, or downloading an existing job ID. Not for starting new jobs.
---
## 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 to recover state across sessions and to inspect or download results for prior Boltz jobs. No payload authoring — this skill only calls `list` / `retrieve` / `download-results` / `download-status`.
Use four modes:
1. Local progress: if the user knows the run name / run dir, prefer `download-status` before remote API calls.
2. List recent jobs: enumerate all six resources, merge, and sort by `created_at` descending.
3. Retrieve one job: use the job ID prefix when known; otherwise probe resources until one succeeds.
4. Resume/download results: run `download-results` with the original run name when possible. Never run `start` again to resume.
ADME jobs use the prefix `adme_pred_*` and show up in Modes 1-2 (`list` / `retrieve`) like the others. ADME has **no** `download-results`/archive step, so Modes 3-4 don't apply — recover its scores by re-running `retrieve` (read `output.molecules[]`) or from the local `run.json`.
Read [references/resume.md](references/resume.md) before recovering a dropped session, mapping job ID prefixes, or choosing a run name for `download-results`. Read [references/api.md](references/api.md) for per-resource `list` columns, `retrieve` fields, and result semantics.
## Command Pattern
```bash
# Replace placeholders with concrete absolute paths before running.
# Local helper: inspect local checkpoint state without API calls.
boltz-api --format json download-status \
--name "<run-name>" \
--root-dir "/absolute/path/boltz-experiments"
# Mode 1: list recent jobs across all 6 resources.
# Note: the CLI emits one JSON object per record (streamed, no {data:[]} wrapper).
# --limit is per-page and the CLI auto-paginates, so cap each explicit command with head.
boltz-api predictions:structure-and-binding list --limit 20 --format jsonl | head -20
boltz-api predictions:adme list --limit 20 --format jsonl | head -20
boltz-api small-molecule:library-screen list --limit 20 --format jsonl | head -20
boltz-api small-molecule:design list --limit 20 --format jsonl | head -20
boltz-api protein:library-screen list --limit 20 --format jsonl | head -20
boltz-api protein:design list --limit 20 --format jsonl | head -20
# Mode 2: retrieve by ID. Pick the resource from the ID prefix in the workflow
# notes above. If the prefix is unknown, run these one at a time until one succeeds.
boltz-api predictions:structure-and-binding retrieve --id "<job-id>" --format json
boltz-api predictions:adme retrieve --id "<job-id>" --format json
boltz-api small-molecule:library-screen retrieve --id "<job-id>" --format json
boltz-api small-molecule:design retrieve --id "<job-id>" --format json
boltz-api protein:library-screen retrieve --id "<job-id>" --format json
boltz-api protein:design retrieve --id "<job-id>" --format json
# Mode 3: resume download. Use the agent runtime's managed long-running command mode.
boltz-api download-results \
--id "<job-id>" --name "<run-name>" \
--root-dir "/absolute/path/boltz-experiments" \
--poll-interval-seconds 30
```
## Always Do This
- If the user has a run name / slug or run dir and only wants local downloader state, prefer `download-status` before `retrieve`.
- Use an absolute output root and keep passing it through `--roPreview of the first 4,000 characters. Read full instructions →
Referenced files: 3 — file references are metadata, not package contents.
---
name: boltz-cli-setup
description: Boltz CLI setup and auth. Use when installing, updating, verifying, or authenticating `boltz-api`, or fixing missing CLI, PATH, sandbox, browser login, or auth errors.
---
# Boltz CLI Setup
Use this skill for `boltz-api` installation, version, PATH, and authentication issues. The workflow skills assume `boltz-api` is already installed.
## Verify Installation
Check that the CLI is available:
```sh
boltz-api --version
```
If `boltz-api` is missing or too old, prefer a version-pinned release artifact
whose checksum or signature can be verified. If Boltz does not publish one for
the user's platform, its official installer is the fallback.
Before downloading or running either installer, show the exact platform command
and obtain the user's explicit confirmation. Explain that the command downloads
mutable remote code, executes it as the user outside the sandbox, and therefore
trusts `install.boltz.bio` at execution time. A general request to use or install
Boltz is not confirmation for this specific risk.
macOS and Linux:
```sh
curl -fsSL https://install.boltz.bio/boltz-api/install.sh | sh
```
Windows PowerShell:
```powershell
irm https://install.boltz.bio/boltz-api/install.ps1 | iex
```
The installer updates an existing `boltz-api` on `PATH`. If no binary is found, it installs to a user-local bin directory. Add the installed binary to `PATH` if `boltz-api --version` is still not found after install.
The sandbox can block browser login, OAuth callbacks, temp files, credential
storage, and user-wide install paths. Request the host sandbox bypass/escalation
needed for installation only after the installer confirmation above. The host
approval must cover the exact command; do not treat an ordinary setup request as
authorization to execute mutable remote code outside the sandbox.
Read [references/sandbox.md](references/sandbox.md) when an agent sandbox blocks the installer, browser auto-open, OAuth callback, credential storage, temp files, or global install path.
## Authenticate
Check the current auth state with:
```sh
boltz-api auth status
```
If `auth status` reports unauthenticated, or any Boltz command fails because authentication is missing or expired, start device-code login on the user's behalf before retrying:
```sh
boltz-api auth login --device-code
```
Do not ask the user for permission before starting device-code login; relaying the login URL/code and waiting for the CLI to complete is part of auth recovery. When sharing the authentication login URL/code, tell the user to use exactly `boltz-api auth login --device-code`.
For auth recovery, assume the CLI can auto-open the browser and run the exact command above. In sandboxed environments, request the host sandbox bypass/escalation needed for browser auto-open, OAuth callbacks, credential storage, or temp files.
For automation, an API key is still supported when it is already provisioned in
the environment:
```sh
test -n "${BOLTZ_API_KEY:+configured}" && echo "BOLTZ_API_KEY is configured"
```
Never ask the user to paste an API key into chat or a command, and never print,
log, or persist it in shell history or generated files. If the variable is not
already provisioned, direct the user to their host's secret-management facility.
## Version Checks
Do not hard-code expected commands or minimum versions in this skill. Treat the CLI's own update check as the source of truth.
When `boltz-api` reports that an update is available or required, relay that message and the install command it provides. The CLI may get this from a Boltz-hosted version metadata endpoint such as `/cli/version`, returning latest version, minimum supported version, whether an update is required, and platform-appropriate install instructions.
If a user asks why the CLI thinks it is stale, explain the split:
- GitHub Releases define which CLI binaries are available to install.
- The Boltz version endpoint defines API compatibility, including the Preview of the first 4,000 characters. Read full instructions →
Referenced files: 2 — file references are metadata, not package contents.
--- name: boltz-protein-design description: 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. --- ## 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](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` —
Preview of the first 4,000 characters. Read full instructions →
Referenced files: 11 — file references are metadata, not package contents.
---
name: boltz-protein-screen
description: Screen existing protein binders with Boltz. Use when ranking a supplied protein, peptide, antibody, nanobody, or binder library against a target. Not for designing new proteins or screening small molecules.
---
## 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 already has candidate proteins / peptides / antibodies / nanobodies.
1. Normalize the binder library into `proteins` — a list of candidate complexes. For a simple sequence library each entry has one protein entity; multi-chain candidates (antibody heavy+light) are also allowed.
2. Pick the target variant:
- `structure_template` — user has a CIF/PDB file or URL; select which chains are polymer vs ligand, which residues to keep (`crop_residues`), and optionally `epitope_residues` / `flexible_residues`.
- `no_template` — user has only sequences; pass them as `target.entities` plus optional `epitope_residues`.
3. Don't add `bonds` / `constraints` unless the user asks for geometry constraints.
4. Author the payload YAML or JSON, run `estimate-cost`, show the USD cost, wait for explicit confirmation.
5. `start` to submit. Capture the ID.
6. 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.
7. Rank hits 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](references/results.md) for output layout and metric details.
## Command Pattern
```bash
# Replace placeholders with concrete absolute paths before running.
# Use a short descriptive run name, for example: protein-screen-<target>-<library>-v1
boltz-api protein:library-screen estimate-cost \
--input @yaml:///absolute/path/payload.yaml
boltz-api protein:library-screen 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 30
```
Payload keys are `proteins`, `target` — API body field names.
## Always Do This
- For `structure_template`, embed CIF/PDB bytes with `@data:///abs/path/target.cif` inside the `structure.data` field. Don't use bare `@path` (automatic file-type detection once senPreview of the first 4,000 characters. Read full instructions →
Referenced files: 3 — file references are metadata, not package contents.
---
name: boltz-small-molecule-adme
description: Predict Tier-1 ADME/ADMET for small molecules with Boltz from bare SMILES — no target, no docking. Use when the user wants solubility, permeability, or lipophilicity/logD for a molecule or list of molecules. Not for ranking molecules against a protein target (use boltz-small-molecule-screen, which already returns ADME free).
---
## 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 for standalone ADME triage on SMILES the user already has. No protein target is involved. If the user is also screening or docking those molecules against a target, prefer `boltz-small-molecule-screen` — it returns the same ADME block free as part of the screen.
1. Normalize the molecules from raw SMILES, a CSV (auto-detect the SMILES column), `.smi`, or `.txt` into the `molecules` list. Each entry is `{smiles, id?}`; the optional `id` is echoed back as `external_id` on each result so you can map results to inputs.
2. **Hard cap: 128 molecules per request.** If the list exceeds 128, split into batches of ≤128 and submit one request per batch (suffix the run name, for example `-b1`, `-b2`), then merge results. Never send more than 128 in one call — the API rejects it with `VALIDATION_ERROR: input.molecules must contain at most 128 items`.
3. Author the payload YAML or JSON, run `estimate-cost`, show the USD cost, wait for explicit confirmation. ADME is priced at **$0.01 per molecule** (size-independent); `estimate-cost` returns the authoritative total — always quote it.
4. `run` to submit and wait — ADME finishes in seconds, so it is synchronous and needs no background polling. `run` persists results locally under `--root-dir/<run-name>/`.
5. Report from `<output-root>/<run-name>/run.json` → `output.molecules[]`. For each molecule show `external_id` (or `smiles`), `solubility`, `permeability`, and `lipophilicity`. The three values live under each molecule's `adme` object. Call out any molecule with `status: failed` and its `error` (an object `{code, message}`, e.g. code `adme_enumeration_failed`, message `Invalid SMILES`) — `adme` is `null` there; one bad SMILES fails only that molecule, not the batch. Read [references/results.md](references/results.md) for the output layout and [references/api.md](references/api.md) for the payload and batching details.
ADME values are approximate estimates for triage and ranking, not absolute measurements.
## Command Pattern
```bash
# Replace placeholders with concrete absolute paths before running.
# Use a short descriptive run name, for example: adme-<library>-v1
boltz-api predictions:adme estimate-cost \
--model adme-v1 --input @yaml:///absolute/path/payload.yaml
# `run` is synchronous (submit + wait + persist) and finishes in seconds — no background mode needed.
# Claude Code: run as a normal Bash command. Codex: run as a foreground shell command; if Codex
# returns a session_id because it is still running, poll it. Do not append "&" or use nohup in Codex.
boltz-api predictions:adme run \
--model adme-v1 \
--idempotency-key "<run-name>" \
--input @yaml:///absolute/path/payload.yaml \
--name "<run-name>" \
--root-dir "/absolute/path/boltz-experiments" \
--poll-interval-seconds 5
# -> /absolute/path/boltz-experiments/<run-name>/run.json (output.molecules[].adme)
```
Payload is just a `molecules` list — the API body field name, not the direct CLI flag. `--model adme-v1` is required.
## Always Do This
- Keep payload field names exactly as the API body Preview of the first 4,000 characters. Read full instructions →
Referenced files: 3 — file references are metadata, not package contents.
---
name: boltz-small-molecule-design
description: Design new small-molecule binders with Boltz. Use when generating novel ligands or hits for a target without a fixed compound library. Not for screening existing molecules or one-off docking.
---
## 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 small-molecule binders (no existing library).
1. Normalize the target: one or more protein sequences into `target.entities`, plus optional `pocket_residues` (0-based) and/or `reference_ligands` (known binders to help locate the pocket).
2. Pick `num_molecules` — valid range **10 to 1,000,000** (server rejects outside it). If the user says fewer than 10, explain the floor and propose 10.
3. Only add `chemical_space` (e.g. `"enamine_real"`) if the user explicitly wants generation restricted to synthesizable molecules within that library.
4. Supported optional features include `chemical_space` and `molecule_filters`; only add them on explicit request. Read [references/api.md](references/api.md) for exact shapes and filter options.
5. Author the payload YAML or JSON, run `estimate-cost`, show the USD cost, wait for explicit confirmation. Cost is a flat $0.025 per molecule (size-independent); still quote `estimated_cost_usd` from the response as the authoritative total.
6. `start` to submit (synchronous). Capture the ID.
7. Launch `download-results` with the agent runtime's background/non-blocking command facility; it polls, paginates, downloads per-hit structures, and exits when terminal. 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.
8. Rank hits from `<output-root>/<run-name>/results/index.jsonl` by `binding_confidence` for hit discovery or `optimization_score` for lead optimization. Each generated molecule also carries a free `adme` block (`solubility`, `permeability`, `lipophilicity`) — surface it for developability triage when the user cares about ADME, or when a top hit looks risky. Read [references/results.md](references/results.md) for output layout and metric details.
## Command Pattern
```bash
# Replace placeholders with concrete absolute paths before running.
# Use a short descriptive run name, for example: sm-design-<target>-<batch>-v1
boltz-api small-molecule:design estimate-cost \
--input @yaml:///absolute/path/payload.yaml
boltz-api small-molecule: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-rPreview of the first 4,000 characters. Read full instructions →
Referenced files: 3 — file references are metadata, not package contents.
---
name: boltz-small-molecule-screen
description: Screen existing small-molecule libraries with Boltz. Use when docking, scoring, or ranking a supplied SMILES or compound library against a target; also returns free Tier-1 ADME/ADMET (solubility, permeability, lipophilicity/logD) per molecule. Not for de novo molecule design, one-off docking, or ADME on bare SMILES with no target (use boltz-small-molecule-adme).
---
## 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 already has candidate molecules.
1. Normalize the library from raw SMILES, a CSV (auto-detect the SMILES column), `.smi`, or `.txt` into the `molecules` list. Each entry is `{smiles, id?}`; the optional `id` is echoed back as `external_id` on each result.
2. Normalize the target: one or more protein sequences into `target.entities`, plus optional `pocket_residues` (0-based) and/or `reference_ligands` (SMILES of known binders to help locate the pocket).
3. Keep default server-side filtering unless the user asks for custom filters — only add `molecule_filters` on explicit request.
4. Author the payload YAML or JSON, run `estimate-cost`, show the USD cost, wait for explicit confirmation.
5. `start` to submit (synchronous). Capture the ID.
6. Launch `download-results` with the agent runtime's background/non-blocking command facility — it polls, paginates `list-results`, downloads every per-hit structure, and exits when terminal. 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.
7. When done, rank from `<output-root>/<run-name>/results/index.jsonl`. Sort by `binding_confidence` for hit discovery or `optimization_score` for lead optimization; these are parallel intents, not a fallback hierarchy. Report the top 5-10 hits with `smiles`, the chosen ranking metric, key confidence metrics, and structure path. Each result also carries a free `adme` block (`solubility`, `permeability`, `lipophilicity`) — include it for developability triage when the user cares about ADME, or when a top hit looks risky. Read [references/results.md](references/results.md) for output layout, metrics, ADME, and filtered-input accounting.
## Command Pattern
```bash
# Replace placeholders with concrete absolute paths before running.
# Use a short descriptive run name, for example: sm-screen-<target>-<library>-v1
boltz-api small-molecule:library-screen estimate-cost \
--input @yaml:///absolute/path/payload.yaml
boltz-api small-molecule:library-screen 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 thePreview of the first 4,000 characters. Read full instructions →
Referenced files: 3 — file references are metadata, not package contents.
---
name: boltz-structure-and-binding
description: Predict structures and binding for one defined complex with Boltz. Use when folding a protein, RNA, DNA, or ligand complex, docking one ligand, predicting an interface, or scoring binding. Not for screening libraries or design.
---
## 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 for one defined complex, not a library workflow.
1. Normalize the inputs into `entities`. Each entity is **`{type, chain_ids, value}`** — note plural `chain_ids` (an array, even for one chain) and the field is `value`, **not** `sequence`:
```json
{"entities": [{"type": "protein", "chain_ids": ["A"], "value": "MKTAYIAKQRQISFVKSHFSRQ"}]}
```
`type` is one of `protein | rna | dna | ligand_smiles | ligand_ccd`. Chain IDs go in entity order (`A`, `B`, `C`, …) unless the user specifies otherwise. Read `references/api.md` for per-type field variants (`cyclic`, `modifications`, ligand CCD codes, etc.) **before** authoring your first payload — agent guesses like `sequence:` or `chain_id: "A"` (singular) fail with unclear 400 errors.
2. If the user wants binding metrics, add a flat `binding` block with an explicit `type` field. For ligand-protein binding use:
```yaml
binding:
type: ligand_protein_binding
binder_chain_id: B
```
For protein-protein binding use:
```yaml
binding:
type: protein_protein_binding
binder_chain_ids: [B]
```
Do not nest the variant name under `binding` (for example, no `binding.ligand_protein_binding` object).
3. Supported optional features include `constraints`, `bonds`, `modifications`, `model_options`, and binding metrics; only add them if the user asks. Read [references/api.md](references/api.md) for exact shapes and examples.
4. Author the payload YAML or JSON, run `estimate-cost`, show the USD cost, wait for explicit confirmation.
5. `start` to submit (synchronous). Capture the ID.
6. Launch `download-results` with the agent runtime's background/non-blocking command facility so polling + download continue without blocking the agent session. 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.
## Command Pattern
```bash
# Replace placeholders with concrete absolute paths before running.
# Use a short descriptive run name, for example: sab-<target>-<ligand>-v1
# 1. estimate
boltz-api predictions:structure-and-binding estimate-cost \
--model boltz-2.1 \
--input @yaml:///absolute/path/payload.yaml
# 2. confirm with user, then submit
boltz-api predictions:structure-and-binding start \
--model boltz-2.1 \
--idempotency-key "<run-name>" \
--input @yaml:///absolute/path/payload.yaml \
--raw-output --transform id
# 3. Copy the printed job ID into this command, then launch it in the agent
# runtime's background/non-blocking moPreview of the first 4,000 characters. Read full instructions →
Referenced files: 3 — file references are metadata, not package contents.
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Package observed Nov 6, 2026.
Plugin_146eca281b788191ba8a689a3a96f977
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