API Reference

Small Molecule

Design

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Resume a stopped small molecule design run

client.SmallMolecule.Design.Resume(ctx, id) (*SmallMoleculeDesignResumeResponse, error)

POST/compute/v1/small-molecule/design/{id}/resume

Resume a stopped small molecule design run from its last checkpoint

ParametersExpand Collapse

id string

ReturnsExpand Collapse

type SmallMoleculeDesignResumeResponse struct{…}

A small molecule design pipeline run that generates novel molecules

ID string

Unique SmDesignRun identifier

CompletedAt Time

formatdate-time

CreatedAt Time

formatdate-time

DataDeletedAt Time

When the input, output, and result data was permanently deleted. Null if data has not been deleted.

formatdate-time

DeprecatedEngine Boltzmol

Use pipeline instead.

Deprecated. Use pipeline instead.

DeprecatedEngineVersion String1_0

Use pipeline_version instead.

Deprecated. Use pipeline_version instead.

Error SmallMoleculeDesignResumeResponseError

Code string

Machine-readable error code

Message string

Human-readable error message

Details anyOptional

Additional field-level error details keyed by input path, when available.

Input SmallMoleculeDesignResumeResponseInput

Pipeline input (null if data deleted)

NumMolecules int64

Number of molecules to generate. Must be between 10 and 1,000,000.

minimum10

maximum1000000

Target SmallMoleculeDesignResumeResponseInputTarget

Target protein sequences for small molecule design or screening.

Entities []SmallMoleculeDesignResumeResponseInputTargetEntity

Protein entities defining the target structure. Each entity represents a protein chain.

ChainIDs []string

Chain IDs for this entity

Type Protein

Value string

Amino acid sequence (one-letter codes)

Cyclic boolOptional

Whether the sequence is cyclic

Modifications []SmallMoleculeDesignResumeResponseInputTargetEntityModificationOptional

CCD post-translational modifications. Optional; defaults to an empty list when omitted. SMILES modifications are not supported.

ResidueIndex int64

0-based index of the residue to modify

minimum0

Type Ccd

Modification format. Only CCD polymer modifications are supported.

Value string

CCD code from RCSB PDB (e.g. ‘MSE’ for selenomethionine, ‘SEP’ for phosphoserine)

Bonds []SmallMoleculeDesignResumeResponseInputTargetBondOptional

Covalent bond constraints between atoms in the target complex. Ligand atom references support CCD atom names and explicitly atom-mapped SMILES atoms.

Atom1 SmallMoleculeDesignResumeResponseInputTargetBondAtom1Union

Ligand atom reference for a CCD atom or an explicitly atom-mapped SMILES atom.

One of the following:

type SmallMoleculeDesignResumeResponseInputTargetBondAtom1LigandAtomResponse struct{…}

Ligand atom reference for a CCD atom or an explicitly atom-mapped SMILES atom.

AtomName string

Atom name. For ligand_ccd, use the standardized CIF atom name. For ligand_smiles, explicitly label the atom with numeric atom-map notation: [C:1] is referenced as C1 and [O:2] as O2. The resulting name must be unique within the molecule and at most four characters.

ChainID string

Chain ID containing the atom

Type LigandAtom

type SmallMoleculeDesignResumeResponseInputTargetBondAtom1PolymerAtomResponse struct{…}

AtomName string

Standardized atom name (verifiable in CIF file on RCSB)

ChainID string

Chain ID containing the atom

ResidueIndex int64

0-based residue index

minimum0

Type PolymerAtom

Atom2 SmallMoleculeDesignResumeResponseInputTargetBondAtom2Union

Ligand atom reference for a CCD atom or an explicitly atom-mapped SMILES atom.

One of the following:

type SmallMoleculeDesignResumeResponseInputTargetBondAtom2LigandAtomResponse struct{…}

Ligand atom reference for a CCD atom or an explicitly atom-mapped SMILES atom.

AtomName string

Atom name. For ligand_ccd, use the standardized CIF atom name. For ligand_smiles, explicitly label the atom with numeric atom-map notation: [C:1] is referenced as C1 and [O:2] as O2. The resulting name must be unique within the molecule and at most four characters.

ChainID string

Chain ID containing the atom

Type LigandAtom

type SmallMoleculeDesignResumeResponseInputTargetBondAtom2PolymerAtomResponse struct{…}

AtomName string

Standardized atom name (verifiable in CIF file on RCSB)

ChainID string

Chain ID containing the atom

ResidueIndex int64

0-based residue index

minimum0

Type PolymerAtom

Constraints []SmallMoleculeDesignResumeResponseInputTargetConstraintUnionOptional

Structural constraints (pocket and contact). Ligand atom references support CCD atom names and explicitly atom-mapped SMILES atoms.

One of the following:

type SmallMoleculeDesignResumeResponseInputTargetConstraintPocketConstraintResponse struct{…}

Constrains the binder to interact with specific pocket residues on the target.

BinderChainID string

Chain ID of the binder molecule

ContactResidues map[string, []int64]

Binding pocket residues keyed by chain ID. Each key is a chain ID (e.g. “A”) and the value is an array of 0-indexed residue indices that define the pocket on that chain.

MaxDistanceAngstrom float64

Maximum allowed distance in Angstroms between binder and pocket residues. Typical range: 4-8 A.

Type Pocket

Force boolOptional

Whether to force the constraint

type SmallMoleculeDesignResumeResponseInputTargetConstraintContactConstraintResponse struct{…}

Maximum-distance contact constraint between two polymer residues or ligand atoms.

MaxDistanceAngstrom float64

Maximum distance in Angstroms

Token1 SmallMoleculeDesignResumeResponseInputTargetConstraintContactConstraintResponseToken1Union

Ligand contact token for a CCD atom or an explicitly atom-mapped SMILES atom.

One of the following:

type SmallMoleculeDesignResumeResponseInputTargetConstraintContactConstraintResponseToken1PolymerContactTokenResponse struct{…}

ChainID string

Chain ID

ResidueIndex int64

0-based residue index

minimum0

Type PolymerContact

type SmallMoleculeDesignResumeResponseInputTargetConstraintContactConstraintResponseToken1LigandContactTokenResponse struct{…}

Ligand contact token for a CCD atom or an explicitly atom-mapped SMILES atom.

AtomName string

Atom name. For ligand_ccd, use the standardized CIF atom name. For ligand_smiles, explicitly label the atom with numeric atom-map notation: [C:1] is referenced as C1 and [O:2] as O2. The resulting name must be unique within the molecule and at most four characters.

ChainID string

Chain ID

Type LigandContact

Token2 SmallMoleculeDesignResumeResponseInputTargetConstraintContactConstraintResponseToken2Union

Ligand contact token for a CCD atom or an explicitly atom-mapped SMILES atom.

One of the following:

type SmallMoleculeDesignResumeResponseInputTargetConstraintContactConstraintResponseToken2PolymerContactTokenResponse struct{…}

ChainID string

Chain ID

ResidueIndex int64

0-based residue index

minimum0

Type PolymerContact

type SmallMoleculeDesignResumeResponseInputTargetConstraintContactConstraintResponseToken2LigandContactTokenResponse struct{…}

Ligand contact token for a CCD atom or an explicitly atom-mapped SMILES atom.

AtomName string

Atom name. For ligand_ccd, use the standardized CIF atom name. For ligand_smiles, explicitly label the atom with numeric atom-map notation: [C:1] is referenced as C1 and [O:2] as O2. The resulting name must be unique within the molecule and at most four characters.

ChainID string

Chain ID

Type LigandContact

Type Contact

Force boolOptional

Whether to force the constraint

PocketResidues map[string, []int64]Optional

Binding pocket residues, keyed by chain ID. Each key is a chain ID (e.g. “A”) and the value is an array of 0-indexed residue indices that define the binding pocket on that chain. When provided, these residues guide pocket extraction and add a derived pocket constraint during affinity predictions. That derived constraint remains separate from any explicit pocket constraints in target.constraints. When omitted, the model auto-detects the pocket.

ReferenceLigands []stringOptional

Reference ligands as SMILES strings that help the model identify the binding pocket. When omitted, a set of drug-like default ligands is used for pocket detection.

Type stringOptional

Target is defined directly by protein sequences rather than a structure template.

ChemicalSpace SmallMoleculeDesignResumeResponseInputChemicalSpaceOptional

Chemical space to constrain generated molecules. Use ‘enamine_real’ for the Enamine REAL chemical space or ‘none’ to disable chemical-space filtering.

One of the following:

const SmallMoleculeDesignResumeResponseInputChemicalSpaceEnamineReal SmallMoleculeDesignResumeResponseInputChemicalSpace = "enamine_real"

const SmallMoleculeDesignResumeResponseInputChemicalSpaceNone SmallMoleculeDesignResumeResponseInputChemicalSpace = "none"

IdempotencyKey stringOptional

Client-provided key to prevent duplicate submissions on retries

maxLength255

MoleculeFilters SmallMoleculeDesignResumeResponseInputMoleculeFiltersOptional

Molecule filtering configuration. Controls both Boltz built-in SMARTS filtering and custom filters.

BoltzSmartsCatalogFilterLevel SmallMoleculeDesignResumeResponseInputMoleculeFiltersBoltzSmartsCatalogFilterLevelOptional

Controls the stringency of Boltz’s built-in SMARTS structural alert filtering, which removes molecules matching known problematic substructures. ‘recommended’ (default): applies a curated set of alerts balancing safety and hit rate. ‘extra’: adds additional alerts beyond the recommended set for stricter filtering. ‘aggressive’: applies the most comprehensive alert set — may reject viable molecules. ‘disabled’: turns off Boltz SMARTS filtering entirely; only custom_filters will be applied.

One of the following:

const SmallMoleculeDesignResumeResponseInputMoleculeFiltersBoltzSmartsCatalogFilterLevelRecommended SmallMoleculeDesignResumeResponseInputMoleculeFiltersBoltzSmartsCatalogFilterLevel = "recommended"

const SmallMoleculeDesignResumeResponseInputMoleculeFiltersBoltzSmartsCatalogFilterLevelExtra SmallMoleculeDesignResumeResponseInputMoleculeFiltersBoltzSmartsCatalogFilterLevel = "extra"

const SmallMoleculeDesignResumeResponseInputMoleculeFiltersBoltzSmartsCatalogFilterLevelAggressive SmallMoleculeDesignResumeResponseInputMoleculeFiltersBoltzSmartsCatalogFilterLevel = "aggressive"

const SmallMoleculeDesignResumeResponseInputMoleculeFiltersBoltzSmartsCatalogFilterLevelDisabled SmallMoleculeDesignResumeResponseInputMoleculeFiltersBoltzSmartsCatalogFilterLevel = "disabled"

CustomFilters []SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterUnionOptional

Custom filters to apply. Molecules must pass all filters (AND logic).

One of the following:

type SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterLipinskiFilterResponse struct{…}

Lipinski’s Rule of Five filter. Rejects molecules that violate drug-likeness criteria based on molecular weight, LogP, hydrogen bond donors, and hydrogen bond acceptors.

MaxHba float64

Maximum number of hydrogen bond acceptors. Lipinski threshold: 10

MaxHbd float64

Maximum number of hydrogen bond donors. Lipinski threshold: 5

MaxLogp float64

Maximum LogP. Lipinski threshold: 5

MaxMw float64

Maximum molecular weight (Da). Lipinski threshold: 500

Type LipinskiFilter

AllowSingleViolation boolOptional

If true, one rule violation is allowed (classic Rule of Five). Defaults to false (all rules must pass).

type SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterRdkitDescriptorFilterResponse struct{…}

Filter molecules by RDKit molecular descriptors. Each descriptor is constrained to a min/max range. Only descriptors you provide are checked — omitted descriptors are unconstrained.

Type RdkitDescriptorFilter

FractionCsp3 SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterRdkitDescriptorFilterResponseFractionCsp3Optional

Min/max range constraint for an RDKit molecular descriptor

Max float64Optional

Maximum allowed value (inclusive)

Min float64Optional

Minimum allowed value (inclusive)

MolLogp SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterRdkitDescriptorFilterResponseMolLogpOptional

Min/max range constraint for an RDKit molecular descriptor

Max float64Optional

Maximum allowed value (inclusive)

Min float64Optional

Minimum allowed value (inclusive)

MolWt SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterRdkitDescriptorFilterResponseMolWtOptional

Min/max range constraint for an RDKit molecular descriptor

Max float64Optional

Maximum allowed value (inclusive)

Min float64Optional

Minimum allowed value (inclusive)

NumAromaticRings SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterRdkitDescriptorFilterResponseNumAromaticRingsOptional

Min/max range constraint for an RDKit molecular descriptor

Max float64Optional

Maximum allowed value (inclusive)

Min float64Optional

Minimum allowed value (inclusive)

NumHAcceptors SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterRdkitDescriptorFilterResponseNumHAcceptorsOptional

Min/max range constraint for an RDKit molecular descriptor

Max float64Optional

Maximum allowed value (inclusive)

Min float64Optional

Minimum allowed value (inclusive)

NumHDonors SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterRdkitDescriptorFilterResponseNumHDonorsOptional

Min/max range constraint for an RDKit molecular descriptor

Max float64Optional

Maximum allowed value (inclusive)

Min float64Optional

Minimum allowed value (inclusive)

NumHeteroatoms SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterRdkitDescriptorFilterResponseNumHeteroatomsOptional

Min/max range constraint for an RDKit molecular descriptor

Max float64Optional

Maximum allowed value (inclusive)

Min float64Optional

Minimum allowed value (inclusive)

NumRings SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterRdkitDescriptorFilterResponseNumRingsOptional

Min/max range constraint for an RDKit molecular descriptor

Max float64Optional

Maximum allowed value (inclusive)

Min float64Optional

Minimum allowed value (inclusive)

NumRotatableBonds SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterRdkitDescriptorFilterResponseNumRotatableBondsOptional

Min/max range constraint for an RDKit molecular descriptor

Max float64Optional

Maximum allowed value (inclusive)

Min float64Optional

Minimum allowed value (inclusive)

Tpsa SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterRdkitDescriptorFilterResponseTpsaOptional

Min/max range constraint for an RDKit molecular descriptor

Max float64Optional

Maximum allowed value (inclusive)

Min float64Optional

Minimum allowed value (inclusive)

type SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmartsCustomFilterResponse struct{…}

Filter molecules by custom SMARTS patterns. Molecules matching any pattern are rejected.

Patterns []string

SMARTS patterns. Molecules matching any pattern are rejected.

Type SmartsCustomFilter

type SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmartsCatalogFilterResponse struct{…}

Filter molecules using a predefined SMARTS catalog of structural alerts.

Catalog string

Predefined SMARTS catalog to apply. PAINS, BRENK, ChEMBL, and NIH catalogs reject known problematic substructures.

One of the following:

const SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmartsCatalogFilterResponseCatalogPains SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmartsCatalogFilterResponseCatalog = "PAINS"

const SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmartsCatalogFilterResponseCatalogPainsA SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmartsCatalogFilterResponseCatalog = "PAINS_A"

const SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmartsCatalogFilterResponseCatalogPainsB SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmartsCatalogFilterResponseCatalog = "PAINS_B"

const SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmartsCatalogFilterResponseCatalogPainsC SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmartsCatalogFilterResponseCatalog = "PAINS_C"

const SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmartsCatalogFilterResponseCatalogBrenk SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmartsCatalogFilterResponseCatalog = "BRENK"

const SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmartsCatalogFilterResponseCatalogChembl SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmartsCatalogFilterResponseCatalog = "CHEMBL"

const SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmartsCatalogFilterResponseCatalogChemblBms SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmartsCatalogFilterResponseCatalog = "CHEMBL_BMS"

const SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmartsCatalogFilterResponseCatalogChemblDundee SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmartsCatalogFilterResponseCatalog = "CHEMBL_Dundee"

const SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmartsCatalogFilterResponseCatalogChemblGlaxo SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmartsCatalogFilterResponseCatalog = "CHEMBL_Glaxo"

const SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmartsCatalogFilterResponseCatalogChemblInpharmatica SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmartsCatalogFilterResponseCatalog = "CHEMBL_Inpharmatica"

const SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmartsCatalogFilterResponseCatalogChemblLint SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmartsCatalogFilterResponseCatalog = "CHEMBL_LINT"

const SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmartsCatalogFilterResponseCatalogChemblMlsmr SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmartsCatalogFilterResponseCatalog = "CHEMBL_MLSMR"

const SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmartsCatalogFilterResponseCatalogChemblSureChEmbl SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmartsCatalogFilterResponseCatalog = "CHEMBL_SureChEMBL"

const SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmartsCatalogFilterResponseCatalogNih SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmartsCatalogFilterResponseCatalog = "NIH"

Type SmartsCatalogFilter

type SmallMoleculeDesignResumeResponseInputMoleculeFiltersCustomFilterSmilesRegexFilterResponse struct{…}

Filter molecules by regex patterns on their SMILES representation.

Patterns []string

Regex patterns applied to SMILES strings. Molecules matching any pattern are rejected.

Type SmilesRegexFilter

WorkspaceID stringOptional

Target workspace ID (admin keys only; ignored for workspace keys)

Livemode bool

Whether this resource was created with a live API key.

Pipeline Boltzmol

Pipeline used for small molecule design

PipelineVersion String1_0

Pipeline version used for small molecule design

Progress SmallMoleculeDesignResumeResponseProgress

NumMoleculesGenerated int64

Number of molecules generated so far

minimum0

TotalMoleculesToGenerate int64

Total number of molecules requested

minimum1

LatestResultID stringOptional

ID of the most recently generated result

StartedAt Time

formatdate-time

Status SmallMoleculeDesignResumeResponseStatus

One of the following:

const SmallMoleculeDesignResumeResponseStatusPending SmallMoleculeDesignResumeResponseStatus = "pending"

const SmallMoleculeDesignResumeResponseStatusRunning SmallMoleculeDesignResumeResponseStatus = "running"

const SmallMoleculeDesignResumeResponseStatusSucceeded SmallMoleculeDesignResumeResponseStatus = "succeeded"

const SmallMoleculeDesignResumeResponseStatusFailed SmallMoleculeDesignResumeResponseStatus = "failed"

const SmallMoleculeDesignResumeResponseStatusStopped SmallMoleculeDesignResumeResponseStatus = "stopped"

StoppedAt Time

formatdate-time

WorkspaceID string

Workspace ID

IdempotencyKey stringOptional

Client-provided idempotency key

Resume a stopped small molecule design run

Go

HTTP

TypeScript

Python

Go

CLI Tool

package main

import (
  "context"
  "fmt"

  "github.com/boltz-bio/boltz-api-go"
  "github.com/boltz-bio/boltz-api-go/option"
)

func main() {
  client := boltzapi.NewClient(
    option.WithAPIKey("My API Key"),
  )
  response, err := client.SmallMolecule.Design.Resume(context.TODO(), "id")
  if err != nil {
    panic(err.Error())
  }
  fmt.Printf("%+v\n", response.ID)
}

200 example

{
  "id": "id",
  "completed_at": "2019-12-27T18:11:19.117Z",
  "created_at": "2019-12-27T18:11:19.117Z",
  "data_deleted_at": "2019-12-27T18:11:19.117Z",
  "engine": "boltzmol",
  "engine_version": "1.0",
  "error": {
    "code": "code",
    "message": "message",
    "details": {}
  },
  "input": {
    "num_molecules": 10,
    "target": {
      "entities": [
        {
          "chain_ids": [
            "string"
          ],
          "type": "protein",
          "value": "value",
          "cyclic": true,
          "modifications": [
            {
              "residue_index": 0,
              "type": "ccd",
              "value": "value"
            }
          ]
        }
      ],
      "bonds": [
        {
          "atom1": {
            "atom_name": "atom_name",
            "chain_id": "chain_id",
            "type": "ligand_atom"
          },
          "atom2": {
            "atom_name": "atom_name",
            "chain_id": "chain_id",
            "type": "ligand_atom"
          }
        }
      ],
      "constraints": [
        {
          "binder_chain_id": "binder_chain_id",
          "contact_residues": {
            "A": [
              42,
              43,
              44,
              67,
              68,
              69
            ]
          },
          "max_distance_angstrom": 0,
          "type": "pocket",
          "force": true
        }
      ],
      "pocket_residues": {
        "A": [
          42,
          43,
          44,
          67,
          68,
          69
        ]
      },
      "reference_ligands": [
        "string"
      ],
      "type": "no_template"
    },
    "chemical_space": "enamine_real",
    "idempotency_key": "idempotency_key",
    "molecule_filters": {
      "boltz_smarts_catalog_filter_level": "recommended",
      "custom_filters": [
        {
          "max_hba": 0,
          "max_hbd": 0,
          "max_logp": 0,
          "max_mw": 0,
          "type": "lipinski_filter",
          "allow_single_violation": true
        }
      ]
    },
    "workspace_id": "workspace_id"
  },
  "livemode": true,
  "pipeline": "boltzmol",
  "pipeline_version": "1.0",
  "progress": {
    "num_molecules_generated": 0,
    "total_molecules_to_generate": 1,
    "latest_result_id": "latest_result_id"
  },
  "started_at": "2019-12-27T18:11:19.117Z",
  "status": "pending",
  "stopped_at": "2019-12-27T18:11:19.117Z",
  "workspace_id": "workspace_id",
  "idempotency_key": "idempotency_key"
}

Returns Examples

200 example

{
  "id": "id",
  "completed_at": "2019-12-27T18:11:19.117Z",
  "created_at": "2019-12-27T18:11:19.117Z",
  "data_deleted_at": "2019-12-27T18:11:19.117Z",
  "engine": "boltzmol",
  "engine_version": "1.0",
  "error": {
    "code": "code",
    "message": "message",
    "details": {}
  },
  "input": {
    "num_molecules": 10,
    "target": {
      "entities": [
        {
          "chain_ids": [
            "string"
          ],
          "type": "protein",
          "value": "value",
          "cyclic": true,
          "modifications": [
            {
              "residue_index": 0,
              "type": "ccd",
              "value": "value"
            }
          ]
        }
      ],
      "bonds": [
        {
          "atom1": {
            "atom_name": "atom_name",
            "chain_id": "chain_id",
            "type": "ligand_atom"
          },
          "atom2": {
            "atom_name": "atom_name",
            "chain_id": "chain_id",
            "type": "ligand_atom"
          }
        }
      ],
      "constraints": [
        {
          "binder_chain_id": "binder_chain_id",
          "contact_residues": {
            "A": [
              42,
              43,
              44,
              67,
              68,
              69
            ]
          },
          "max_distance_angstrom": 0,
          "type": "pocket",
          "force": true
        }
      ],
      "pocket_residues": {
        "A": [
          42,
          43,
          44,
          67,
          68,
          69
        ]
      },
      "reference_ligands": [
        "string"
      ],
      "type": "no_template"
    },
    "chemical_space": "enamine_real",
    "idempotency_key": "idempotency_key",
    "molecule_filters": {
      "boltz_smarts_catalog_filter_level": "recommended",
      "custom_filters": [
        {
          "max_hba": 0,
          "max_hbd": 0,
          "max_logp": 0,
          "max_mw": 0,
          "type": "lipinski_filter",
          "allow_single_violation": true
        }
      ]
    },
    "workspace_id": "workspace_id"
  },
  "livemode": true,
  "pipeline": "boltzmol",
  "pipeline_version": "1.0",
  "progress": {
    "num_molecules_generated": 0,
    "total_molecules_to_generate": 1,
    "latest_result_id": "latest_result_id"
  },
  "started_at": "2019-12-27T18:11:19.117Z",
  "status": "pending",
  "stopped_at": "2019-12-27T18:11:19.117Z",
  "workspace_id": "workspace_id",
  "idempotency_key": "idempotency_key"
}