structure-prediction-boltz-2

name	structure-prediction-boltz-2
description	Structure prediction using Boltz-2, an open biomolecular structure predictor. Use this skill when: (1) Predicting protein complex structures, (2) Validating designed binders, (3) Predicting protein-ligand complexes, (4) Using local GPU resources. For protein complex binding affinity evaluation, use prodigy.
license	MIT
category	design-tools
tags	["structure-prediction","protein complex","protein-ligand complex"]

Boltz-2 Structure Prediction

Prerequisites

Requirement	Minimum	Recommended
Python	3.10+	3.10
CUDA	12.0+	12.2
GPU VRAM	24GB	80GB (A800)
RAM	32GB	64GB

How to run

Local installation

pip install boltz[cuda] -U -i

Predict protein complex structure

import os, yaml, subprocess

def predict_protein_complex_structure(sequence_1, sequence_2, project_dir):
    """
    :param sequence_1: sequence of the first protein
    :param sequence_2: sequence of the second protein
    :param project_dir: path to the project
    :return structure of the protein complex in PDB format
    """
    # init project dir
    os.makedirs(project_dir, exist_ok=True)
    log_file = os.join(project_dir, 'log.txt')
    # init input yaml file
    data = {
        "sequences": [
            {
                "protein": {
                    "id": "A",
                    "sequence": sequence_1,
                    "msa": "empty"
                }
            },
            {
                "protein": {
                    "id": "B",
                    "sequence": sequence_2,
                    "msa": "empty"
                }
            },
        ]
    }
    input_file = os.path.join(project_dir, "input.yaml")
    with open(input_file, "w") as f:
        yaml.dump(data, f)
    # init output file
    output_dir = os.path.join(project_dir, "boltz")
    # prediction
    command = [
        'boltz', 'predict', input_file,
        "--out_dir", output_dir,
        '--use_msa_server',
        '--output_format', "pdb",
        "--seed", "42"
    ]
    with open(log_file, 'a') as f:
        process = subprocess.Popen(command, stdout=f, stderr=f, env=self.env)
        process.communicate()
    process.terminate()
    try:
        process.wait(timeout=5)
    except subprocess.TimeoutExpired:
        process.kill() 
        process.wait()

    # extract structure
    with open(os.path.join(output_dir, "boltz_results_input", "predictions", "input", "input_model_0.pdb"), 'r') as f:
        pred_struc = f.read()

    return pred_struc

# Predict protein complex structure for sequence_1 and sequence_2
# pred_structure is the structure prediction in PDB format
pred_structure = predict_protein_complex_structure(sequence_1, sequence_2, project_dir)

Predict protein ligand complex structure and IC50

import os, yaml, subprocess

def predict_protein_ligand_complex_affinity(sequence, smiles, project_dir):
    """
    :param sequence: sequence of the first protein
    :param smiles: SMILES string of the ligand
    :param project_dir: path to the project
    :return pred_struct: structure of protein-ligand complex in PDB format
    :return pred_ic50: binding affinity prediction of the protein-ligand complex
    """
    # init project dir
    os.makedirs(project_dir, exist_ok=True)
    log_file = os.join(project_dir, 'log.txt')
    # init input yaml file
    data = {
        "sequences": [
            {
                "protein": {
                    "id": "A",
                    "sequence": sequence,
                    "msa": "empty"
                }
            },
            {
                "ligand":{
                    "id": "B",
                    "smiles": smiles,
                }
            }
        ],
        "properties": [
            {
                "affinity":{
                    "binder": "B"
                }
            }
        ]
    }
    input_file = os.path.join(project_dir, "input.yaml")
    with open(input_file, "w") as f:
        yaml.dump(data, f)

    # init output file
    output_dir = os.path.join(project_dir, "boltz")
    # prediction
    command = [
        'boltz', 'predict', input_file,
        "--out_dir", output_dir,
        '--use_msa_server',
        , ,
        , 
    ]
     (log_file, )  f:
        process = subprocess.Popen(command, stdout=f, stderr=f, env=.env)
        process.communicate()
    process.terminate()
    :
        process.wait(timeout=)
     subprocess.TimeoutExpired:
        process.kill() 
        process.wait()

    
     (os.path.join(output_dir, , , , ), )  f:
        pred_ic50 = ( - json.load(f)[]) * 
    
     (os.path.join(output_dir, , , , ), )  f:
        pred_struc = f.read()

     pred_struc, pred_ic50




pred_structure, pred_ic50 = predict_protein_ligand_complex_affinity(sequence, smiles, project_dir):

Output format

Protein complex structure prediction

project_dir/boltz/boltz_results_input/predictions/input/
├── input_model_0.pdb               # structure prediction (PDB format)
├── confidence_input_model_0.json   # pTM, ipTM
├── pae_input_model_0.npz           # PAE matrix
└── plddt_input_model_0.npz         # pLDDT matrix

Protein-ligand complex structure prediction

project_dir/boltz/boltz_results_input/predictions/input/
├── input_model_0.pdb               # structure prediction (PDB format)
└── affinity_input.json             # affinity_pred_value

Decision tree

Should I use Boltz-2?
│
└─ What are you predicting?
   ├─ Structure prediction for general protein-protein complex → boltz-2 ✓
   ├─ Structure prediction for protein-ligand complex → boltz-2 ✓
   ├─ Antibody and nanobody structure prediction → tfold
   └─ Antigen-antibody structure prediction → tfold

Typical performance

Campaign Size	Time (L40S)	Cost (Modal)	Notes
100 complexes	30-45 min	~$8	Standard validation
500 complexes	2-3h	~$35	Large campaign
1000 complexes	4-6h	~$70	Comprehensive

Per-complex: ~15-30s for typical binder-target complex.

Next: Evaluate protein complex binding affinity with prodigy.