internscience/scp/boltz2-binding-affinity

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Predict protein-ligand binding affinity using Boltz-2 model to assess molecular interactions and binding probability for drug discovery.

Install

npx vskill@latest install internscience/scp/boltz2-binding-affinity

SKILL.md

Boltz-2 Protein-Ligand Binding Affinity Prediction

Usage

1. MCP Server Definition
python
import asyncio
import json
from mcp.client.streamable_http import streamablehttp_client
from mcp import ClientSession
class DrugSDAClient:
"""DrugSDA-Model MCP Client"""
def __init__(self, server_url: str, api_key: str):
self.server_url = server_url
self.api_key = api_key
self.session = None
async def connect(self):
"""Establish connection and initialize session"""
print(f"server url: {self.server_url}")
try:
self.transport = streamablehttp_client(
url=self.server_url,
headers={"SCP-HUB-API-KEY": self.api_key}
)
self.read, self.write, self.get_session_id = await self.transport.__aenter__()
self.session_ctx = ClientSession(self.read, self.write)
self.session = await self.session_ctx.__aenter__()
await self.session.initialize()
session_id = self.get_session_id()
print(f"✓ connect success")
return True
except Exception as e:
print(f"✗ connect failure: {e}")
import traceback
traceback.print_exc()
return False
async def disconnect(self):
"""Disconnect from server"""
try:
if self.session:
await self.session_ctx.__aexit__(None, None, None)
if hasattr(self, 'transport'):
await self.transport.__aexit__(None, None, None)
print("✓ already disconnect")
except Exception as e:
print(f"✗ disconnect error: {e}")
def parse_result(self, result):
"""Parse MCP tool call result"""
try:
if hasattr(result, 'content') and result.content:
content = result.content[0]
if hasattr(content, 'text'):
return json.loads(content.text)
return str(result)
except Exception as e:
return {"error": f"parse error: {e}", "raw": str(result)}
2. Boltz-2 Binding Affinity Workflow

This workflow predicts protein-ligand binding affinity using the Boltz-2 deep learning model, providing affinity probabilities and 3D complex structures.

Workflow Steps:

  1. Prepare Input - Define protein sequence and SMILES list for ligands
  2. Run Boltz-2 Prediction - Calculate binding affinity probability for each ligand
  3. Analyze Results - Extract affinity scores and structure files

Implementation:

python
## Initialize client
client = DrugSDAClient(
"https://scp.intern-ai.org.cn/api/v1/mcp/3/DrugSDA-Model",
"<your-api-key>"
)
if not await client.connect():
print("connection failed")
exit()
## Input: Protein sequence and ligand SMILES
sequence = 'PIVQNLQGQMVHQCISPRTLNAWVKVVEEKAFSPEVIPMFSALSCGATPQDLNTMLNTVGGHQAAMQMLKETINEEAAEWDRLHPVHAGPIAPGQMREPRGSDIAGTTSTLQEQIGWMTHNPPIPVGEIYKRWIILGLNKIVRMYSPTSILDIRQGPKEPFRDYVDRFYKTLRAEQASQEVKNAATETLLVQNANPDCKTILKALGPGATLEEMMTACQG'
protein = [{'chain': 'A', 'sequence': sequence}]
smiles_list = ['N[C@@H](Cc1ccc(O)cc1)C(=O)O', "CC(C)C1=CC=CC=C1"]
## Execute Boltz-2 binding affinity prediction
result = await client.session.call_tool(
"boltz_binding_affinity",
arguments={
"protein": protein,
"smiles_list": smiles_list
}
)
result_data = client.parse_result(result)
boltz_res = result_data["boltz_res"]
## Display results
for i, item in enumerate(boltz_res, 1):
print(f"{i}. SMILES: {item['smiles']}")
print(f" Affinity Probability: {item['affinity_probability']:.4f}")
print(f" Structure File: {item['cif_file']}\n")
await client.disconnect()
Tool Descriptions

DrugSDA-Model Server:

  • boltz_binding_affinity: Predict protein-ligand binding affinity using Boltz-2
  • Args:
  • protein (list): List of protein chains with sequence information
  • Each chain: {'chain': str, 'sequence': str}
  • smiles_list (list): List of ligand SMILES strings
  • Returns:
  • boltz_res (list): List of binding predictions
  • smiles (str): Ligand SMILES string
  • affinity_probability (float): Binding affinity probability (0-1)
  • cif_file (str): Path to predicted complex structure
Input/Output

Input:

  • protein: List of protein chains
  • chain: Chain identifier (e.g., 'A', 'B')
  • sequence: Amino acid sequence in single-letter code
  • smiles_list: List of SMILES strings for ligand molecules

Output:

  • List of binding predictions, each containing:
  • smiles: Ligand SMILES string
  • affinity_probability: Binding probability (0-1, higher is better)
  • cif_file: Path to predicted protein-ligand complex structure in CIF format
Affinity Interpretation
  • Probability > 0.5: Strong binding likelihood
  • Probability 0.3-0.5: Moderate binding potential
  • Probability < 0.3: Weak or no binding expected
Use Cases
  • Virtual screening of compound libraries
  • Lead optimization in drug discovery
  • Protein-ligand binding mode prediction
  • Structure-based drug design
  • Comparative binding analysis across ligands
Performance Notes
  • Execution time: 30-120 seconds per ligand depending on protein size
  • Protein length: Best for proteins <1000 amino acids
  • Multiple ligands: Processes sequentially, allow sufficient time
  • Structure output: CIF files can be visualized in PyMOL, ChimeraX, or similar tools

Security

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  • Model reviewPassed

Quality evaluation

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Source

Popularity

Repository stars
150
Repository forks
10
7-day trend score
25

Stars and forks are for the whole GitHub repository, not this skill alone. Refreshed 19 Mar 2026, 7 months ago.

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