Biomolecular Complexes / Diffusion ModelingFree5 / 5.0 (編集部検証済み)

AlphaFold 3 Web Server

Unified Diffusion-Based Prediction of Proteins, DNA, RNA, Ligands & Ions

Google DeepMind and Isomorphic Labs' transformative foundation model for universal biomolecular complex prediction.

Developed by:Google DeepMind & Isomorphic Labs
#AlphaFold 3#Protein-DNA Complex#RNA Secondary & 3D#Small Molecule Ligands#DeepMind#Diffusion Model
Open Official ToolRead Research Paper
✓ Free Web Access • Safe & Verified

Technical Overview & Biological Significance

AlphaFold 3 represents a fundamental paradigm shift from AlphaFold 2. By replacing traditional structural geometry modules with a raw atomic diffusion architecture (Pairformer + Diffusion Module), AlphaFold 3 predicts atomic coordinates across all biomolecular classes—proteins, nucleic acids (DNA/RNA), post-translational modifications (PTMs), ions, and drug-like small-molecule ligands—simultaneously within a single unified network.

The Biological Challenge Solved

Biological processes are governed by intricate multi-component macromolecular assemblies (e.g. CRISPR-Cas9 bound to guide RNA and target DNA, or transcription factors docked to enhancer motifs). Previous computational methods were siloed, requiring separate pipelines for protein folding, RNA folding, and small-molecule docking, often failing at multi-molecular interfaces.

Key Computational Capabilities

1

Universal Biomolecular Interaction

Simultaneously folds and docks multi-chain proteins, DNA duplexes, RNA stem-loops, chemical ligands, and metal ions.

2

Diffusion-Based Direct Coordinate Generation

Operates directly on 3D atomic coordinates via denoising diffusion, accurately resolving disordered loops, stereochemistry, and bond lengths.

3

Interface Prediction Metrics (ipTM & pTM)

Provides rigorous per-interface predicted TM-scores (ipTM), allowing researchers to differentiate true biological binders from non-specific artifacts.

4

Extensive Chemical & PTM Support

Supports standard post-translational modifications including glycosylation, phosphorylation, methylation, and modified bases.

Executable Commands & API Usage

Define multi-chain protein-DNA-ligand complexes for submission to the AlphaFold 3 Web Server:

python
terminal - bio_query_alphafold3.py
# AlphaFold 3 Complex Job Specification JSON
import json

job_config = {
    "name": "Transcription_Factor_DNA_Complex",
    "modelSeeds": [1],
    "sequences": [
        {
            "proteinChain": {
                "sequence": "MVRKTVRQERLKSIVRILERSKEPVSGAQLAEELSVSRQVIVQDIA",
                "count": 2  # Homodimer
            }
        },
        {
            "dnaSequence": {
                "sequence": "ATGCGTACCGGATCC",
                "count": 1
            }
        }
    ]
}

print(json.dumps(job_config, indent=2))

Input Specifications & Inference Results

Query Input Format
Multi-Entity Sequences (Protein + DNA/RNA + Ligand SMILES)
Entity 1: Protein Chain A (p53 DNA-binding domain, 190 residues)
Entity 2: Double-stranded DNA Target (GGCAAGTTAGGGCAAGTTAG)
Entity 3: Zinc Ion (ZN) cofactor

Users specify amino acid sequences, nucleotide sequences, and chemical identifiers for multi-component folding.

Predicted Output Stream
mmCIF File + Summary Confidence Metrics
{
  "ranking_score": 0.892,
  "ptm": 0.915,
  "iptm": 0.867,
  "fraction_disordered": 0.08,
  "chain_pair_iptm": {
    "[A, B]": 0.92,
    "[A, DNA]": 0.87
  }
}

Calibrated quantitative scores ready for downstream analysis.

Biological Result Interpretation Guide

How researchers interpret confidence thresholds, fold-change values, and functional impact:

ipTM > 0.80
High-Confidence Molecular Interaction

The predicted multi-molecular binding interface is highly reliable, suitable for rational drug discovery or mutagenesis experiments.

0.60 < ipTM < 0.80
Probable Binding / Requires Validation

Overall topology is plausible; active site residues should be cross-referenced with experimental conservation or mutagenesis data.

ipTM < 0.50
Unlikely Binding / Non-Specific Contact

The model does not find strong co-evolutionary or physicochemical evidence for a stable interaction under physiological conditions.

AlphaFold 3 Web Server vs. Traditional Computational Methods

DimensionAlphaFold 3 Web Server (This Tool)Traditional Pipelines
Multi-Entity ComplexEnd-to-end (Protein + RNA + DNA + Ligand)Separate rigid-body docking (AutoDock / HADDOCK)
Protein-Nucleic Acid AccuracyState-of-the-art atomic resolutionOften requires experimental cryo-EM constraints
ArchitectureDiffusion network on raw coordinatesEvoformer + invariant coordinate frames

Frequently Asked Questions (FAQ)

How do I access AlphaFold 3?

You can use the free AlphaFold Server at alphafoldserver.com with a standard Google account. It requires zero GPU setup and delivers full 3D models in minutes.

Can AlphaFold 3 predict DNA-protein binding specificity?

Yes, AlphaFold 3 exhibits remarkable accuracy in placing transcription factors into DNA major and minor grooves with correct base-specific hydrogen bonding.