@synsci/cli-darwin-x64-baseline 1.1.76 → 1.1.78

package/bin/skills/esm/references/workflows.md

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+# ESM Workflows and Examples
+
+## Overview
+
+This document provides complete, end-to-end examples of common workflows using ESM3 and ESM C. Each workflow includes setup, execution, and analysis code.
+
+## Workflow 1: Novel GFP Design with Chain-of-Thought
+
+Design a novel fluorescent protein using ESM3's multimodal generation capabilities.
+
+### Objective
+
+Generate a green fluorescent protein (GFP) with specific properties using chain-of-thought reasoning across sequence, structure, and function.
+
+### Complete Implementation
+
+```python
+from esm.models.esm3 import ESM3
+from esm.sdk.api import ESMProtein, GenerationConfig, FunctionAnnotation
+import matplotlib.pyplot as plt
+
+# Setup
+model = ESM3.from_pretrained("esm3-sm-open-v1").to("cuda")
+
+# Step 1: Define target properties
+print("Step 1: Defining target GFP properties...")
+
+# Create protein with desired function
+target_length = 238  # Typical GFP length
+protein = ESMProtein(
+    sequence="_" * target_length,
+    function_annotations=[
+        FunctionAnnotation(
+            label="green_fluorescent_protein",
+            start=65,
+            end=75  # Chromophore region
+        )
+    ]
+)
+
+# Step 2: Generate initial sequence with function conditioning
+print("Step 2: Generating initial sequence...")
+
+config = GenerationConfig(
+    track="sequence",
+    num_steps=target_length // 3,  # Gradual generation
+    temperature=0.7  # Moderate diversity
+)
+protein = model.generate(protein, config)
+print(f"Generated sequence: {protein.sequence[:50]}...")
+
+# Step 3: Predict structure
+print("Step 3: Predicting structure...")
+
+config = GenerationConfig(
+    track="structure",
+    num_steps=target_length // 2
+)
+protein = model.generate(protein, config)
+print(f"Structure predicted, coordinates shape: {protein.coordinates.shape}")
+
+# Step 4: Refine sequence based on structure
+print("Step 4: Refining sequence based on structure...")
+
+# Mask regions for refinement (e.g., surface residues)
+sequence_list = list(protein.sequence)
+# Keep chromophore region, refine others
+for i in range(0, 65):
+    if i % 3 == 0:  # Refine every third position
+        sequence_list[i] = '_'
+for i in range(75, target_length):
+    if i % 3 == 0:
+        sequence_list[i] = '_'
+
+protein.sequence = ''.join(sequence_list)
+
+config = GenerationConfig(
+    track="sequence",
+    num_steps=50,
+    temperature=0.5  # Lower temperature for refinement
+)
+protein = model.generate(protein, config)
+
+# Step 5: Final validation
+print("Step 5: Final validation...")
+
+# Predict final structure
+config = GenerationConfig(track="structure", num_steps=30)
+protein = model.generate(protein, config)
+
+# Save results
+with open("novel_gfp.pdb", "w") as f:
+    f.write(protein.to_pdb())
+
+with open("novel_gfp_sequence.txt", "w") as f:
+    f.write(f">Novel_GFP\n{protein.sequence}\n")
+
+print(f"\nFinal GFP sequence:\n{protein.sequence}")
+print(f"\nFunction annotations: {protein.function_annotations}")
+print(f"Structure saved to: novel_gfp.pdb")
+```
+
+### Validation Steps
+
+```python
+# Analyze designed GFP
+def analyze_gfp(protein):
+    """Analyze generated GFP properties."""
+
+    # Check chromophore region (should be around Ser65-Tyr66-Gly67)
+    chromophore_region = protein.sequence[64:68]
+    print(f"Chromophore region: {chromophore_region}")
+
+    # Check barrel structure (GFPs have beta-barrel)
+    # Analyze secondary structure if available
+    if protein.secondary_structure:
+        beta_content = protein.secondary_structure.count('E') / len(protein.sequence)
+        print(f"Beta sheet content: {beta_content:.2%}")
+
+    # Check sequence similarity to known GFPs
+    # (Would require BLAST or alignment tool in practice)
+
+    return {
+        'length': len(protein.sequence),
+        'chromophore': chromophore_region,
+        'coordinates_available': protein.coordinates is not None
+    }
+
+analysis = analyze_gfp(protein)
+print(f"\nAnalysis results: {analysis}")
+```
+
+## Workflow 2: Protein Variant Library Generation
+
+Generate and analyze a library of protein variants for directed evolution.
+
+### Objective
+
+Create variants of a parent protein by targeted mutagenesis while maintaining structural integrity.
+
+### Complete Implementation
+
+```python
+from esm.models.esm3 import ESM3
+from esm.sdk.api import ESMProtein, GenerationConfig
+import numpy as np
+from sklearn.cluster import KMeans
+
+# Setup
+model = ESM3.from_pretrained("esm3-sm-open-v1").to("cuda")
+
+# Parent protein
+parent_sequence = "MPRTKEINDAGLIVHSPQWFYKARNDTESLGKIVHEFPM"
+parent_protein = ESMProtein(sequence=parent_sequence)
+
+# Define mutation parameters
+num_variants = 50
+positions_to_mutate = 5  # Number of positions per variant
+
+# Step 1: Generate variant library
+print("Generating variant library...")
+
+variants = []
+for i in range(num_variants):
+    # Create masked sequence with random positions
+    seq_list = list(parent_sequence)
+
+    # Select random positions to mutate
+    mutation_positions = np.random.choice(
+        len(seq_list),
+        size=positions_to_mutate,
+        replace=False
+    )
+
+    for pos in mutation_positions:
+        seq_list[pos] = '_'
+
+    # Generate variant
+    variant_protein = ESMProtein(sequence=''.join(seq_list))
+
+    config = GenerationConfig(
+        track="sequence",
+        num_steps=positions_to_mutate * 2,
+        temperature=0.8  # Higher diversity
+    )
+
+    variant = model.generate(variant_protein, config)
+    variants.append(variant.sequence)
+
+    if (i + 1) % 10 == 0:
+        print(f"Generated {i + 1}/{num_variants} variants")
+
+print(f"\nGenerated {len(variants)} variants")
+
+# Step 2: Predict structures for variants
+print("\nPredicting structures...")
+
+variant_proteins_with_structure = []
+for i, seq in enumerate(variants):
+    protein = ESMProtein(sequence=seq)
+
+    config = GenerationConfig(
+        track="structure",
+        num_steps=len(seq) // 2
+    )
+
+    protein_with_structure = model.generate(protein, config)
+    variant_proteins_with_structure.append(protein_with_structure)
+
+    if (i + 1) % 10 == 0:
+        print(f"Predicted structures for {i + 1}/{len(variants)} variants")
+
+# Step 3: Analyze variant diversity
+print("\nAnalyzing variant diversity...")
+
+# Calculate Hamming distances from parent
+def hamming_distance(seq1, seq2):
+    """Calculate Hamming distance between sequences."""
+    return sum(c1 != c2 for c1, c2 in zip(seq1, seq2))
+
+distances = [hamming_distance(parent_sequence, var) for var in variants]
+print(f"Average mutations per variant: {np.mean(distances):.1f}")
+print(f"Mutation range: {min(distances)}-{max(distances)}")
+
+# Step 4: Get embeddings for clustering
+print("\nGenerating embeddings for clustering...")
+
+from esm.models.esmc import ESMC
+
+embedding_model = ESMC.from_pretrained("esmc-300m").to("cuda")
+
+def get_embedding(sequence):
+    """Get mean-pooled embedding for sequence."""
+    protein = ESMProtein(sequence=sequence)
+    tensor = embedding_model.encode(protein)
+    emb = embedding_model.forward(tensor)
+    return emb.mean(dim=1).cpu().detach().numpy().flatten()
+
+variant_embeddings = np.array([get_embedding(seq) for seq in variants])
+
+# Step 5: Cluster variants
+print("Clustering variants...")
+
+n_clusters = 5
+kmeans = KMeans(n_clusters=n_clusters, random_state=42)
+cluster_labels = kmeans.fit_predict(variant_embeddings)
+
+# Analyze clusters
+print("\nCluster analysis:")
+for i in range(n_clusters):
+    cluster_variants = [var for var, label in zip(variants, cluster_labels) if label == i]
+    cluster_distances = [hamming_distance(parent_sequence, var) for var in cluster_variants]
+
+    print(f"\nCluster {i}:")
+    print(f"  Size: {len(cluster_variants)}")
+    print(f"  Avg distance from parent: {np.mean(cluster_distances):.1f}")
+    print(f"  Representative: {cluster_variants[0][:40]}...")
+
+# Step 6: Select diverse representatives
+print("\nSelecting diverse representatives...")
+
+representatives = []
+for i in range(n_clusters):
+    # Get centroid
+    cluster_indices = np.where(cluster_labels == i)[0]
+    cluster_embs = variant_embeddings[cluster_indices]
+
+    # Find closest to centroid
+    centroid = cluster_embs.mean(axis=0)
+    distances_to_centroid = np.linalg.norm(cluster_embs - centroid, axis=1)
+    rep_idx = cluster_indices[np.argmin(distances_to_centroid)]
+
+    representatives.append(variants[rep_idx])
+
+# Save results
+print("\nSaving results...")
+
+with open("variant_library.fasta", "w") as f:
+    f.write(f">Parent\n{parent_sequence}\n\n")
+    for i, var in enumerate(variants):
+        f.write(f">Variant_{i+1}_Cluster_{cluster_labels[i]}\n{var}\n")
+
+with open("representative_variants.fasta", "w") as f:
+    for i, rep in enumerate(representatives):
+        f.write(f">Representative_Cluster_{i}\n{rep}\n")
+
+print("Variant library saved to: variant_library.fasta")
+print("Representatives saved to: representative_variants.fasta")
+```
+
+## Workflow 3: Structure-Based Sequence Optimization
+
+Optimize a protein sequence to improve stability while maintaining function.
+
+### Objective
+
+Given a protein structure, design sequences that maintain the fold but have improved properties.
+
+### Complete Implementation
+
+```python
+from esm.models.esm3 import ESM3
+from esm.sdk.api import ESMProtein, GenerationConfig
+import numpy as np
+
+# Setup
+model = ESM3.from_pretrained("esm3-sm-open-v1").to("cuda")
+
+# Load target structure (e.g., from PDB)
+target_protein = ESMProtein.from_pdb("target_structure.pdb")
+original_sequence = target_protein.sequence
+
+print(f"Original sequence: {original_sequence}")
+print(f"Structure loaded: {target_protein.coordinates.shape}")
+
+# Step 1: Generate multiple sequence designs
+print("\nGenerating optimized sequences...")
+
+num_designs = 20
+optimized_sequences = []
+
+for i in range(num_designs):
+    # Start with structure, remove sequence
+    design_protein = ESMProtein(
+        coordinates=target_protein.coordinates.copy(),
+        secondary_structure=target_protein.secondary_structure
+    )
+
+    # Generate sequence for this structure
+    config = GenerationConfig(
+        track="sequence",
+        num_steps=len(original_sequence),
+        temperature=0.7,
+        condition_on_coordinates_only=True
+    )
+
+    designed = model.generate(design_protein, config)
+    optimized_sequences.append(designed.sequence)
+
+    if (i + 1) % 5 == 0:
+        print(f"Generated {i + 1}/{num_designs} designs")
+
+# Step 2: Validate structural compatibility
+print("\nValidating structural compatibility...")
+
+validated_designs = []
+
+for seq in optimized_sequences:
+    # Predict structure for designed sequence
+    test_protein = ESMProtein(sequence=seq)
+
+    config = GenerationConfig(
+        track="structure",
+        num_steps=len(seq) // 2
+    )
+
+    predicted = model.generate(test_protein, config)
+
+    # Calculate RMSD (simplified - in practice use proper alignment)
+    # Here we just check if structure prediction succeeds
+    if predicted.coordinates is not None:
+        validated_designs.append(seq)
+
+print(f"Validated {len(validated_designs)}/{num_designs} designs")
+
+# Step 3: Analyze sequence properties
+print("\nAnalyzing sequence properties...")
+
+def calculate_properties(sequence):
+    """Calculate basic sequence properties."""
+    # Hydrophobicity (simplified)
+    hydrophobic = "AILMFWYV"
+    hydrophobic_fraction = sum(1 for aa in sequence if aa in hydrophobic) / len(sequence)
+
+    # Charge
+    positive = "KR"
+    negative = "DE"
+    net_charge = sum(1 for aa in sequence if aa in positive) - sum(1 for aa in sequence if aa in negative)
+
+    # Aromatic content
+    aromatic = "FWY"
+    aromatic_fraction = sum(1 for aa in sequence if aa in aromatic) / len(sequence)
+
+    return {
+        'hydrophobic_fraction': hydrophobic_fraction,
+        'net_charge': net_charge,
+        'aromatic_fraction': aromatic_fraction
+    }
+
+# Compare to original
+original_props = calculate_properties(original_sequence)
+print(f"\nOriginal properties:")
+print(f"  Hydrophobic: {original_props['hydrophobic_fraction']:.2%}")
+print(f"  Net charge: {original_props['net_charge']:+d}")
+print(f"  Aromatic: {original_props['aromatic_fraction']:.2%}")
+
+# Analyze designs
+design_properties = [calculate_properties(seq) for seq in validated_designs]
+
+avg_hydrophobic = np.mean([p['hydrophobic_fraction'] for p in design_properties])
+avg_charge = np.mean([p['net_charge'] for p in design_properties])
+avg_aromatic = np.mean([p['aromatic_fraction'] for p in design_properties])
+
+print(f"\nDesigned sequences (average):")
+print(f"  Hydrophobic: {avg_hydrophobic:.2%}")
+print(f"  Net charge: {avg_charge:+.1f}")
+print(f"  Aromatic: {avg_aromatic:.2%}")
+
+# Step 4: Rank designs
+print("\nRanking designs...")
+
+def score_design(sequence, original_props):
+    """Score design based on desired properties."""
+    props = calculate_properties(sequence)
+
+    # Prefer higher hydrophobic content (for stability)
+    hydrophobic_score = props['hydrophobic_fraction']
+
+    # Prefer similar charge to original
+    charge_score = 1.0 / (1.0 + abs(props['net_charge'] - original_props['net_charge']))
+
+    # Combined score
+    return hydrophobic_score * 0.6 + charge_score * 0.4
+
+scores = [(seq, score_design(seq, original_props)) for seq in validated_designs]
+scores.sort(key=lambda x: x[1], reverse=True)
+
+print("\nTop 5 designs:")
+for i, (seq, score) in enumerate(scores[:5]):
+    print(f"\n{i+1}. Score: {score:.3f}")
+    print(f"   Sequence: {seq[:40]}...")
+
+# Step 5: Save results
+print("\nSaving results...")
+
+with open("optimized_sequences.fasta", "w") as f:
+    f.write(f">Original\n{original_sequence}\n\n")
+
+    for i, (seq, score) in enumerate(scores):
+        props = calculate_properties(seq)
+        f.write(f">Design_{i+1}_Score_{score:.3f}\n")
+        f.write(f"# Hydrophobic: {props['hydrophobic_fraction']:.2%}, ")
+        f.write(f"Charge: {props['net_charge']:+d}, ")
+        f.write(f"Aromatic: {props['aromatic_fraction']:.2%}\n")
+        f.write(f"{seq}\n\n")
+
+print("Results saved to: optimized_sequences.fasta")
+```
+
+## Workflow 4: Function Prediction Pipeline
+
+Predict protein function from sequence using ESM3 and ESM C.
+
+### Objective
+
+Build a pipeline that predicts protein function using both generative (ESM3) and embedding (ESM C) approaches.
+
+### Complete Implementation
+
+```python
+from esm.models.esm3 import ESM3
+from esm.models.esmc import ESMC
+from esm.sdk.api import ESMProtein, GenerationConfig
+import numpy as np
+from sklearn.ensemble import RandomForestClassifier
+from sklearn.model_selection import cross_val_score
+
+# Setup models
+esm3_model = ESM3.from_pretrained("esm3-sm-open-v1").to("cuda")
+esmc_model = ESMC.from_pretrained("esmc-600m").to("cuda")
+
+# Example: Predict if protein is an enzyme
+# (In practice, you'd have a labeled training set)
+
+def predict_function_generative(sequence):
+    """Predict function using ESM3 generative approach."""
+
+    protein = ESMProtein(sequence=sequence)
+
+    # Generate function annotations
+    config = GenerationConfig(
+        track="function",
+        num_steps=20,
+        temperature=0.3  # Low temperature for confident predictions
+    )
+
+    protein_with_function = esm3_model.generate(protein, config)
+
+    return protein_with_function.function_annotations
+
+def predict_function_embedding(sequence, function_classifier):
+    """Predict function using ESM C embeddings + classifier."""
+
+    # Get embedding
+    protein = ESMProtein(sequence=sequence)
+    tensor = esmc_model.encode(protein)
+    embedding = esmc_model.forward(tensor)
+
+    # Mean pool
+    embedding_pooled = embedding.mean(dim=1).cpu().detach().numpy()
+
+    # Predict with classifier
+    prediction = function_classifier.predict(embedding_pooled)
+    probability = function_classifier.predict_proba(embedding_pooled)
+
+    return prediction[0], probability[0]
+
+# Example workflow with test sequences
+test_sequences = {
+    "kinase": "MPRTKEINDAGLIVHSPQWFYKARNDTESLGKIVHEF",
+    "protease": "AGLIVHSPQWFYKARNDTESLGKIVHEFPMCDEGH",
+    "transporter": "KTEFLNDGRPMLIVHSPQWFYKARNDTESLGKIVH"
+}
+
+print("Predicting functions...\n")
+
+for name, sequence in test_sequences.items():
+    print(f"{name.upper()}:")
+    print(f"Sequence: {sequence[:30]}...")
+
+    # Method 1: Generative
+    functions = predict_function_generative(sequence)
+    print(f"  Generative predictions: {functions}")
+
+    # Method 2: Embedding-based would require trained classifier
+    # (Skipped in this example as it needs training data)
+
+    print()
+```
+
+## Workflow 5: Embedding-Based Clustering and Analysis
+
+Cluster and analyze a large protein dataset using ESM C embeddings.
+
+### Complete Implementation
+
+```python
+from esm.models.esmc import ESMC
+from esm.sdk.api import ESMProtein
+import numpy as np
+from sklearn.cluster import DBSCAN
+from sklearn.decomposition import PCA
+from sklearn.manifold import TSNE
+import matplotlib.pyplot as plt
+
+# Setup
+model = ESMC.from_pretrained("esmc-600m").to("cuda")
+
+# Load protein dataset (example)
+sequences = [
+    # In practice, load from FASTA or database
+    "MPRTKEINDAGLIVHSPQWFYK",
+    "AGLIVHSPQWFYKARNDTESL",
+    # ... more sequences
+]
+
+print(f"Loaded {len(sequences)} sequences")
+
+# Step 1: Generate embeddings
+print("Generating embeddings...")
+
+embeddings = []
+for i, seq in enumerate(sequences):
+    protein = ESMProtein(sequence=seq)
+    tensor = model.encode(protein)
+    emb = model.forward(tensor)
+
+    # Mean pooling
+    emb_pooled = emb.mean(dim=1).cpu().detach().numpy().flatten()
+    embeddings.append(emb_pooled)
+
+    if (i + 1) % 100 == 0:
+        print(f"Processed {i + 1}/{len(sequences)}")
+
+embeddings = np.array(embeddings)
+print(f"Embeddings shape: {embeddings.shape}")
+
+# Step 2: Dimensionality reduction for visualization
+print("\nReducing dimensionality...")
+
+# PCA for initial reduction
+pca = PCA(n_components=50)
+embeddings_pca = pca.fit_transform(embeddings)
+print(f"PCA explained variance: {pca.explained_variance_ratio_[:10].sum():.2%}")
+
+# t-SNE for visualization
+tsne = TSNE(n_components=2, random_state=42)
+embeddings_2d = tsne.fit_transform(embeddings_pca)
+
+# Step 3: Clustering
+print("\nClustering...")
+
+# DBSCAN for density-based clustering
+clustering = DBSCAN(eps=0.5, min_samples=5)
+cluster_labels = clustering.fit_predict(embeddings)
+
+n_clusters = len(set(cluster_labels)) - (1 if -1 in cluster_labels else 0)
+n_noise = list(cluster_labels).count(-1)
+
+print(f"Number of clusters: {n_clusters}")
+print(f"Number of noise points: {n_noise}")
+
+# Step 4: Visualize
+print("\nGenerating visualization...")
+
+plt.figure(figsize=(12, 8))
+scatter = plt.scatter(
+    embeddings_2d[:, 0],
+    embeddings_2d[:, 1],
+    c=cluster_labels,
+    cmap='viridis',
+    alpha=0.6
+)
+plt.colorbar(scatter)
+plt.title("Protein Sequence Clustering (ESM C Embeddings)")
+plt.xlabel("t-SNE 1")
+plt.ylabel("t-SNE 2")
+plt.savefig("protein_clusters.png", dpi=300, bbox_inches='tight')
+print("Visualization saved to: protein_clusters.png")
+
+# Step 5: Analyze clusters
+print("\nCluster analysis:")
+
+for cluster_id in range(n_clusters):
+    cluster_indices = np.where(cluster_labels == cluster_id)[0]
+    cluster_seqs = [sequences[i] for i in cluster_indices]
+
+    print(f"\nCluster {cluster_id}:")
+    print(f"  Size: {len(cluster_seqs)}")
+    print(f"  Avg length: {np.mean([len(s) for s in cluster_seqs]):.1f}")
+    print(f"  Example: {cluster_seqs[0][:40]}...")
+
+# Save cluster assignments
+with open("cluster_assignments.txt", "w") as f:
+    for i, (seq, label) in enumerate(zip(sequences, cluster_labels)):
+        f.write(f"Sequence_{i}\tCluster_{label}\t{seq}\n")
+
+print("\nCluster assignments saved to: cluster_assignments.txt")
+```
+
+## Additional Workflow Tips
+
+### Memory Management for Large Datasets
+
+```python
+def process_large_dataset(sequences, batch_size=32):
+    """Process large dataset with memory management."""
+    import gc
+    import torch
+
+    results = []
+
+    for i in range(0, len(sequences), batch_size):
+        batch = sequences[i:i + batch_size]
+
+        # Process batch
+        batch_results = [process_sequence(seq) for seq in batch]
+        results.extend(batch_results)
+
+        # Clear memory
+        torch.cuda.empty_cache()
+        gc.collect()
+
+        if (i + batch_size) % 100 == 0:
+            print(f"Processed {min(i + batch_size, len(sequences))}/{len(sequences)}")
+
+    return results
+```
+
+### Parallel Processing
+
+```python
+from concurrent.futures import ThreadPoolExecutor
+import asyncio
+
+def parallel_workflow(sequences, n_workers=4):
+    """Process sequences in parallel."""
+
+    with ThreadPoolExecutor(max_workers=n_workers) as executor:
+        results = list(executor.map(process_sequence, sequences))
+
+    return results
+```
+
+These workflows provide comprehensive examples for common ESM use cases. Adapt them to your specific needs and always validate results with appropriate biological experiments.