Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
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Structure similarity search with Foldseek. Use this skill when: (1) Finding similar structures in PDB/AFDB databases, (2) Structural homology search, (3) Database queries by 3D structure, (4) Finding remote homologs not detected by sequence, (5) Clustering structures by similarity. For sequence similarity, use uniprot BLAST. For structure prediction, use chai or boltz.
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See how to installReview the instructions the agent will receive before you install.
| Requirement | Minimum | Recommended |
|---|---|---|
| Python | 3.8+ | 3.10 |
| RAM | 8GB | 16GB |
| Disk | 10GB | 50GB (for local databases) |
Note: Foldseek can run locally or via web server. No GPU required.
# Upload structure to web server
curl -X POST "https://search.foldseek.com/api/ticket" \
-F "q=@query.pdb" \
-F "database[]=afdb50" \
-F "database[]=pdb100"
# Install Foldseek
conda install -c conda-forge -c bioconda foldseek
# Search PDB
foldseek easy-search query.pdb /path/to/pdb100 results.m8 tmp/
# Search AlphaFold DB
foldseek easy-search query.pdb /path/to/afdb50 results.m8 tmp/
import subprocess
import pandas as pd
def foldseek_search(query_pdb, database, output="results.m8"):
"""Run Foldseek search."""
subprocess.run([
"foldseek", "easy-search",
query_pdb, database, output, "tmp/",
"--format-output", "query,target,pident,alnlen,evalue,bits"
])
return pd.read_csv(output, sep="\t",
names=["query", "target", "pident", "alnlen", "evalue", "bits"])
| Parameter | Default | Description |
|---|---|---|
--min-seq-id | 0.0 | Minimum sequence identity |
-e | 0.001 | E-value threshold |
--alignment-type | 2 | 0=3Di, 1=TM, 2=3Di+AA |
--max-seqs | 300 | Max hits to pass through prefilter; reducing this affects sensitivity |
| Database | Description | Size |
|---|---|---|
pdb100 | PDB clustered at 100% | ~200K structures |
afdb50 | AlphaFold DB at 50% | ~67M structures |
swissprot | SwissProt structures | ~500K structures |
cath50 | CATH domains | ~50K domains |
# results.m8 (tabular)
query target pident alnlen evalue bits
query 1abc_A 85.2 120 1e-45 180.5
query 2def_B 72.1 115 1e-32 145.2
$ foldseek easy-search query.pdb pdb100 results.m8 tmp/
[INFO] Loading database: pdb100 (194,527 entries)
[INFO] Searching...
[INFO] Found 127 hits
Top 5 hits:
1. 1abc_A - 85.2% identity, E=1e-45
2. 2def_B - 72.1% identity, E=1e-32
3. 3ghi_C - 68.5% identity, E=1e-28
4. 4jkl_A - 55.3% identity, E=1e-18
5. 5mno_B - 42.1% identity, E=1e-10
Should I use Foldseek?
│
├─ What are you searching?
│ ├─ By 3D structure → Foldseek ✓
│ ├─ By sequence → Use BLAST (uniprot skill)
│ └─ Both → Run both, compare results
│
└─ What do you need?
├─ Find structural homologs → Foldseek ✓
├─ Remote homolog detection → Foldseek ✓
├─ Structural clustering → Foldseek ✓
└─ Functional annotation → Cross-reference with UniProt
# Compare your design to PDB
foldseek easy-search design.pdb pdb100 similar_natural.m8 tmp/
# Ensure design is novel (low similarity to known)
foldseek easy-search design.pdb afdb50 novelty.m8 tmp/
# Novel if: top hit identity < 30%
# Find scaffolds for motif grafting
foldseek easy-search motif.pdb pdb100 scaffolds.m8 tmp/ \
--min-seq-id 0.0 -e 10
wc -l results.m8 # Number of hits
No hits: Lower e-value threshold, try larger database Too many hits: Increase min-seq-id threshold Slow search: Use smaller database
| Error | Cause | Fix |
|---|---|---|
Database not found | Wrong path | Check database location |
Invalid PDB | Malformed structure | Validate PDB format |
Out of memory | Large database | Use more RAM or web server |
Next: Download hits with pdb skill → use for scaffold design.
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Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
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Validate protein designs using AlphaFold2 structure prediction. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm. For QC thresholds, use protein-qc.
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AlphaFold2 / AlphaFold-Multimer structure prediction for validation and confidence scoring. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm2-sequence-scoring. For QC thresholds, use protein-design-qc.
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Workflow for event-level and isoform-level splicing analysis with sashimi-ready outputs and splice QC.
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ATAC-seq processing with assay QC, MACS3 peak calling, consensus peak matrices, differential accessibility, and motif or footprint follow-up.
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End-to-end binder design using BindCraft hallucination. Use this skill when: (1) Designing protein binders with built-in AF2 validation, (2) Running production-quality binder campaigns, (3) Using different design protocols (fast, default, slow), (4) Need joint backbone and sequence optimization, (5) Want high experimental success rate. For backbone-only generation, use rfdiffusion. For QC thresholds, use protein-qc. For tool selection guidance, use binder-design.
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