| name | foldseek |
| description | 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 chai1-structure-prediction or boltz-structure-prediction.
|
| license | MIT |
| category | utilities |
| tags | ["search","structure","database","similarity"] |
Foldseek Structure Search
Prerequisites
| Requirement | Minimum | Recommended |
|---|
| Python | 3.8+ | 3.10 |
| RAM | 8GB | 16GB |
| Disk | 10GB | 50GB (for local databases) |
How to run
Note: Foldseek can run locally or via web server. No GPU required.
Option 1: Web Server (Quick; rate-limited, use sparingly)
curl -X POST "https://search.foldseek.com/api/ticket" \
-F "q=@query.pdb" \
-F "database[]=afdb50" \
-F "database[]=pdb100"
Option 2: Local installation
conda install -c conda-forge -c bioconda foldseek
foldseek easy-search query.pdb /path/to/pdb100 results.m8 tmp/
foldseek easy-search query.pdb /path/to/afdb50 results.m8 tmp/
Option 3: Python API
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"])
Key parameters
| 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 |
Databases
| 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 |
Output format
# 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
Sample output
Successful run
$ 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
Decision tree
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
Common use cases
Find similar designs
foldseek easy-search design.pdb pdb100 similar_natural.m8 tmp/
Novelty check
foldseek easy-search design.pdb afdb50 novelty.m8 tmp/
Scaffold search
foldseek easy-search motif.pdb pdb100 scaffolds.m8 tmp/ \
--min-seq-id 0.0 -e 10
Verify
wc -l results.m8
Troubleshooting
No hits: Lower e-value threshold, try larger database
Too many hits: Increase min-seq-id threshold
Slow search: Use smaller database
Error interpretation
| 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.
Inputs
- One or more query structures in PDB or mmCIF format.
- A chosen database target such as PDB, AFDB, or a local structural collection.
- Search settings like sensitivity, output mode, and result count.
Outputs
- Ranked structural hits with alignment statistics and hit annotations.
- Evidence about novelty, scaffold reuse, or remote structural homology.
- Candidate templates or analogs to inspect with
pdb or follow up in design decisions.
Next Step
Inspect the top structural hits with pdb, then use the results to refine scaffold choice or novelty claims.