| name | structural-biology |
| description | Structure retrieval, confidence-aware AlphaFold DB usage, coordinate download, PAE and pLDDT interpretation, and structure-guided biological annotation. |
| tool_type | python |
| primary_tool | AlphaFold DB |
Structural Biology
Version Compatibility
Reference examples assume:
biopython 1.84+
- AlphaFold DB public API current format
- optional visualization stack such as
py3Dmol or PyMOL
Verify before use:
- Python:
python -c "import Bio; print(Bio.__version__)"
Overview
Use this skill when the task is:
- retrieving AlphaFold-predicted structures by UniProt accession
- downloading coordinate and confidence files
- reading pLDDT or PAE to judge confidence
- mapping sequence findings onto structure
When To Use This Skill
- a UniProt accession or known protein target exists
- experimental structure is absent or incomplete
- the user needs confidence-aware structural interpretation
Quick Route
- known UniProt accession: query AlphaFold DB first
- novel designed sequence without AlphaFold DB entry: use a separate prediction workflow such as ColabFold
- structure interpretation request: always inspect pLDDT and PAE before making mechanistic claims
Progressive Disclosure
Expected Inputs
- UniProt accession or sequence context
- optional residue list, mutation list, or ligand site hypothesis
Expected Outputs
results/structures/AF-<accession>.cif
results/structures/AF-<accession>.pdb
results/confidence/AF-<accession>-confidence.json
results/confidence/AF-<accession>-pae.json
figures/AF-<accession>-pae.png
Starter Pattern
from Bio.PDB import alphafold_db
prediction = next(alphafold_db.get_predictions("P00520"))
cif_path = alphafold_db.download_cif_for(prediction, directory="results/structures")
print(cif_path)
Confidence Thresholds
pLDDT
| pLDDT | Interpretation |
|---|
> 90 | very high confidence |
70-90 | good backbone confidence |
50-70 | low confidence |
< 50 | likely disorder or unreliable local structure |
PAE
| PAE | Interpretation |
|---|
< 5 Å | confident relative positioning |
5-15 Å | moderate uncertainty |
> 15 Å | domain orientation may be unreliable |
Workflow
1. Choose the structure source
- experimental structure if available and suitable
- AlphaFold DB for known proteins with UniProt accessions
- separate prediction workflow for novel sequences
2. Retrieve coordinates and confidence files
Download:
mmCIF or PDB
- confidence JSON
- PAE JSON
3. Inspect confidence before interpretation
Do not map mutations or infer interfaces from low-confidence regions without saying so.
4. Annotate the biological question
Map domains, active sites, mutations, motifs, or interfaces onto the structure.
5. Export reusable artifacts
Save coordinates, confidence files, and a PAE heatmap or equivalent summary.
Output Artifacts
results/
├── structures/
│ ├── AF-P00520-F1-model_v4.cif
│ └── AF-P00520-F1-model_v4.pdb
└── confidence/
├── AF-P00520-F1-confidence_v4.json
└── AF-P00520-F1-predicted_aligned_error_v4.json
figures/
└── AF-P00520-F1-pae.png
Quality Review
- pLDDT must be reviewed before claiming local residue geometry is trustworthy
- PAE must be reviewed before claiming domain-domain arrangement is trustworthy
- residue numbering and chain mapping must be checked before mutation interpretation
- low-confidence or disordered regions should be labeled explicitly
Anti-Patterns
- treating every AlphaFold region as equally reliable
- ignoring PAE when discussing domain orientation
- mapping variants onto mismatched residue numbering
- using AlphaFold DB retrieval as if it were de novo prediction for novel sequences
Related Skills
- Proteomics
- Pathway Analysis
Optional Supplements