| name | kegg-analysis |
| category | data-ai |
| description | Multi-step KEGG bioinformatics workflows — pathway enrichment from gene lists, drug-target investigation, cross-species metabolic comparison, and compound-reaction network exploration. Guides Claude through the full analytical pipeline using KEGG MCP tools. |
KEGG Bioinformatics Analysis
This skill orchestrates multi-step biological analyses using the KEGG MCP server tools. It transforms raw gene lists, drug names, or pathway IDs into structured biological insights.
When to Use This Skill
- Performing pathway enrichment analysis on a gene list
- Investigating a drug's mechanism of action, targets, and interactions
- Comparing metabolic pathways across species
- Tracing compound-reaction networks
- Mapping genes to functional modules and ortholog groups
What This Skill Does
- Identifies the analysis type from the user's input (enrichment, drug, comparison, network)
- Resolves identifiers — maps gene symbols, drug names, or pathway IDs to KEGG entries
- Retrieves cross-linked data — follows relationships across KEGG databases
- Aggregates and ranks results — counts pathway hits, scores conservation, groups by function
- Synthesizes biological context — explains significance, not just IDs
How to Use
Pathway Enrichment
Analyze these genes for pathway enrichment in human: BRCA1, TP53, EGFR, KRAS, PIK3CA
Workflow:
search_genes for each gene in the target organism (e.g., hsa)
get_gene_info to confirm identity and get KEGG gene IDs
find_related_entries to get pathway associations per gene
- Aggregate: count how many input genes map to each pathway
get_pathway_info for top pathways
render_pathway_ascii for visual context
- Report ranked pathways with p-value proxy (gene count / pathway size)
Drug Target Investigation
Investigate metformin: targets, pathways, and interactions
Workflow:
search_drugs to find the KEGG drug entry
get_drug_info for targets, classification, and metabolism
search_genes for each target gene
find_related_entries to get target pathways
get_drug_interactions for DDI screening
- Synthesize mechanism-of-action summary
Cross-Species Comparison
Compare glycolysis (map00010) between human, E. coli, and yeast
Workflow:
get_pathway_info for organism-specific variants (hsa00010, eco00010, sce00010)
get_pathway_genes for each organism
get_gene_orthologs to identify conserved vs. species-specific enzymes
get_pathway_compounds to compare metabolite pools
render_pathway_ascii for each organism
- Report conservation matrix and unique adaptations
Example
User: "What pathways are enriched in this gene set: SOD1, SOD2, CAT, GPX1, PRDX1?"
Output:
Pathway Enrichment Results (Homo sapiens)
Top Pathways:
1. hsa04146 Peroxisome (4/5 genes) — organelle for fatty acid oxidation and ROS detox
2. hsa04216 Ferroptosis (3/5 genes) — iron-dependent cell death regulated by GPX
3. hsa05022 Pathways of neurodegeneration (3/5 genes) — oxidative damage in ALS, AD, PD
4. hsa00480 Glutathione metabolism (2/5 genes) — GSH-dependent antioxidant system
Biological Context:
All 5 genes encode antioxidant enzymes. The enrichment in Peroxisome
and Ferroptosis pathways reflects their central role in reactive oxygen
species (ROS) detoxification. The neurodegeneration hit is consistent
with oxidative stress as a driver of SOD1-linked ALS.
Tips
- Provide organism context (human, mouse, E. coli) for faster resolution
- Use standard gene symbols — KEGG resolves HGNC symbols for human
- For large gene lists (>20), batch with
batch_entry_lookup (max 50 per call)
- Cross-reference with
convert_identifiers to bridge UniProt, NCBI Gene, or PDB IDs
- Use
find_related_entries to discover unexpected connections between databases