tooluniverse-kegg-disease-drug

name	tooluniverse-kegg-disease-drug
description	KEGG-based disease-drug-variant network research. Connects diseases to causal genes, drugs to molecular targets, and variants to pathways using KEGG's editorially curated databases (KEGG Disease, Drug, Network, Variant, Pathway). Use for drug repurposing via shared pathways, mechanistic disease-gene-drug networks, and pathway-based target discovery. Distinguishes direct (binding) vs indirect (pathway co-membership) drug-target relationships.
triggers	[{"keywords":["KEGG disease","KEGG drug","KEGG network","KEGG variant","disease genes","drug targets"]},{"patterns":["KEGG .* disease","KEGG .* drug","disease.*drug.*variant","KEGG network"]}]

KEGG Disease-Drug-Variant Research

Systematic exploration of disease-drug-variant relationships using KEGG's curated databases.

Reasoning Strategy

KEGG maps diseases to pathways and drugs to targets, but the real value is in the connections — which pathways link a disease gene to a drug target? This is a network question, not a simple lookup. A gene appearing in a KEGG disease entry has been editorially reviewed as mechanistically relevant; a drug entry with a confirmed target is more reliable than one inferred from pathway co-membership. When using KEGG for drug repurposing, always ask: is the drug-target relationship direct (the drug binds the gene product) or indirect (the drug affects a pathway that contains the gene)? Direct relationships are far stronger evidence. KEGG coverage is not exhaustive — absence from KEGG does not mean absence of biological involvement; complement with Reactome, WikiPathways, or CTD for broader coverage. ID namespace differences are a frequent source of errors: KEGG uses its own gene IDs (e.g., hsa:7157 for TP53), so always convert external IDs before querying KEGG-specific tools.

LOOK UP DON'T GUESS: Do not assume KEGG disease IDs, drug IDs, or gene IDs from memory — always search first with KEGG_search_disease, KEGG_search_drug, or KEGG_convert_ids. Do not assume which pathways link a disease gene to a drug; use KEGG_link_entries and KEGG_get_network to retrieve the actual connections.

When to Use

• "What genes are associated with [disease] in KEGG?"
• "Find KEGG drugs targeting [gene/pathway]"
• "What variants are linked to [disease] in KEGG?"
• "Show the KEGG disease-gene-drug network for [condition]"
• "Find drugs targeting BRAF variants in cancer"

Tool Inventory (12 tools)

Tool	Key Params	Returns
KEGG_search_disease	keyword	Disease entries matching keyword
KEGG_get_disease	disease_id (e.g., "H00004")	Disease details: genes, drugs, pathways
KEGG_get_disease_genes	disease_id	All genes for a disease
KEGG_search_drug	keyword	Drug entries matching keyword
KEGG_get_drug	drug_id (e.g., "D00123")	Drug details: targets, pathways, metabolism
KEGG_get_drug_targets	drug_id	Molecular targets for a drug
KEGG_search_network	keyword	Network entries (disease-gene-drug)
KEGG_get_network	network_id	Network details and relationships
KEGG_search_variant	keyword	Variant entries matching keyword
KEGG_get_variant	variant_id	Variant details and disease associations
KEGG_convert_ids	source_db, target_db, ids	Convert identifiers between KEGG and external databases (e.g., NCBI Gene ↔ KEGG gene IDs, UniProt ↔ KEGG)
KEGG_link_entries	target_db, source_db_or_ids	Find cross-database relationships (e.g., all genes linked to a pathway, all drugs linked to a disease)

Workflow

Phase 1: Disease Lookup -> Phase 2: Disease Genes -> Phase 3: Drug Search
  -> Phase 4: Drug Targets -> Phase 5: Network/Variant Context -> Report

Phase 1: Disease Lookup

Search and retrieve KEGG disease entries.

# Search for cancer-related diseases
diseases = tu.tools.KEGG_search_disease(keyword="breast cancer")
# Get details for a specific disease
disease = tu.tools.KEGG_get_disease(disease_id="H00031")

Phase 2: Disease Genes

Get genes associated with a KEGG disease entry.

genes = tu.tools.KEGG_get_disease_genes(disease_id="H00031")

Phase 3: Drug Search

Find KEGG drugs by name, target, or keyword.

drugs = tu.tools.KEGG_search_drug(keyword="vemurafenib")
drug_detail = tu.tools.KEGG_get_drug(drug_id="D09996")

Phase 4: Drug Targets

Get molecular targets for a drug.

targets = tu.tools.KEGG_get_drug_targets(drug_id="D09996")

Phase 5: Network & Variant Context

Explore disease-gene-drug networks and variant annotations.

# Search networks linking disease, genes, and drugs
networks = tu.tools.KEGG_search_network(keyword="BRAF melanoma")
network = tu.tools.KEGG_get_network(network_id="N00001")

# Search and get variant details
variants = tu.tools.KEGG_search_variant(keyword="BRAF V600E")
variant = tu.tools.KEGG_get_variant(variant_id="hsa:BRAF")

Example Workflow: Find Drugs Targeting BRAF Variants in Cancer

from tooluniverse import ToolUniverse
tu = ToolUniverse()
tu.load_tools()

# 1. Find BRAF-related diseases
diseases = tu.tools.KEGG_search_disease(keyword="BRAF")

# 2. Get disease genes for melanoma
genes = tu.tools.KEGG_get_disease_genes(disease_id="H00038")

# 3. Search for BRAF-targeting drugs
drugs = tu.tools.KEGG_search_drug(keyword="BRAF inhibitor")

# 4. Get targets for vemurafenib
targets = tu.tools.KEGG_get_drug_targets(drug_id="D09996")

# 5. Get BRAF variant info
variants = tu.tools.KEGG_search_variant(keyword="BRAF V600E")

# 6. Explore disease-gene-drug network
networks = tu.tools.KEGG_search_network(keyword="BRAF melanoma")

ID Conversion & Cross-Linking

Use KEGG_convert_ids to map between KEGG identifiers and external databases before or after lookups:

# Convert NCBI Gene IDs to KEGG gene IDs for human (hsa)
result = tu.tools.KEGG_convert_ids(source_db="ncbi-geneid", target_db="hsa", ids=["672", "675"])

# Convert UniProt accessions to KEGG entries
result = tu.tools.KEGG_convert_ids(source_db="up", target_db="hsa", ids=["P38398"])

Use KEGG_link_entries to retrieve relationships between KEGG databases:

# Find all KEGG pathway IDs that contain a given gene
result = tu.tools.KEGG_link_entries(target_db="pathway", source_db_or_ids="hsa:7157")

# Find all genes linked to a specific pathway
result = tu.tools.KEGG_link_entries(target_db="hsa", source_db_or_ids="path:hsa05210")

These tools are especially useful when you have external IDs (Entrez Gene, UniProt, ChEMBL) and need to bridge into KEGG's namespace, or when you want a complete gene-pathway or drug-disease adjacency list.

Integration with Other Skills

• Pathway details: Use tooluniverse-systems-biology for Reactome/WikiPathways cross-ref
• Drug mechanisms: Use tooluniverse-drug-mechanism-research for ChEMBL/DailyMed MOA
• Clinical variants: Use tooluniverse-cancer-variant-interpretation for CIViC/ClinVar
• Drug safety: Use tooluniverse-adverse-event-detection for FAERS data

Reasoning Framework for Result Interpretation

Evidence Grading

Grade	Criteria	Example
Strong	KEGG disease entry with curated gene list, drug with confirmed target, pathway mechanistically linked	H00031 (breast cancer) with BRCA1/BRCA2 genes, D09996 (vemurafenib) targeting BRAF
Moderate	Disease-gene link in KEGG but no drug-target validation, or network entry without variant data	KEGG disease entry lists gene, but drug targets are inferred from pathway membership
Weak	Keyword search hit only, no curated disease-gene-drug relationship in KEGG	Drug found by name search but not linked to the disease in KEGG network
Insufficient	No KEGG entries found, or only cross-database ID conversion available	Rare disease not curated in KEGG Disease

Interpretation Guidance

• KEGG pathway significance: KEGG pathways are manually curated maps of molecular interactions. A gene appearing in a KEGG disease pathway has been editorially reviewed as relevant to that disease mechanism. However, KEGG coverage is not exhaustive -- absence from KEGG does not mean absence of involvement. Cross-reference with Reactome or WikiPathways for broader coverage.
• Disease-drug network interpretation: KEGG Network entries (N-codes) link diseases, genes, and drugs in mechanistic triangles. A drug targeting a gene in a disease network has a curated rationale for therapeutic relevance. The network structure distinguishes direct targets (drug binds gene product) from pathway-level connections (drug affects pathway containing the gene). Prioritize direct target relationships for drug repurposing hypotheses.
• Variant impact assessment: KEGG Variant entries are curated for clinical significance (often cancer driver mutations). A variant listed in KEGG with a linked drug entry indicates an established pharmacogenomic or precision oncology relationship (e.g., BRAF V600E linked to vemurafenib). Variants not in KEGG may still be clinically relevant -- cross-reference with ClinVar and CIViC.
• ID conversion caveat: KEGG uses its own gene ID namespace (e.g., hsa:7157 for TP53). Always use KEGG_convert_ids to map from external IDs (NCBI Gene, UniProt) before querying KEGG-specific tools. Failed conversions may indicate the gene is not in KEGG's curated set.
• Drug entry completeness: KEGG Drug entries vary in detail. Approved drugs typically have full target, pathway, and metabolism information. Investigational compounds may have partial entries. Check the drug's "Target" and "Pathway" fields for completeness before drawing conclusions.

Synthesis Questions

1. Does the KEGG disease entry list the gene of interest with a direct mechanistic role, or is the gene only peripherally connected through a shared pathway?
2. For drug-target relationships, is the target confirmed by KEGG Network (direct link), or inferred from pathway co-membership?
3. Are there KEGG variant entries linking specific mutations to drug response, supporting precision medicine applications?
4. Does the KEGG disease-gene-drug network for the condition align with evidence from other curated sources (CIViC, OncoKB, DrugBank)?
5. If KEGG has limited entries for the query, which complementary databases (Reactome, WikiPathways, CTD) should be consulted to fill gaps?

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Output

Markdown report with:

1. Disease summary (KEGG ID, name, associated genes/pathways)
2. Gene list with KEGG gene IDs and symbols
3. Drug candidates with targets and mechanisms
4. Network relationships (disease-gene-drug triangles)
5. Variant annotations if available