Tooluniverse Binder Discovery

Small Molecule Binder Discovery Strategy

Systematic discovery of novel small molecule binders using 60+ ToolUniverse tools across druggability assessment, known ligand mining, similarity expansion, ADMET filtering, and synthesis feasibility.

LOOK UP DON'T GUESS - Always retrieve actual data from tools before drawing conclusions. Do not assume druggability, binding sites, or compound properties based on target class alone.

KEY PRINCIPLES:

1. Report-first approach - Create report file FIRST, then populate progressively
2. Target validation FIRST - Confirm druggability before compound searching
3. Multi-strategy approach - Combine structure-based and ligand-based methods
4. ADMET-aware filtering - Eliminate poor compounds early
5. Evidence grading - Grade candidates by supporting evidence
6. Actionable output - Provide prioritized candidates with rationale
7. English-first queries - Always use English terms in tool calls. Respond in the user's language

Binding Site Reasoning (Start Here)

Before any tool call, reason about the target's structural biology:

Is the binding site a well-defined pocket (small molecule accessible) or a flat protein-protein interface (needs peptide/macrocycle)? This determines your screening strategy.

• Enzymes with active sites (proteases, kinases, ATPases): deep, well-defined pockets. Classic small molecule territory. Prioritize co-crystal structure search and known inhibitor scaffold analysis.
• GPCRs and ion channels: transmembrane pockets. Structure often available; start with GPCRdb and GtoPdb for known pharmacology.
• Nuclear receptors: deep hydrophobic pockets. Excellent small molecule tractability; ligand-based methods are well-powered.
• Protein-protein interfaces: flat, large contact surface. Small molecules rarely compete effectively unless there is a "hot spot" cavity. Check whether any allosteric pockets exist before committing to small molecule strategy. Warn the user if no pocket is found. If the target is a known molecular-glue-degrader neosubstrate (or the goal is to induce a new PPI rather than block an existing pocket), check MolGlueDB_search_compounds/MolGlueDB_get_compound for known glue chemotypes before declaring the target undruggable by small molecules.
• Intrinsically disordered regions: essentially no direct small molecule approach. Redirect to peptide strategies, or check MolGlueDB_search_compounds in case the target is a documented molecular-glue neosubstrate.
• Scaffolding / adaptor proteins: assess co-crystal structures for unexpected pockets before declaring undruggable.

Use this reasoning to select phases and warn the user about challenges before executing a full workflow.

Critical Workflow Requirements

1. Report-First Approach (MANDATORY)

DO NOT show search process or tool outputs to the user. Instead:

1. Create the report file FIRST - Before any data collection:

• File name: [TARGET]_binder_discovery_report.md
• Initialize with all section headers from the template (see REPORT_TEMPLATE.md)
• Add placeholder text: [Researching...] in each section

1. Progressively update the report - As you gather data, update each section immediately.

1. Output separate data files:

• [TARGET]_candidate_compounds.csv - Prioritized compounds with SMILES, scores
• [TARGET]_bibliography.json - Literature references (optional)

2. Citation Requirements (MANDATORY)

Every piece of information MUST include its source:

Example: *Source: ChEMBL via ChEMBL_get_target_activities (CHEMBL203)*

Workflow Overview

Phases in order:

• Phase 0: Tool verification (check parameter names with get_tool_info)
• Phase 1: Target validation — resolve IDs, assess druggability, identify binding sites, predict structure if needed
• Phase 2: Known ligand mining — ChEMBL, BindingDB, GtoPdb, PubChem BioAssay, chemical probes; SAR analysis
• Phase 3: Structure analysis — PDB co-crystals, EMDB (membrane targets), binding pocket characterization
• Phase 3.5: Docking validation — dock reference inhibitor to validate pocket geometry
• Phase 4: Compound expansion — similarity/substructure search (seeds: 3-5 diverse actives) + de novo generation
• Phase 5: ADMET filtering — physicochemical, bioavailability, toxicity, CYP, structural alerts
• Phase 6: Candidate docking and prioritization — score and rank top 20
• Phase 6.5: Literature evidence — PubMed, EuropePMC, OpenAlex
• Phase 7: Report synthesis and delivery

Phase 0: Tool Verification

CRITICAL: Verify tool parameters before calling unfamiliar tools.

tool_info = tu.tools.get_tool_info(tool_name="ChEMBL_get_target_activities")

Common parameter corrections (verify with get_tool_info if uncertain):

• OpenTargets_*: ensemblId (camelCase); ADMETAI_*: smiles must be a list
• NvidiaNIM_alphafold2 (requires NVIDIA_API_KEY env var; free key at build.nvidia.com): sequence not seq; NvidiaNIM_genmol (requires NVIDIA_API_KEY env var; free key at build.nvidia.com): SMILES must contain [*{min-max}]
• NvidiaNIM_boltz2 (requires NVIDIA_API_KEY env var; free key at build.nvidia.com): polymers=[{"molecule_type": "protein", "sequence": "..."}]

Phase 1: Target Validation

1.1 Identifier Resolution

Resolve all IDs upfront and store for downstream queries:

1. UniProt_search(query=target_name, organism="human") -> UniProt accession
2. MyGene_query_genes(q=gene_symbol, species="human") -> Ensembl gene ID
3. ChEMBL_search_targets(query=target_name, organism="Homo sapiens") -> ChEMBL target ID
4. GtoPdb_search_targets(query=target_name) -> GtoPdb ID (if GPCR/channel/enzyme)

1.2 Druggability Assessment

Use multi-source triangulation:

• OpenTargets_get_target_tractability_by_ensemblID(ensemblId) - tractability bucket
• DGIdb_get_gene_druggability(genes=[gene_symbol]) - druggability categories
• OpenTargets_get_target_classes_by_ensemblID(ensemblId) - target class
• For GPCRs: GPCRdb_get_protein + GPCRdb_get_ligands + GPCRdb_get_structures
• For antibody landscape: TheraSAbDab_search_by_target(target=target_name)

Decision Point: If no tractability data and binding site reasoning suggests PPI or disordered region, explicitly warn the user before proceeding.

1.3 Binding Site Analysis

• ChEMBL_search_binding_sites(target_chembl_id)
• get_binding_affinity_by_pdb_id(pdb_id) for co-crystallized ligands
• InterPro_get_protein_domains(accession) for domain architecture

1.4 Structure Prediction (NVIDIA NIM)

Requires NVIDIA_API_KEY. Two options:

• AlphaFold2: NvidiaNIM_alphafold2(sequence, algorithm="mmseqs2") - high accuracy, 5-15 min
• ESMFold: ESMFold_predict_structure(sequence) - fast (~30s), max 1024 AA

pLDDT guidance: >=90 very high confidence, 70-90 confident, <70 use with caution. Low pLDDT in the putative binding region undermines docking reliability.

Phase 2: Known Ligand Mining

Priority order for bioactivity data:

1. ChEMBL_get_target_activities - curated, SAR-ready
2. BindingDB_get_ligands_by_uniprot - direct Ki/Kd with literature links
3. GtoPdb_search_ligands - pharmacology focus (GPCRs, channels)
4. PubChem_search_assays_by_target_gene - HTS screens, novel scaffolds
5. OpenTargets_get_chemical_probes_by_target_ensemblID - validated probes
6. MolGlueDB_search_compounds - molecular glue degraders specifically (small molecules that induce a novel protein-protein interaction rather than occupy a conventional pocket); check this when the target has no tractable pocket but is a known or candidate neosubstrate

Key steps:

1. Filter to IC50/Ki/Kd < 10 uM; retrieve molecule details for top actives
2. Identify chemical probes and approved drugs
3. Analyze SAR: common scaffolds, key modifications
4. Check off-target selectivity: BindingDB_get_targets_by_compound