virtual-screening

Version Compatibility

Reference examples tested with: AutoDock Vina 1.2.5+, SMINA 2020-12+, GNINA 1.1+, RDKit 2024.09+, meeko 0.5+, P2Rank 2.4+, ProDy 2.4+, pdb2pqr 3.6+.

Before using code patterns, verify installed versions match. If versions differ:

• Python: pip show <package> then help(module.function) to check signatures
• CLI: vina --version; gnina --version; smina --version

If code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.

Virtual Screening

Hard rules

1. No fabricated citations. Every cited work must resolve to a verifiable
2. No claim without provenance. Every quantitative or factual claim
3. No silent failure. Every script invocation, API call, or tool use must declare its exit status and what to do on non-zero. A skill that silently swallows errors is a violation.

When to use

Load this skill when the user asks a question that matches its declared trigger conditions (see the frontmatter description for the most common ones). Do not load it for questions outside its scope — defer to the appropriate ORS skill instead.

When NOT to use

Do not load this skill if the question is in a sibling skill's domain (see ## Cross-references), if the user explicitly asks for a different tool, or if the task is outside the skill's declared category.

Docking Tool Taxonomy

Decision: For most screens, GNINA 1.1 with CNN scoring is the modern default (better than Vina on every benchmark; 30s/ligand on GPU). For >1M library scale, hierarchical Vina -> GNINA -> MM/GBSA. For cross-docking (predicted target structure or apo-holo), GNINA's CNN scoring transfers better than Vina.

Decision Tree by Scenario

Receptor Preparation

Goal: Convert a protein PDB into a docking-ready format with correct protonation, missing atoms, and removed waters.

Approach: Strip ligands and waters -> fill missing atoms (PROPKA or pdbfixer) -> add hydrogens at pH 7.4 (PDB2PQR / Reduce) -> assign partial charges -> convert to PDBQT (Open Babel).

import subprocess

def prepare_receptor(pdb_in, pdbqt_out, pH=7.4, remove_het=True):
    base = pdb_in.replace('.pdb', '')
    fixed = f'{base}_fixed.pdb'
    propka_pdb = f'{base}_propka.pdb'

    if remove_het:
        with open(pdb_in) as fin, open(f'{base}_clean.pdb', 'w') as fout:
            for line in fin:
                if line.startswith('HETATM') and 'HOH' in line:
                    continue
                if line.startswith('HETATM'):
                    continue
                fout.write(line)

    subprocess.run(['pdb2pqr', '--ff=AMBER', f'--with-ph={pH}',
                    f'{base}_clean.pdb', propka_pdb], check=True)
    subprocess.run(['obabel', propka_pdb, '-O', pdbqt_out,
                    '-xr', '--partialcharge', 'gasteiger'], check=True)
    return pdbqt_out

Common pitfall: Forgetting to add hydrogens at protein pH (7.4) but using pH 7.0 ligand charges. Hist mistakenly protonated. Use PROPKA + manual review of catalytic residues.

Ligand Preparation

Goal: Generate a 3D, docking-ready ligand file from SMILES with appropriate protonation and conformation.

Approach: Protonate at pH 7.4 with Chem.MolFromSmiles then rdMolStandardize.Uncharger -> embed 3D with ETKDGv3 -> minimize with MMFF94 -> assign Gasteiger charges -> write PDBQT with meeko.

from rdkit import Chem
from rdkit.Chem import AllChem
from rdkit.Chem.MolStandardize import rdMolStandardize
from meeko import MoleculePreparation, PDBQTWriterLegacy

def prepare_ligand(smiles, pdbqt_out):
    mol = Chem.MolFromSmiles(smiles)
    uncharger = rdMolStandardize.Uncharger()
    mol = uncharger.uncharge(mol)
    mol = Chem.AddHs(mol)
    AllChem.EmbedMolecule(mol, AllChem.ETKDGv3())
    AllChem.MMFFOptimizeMolecule(mol)

    mk_prep = MoleculePreparation()
    setups = mk_prep.prepare(mol)
    pdbqt_text, is_ok, err = PDBQTWriterLegacy.write_string(setups[0])
    if not is_ok:
        raise RuntimeError(f'meeko PDBQT export failed: {err}')
    with open(pdbqt_out, 'w') as f:
        f.write(pdbqt_text)
    return pdbqt_out

meeko (AutoDock developers' tool) handles torsion tree creation, rotamer flagging, and PDBQT writing -- preferred over Open Babel's PDBQT writer. Note: meeko 0.5+ separated the writer (PDBQTWriterLegacy) from MoleculePreparation; older code using prep.write_pdbqt_file() is deprecated.

Binding Site Detection

When the binding pocket is not known (apo target, novel allosteric site):

prank predict -f receptor.pdb -o pockets/

P2Rank output <receptor>_predictions.csv lists pocket centers with scores. Pocket 1 (highest score) is typically the orthosteric site for known protein families.

Vina Docking (Single Ligand)

# AutoDock Vina Python API requires Vina 1.2+; for Vina 1.1 use subprocess CLI:
# subprocess.run(['vina', '--receptor', ..., '--ligand', ..., '--center_x', ...], check=True)
from vina import Vina

def dock_single(receptor_pdbqt, ligand_pdbqt, center, box_size,
                exhaustiveness=8, n_poses=10):
    v = Vina(sf_name='vina')
    v.set_receptor(receptor_pdbqt)
    v.set_ligand_from_file(ligand_pdbqt)
    v.compute_vina_maps(center=center, box_size=box_size)
    v.dock(exhaustiveness=exhaustiveness, n_poses=n_poses)
    return v.energies(), v.poses()

Exhaustiveness:

• 8: default, ~30s/ligand, acceptable for screening
• 16: ~60s/ligand, lead-like prioritization
• 32: ~2 min/ligand, top-hit re-docking
• 64: ~4 min/ligand, production / co-crystal comparison

Vina pose RMSD lower bound rmsd_lb and upper bound rmsd_ub are NOT pose-vs-reference RMSDs; they are bounds on the conformational space sampled. Use external RMSD to a reference pose for accuracy QC.

GNINA with CNN Scoring (modern default)

gnina -r receptor.pdb -l ligand.sdf \
      --autobox_ligand reference_ligand.sdf \
      --cnn_scoring rescore \
      -o poses.sdf.gz \
      --num_modes 9 --exhaustiveness 8

--cnn_scoring:

• rescore (default): Vina sampling + CNN scoring (best validated)
• refinement: CNN refines top Vina pose
• metrorefine: Metropolis-style CNN refinement (slower, ~10% better pose accuracy)
• none: Vina-only (use SMINA equivalently)

--autobox_ligand: define box from reference ligand SDF/PDB. Otherwise specify --center_x/y/z + --size_x/y/z.

Critical: GNINA's CNN was trained on PDBbind 2019; performance on novel chemotypes outside this distribution is reduced. Validate with a known co-crystal redock if possible.

Virtual Screening Pipeline (Hierarchical)

Goal: Screen 10M-compound library down to top-1k candidates for follow-up.

Approach: Three-stage filter:

import pandas as pd
from concurrent.futures import ProcessPoolExecutor

# Stub helpers to be implemented per project; see the cross-referenced skills.
def drug_like_filter(df):
    raise NotImplementedError('See chemoinformatics/admet-prediction (Lipinski+Veber+PAINS)')
def vina_dock(smi, receptor_pdbqt, center, box):
    raise NotImplementedError('Wrap dock_single() above; return best affinity')
def gnina_rescore(smi, receptor_pdbqt, center, box):
    raise NotImplementedError('Wrap gnina --cnn_scoring rescore subprocess call')
def pose_validate(df):
    raise NotImplementedError('See chemoinformatics/pose-validation (PoseBusters)')

def vs_pipeline(library_smi, receptor_pdbqt, center, box, output_dir, n_workers=16):
    df = pd.read_csv(library_smi)
    df_stage1 = drug_like_filter(df)  # ~10x reduction

    with ProcessPoolExecutor(max_workers=n_workers) as ex:
        affinities = list(ex.map(
            lambda smi: vina_dock(smi, receptor_pdbqt, center, box),
            df_stage1['smiles']))
    df_stage1['vina_affinity'] = affinities
    df_stage2 = df_stage1.nsmallest(int(len(df_stage1) * 0.01), 'vina_affinity')

    df_stage2['gnina_affinity'] = df_stage2['smiles'].apply(
        lambda smi: gnina_rescore(smi, receptor_pdbqt, center, box))
    df_stage3 = df_stage2.nsmallest(1000, 'gnina_affinity')

    return pose_validate(df_stage3)

For 10M-compound libraries (ZINC22, Enamine REAL), use slurm-orchestrated parallel docking. Single-node GPU GNINA: ~3000 ligands/day. SLURM cluster (50 nodes): ~150k ligands/day.

Ultralarge Library Screening (ZINC22, Enamine REAL)

For ultralarge VS:

1. Pre-filter to drug-like (Lipinski + Ro5 + PAINS) -> typically 10-20x reduction
2. Pre-filter by 2D similarity to known actives (Tanimoto >= 0.4 via ECFP4) -> 100x reduction
3. Vina dock the filtered subset
4. Rescore top 1% with GNINA
5. Rescore top 0.1% with MM/GBSA or FEP

Lyu et al. 2019 ZINC15 ultralarge VS gold standard: 138M docked, top 96 hits picked, 13 nM-µM actives.

Per-Tool Failure Modes

Vina -- cross-dock failure

Trigger: Receptor structure not the holo (co-crystal with ligand from another binder).

Mechanism: Vina pose accuracy degrades 2-3x from self-dock (RMSD<=2A 70%) to cross-dock (RMSD<=2A 30%).

Symptom: Top-ranked pose makes no geometric sense; key contacts missing.

Fix: GNINA CNN scoring or ensemble docking. For genuine apo, predict holo with AlphaFold3 / Boltz-1 then dock.

GNINA CNN -- novel chemotype out-of-distribution

Trigger: Ligand chemotype not in PDBbind training.

Mechanism: CNN scoring overfits to PDBbind chemotypes; novel macrocycle / peptide / PROTAC scores poorly.

Symptom: Affinity prediction far worse than Vina alone.

Fix: Use --cnn_scoring rescore (sampling still by Vina) rather than CNN sampling. Validate against co-crystal of close analog.

Box too small

Trigger: Binding box defined tightly around small ligand reference.

Mechanism: Vina explores only within the box; large analogs cannot fit. " Symptom: Many ligands report "no valid pose"; chemotype-biased hits.

Fix: Add padding 5-10 A beyond reference ligand bounding box. For unknown ligand size, use 25x25x25 A.

Multi-pocket protein -- wrong site

Trigger: Protein has multiple binding sites (orthosteric + allosteric).

Mechanism: P2Rank or AutoBox picks the most "drugable" pocket; not always the desired one.

Symptom: Hits dock in wrong pocket; SAR confusing.

Fix: Verify pocket from co-crystal data; explicitly set center_x/y/z from known ligand centroid.

DiffDock-L -- PoseBusters invalid

Trigger: Default DiffDock-L output for any receptor.

Mechanism: Diffusion generates poses without physical-validity loss; ~50% fail planarity / stereochemistry / vdW overlap tests.

Symptom: Poses look reasonable but fail PoseBusters checks.

Fix: Filter to PB-valid (PoseBusters); rescore with GNINA. See chemoinformatics/pose-validation.

Wrong ionization state

Trigger: Ligand or receptor residues protonated incorrectly at pH 7.4.

Mechanism: Aspartate/glutamate/histidine protonation depends on local environment; default protonation may be wrong.

Symptom: Salt bridges missing; poses misranked.

Fix: Run PROPKA on receptor (cabinet residue pKas); for catalytic His, manually inspect rotamer state.

Reconciliation: Vina vs GNINA Disagreement

Common Errors

References

• Trott & Olson, J. Comput. Chem. 31:455 -- AutoDock Vina.
• Eberhardt et al., J. Chem. Inf. Model. 61:3891 -- Vina 1.2 features.
• Quiroga & Villarreal, PLoS ONE 11:e0155183 -- Vinardo scoring.
• McNutt et al., J. Cheminformatics 13:43 -- GNINA 1.0 CNN docking.
• Buttenschoen et al., Chem. Sci. 15:3130 -- PoseBusters (DL methods fail).
• Lyu et al., Nature 566:224 -- ultralarge VS proof-of-concept.
• Krivak & Hoksza, J. Cheminformatics 10:39 -- P2Rank.
• Forli et al., Nat. Protoc. 11:905 -- AutoDockTools / meeko.

Related Skills

• chemoinformatics/molecular-io - Parse ligands
• chemoinformatics/conformer-generation - Generate 3D for ligand prep
• chemoinformatics/molecular-standardization - Canonicalize before docking
• chemoinformatics/pose-validation - PoseBusters physical-validity QC
• chemoinformatics/docking-rescoring - DiffDock-L + GNINA hybrid
• chemoinformatics/covalent-design - Covalent docking
• chemoinformatics/free-energy-calculations - FEP for refined affinity
• chemoinformatics/admet-prediction - Filter library before docking
• structural-biology/structure-io - PDB / mmCIF handling
• structural-biology/modern-structure-prediction - AlphaFold3 / Boltz-1 for apo receptors

Cross-references

Other skills in this category:

• admet-prediction
• conformer-generation
• covalent-design
• docking-rescoring
• free-energy-calculations
• generative-design
• molecular-descriptors
• molecular-io
• molecular-standardization
• pharmacophore-modeling
• pose-validation
• protac-degraders
• qsar-modeling
• retrosynthesis
• scaffold-analysis
• shape-similarity
• similarity-searching
• substructure-search

Changelog

• 1.1.0 (migration) — Bulk-migrated to v0.4.0 schema: canonical metadata block, base Hard rules, Cross-references. Body content unchanged; author should review and fill in any domain-specific extensions to the Hard rules.
• 1.0.0 — Initial release.