生成图文并茂的分析报告/实验报告/质检报告(固定模版)。当用户要求"生成报告/总结报告/实验报告/质检报告/QC报告",或分析流程收尾需要交付报告时使用。报告必须基于真实分析输出,包含固定章节结构、关键指标表格和真实结果图。
日本語の概要は準備中です。原文の説明を表示しています。
Validates docked / generated protein-ligand poses using PoseBusters physical-validity tests, strain energy quantification, geometric checks (planarity, vdW overlap, bond/angle distortion), and pose-energy reasonableness. Filters AI-docking outputs (DiffDock, EquiBind, NeuralPLexer) where ~50% of poses fail physical-validity tests. Use when QC-ing docking results, comparing classical vs ML docking outputs, or filtering pose lists before SAR analysis.
インストールする前に、エージェントに与えられる指示の中身を確認できます。
Reference examples tested with: PoseBusters 0.6+, RDKit 2024.09+, pandas 2.2+, posecheck 0.5+ (optional).
Before using code patterns, verify installed versions match. If versions differ:
pip show <package> then help(module.function) to check signaturesIf code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.
Test docked or AI-generated protein-ligand poses for physical plausibility. PoseBusters (Buttenschoen 2024) is the modern gold standard: a suite of geometric, chemical, and energetic checks that flag implausible poses (planar aromatic rings now non-planar, vdW clashes, broken bonds, wrong chirality, unrealistic torsions). The PoseBusters benchmark showed that AI-based docking methods (DiffDock, EquiBind, TANKBind) produce ~50% physically-invalid poses despite reporting good RMSD; classical methods (Vina, GOLD) produce ~5-15% invalid. PB-valid status is therefore essential for downstream SAR, FEP setup, or generative model training.
For docking, see chemoinformatics/virtual-screening. For ML docking specifically, see chemoinformatics/ml-docking-rescoring.
PoseBusters runs ~20 individual checks grouped into:
| Check group | What it tests | Threshold |
|---|---|---|
| Sanity | Ligand chemical sanity | RDKit sanitization passes |
| Bond lengths | Bond lengths within reference | < 2 std from RDKit defaults |
| Bond angles | Bond angles within reference | < 2 std from RDKit defaults |
| Internal steric | No intra-ligand vdW clash | vdW overlap < 1.0 Å |
| Aromatic ring planarity | Aromatic rings planar | < 0.25 Å RMS deviation |
| Double-bond stereo | Z/E preserved | Match input SMILES |
| Internal energy | Strain not absurd | UFF energy < 100 kcal/mol typical |
| Volume overlap | vdW overlap with protein | < 7.5% of ligand vdW volume |
| Distance to protein | Not floating in solvent | Closest contact < 5 Å |
| Chirality | R/S preserved from input | Match input SMILES |
A pose passing ALL tests is "PB-valid". Combined PB-valid + RMSD <= 2 Å is the modern criterion.
| Workflow | PoseBusters use | Action |
|---|---|---|
| Self-docking (validating method) | Required | Compare PB-valid + RMSD <= 2A |
| Cross-docking | Required | PB-valid + RMSD <= 2A; account for protein flexibility |
| Virtual screening top hits | Required | Filter to PB-valid before MM/GBSA / FEP |
| AI docking (DiffDock, etc.) | Mandatory | Often 50% fail; otherwise can't compare to classical |
| Generated structures (RFdiffusion) | Required | Generation often produces clashes |
| Boltz-2 / AlphaFold3 ligand poses | Recommended | Same family of issues; less frequent than DiffDock |
| Production FEP setup | Required | Strain in input pose breaks FEP convergence |
from posebusters import PoseBusters
bust = PoseBusters(config='redock')
results = bust.bust(
mol_pred='predicted.sdf',
mol_true='reference.sdf',
mol_cond='receptor.pdb',
)
config options and included checks:
| Config | Includes | When to use |
|---|---|---|
redock | All checks + RMSD vs reference + protein vdW overlap | Self-docking benchmarks, retrospective validation |
dock | All checks except RMSD reference | Blind docking, prospective virtual screening |
mol | Intra-ligand only (sanity, bonds, angles, rings, stereo, energy) | Conformer QC; no protein context |
Output DataFrame columns include: mol_pred_loaded, sanitization, all_atoms_connected, bond_lengths, bond_angles, internal_steric_clash, aromatic_ring_flatness, double_bond_flatness, internal_energy, protein_flexibility, minimum_distance_to_protein, minimum_distance_to_organic_cofactors, minimum_distance_to_inorganic_cofactors, volume_overlap_with_protein, volume_overlap_with_organic_cofactors, volume_overlap_with_inorganic_cofactors. All bool; True = pass.
Output: DataFrame with one column per check, one row per pose, boolean pass/fail.
Goal: Programmatically validate a docked-pose SDF against a receptor PDB and produce a PB-valid filter.
Approach: Instantiate PoseBusters(config='dock'), call bust() on the SDF + PDB pair, and AND-aggregate all boolean check columns into a single pb_valid flag.
from posebusters import PoseBusters
import pandas as pd
bust = PoseBusters(config='dock')
results = bust.bust(
mol_pred='/path/to/docked_poses.sdf',
mol_cond='/path/to/receptor.pdb',
)
results['pb_valid'] = results.iloc[:, 4:].all(axis=1)
valid = results[results['pb_valid']]
print(f'{len(valid)} / {len(results)} poses are PB-valid')
Beyond binary PB-valid, quantitative strain energy distinguishes "marginal" from "egregious" poses.
Goal: Quantify how far each docked pose is from its lowest-energy free conformer in MMFF94 energy units.
Approach: Generate a reference conformer ensemble (ETKDGv3 + MMFF94), take the global minimum energy as baseline, and report docked_energy - min_ref_energy as strain.
from rdkit import Chem
from rdkit.Chem import AllChem
def ligand_strain(docked_sdf, n_ref=20):
suppl = Chem.SDMolSupplier(docked_sdf, removeHs=False)
strains = []
for docked in suppl:
if docked is None:
continue
smi = Chem.MolToSmiles(docked)
ref = Chem.MolFromSmiles(smi)
ref = Chem.AddHs(ref)
AllChem.EmbedMultipleConfs(ref, numConfs=n_ref, params=AllChem.ETKDGv3())
AllChem.MMFFOptimizeMoleculeConfs(ref)
ref_energies = []
for c in range(ref.GetNumConformers()):
ff = AllChem.MMFFGetMoleculeForceField(
ref,
AllChem.MMFFGetMoleculeProperties(ref),
confId=c
)
ref_energies.append(ff.CalcEnergy())
min_ref = min(ref_energies)
docked_ff = AllChem.MMFFGetMoleculeForceField(
docked,
AllChem.MMFFGetMoleculeProperties(docked)
)
docked_e = docked_ff.CalcEnergy() if docked_ff else None
strains.append({
'min_ref_energy': min_ref,
'docked_energy': docked_e,
'strain': docked_e - min_ref if docked_e else None,
})
return strains
Strain interpretation:
10 kcal/mol: implausible without exceptional binding
(Boström 1998 showed bioactive ligands have median strain ~2-4 kcal/mol.)
PoseBusters limit: protein-ligand vdW overlap < 7.5% of ligand vdW volume. Computed via:
def vdw_overlap_fraction(ligand_pdb, protein_pdb):
from rdkit import Chem
from rdkit.Chem import AllChem
# Use RDKit AllChem.UFFGetMoleculeForceField for vdW radii
# Compute pairwise distances, sum overlap volume
# (full implementation in PoseBusters; this is a sketch)
return overlap_fraction
In practice, PoseBusters' bust(...) does this automatically.
import numpy as np
def aromatic_planarity(mol):
deviations = []
for ring in mol.GetRingInfo().AtomRings():
ring_atoms = [mol.GetAtomWithIdx(i) for i in ring]
if not all(a.GetIsAromatic() for a in ring_atoms):
continue
coords = np.array([mol.GetConformer().GetAtomPosition(i)
for i in ring])
centroid = coords.mean(axis=0)
centered = coords - centroid
_, s, vh = np.linalg.svd(centered)
normal = vh[-1]
deviation = np.abs(centered @ normal).max()
deviations.append(deviation)
return max(deviations) if deviations else 0
Aromatic ring deviation > 0.25 Å is implausible; flag.
Trigger: Default DiffDock-L on chiral ligand.
Mechanism: Diffusion sampling can invert stereocenters; not constrained by training.
Symptom: PoseBusters chirality check fails; SMILES from pose != input SMILES.
Fix: Filter to PB-valid; rerun with constrained stereo if supported.
Trigger: EquiBind single-shot pose prediction.
Mechanism: Equivariant NN does not preserve ring planarity.
Symptom: Aromatic rings buckled.
Fix: Post-relax with UFF/MMFF94 minimization before downstream use.
Trigger: TANKBind pose in tight pocket.
Mechanism: Distance prediction not constrained to vdW radii.
Symptom: PoseBusters vdW overlap fails.
Fix: Post-process with constrained energy minimization (UFF + frozen heavy atoms 10% relaxation).
Trigger: Cofactor-bound complex.
Mechanism: Model trained on bond-length distribution; uncommon ligand pushes outside training distribution.
Symptom: Bond lengths >2 std from RDKit reference.
Fix: Post-relax with MMFF94 (constrained to maintain pose).
Trigger: Highly constrained pocket; flexible ligand.
Mechanism: Vina exhaustiveness limits sampling; not enough rotation search.
Symptom: Strain energy > 8 kcal/mol but pose passes PoseBusters geometric.
Fix: Re-dock with exhaustiveness=32; or post-relax pose with UFF inside pocket.
| RMSD <= 2A | PB-valid | Action |
|---|---|---|
| Yes | Yes | High confidence; use for SAR |
| Yes | No | RMSD-good but unphysical; re-relax |
| No | Yes | Physical but wrong binding mode; consider ensemble |
| No | No | Both wrong; reject |
In DiffDock benchmarks, ~25% of poses are RMSD <= 2A AND PB-valid; ~25% RMSD <= 2A but NOT PB-valid (the "false success" rate of AI methods).
import pandas as pd
from posebusters import PoseBusters
def pose_qc_pipeline(docked_sdfs, receptor_pdb):
bust = PoseBusters(config='dock')
all_results = []
for sdf in docked_sdfs:
r = bust.bust(mol_pred=sdf, mol_cond=receptor_pdb)
r['pb_valid'] = r.iloc[:, 4:].all(axis=1)
r['source'] = sdf
all_results.append(r)
df = pd.concat(all_results)
df['rank'] = df.groupby('source')['pb_valid'].cumsum()
valid_top = df[df['pb_valid']].groupby('source').head(1)
return valid_top
| Symptom | Cause | Fix |
|---|---|---|
| PoseBusters reports None | Sanitize failed on input pose | Standardize before docking; check SDF format |
| RMSD not computed | No reference provided | Pass mol_true parameter |
| All checks pass for invalid pose | Wrong receptor file format | Use PDB with hydrogens; PDBQT may not work |
| vdW overlap false positive on covalent | Covalent bond counted as clash | Use covalent docking-specific validation |
| Strain calculation slow | Too many reference conformers | Reduce n_ref to 5-10 |
| Posebusters config error | Wrong config name | Options: redock, dock, mol |
| posecheck unavailable | Different tool, similar purpose | pip install posecheck for alternative |
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概要と使いどころ
生成图文并茂的分析报告/实验报告/质检报告(固定模版)。当用户要求"生成报告/总结报告/实验报告/质检报告/QC报告",或分析流程收尾需要交付报告时使用。报告必须基于真实分析输出,包含固定章节结构、关键指标表格和真实结果图。
日本語の概要は準備中です。原文の説明を表示しています。
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日本語の概要は準備中です。原文の説明を表示しています。
Trim PCR primers from aligned reads in amplicon-panel BAMs using samtools ampliconclip. Use when processing SARS-CoV-2 ARTIC, hereditary cancer panels, ctDNA hot-spot panels, or any amplicon assay where primer-derived bases would falsely confirm reference at primer footprints.
日本語の概要は準備中です。原文の説明を表示しています。
Filter alignments by flags, mapping quality, and regions using samtools view and pysam. Use when extracting specific reads, removing low-quality alignments, or subsetting to target regions.
日本語の概要は準備中です。原文の説明を表示しています。
Create and use BAI/CSI indices for BAM/CRAM files using samtools and pysam. Use when enabling random access to alignment files or fetching specific genomic regions.
日本語の概要は準備中です。原文の説明を表示しています。
Read, write, and convert multiple sequence alignment files using Biopython Bio.AlignIO. Supports Clustal, PHYLIP, Stockholm, FASTA, Nexus, and other alignment formats for phylogenetics and conservation analysis. Use when reading, writing, or converting alignment file formats.
日本語の概要は準備中です。原文の説明を表示しています。