FAIRMol

OHD_TC1_167

Pose ID 9572 Compound 4315 Pose 86

DB fairmolDocking pose analysis is being read from this database.
Molecular metrics status: done
RDKit SASA-based burial metrics are cached.
SASA cached
T15
T. brucei TR (Dimer cleft site) T. brucei Dimer cleft site
Ligand OHD_TC1_167
PDB9IFF

3D complex viewer

Strict H-bonds Permissive H-bonds
Viewer legend
Protein receptor
Pocket residues
Cofactor context
Docked ligand
Overall assessment
Reject SASA cached
Likely artefact or unreliable pose
Binding strong Geometry medium Native strong SASA done
Strain ΔE
35.8 kcal/mol
Protein clashes
1
Internal clashes
1
Native overlap
contact recall 0.62, Jaccard 0.42
Burial
76%
Hydrophobic fit
90%
Reason: no major geometry red flags detected
1 protein-contact clashes 48% of hydrophobic surface appears solvent-exposed (11/23 atoms). Partial exposure is common but may limit selectivity and membrane permeability.
Molecular report
Full metrics ↗
Reject Multiple quality flags — this pose should be deprioritised or discarded.
✓ Excellent LE (-0.889 kcal/mol/HA) ✓ Good fit quality (FQ -8.57) ✓ Good H-bonds (3 bonds) ✓ Deep burial (76% SASA buried) ✓ Lipophilic contacts well-matched (90%) ✗ Very high strain energy (35.8 kcal/mol) ✗ Geometry warnings ✗ Protein-contact clashes (5) ✗ Many internal clashes (17)
Score
-26.658
kcal/mol
LE
-0.889
kcal/mol/HA
Fit Quality
-8.57
FQ (Leeson)
HAC
30
heavy atoms
MW
426
Da
LogP
2.61
cLogP
Final rank
1.8246
rank score
Inter norm
-0.848
normalised
Contacts
14
H-bonds 5
Strain ΔE
35.8 kcal/mol
SASA buried
76%
Lipo contact
90% BSA apolar/total
SASA unbound
690 Ų
Apolar buried
472 Ų

Interaction summary

HBD 2 HBA 1 HY 8 PI 0 CLASH 1

HBD/HBA · H-bonds (geometric)

HBD = ligand donates H · HBA = ligand accepts H · ~ = weak (≥110°). Mode: permissive. Residues: 3.

PI · π–π interactions

No pi · π–π interactions detected for this pose.

HY · Hydrophobic contacts

CLASH · Clashes

Native ligand reference

★ reference
Interaction fingerprint calculated directly from the uploaded native ligand without docking. Current H-bond mode: permissive.
Name9IFFContacts13
PoseOpen native poseHB0
IFP residues
ALA209 ARG74 ASN208 GLY214 GLY215 GLY85 LEU73 LYS211 MET70 PHE83 PRO212 PRO213 VAL88
Current overlap8Native recall0.62
Jaccard0.42RMSD-
HB strict0Strict recall-
HB same residue+role0HB role recall-
HB same residue0HB residue recall-

Protein summary

489 residues
Protein targetT15Atoms7420
Residues489Chains1
Residue summaryVAL:768; LYS:704; LEU:703; ILE:532; GLU:450; THR:434; ARG:408; PHE:400; ALA:390; ASN:350; PRO:350; GLY:336; SER:319; TYR:294; ASP:264; MET:204

All stored poses for this docking hit

PoseFinal rankInter normScoreHBCTCT overlapCT recallHB role rec.RMSDExcluded
86 1.8246263809689578 -0.847733 -26.6577 5 14 8 0.62 - - no Current

Molecular metrics

RDKit SASA burial, strain energy (MMFF94s), ligand efficiency and fit quality for this docking pose.
✓ Metrics available

Scoring & efficiency

Docking score -26.658kcal/mol
Ligand efficiency (LE) -0.8886kcal/mol/HA
Score / heavy atom count
Fit quality (FQ) -8.572
LE / (0.072 + 0.95/HAC) — Leeson & Springthorpe
Heavy atom count 30HA

Physicochemical properties

Molecular weight 425.9Da
Lipinski: ≤ 500 Da
LogP (cLogP) 2.61
Lipinski: ≤ 5
Rotatable bonds 7

Conformational strain (MMFF94s)

Strain energy (ΔE) 35.82kcal/mol
< 5 good · 5–10 marginal · > 10 problematic
Docked FF energy 188.45kcal/mol
Minimised FF energy 152.63kcal/mol

SASA & burial

✓ computed
SASA (unbound) 690.2Ų
Total solvent-accessible surface area of free ligand
BSA total 527.3Ų
Buried surface area upon binding
BSA apolar 472.0Ų
Hydrophobic contacts buried
BSA polar 55.2Ų
Polar contacts buried
Fraction buried 76.4%
> 60 % indicates good pocket engagement
Lipophilic contact ratio 89.5%
BSA apolar / BSA total — high = hydrophobic driver
Δ Non-polar SASA -3106.5Ų
SASA_nonpolar(complex) − SASA_nonpolar(receptor) − SASA_nonpolar(ligand free). Negative = non-polar surface buried upon binding. Requires full polarity-decomposed SASA computation.
Receptor non-polar SASA 4005.2Ų
Non-polar SASA of receptor alone (VdW proxy, nonpolar atoms only)
Complex non-polar SASA 1523.6Ų
Non-polar SASA of full complex (VdW proxy, nonpolar atoms only)