FAIRMol

OHD_Leishmania_310

Pose ID 12970 Compound 1186 Pose 117

DB Docking_panel_21Docking pose analysis is being read from this database.
Molecular metrics status: done
Cached molecular metrics are available for this pose.
Metrics cached · SASA missing

py3Dmol interaction viewer

Left: interactive complex viewer. Right: clickable PLIP-like interaction summary. Clicking an interaction thickens and highlights it in the 3D view.
Strict H-bonds Permissive H-bonds
Molecular report
Full metrics ↗
Reject Multiple quality flags — this pose should be deprioritised or discarded.
✓ Excellent LE (-1.232 kcal/mol/HA) ✓ Good fit quality (FQ -11.49) ✓ Strong H-bond network (11 bonds) ✗ Very high strain energy (26.4 kcal/mol) ✗ Geometry warnings ✗ Protein contact clashes ℹ SASA not computed
Score
-33.263
kcal/mol
LE
-1.232
kcal/mol/HA
Fit Quality
-11.49
FQ (Leeson)
HAC
27
heavy atoms
MW
360
Da
LogP
2.42
cLogP
Strain ΔE
26.4 kcal/mol
SASA buried
computing…
Overall: Promising but geometrically suspicious
Binding evidence: strong
Native-like contacts: strong
Ligand efficiency: excellent
Geometry reliability: low
Reason: geometry warning, clashes, protein contact clashes, strain 26.4 kcal/mol

Interaction summary

Collapsible panels
H-bonds 11 Hydrophobic 24 π–π 4 Clashes 9 Severe clashes 0
Final rank5.993552217946947Score-33.2626
Inter norm-1.45916Intra norm0.227212
Top1000noExcludedno
Contacts19H-bonds11
Artifact reasongeometry warning; 16 clashes; 9 protein contact clashes; high strain Δ 35.9
ResiduesA:ALA96;A:ARG14;A:ASP161;A:CYS168;A:GLY205;A:LEU208;A:LEU209;A:LEU263;A:LYS178;A:MET163;A:MET213;A:NAP301;A:PHE97;A:PRO210;A:SER207;A:SER95;A:TRP221;A:TYR174;A:VAL206

Protein summary

258 residues
Protein targetT08Atoms3881
Residues258Chains2
Residue summaryLEU:437; VAL:433; ALA:361; ARG:288; ILE:266; GLU:210; LYS:198; SER:198; ASN:182; THR:154; GLN:153; PHE:140; PRO:140; TYR:126; GLY:112; HIS:103

Native ligand reference

★ reference
Interaction fingerprint calculated directly from the uploaded native ligand without docking. Current H-bond mode: strict.
NameTbPTR1_cW_6RX6_ReadyContacts19
PoseOpen native poseH-bonds6
IFP residuesA:ARG14; A:ASP161; A:CYS168; A:GLY205; A:LEU208; A:LEU209; A:LYS178; A:MET213; A:NAP301; A:PHE171; A:PHE97; A:PRO210; A:PRO99; A:SER207; A:SER95; A:TRP221; A:TYR174; A:TYR98; A:VAL206
Current overlap16Native recall0.84
Jaccard0.73RMSD-
H-bond strict4Strict recall0.67
H-bond same residue+role3Role recall0.60
H-bond same residue4Residue recall0.80

Hydrogen bonds

Mode: strict. Count shows atom-level H-bonds; unique residues in summary: 0.

π–π interactions

Native π–π recall is disabled because no explicit native π–π reference was stored.

Hydrophobic contacts

Clashes

All stored poses for this docking hit

PoseFinal rankInter normScoreHBContactsNative overlapNative recallHB role recallRMSDExcluded
1295 4.630936644762207 -0.944168 -25.3759 8 17 0 0.00 0.00 - no Open
1036 4.645077071742692 -1.45049 -32.341 12 17 15 0.79 0.60 - no Open
145 5.219792930285267 -0.966783 -22.6379 4 18 0 0.00 0.00 - no Open
102 5.681449860451923 -1.59413 -34.7747 10 20 15 0.79 0.60 - no Open
117 5.993552217946947 -1.45916 -33.2626 11 19 16 0.84 0.60 - no Current
887 6.219769498690958 -1.58597 -34.0011 11 20 15 0.79 0.60 - no Open

Molecular metrics

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

Scoring & efficiency

Docking score -33.263kcal/mol
Ligand efficiency (LE) -1.2319kcal/mol/HA
Score / heavy atom count
Fit quality (FQ) -11.494
LE / (0.072 + 0.95/HAC) — Leeson & Springthorpe
Heavy atom count 27HA

Physicochemical properties

Molecular weight 360.4Da
Lipinski: ≤ 500 Da
LogP (cLogP) 2.42
Lipinski: ≤ 5
Rotatable bonds 6

Conformational strain (MMFF94s)

Strain energy (ΔE) 26.35kcal/mol
< 5 good · 5–10 marginal · > 10 problematic
Docked FF energy 84.63kcal/mol
Minimised FF energy 58.28kcal/mol

SASA & burial (FreeSASA)

not yet run
SASA has not been computed yet for this pose. Queue a background recompute to populate FreeSASA burial metrics without blocking the page.