Docking pose detail

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 ↗

Weak Marginal quality. Consider only alongside better-scoring alternatives.

✓ Excellent LE (-0.826 kcal/mol/HA) ✓ Good fit quality (FQ -7.50) ✗ Moderate strain (8.3 kcal/mol) ✗ Geometry warnings ✗ Protein contact clashes ℹ SASA not computed

Score

-20.640

kcal/mol

-0.826

kcal/mol/HA

Fit Quality

-7.50

FQ (Leeson)

HAC

heavy atoms

369

LogP

5.24

cLogP

Strain ΔE

8.3 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

Interaction summary

Collapsible panels

H-bonds 2 Hydrophobic 24 π–π 2 Clashes 8 Severe clashes 0

Final rank	3.0067114732215336	Score	-20.64
Inter norm	-0.831668	Intra norm	0.00606679
Top1000	no	Excluded	no
Contacts	18	H-bonds	2
Artifact reason	geometry warning; 6 clashes; 8 protein contact clashes
Residues	A:ALA10;A:ASN65;A:ASP22;A:GLU31;A:GLY21;A:ILE61;A:ILE8;A:LEU23;A:NAP201;A:PHE32;A:PHE35;A:PRO62;A:SER60;A:THR137;A:THR57;A:TYR122;A:VAL116;A:VAL9

Protein summary

200 residues

Protein target	T02	Atoms	3128
Residues	200	Chains	2
Residue summary	LYS:374; LEU:361; GLU:240; VAL:224; ARG:192; PHE:180; ILE:171; PRO:168; ASN:140; SER:132; TYR:126; GLN:119; ASP:108; MET:102; THR:98; GLY:91

Native ligand reference

★ reference

Interaction fingerprint calculated directly from the uploaded native ligand without docking. Current H-bond mode: strict.

Name	5SD8	Contacts	21
Pose	Open native pose	H-bonds	5
IFP residues	A:ALA10; A:ASN65; A:ASP22; A:GLN36; A:GLU31; A:GLY117; A:GLY21; A:ILE61; A:ILE8; A:LEU23; A:LEU68; A:NAP201; A:PHE32; A:PHE35; A:PRO62; A:SER60; A:THR137; A:THR57; A:TYR122; A:VAL116; A:VAL9
Current overlap	18	Native recall	0.86
Jaccard	0.86	RMSD	-
H-bond strict	0	Strict recall	0.00
H-bond same residue+role	0	Role recall	0.00
H-bond same residue	0	Residue recall	0.00

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

Pose	Final rank	Inter norm	Score	HB	Contacts	Native overlap	Native recall	HB role recall	RMSD	Excluded
324	1.6967939970426513	-0.921832	-22.128	1	19	0	0.00	0.00	-	no	Open
326	2.771138176985468	-0.964171	-22.6455	4	15	0	0.00	0.00	-	no	Open
523	2.7959168604666766	-1.027	-23.8075	1	19	18	0.86	0.20	-	no	Open
323	2.8198475822866444	-0.98054	-22.6816	2	19	0	0.00	0.00	-	no	Open
325	3.0054407329624984	-1.14312	-26.6474	3	20	0	0.00	0.00	-	no	Open
524	3.0067114732215336	-0.831668	-20.64	2	18	18	0.86	0.00	-	no	Current
525	3.879406804448658	-1.03853	-24.7997	1	22	20	0.95	0.20	-	yes	Open
522	5.369933234137985	-0.850796	-20.4426	1	19	18	0.86	0.20	-	yes	Open

Molecular metrics

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

✓ Metrics available

Scoring & efficiency

Docking score -20.640kcal/mol

Ligand efficiency (LE) -0.8256kcal/mol/HA

Score / heavy atom count

Fit quality (FQ) -7.505

LE / (0.072 + 0.95/HAC) — Leeson & Springthorpe

Heavy atom count 25HA

Physicochemical properties

Molecular weight 369.3Da

Lipinski: ≤ 500 Da

LogP (cLogP) 5.24

Lipinski: ≤ 5

Rotatable bonds 4

Conformational strain (MMFF94s)

Strain energy (ΔE) 8.26kcal/mol

< 5 good · 5–10 marginal · > 10 problematic

Docked FF energy 46.84kcal/mol

Minimised FF energy 38.58kcal/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.

OHD_TC1_133