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 ↗

Reject Multiple quality flags — this pose should be deprioritised or discarded.

✓ Excellent LE (-0.583 kcal/mol/HA) ✓ Good fit quality (FQ -6.01) ✗ Very high strain energy (28.6 kcal/mol) ✗ Geometry warnings ✗ Protein contact clashes ℹ SASA not computed

Score

-22.161

kcal/mol

-0.583

kcal/mol/HA

Fit Quality

-6.01

FQ (Leeson)

HAC

heavy atoms

511

LogP

5.13

cLogP

Strain ΔE

28.6 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 28.6 kcal/mol

Interaction summary

Collapsible panels

H-bonds 1 Hydrophobic 24 π–π 2 Clashes 12 Severe clashes 0

Final rank	57.394287382956804	Score	-22.1612
Inter norm	-0.593475	Intra norm	0.0102856
Top1000	no	Excluded	no
Contacts	14	H-bonds	1
Artifact reason	geometry warning; 22 clashes; 12 protein contact clashes
Residues	A:ARG97;A:ILE45;A:LEU94;A:LYS57;A:LYS95;A:MET53;A:PHE56;A:PHE91;A:PRO50;A:PRO88;A:PRO93;A:SER86;A:THR54;A:VAL87

Protein summary

225 residues

Protein target	T03	Atoms	3428
Residues	225	Chains	2
Residue summary	LEU:380; ARG:360; VAL:272; LYS:264; ALA:240; GLU:240; PRO:224; PHE:180; THR:154; ILE:152; SER:132; TYR:126; GLN:119; ASN:98; GLY:84; NDP:74

Native ligand reference

★ reference

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

Name	3CL9	Contacts	20
Pose	Open native pose	H-bonds	9
IFP residues	A:ALA32; A:ARG97; A:ASP52; A:ILE45; A:LEU94; A:LYS57; A:MET53; A:NDP301; A:PHE56; A:PHE91; A:PRO88; A:SER86; A:THR180; A:THR54; A:THR83; A:TYR162; A:VAL156; A:VAL30; A:VAL31; A:VAL87
Current overlap	11	Native recall	0.55
Jaccard	0.48	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
1364	6.917479352968085	-0.586425	-19.5575	2	21	19	0.95	0.00	-	no	Open
1362	7.932493128258576	-0.578031	-14.5651	1	17	15	0.75	0.00	-	no	Open
1366	7.978866297135433	-0.679046	-18.2764	2	19	14	0.70	0.20	-	no	Open
1361	57.394287382956804	-0.593475	-22.1612	1	14	11	0.55	0.00	-	no	Current
1365	57.55720896347987	-0.568124	-17.6116	3	17	16	0.80	0.00	-	no	Open
1368	57.38209226722004	-0.666651	-13.572	2	15	13	0.65	0.20	-	yes	Open
1363	57.728683315884496	-0.604003	-14.5991	3	17	13	0.65	0.00	-	yes	Open
1367	59.82787887465016	-0.580285	-18.6056	1	18	15	0.75	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 -22.161kcal/mol

Ligand efficiency (LE) -0.5832kcal/mol/HA

Score / heavy atom count

Fit quality (FQ) -6.012

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

Heavy atom count 38HA

Physicochemical properties

Molecular weight 510.6Da

Lipinski: ≤ 500 Da

LogP (cLogP) 5.13

Lipinski: ≤ 5

Rotatable bonds 5

Conformational strain (MMFF94s)

Strain energy (ΔE) 28.64kcal/mol

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

Docked FF energy 92.44kcal/mol

Minimised FF energy 63.80kcal/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.

OSA_Lib_201