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 (-0.568 kcal/mol/HA) ✓ Good fit quality (FQ -5.58) ✗ Very high strain energy (33.0 kcal/mol) ✗ Geometry warnings ℹ SASA not computed

Score

-18.168

kcal/mol

-0.568

kcal/mol/HA

Fit Quality

-5.58

FQ (Leeson)

HAC

heavy atoms

432

LogP

2.38

cLogP

Strain ΔE

33.0 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, strain 33.0 kcal/mol

Interaction summary

Collapsible panels

H-bonds 2 Hydrophobic 24 π–π 2 Clashes 11 Severe clashes 2

Final rank	58.67072341400821	Score	-18.1677
Inter norm	-0.823263	Intra norm	0.255521
Top1000	no	Excluded	yes
Contacts	19	H-bonds	2
Artifact reason	excluded; hard geometry fail; 1 severe clash; 2 protein clashes
Residues	A:ALA32;A:ARG48;A:ARG97;A:ASP52;A:ILE45;A:LEU94;A:LYS57;A:MET53;A:NDP301;A:PHE56;A:PHE91;A:THR180;A:THR83;A:TRP47;A:VAL156;A:VAL30;A:VAL31;A:VAL49;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	16	Native recall	0.80
Jaccard	0.70	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
1666	5.857818074052099	-0.788387	-24.401	2	19	16	0.80	0.20	-	no	Open
1669	6.111696162284338	-0.743191	-21.55	1	10	8	0.40	0.20	-	no	Open
1667	4.407746781727384	-0.703916	-20.8977	1	16	12	0.60	0.00	-	yes	Open
1672	55.39365353157332	-0.616323	-20.7173	0	18	14	0.70	0.00	-	yes	Open
1671	57.67127153356393	-0.724995	-19.5408	2	11	10	0.50	0.20	-	yes	Open
1670	58.67072341400821	-0.823263	-18.1677	2	19	16	0.80	0.00	-	yes	Current
1665	59.67371359637386	-0.70783	-20.6139	2	17	14	0.70	0.20	-	yes	Open
1668	62.045874802677446	-0.671958	-21.0571	1	18	13	0.65	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 -18.168kcal/mol

Ligand efficiency (LE) -0.5677kcal/mol/HA

Score / heavy atom count

Fit quality (FQ) -5.583

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

Heavy atom count 32HA

Physicochemical properties

Molecular weight 431.7Da

Lipinski: ≤ 500 Da

LogP (cLogP) 2.38

Lipinski: ≤ 5

Rotatable bonds 6

Conformational strain (MMFF94s)

Strain energy (ΔE) 33.05kcal/mol

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

Docked FF energy 101.78kcal/mol

Minimised FF energy 68.73kcal/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_238