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An episulfide cation (thiiranium ring) trapped in the active site of hav 3C proteinase inactivated by peptide-based ketone inhibitors

Analyse An episulfide cation (thiiranium ring) trapped in the active site of hav 3C… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2HAL
Type
protein
Length
216 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hepatitis a protease 3C; N-acetyl-leucyl-phenylalanyl-phenylalanyl-glutamate…
EC
3.4.22.28
UniProt
Q81090
Ligands
ACE, BBL, CF0
Pockets
2 · best druggability 0.49

Structure

x-ray diffraction · 2 distinct chains · 18% helix, 49% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHepatitis a protease 3C (EC 3.4.22.28)protein21218% helix, 49% strandQ81090
IN-acetyl-leucyl-phenylalanyl-phenylalanyl-glutamate- fluoromethylketone inhibitorprotein40% helix, 50% strand—

Ligands and binding sites

  • ACE · Acetyl group · ligand · chains A, I
  • BBL · N-[(benzyloxy)carbonyl]-L-alanine · ligand · chains A
  • CF0 · Fluoromethane · ion · chains A, I

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

2 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11220.490.7924empty
2610.310.7521empty

Interfaces

1 interface between chains.

  • A–I · 508 Ų buried · 7 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 covalent, 1 modified (covalent ligand, nonstandard).

Compared structures

  • 2HAL · An episulfide cation (thiiranium ring) trapped in the active site of HAV 3C proteinase… · the same entry in another collection · chain A against A, TM-score 1.00

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