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The structure of chagasin in complex with a cysteine protease clarifies the binding mode and evolution of a new inhibitor family

Analyse The structure of chagasin in complex with a cysteine protease clarifies the… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2OUL
Type
protein
Length
348 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Falcipain 2; Chagasin
EC
3.4.22.-
UniProt
Q9N6S8, Q966X9
Pockets
2 · best druggability 0.52

Structure

x-ray diffraction · 2 distinct chains · 19% helix, 33% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AFalcipain 2 (EC 3.4.22.-)protein24125% helix, 24% strandQ9N6S8
BChagasinprotein1076% helix, 51% strandQ966X9

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11270.520.8126empty
2590.270.7318empty

Interfaces

1 interface between chains.

  • A–B · 1005 Ų buried · 12 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 2OUL · The Structure of Chagasin in Complex with a Cysteine Protease Clarifies the Binding Mode… · the same entry in another collection · chain A against A, TM-score 1.00
  • Q966X9 · AlphaFold monomer V2.0 prediction for chagasin (Q966X9) · a predicted model of the same protein · chain B against A, TM-score 0.98

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