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Crystal structure of human caspase-1 in complex with 4-oxo-3-{6-[4- (quinoxalin-2-yloxy)-benzoylamino]-2-thiophen-2-yl-hexanoylamino}- butyric acid

Analyse Crystal structure of human caspase-1 in complex with 4-oxo-3-{6-[4… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1RWX
Type
protein
Length
266 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Interleukin-1 beta convertase
EC
3.4.22.36
UniProt
P29466
Ligands
YBH
Pockets
1 · best druggability 0.49

Structure

x-ray diffraction · 2 distinct chains · 29% helix, 17% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AInterleukin-1 beta convertase (EC 3.4.22.36)protein17829% helix, 17% strandP29466
BInterleukin-1 beta convertase (EC 3.4.22.36)protein8827% helix, 16% strandP29466

Ligands and binding sites

  • YBH · 4-oxo-3-{6-[4-(quinoxalin-2-yloxy)-benzoylamino]-2-thiophen-2-yl-hexanoylamino}-butyric acid · ligand · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1590.490.8519empty

Interfaces

1 interface between chains.

  • A–B · 2727 Ų buried · 47 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 covalent (covalent ligand).

Compared structures

  • 1RWX · Crystal structure of human caspase-1 in complex with… · the same entry in another collection · chain A against A, TM-score 1.00
  • P29466 · AlphaFold monomer V2.0 prediction for caspase-1 (P29466) · a predicted model of the same protein · chain B against A, TM-score 0.96

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