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Crystal structure of cathepsin S in complex with a nonpeptidic inhibitor.

Analyse Crystal structure of cathepsin S in complex with a nonpeptidic inhibitor. in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2H7J
Type
protein
Length
435 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Cathepsin S
EC
3.4.22.27
UniProt
P25774
Ligands
H7J, P15
Pockets
2 · best druggability 0.69

Structure

x-ray diffraction · 2 distinct chains · 29% helix, 24% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACathepsin S (EC 3.4.22.27)protein21829% helix, 23% strandP25774
BCathepsin S (EC 3.4.22.27)protein21729% helix, 24% strandP25774

Ligands and binding sites

  • H7J · N-[(1S)-1-{1-[(1R,3E)-1-acetylpent-3-en-1-yl]-1H-1,2,3-triazol-4-yl}-1,2-dimethylpropyl]benzamide · ligand · 2 copies · chains A, B
  • P15 · 2,5,8,11,14,17-hexaoxanonadecan-19-ol · ligand · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14710.690.8054H7J, P15
2660.290.7319empty

Interfaces

1 interface between chains.

  • A–B · 779 Ų buried · 10 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 disulfide, 1 covalent (disulfide, covalent ligand).

Compared structures

  • 2H7J · Crystal Structure of Cathepsin S in complex with a Nonpeptidic Inhibitor. · the same entry in another collection · chain A against A, TM-score 1.00
  • P25774 · AlphaFold monomer V2.0 prediction for cathepsin S (P25774) · a predicted model of the same protein · chain A against A, TM-score 1.00

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