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Neutrophil serine protease 4 (PRSS57) with val-leu-lys- chloromethylketone (vlk-cmk)

Analyse Neutrophil serine protease 4 (PRSS57) with val-leu-lys- chloromethylketone… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4Q80
Type
protein
Length
466 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Serine protease 57
EC
3.4.21.-
UniProt
Q6UWY2
Ligands
2YS, NAG
Pockets
3 · best druggability 0.71

Structure

x-ray diffraction · 1 distinct chain · 12% helix, 35% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BSerine protease 57 (EC 3.4.21.-)protein23312% helix, 35% strandQ6UWY2

Ligands and binding sites

  • 2YS · D-valyl-N-[(2S,3S)-7-amino-1-chloro-2-hydroxyheptan-3-yl]-L-leucinamide · ligand · 2 copies · chains A, B
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 7 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18040.710.77752YS
2710.370.7715empty
3550.320.7718empty

Interfaces

1 interface between chains.

  • A–B · 665 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide, 4 covalent, 4 glycan (disulfide, covalent ligand, N-glycosylation).

Compared structures

  • 4Q80 · Neutrophil serine protease 4 (PRSS57) with val-leu-lys-chloromethylketone (VLK-cmk) · the same entry in another collection · chain A against A, TM-score 1.00
  • Q6UWY2 · AlphaFold monomer V2.0 prediction for serine protease 57 (Q6UWY2) · a predicted model of the same protein · chain A against A, TM-score 1.00

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