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Human mesotrypsin complexed with hai-2 kunitz domain 1

Analyse Human mesotrypsin complexed with hai-2 kunitz domain 1 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4U32
Type
protein
Length
278 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Kunitz-type protease inhibitor 2; Trypsin-3
EC
3.4.21.4
UniProt
O43291, P35030
Ligands
NAG, CA
Pockets
2 · best druggability 0.38

Structure

x-ray diffraction · 2 distinct chains · 11% helix, 34% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
XKunitz-type protease inhibitor 2protein5413% helix, 30% strandO43291
ATrypsin-3 (EC 3.4.21.4)protein22411% helix, 35% strandP35030

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · chains X
  • CA · Calcium ion · metal · chains A

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
11080.380.7520empty
2600.290.7419empty

Interfaces

1 interface between chains.

  • X–A · 708 Ų buried · 17 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide, 1 glycan (disulfide, N-glycosylation).

Compared structures

  • 4U32 · Human mesotrypsin complexed with HAI-2 Kunitz domain 1 · the same entry in another collection · chain X against X, TM-score 1.00
  • P35030 · AlphaFold monomer V2.0 prediction for trypsin-3 (P35030) · a predicted model of the same protein · chain A against A, TM-score 0.99
  • O43291 · AlphaFold monomer V2.0 prediction for kunitz-type protease inhibitor 2 (O43291) · a predicted model of the same protein · chain X against A, TM-score 0.96

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