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MolNFT v1 · #89143 · protein

Structure of a human enteropeptidase light chain variant

4DGJ · Enteropeptidase catalytic light chain: “Structure of a human enteropeptidase light chain variant”. X-ray diffraction, 11 pockets (best druggability 0.78). MolNFT v1 #89143 on GenesisL1: 3D structure, binding sites and pockets in…

PDB
4DGJ
Type
protein
Length
938 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Enteropeptidase catalytic light chain
EC
3.4.21.9
UniProt
P98073
Pockets
11 · best druggability 0.78

Structure

x-ray diffraction · 2 distinct chains · 9% helix, 39% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BEnteropeptidase catalytic light chain (EC 3.4.21.9)protein2359% helix, 38% strandP98073
C, DEnteropeptidase catalytic light chain (EC 3.4.21.9)protein2349% helix, 39% strandP98073

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111450.780.80104empty
21580.500.7828empty
31470.480.7834empty
41340.450.7731empty
51290.440.7717empty

Interfaces

5 interfaces between chains.

  • B–C · 703 Ų buried · 12 hydrogen bonds · protein-protein
  • A–D · 638 Ų buried · 4 hydrogen bonds · protein-protein
  • B–D · 423 Ų buried · 4 hydrogen bonds · protein-protein
  • A–C · 371 Ų buried · 2 hydrogen bonds · protein-protein
  • A–B · 106 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 16 disulfide (disulfide).

Compared structures

  • 4DGJ · Structure of a human enteropeptidase light chain variant · the same entry in another collection · chain D against D, TM-score 1.00
  • P98073 · AlphaFold monomer V2.0 prediction for enteropeptidase (P98073) · a predicted model of the same protein · chain D against A, TM-score 0.99

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