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MolNFT v1 · #13379 · protein

Three-dimensional structure of the human transglutaminase 3 enzyme: binding of calcium ions change structure for activation

1L9N · Protein-glutamine glutamyltransferase E3: “Three-dimensional structure of the human transglutaminase 3 enzyme: binding of calcium ions change structure…”. X-ray diffraction, 3 ligands (BGL, CA, CL), 11 pockets (best druggability…

PDB
1L9N
Type
protein
Length
1,346 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Protein-glutamine glutamyltransferase E3
EC
2.3.2.13
UniProt
Q08188
Ligands
BGL, CA, CL
Pockets
11 · best druggability 0.67

Structure

x-ray diffraction · 1 distinct chain · 16% helix, 42% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BProtein-glutamine glutamyltransferase E3 (EC 2.3.2.13)protein67316% helix, 42% strandQ08188

Ligands and binding sites

  • BGL · 2-O-octyl-beta-D-glucopyranose · ligand · 2 copies · chains A, B
  • CA · Calcium ion · metal · 6 copies · chains A, B
  • CL · Chloride ion · ion · 2 copies · chains A, B

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

Pockets

11 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13950.670.8049empty
23770.660.8047empty
33020.660.8133empty
42490.630.8232empty
52340.560.7834empty

Interfaces

1 interface between chains.

  • A–B · 851 Ų buried · 5 hydrogen bonds · protein-protein

Compared structures

  • 1L9N · Three-dimensional structure of the human transglutaminase 3 enzyme: binding of calcium… · the same entry in another collection · chain B against B, TM-score 1.00
  • Q08188 · AlphaFold monomer V2.0 prediction for protein-glutamine gamma- glutamyltransferase E… · a predicted model of the same protein · chain A against A, TM-score 1.00

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