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Transglutaminase2 complexed with GTP

Analyse Transglutaminase2 complexed with GTP in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4PYG
Type
protein
Length
2,055 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.8
Source
Homo sapiens
Molecule
Protein-glutamine gamma-glutamyltransferase 2
EC
2.3.2.13
UniProt
P21980
Ligands
GTP
Pockets
20 · best druggability 0.86

Structure

x-ray diffraction · resolution 2.8 · 1 distinct chain · 15% helix, 39% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, EProtein-glutamine gamma-glutamyltransferase 2 (EC 2.3.2.13)protein68515% helix, 39% strandP21980

Ligands and binding sites

  • GTP · Guanosine-5'-triphosphate · ligand · 3 copies · chains A, B, E

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

Pockets

20 pockets found on a 1 Å grid, 14 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19830.860.87104empty
23050.720.8556empty
34140.700.8255empty
43310.690.8354GTP
51730.680.8734empty

Interfaces

2 interfaces between chains.

  • B–E · 1294 Ų buried · 14 hydrogen bonds · protein-protein
  • A–B · 747 Ų buried · 9 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 disulfide (disulfide).

Compared structures

  • 4PYG · TRANSGLUTAMINASE2 complexed with GTP · the same entry in another collection · chain A against A, TM-score 1.00
  • P21980 · AlphaFold monomer V2.0 prediction for protein-glutamine gamma- glutamyltransferase 2… · a predicted model of the same protein · chain A against A, TM-score 0.98

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