Research workbench
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).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, E | Protein-glutamine gamma-glutamyltransferase 2 (EC 2.3.2.13) | protein | 685 | 15% helix, 39% strand | P21980 |
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.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 983 | 0.86 | 0.87 | 104 | empty |
| 2 | 305 | 0.72 | 0.85 | 56 | empty |
| 3 | 414 | 0.70 | 0.82 | 55 | empty |
| 4 | 331 | 0.69 | 0.83 | 54 | GTP |
| 5 | 173 | 0.68 | 0.87 | 34 | empty |
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
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Every structure of UniProt P21980
- Elsewhere: RCSB PDB 4PYG · PDBe 4PYG · UniProt P21980
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