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Crystal structure of human gitrl
Analyse Crystal structure of human gitrl in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 3B93
- Type
- protein
- Length
- 319 residues
- Chains
- 3
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Tumor necrosis factor ligand superfamily member 18
- UniProt
- Q9UNG2
- Pockets
- 2 · best druggability 0.70
Structure
x-ray diffraction · 3 distinct chains · 0% helix, 51% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Tumor necrosis factor ligand superfamily member 18 | protein | 123 | 0% helix, 49% strand | Q9UNG2 |
| B | Tumor necrosis factor ligand superfamily member 18 | protein | 100 | 0% helix, 54% strand | Q9UNG2 |
| C | Tumor necrosis factor ligand superfamily member 18 | protein | 96 | 0% helix, 50% strand | Q9UNG2 |
Pockets
2 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 641 | 0.70 | 0.78 | 57 | empty |
| 2 | 82 | 0.35 | 0.75 | 12 | empty |
Interfaces
3 interfaces between chains.
- A–C · 790 Ų buried · 6 hydrogen bonds · protein-protein
- B–C · 527 Ų buried · 3 hydrogen bonds · protein-protein
- A–B · 502 Ų buried · 4 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 Q9UNG2
- Elsewhere: RCSB PDB 3B93 · PDBe 3B93 · UniProt Q9UNG2
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