Research workbench
Crystal structure analysis of the GAMMA/DELTA T cell ligand T22
Analyse Crystal structure analysis of the GAMMA/DELTA T cell ligand T22 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 1C16
- Type
- protein
- Length
- 1,430 residues
- Chains
- 8
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- MHC-like protein T22; Protein (beta-2-microglobulin)
- UniProt
- Q31615, P61769
- Pockets
- 20 · best druggability 0.69
Structure
x-ray diffraction · 3 distinct chains · 16% helix, 42% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, C, G | MHC-like protein T22 | protein | 260 | 19% helix, 41% strand | Q31615 |
| B, D, F, H | Protein (beta-2-microglobulin) | protein | 99 | 0% helix, 47% strand | P61769 |
| E | MHC-like protein T22 | protein | 254 | 20% helix, 41% strand | Q31615 |
Pockets
20 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 734 | 0.69 | 0.77 | 62 | empty |
| 2 | 703 | 0.69 | 0.77 | 62 | empty |
| 3 | 704 | 0.69 | 0.77 | 61 | empty |
| 4 | 689 | 0.69 | 0.77 | 63 | empty |
| 5 | 85 | 0.49 | 0.83 | 18 | empty |
Interfaces
6 interfaces between chains.
- G–H · 1248 Ų buried · 18 hydrogen bonds · protein-protein
- E–F · 1247 Ų buried · 16 hydrogen bonds · protein-protein
- A–B · 1228 Ų buried · 17 hydrogen bonds · protein-protein
- C–D · 1227 Ų buried · 15 hydrogen bonds · protein-protein
- A–C · 736 Ų buried · 5 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 16 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 Q31615
- Every structure of UniProt P61769
- Elsewhere: RCSB PDB 1C16 · PDBe 1C16 · UniProt Q31615 · UniProt P61769
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