Research workbench
Human class I MHC HLA-A2 in complex with the peptidomimetic ela-2
Analyse Human class I MHC HLA-A2 in complex with the peptidomimetic ela-2 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 3O3D
- Type
- protein
- Length
- 766 residues
- Chains
- 6
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- HLA class I histocompatibility antigen, a-2 alpha chain; Beta-2-microglobulin…
- UniProt
- P01892, P61769
- Pockets
- 11 · best druggability 0.78
Structure
x-ray diffraction · 3 distinct chains · 20% helix, 41% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, D | HLA class I histocompatibility antigen, a-2 alpha chain | protein | 275 | 28% helix, 39% strand | P01892 |
| B, E | Beta-2-microglobulin | protein | 100 | 0% helix, 49% strand | P61769 |
| C, F | Peptidomimetic ela-2 | protein | 8 | 0% helix, 0% strand | — |
Ligands and binding sites
- GOL · Glycerol · additive · 5 copies · chains A, B, D, E
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
11 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 994 | 0.78 | 0.80 | 86 | GOL |
| 2 | 661 | 0.73 | 0.79 | 73 | GOL |
| 3 | 82 | 0.62 | 0.90 | 17 | empty |
| 4 | 78 | 0.61 | 0.89 | 17 | empty |
| 5 | 160 | 0.53 | 0.79 | 31 | GOL |
Interfaces
5 interfaces between chains.
- A–B · 1429 Ų buried · 19 hydrogen bonds · protein-protein
- D–E · 1405 Ų buried · 20 hydrogen bonds · protein-protein
- A–C · 812 Ų buried · 15 hydrogen bonds · protein-protein
- D–F · 799 Ų buried · 14 hydrogen bonds · protein-protein
- A–D · 589 Ų buried · 13 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 6 disulfide, 4 modified (disulfide, nonstandard).
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 P01892
- Every structure of UniProt P61769
- Elsewhere: RCSB PDB 3O3D · PDBe 3O3D · UniProt P01892 · UniProt P61769
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