Research workbench
Crystal structures of immune receptor complexes
Analyse Crystal structures of immune receptor complexes in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 2PXY
- Type
- protein
- Length
- 608 residues
- Chains
- 5
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- T cell receptor alpha chain; T cell receptor beta chain; H-2 class II histocompatibility…
- UniProt
- Q5R1F5, A2NTY6, P14438, P06344
- Pockets
- 7 · best druggability 0.72
Structure
x-ray diffraction · 5 distinct chains · 11% helix, 46% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | T cell receptor alpha chain | protein | 114 | 3% helix, 51% strand | Q5R1F5 |
| B | T cell receptor beta chain | protein | 111 | 3% helix, 50% strand | A2NTY6 |
| C | H-2 class II histocompatibility antigen, a-U alpha chain | protein | 183 | 14% helix, 44% strand | P14438 |
| D | H-2 class II histocompatibility antigen, a-U beta chain | protein | 189 | 19% helix, 46% strand | P06344 |
| P | Myelin basic protein (mbp)-peptide | protein | 11 | 0% helix, 0% strand | — |
Pockets
7 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 62 | 0.72 | 0.98 | 20 | empty |
| 2 | 315 | 0.58 | 0.77 | 41 | empty |
| 3 | 167 | 0.46 | 0.76 | 20 | empty |
| 4 | 121 | 0.43 | 0.77 | 23 | empty |
| 5 | 106 | 0.38 | 0.75 | 21 | empty |
Interfaces
10 interfaces between chains.
- C–D · 2660 Ų buried · 46 hydrogen bonds · protein-protein
- A–B · 842 Ų buried · 15 hydrogen bonds · protein-protein
- D–P · 628 Ų buried · 13 hydrogen bonds · protein-protein
- C–P · 552 Ų buried · 9 hydrogen bonds · protein-protein
- A–D · 390 Ų buried · 5 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 5 disulfide (disulfide).
Compared structures
- 2PXY · Crystal structures of immune receptor complexes · the same entry in another collection · chain B against B, TM-score 1.00
- P14438 · AlphaFold monomer V2.0 prediction for H-2 class II histocompatibility antigen, a-U alpha… · a predicted model of the same protein · chain C against A, TM-score 0.97
- P06344 · AlphaFold monomer V2.0 prediction for H-2 class II histocompatibility antigen, a-U beta… · a predicted model of the same protein · chain D against A, TM-score 0.88
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 Q5R1F5
- Every structure of UniProt A2NTY6
- Every structure of UniProt P14438
- Every structure of UniProt P06344
- Elsewhere: RCSB PDB 2PXY · PDBe 2PXY · UniProt Q5R1F5 · UniProt A2NTY6 · UniProt P14438 · UniProt P06344
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