Research workbench
Crystal structure of SB27 TCR in complex with the 'restriction triad' mutant HLA-B*3508-13MER
Analyse Crystal structure of SB27 TCR in complex with the 'restriction triad' mutant… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 3KXF
- Type
- protein
- Length
- 3,332 residues
- Chains
- 20
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- HLA class I histocompatibility antigen, B-35 alpha chain; Beta-2-microglobulin; SB27 T…
- UniProt
- P30685, P61769, P03206
- Ligands
- IOD
- Pockets
- 20 · best druggability 0.84
Structure
x-ray diffraction · 5 distinct chains · 12% helix, 43% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, C, K, I | HLA class I histocompatibility antigen, B-35 alpha chain | protein | 276 | 27% helix, 38% strand | P30685 |
| B, F, L, J | Beta-2-microglobulin | protein | 99 | 0% helix, 52% strand | P61769 |
| D, G, N, M | SB27 T cell receptor alpha chain | protein | 204 | 1% helix, 43% strand | — |
| E, H, P, O | SB27 T cell receptor beta chain | protein | 241 | 8% helix, 47% strand | — |
| Q, R, T, S | Peptide from trans-activator protein BZLF1 | protein | 13 | 0% helix, 8% strand | P03206 |
Ligands and binding sites
- IOD · Iodide ion · ion · 24 copies · chains A, B, C, I, D, E, F, G, H, K, L, N, P, J
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
20 pockets found on a 1 Å grid, 20 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1118 | 0.84 | 0.85 | 110 | empty |
| 2 | 942 | 0.82 | 0.83 | 90 | IOD |
| 3 | 932 | 0.77 | 0.80 | 90 | empty |
| 4 | 1038 | 0.77 | 0.79 | 77 | empty |
| 5 | 720 | 0.76 | 0.81 | 63 | IOD |
Interfaces
46 interfaces between chains.
- N–P · 2333 Ų buried · 23 hydrogen bonds · protein-protein
- D–E · 2278 Ų buried · 19 hydrogen bonds · protein-protein
- M–O · 2276 Ų buried · 18 hydrogen bonds · protein-protein
- G–H · 2259 Ų buried · 29 hydrogen bonds · protein-protein
- K–L · 1353 Ų buried · 20 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 32 disulfide (disulfide).
Compared structures
- 3KXF · Crystal Structure of SB27 TCR in complex with the 'restriction triad' mutant… · the same entry in another collection · chain S against S, TM-score 1.00
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 P30685
- Every structure of UniProt P61769
- Every structure of UniProt P03206
- Elsewhere: RCSB PDB 3KXF · PDBe 3KXF · UniProt P30685 · UniProt P61769 · UniProt P03206
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