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T cell receptor-P53-HLA-A2 complex

Analyse T cell receptor-P53-HLA-A2 complex in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6VRM
Type
protein
Length
809 residues
Chains
5
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
MHC class I antigen; Beta-2-microglobulin; T-cell receptor 12-6, alfa chain; TCR 12-6…
UniProt
Q861F7, P61769, P04637
Pockets
9 · best druggability 0.72

Structure

x-ray diffraction · 5 distinct chains · 11% helix, 43% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AMHC class I antigenprotein27326% helix, 39% strandQ861F7
BBeta-2-microglobulinprotein1000% helix, 49% strandP61769
DT-cell receptor 12-6, alfa chainprotein1832% helix, 44% strand—
ETCR 12-6, beta chainprotein2447% helix, 48% strand—
PCellular tumor antigen P53 peptideprotein90% helix, 0% strandP04637

Pockets

9 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110310.720.7684empty
25420.660.7751empty
3940.510.8322empty
41700.480.7730empty
51200.400.7621empty

Interfaces

7 interfaces between chains.

  • D–E · 2076 Ų buried · 23 hydrogen bonds · protein-protein
  • A–B · 1325 Ų buried · 15 hydrogen bonds · protein-protein
  • A–P · 916 Ų buried · 17 hydrogen bonds · protein-protein
  • A–D · 408 Ų buried · 7 hydrogen bonds · protein-protein
  • A–E · 290 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 7 disulfide (disulfide).

Compared structures

  • 6VRM · T cell receptor-p53-HLA-A2 complex · the same entry in another collection · chain A against A, TM-score 1.00
  • P61769 · AlphaFold monomer V2.0 prediction for beta-2-microglobulin (P61769) · a predicted model of the same protein · chain B against A, TM-score 0.98

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