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Crystal structure of human TCR alpha chain-TRAV21-TRAJ8 and beta chain-TRBV7-8

Analyse Crystal structure of human TCR alpha chain-TRAV21-TRAJ8 and beta chain-TRBV7-8 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4WW1
Type
protein
Length
438 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
TCR alpha chain-TRAV21-TRAJ8; TCR beta chain-TRBV7-8
Pockets
3 · best druggability 0.71

Structure

x-ray diffraction · 2 distinct chains · 6% helix, 49% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATCR alpha chain-TRAV21-TRAJ8protein1975% helix, 49% strand—
BTCR beta chain-TRBV7-8protein2417% helix, 49% strand—

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19440.710.7594empty
2790.360.7623empty
3500.330.7917empty

Interfaces

1 interface between chains.

  • A–B · 2097 Ų buried · 24 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 5 disulfide (disulfide).

Compared structures

  • 4WW1 · Crystal structure of human TCR Alpha Chain-TRAV21-TRAJ8 and Beta Chain-TRBV7-8 · the same entry in another collection · chain A against A, TM-score 1.00

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