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1D4 TCR recognition of H2-Ld a1a2 A5 Peptide Complexes

Analyse 1D4 TCR recognition of H2-Ld a1a2 A5 Peptide Complexes in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6L9L
Type
protein
Length
1,242 residues
Chains
8
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.399
Source
Homo sapiens
Molecule
H2-Ld a1a2; T Cell Receptor; Ser-pro-ser-tyr-ala-tyr-his-gln-phe
Pockets
18 · best druggability 0.74

Structure

x-ray diffraction · resolution 2.399 · 4 distinct chains · 15% helix, 42% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, EH2-Ld a1a2protein17538% helix, 32% strand—
C, GT Cell Receptorprotein1984% helix, 43% strand—
D, HT Cell Receptorprotein2398% helix, 50% strand—
B, FSer-pro-ser-tyr-ala-tyr-his-gln-pheprotein90% helix, 0% strand—

Pockets

18 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110920.740.77105empty
25530.700.7980empty
31450.570.8329empty
41120.550.8328empty
51060.540.8428empty

Interfaces

15 interfaces between chains.

  • G–H · 2108 Ų buried · 27 hydrogen bonds · protein-protein
  • C–D · 2087 Ų buried · 30 hydrogen bonds · protein-protein
  • E–F · 908 Ų buried · 21 hydrogen bonds · protein-protein
  • A–B · 900 Ų buried · 19 hydrogen bonds · protein-protein
  • E–G · 398 Ų buried · 1 hydrogen bond · protein-protein

Modifications

Observed in the structure: 12 disulfide (disulfide).

Compared structures

  • 6L9L · 1D4 TCR recognition of H2-ld A1A2 A5 peptide complexes · the same entry in another collection · chain A against A, TM-score 1.00

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