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HLA-B*15:02 complexed with a synthetic peptide

Analyse HLA-B*15:02 complexed with a synthetic peptide in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6VB6
Type
protein
Length
384 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
MHC class I antigen; Beta-2-microglobulin; Synthetic peptide…
UniProt
F4NBQ8, P61769
Pockets
4 · best druggability 0.69

Structure

x-ray diffraction · 3 distinct chains · 20% helix, 41% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AMHC class I antigenprotein27627% helix, 39% strandF4NBQ8
BBeta-2-microglobulinprotein990% helix, 49% strandP61769
CSynthetic peptide thr-val-arg-ala-ser-gly-his-ser-tyrprotein90% helix, 0% strand—

Ligands and binding sites

  • GOL · Glycerol · additive · 2 copies · chains A, B
  • ACT · Acetate ion · additive · chains A, C

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

4 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16380.690.7855GOL
21590.500.7826GOL
31230.480.7918empty
4550.380.8016empty

Interfaces

2 interfaces between chains.

  • A–B · 1301 Ų buried · 18 hydrogen bonds · protein-protein
  • A–C · 891 Ų buried · 22 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 disulfide (disulfide).

Compared structures

  • 6VB6 · HLA-B*15:02 complexed with a synthetic peptide · 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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