GL1X · GenesisL1 explorer

MolNFT v1 · #167109 · protein

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

6VB0 · MHC class I antigen: “HLA-B*15:02 complexed with a synthetic peptide”. X-ray diffraction, 4 pockets (best druggability 0.67). MolNFT v1 #167109 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB
6VB0
Type
protein
Length
385 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 0.67

Structure

x-ray diffraction · 3 distinct chains · 19% helix, 41% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AMHC class I antigenprotein27627% helix, 39% strandF4NBQ8
BBeta-2-microglobulinprotein1000% helix, 49% strandP61769
CSynthetic peptide glu-leu-arg-ala-arg-glu-glu-ser-tyrprotein90% helix, 0% strand—

Ligands and binding sites

  • GOL · Glycerol · additive · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16040.670.7748GOL
21750.500.7729empty
31180.450.7821GOL
4880.410.7815empty

Interfaces

2 interfaces between chains.

  • A–B · 1402 Ų buried · 22 hydrogen bonds · protein-protein
  • A–C · 949 Ų buried · 27 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 disulfide (disulfide).

Compared structures

  • 6VB0 · 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 0.97

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