GL1X · GenesisL1 explorer

MolNFT v1 · #158797 · protein

Structure of HLA-A2:01 with peptide MM92

6O4Z · MHC class I antigen: “Structure of HLA-A2:01 with peptide MM92”. X-ray diffraction, 2 ligands (NA, SO4), 5 pockets (best druggability 0.67). MolNFT v1 #158797 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB
6O4Z
Type
protein
Length
382 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
MHC class I antigen; Beta-2-microglobulin; MM92
UniProt
U5YJM1, P61769
Ligands
NA, SO4
Pockets
5 · best druggability 0.67

Structure

x-ray diffraction · 3 distinct chains · 19% helix, 42% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AMHC class I antigenprotein27426% helix, 40% strandU5YJM1
BBeta-2-microglobulinprotein990% helix, 49% strandP61769
CMM92protein90% helix, 0% strand—

Ligands and binding sites

  • NA · Sodium ion · metal · 6 copies · chains A, B
  • SO4 · Sulfate ion · ion · chains B
  • GOL · Glycerol · additive · 3 copies · chains A, B, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15140.670.7843GOL
2500.430.8417GOL
3730.410.8017empty
4780.360.7715empty
5810.350.7615empty

Interfaces

2 interfaces between chains.

  • A–B · 1283 Ų buried · 23 hydrogen bonds · protein-protein
  • A–C · 815 Ų buried · 12 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 disulfide (disulfide).

Compared structures

  • 6O4Z · Structure of HLA-A2:01 with peptide MM92 · 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 0.99

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