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Crystal structure of HLA-G presenting kgppaaltl peptide

Analyse Crystal structure of HLA-G presenting kgppaaltl peptide in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3KYN
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; Kgppaaltl peptide
UniProt
Q9MYA2, P61769
Ligands
CO, CL
Pockets
5 · best druggability 0.70

Structure

x-ray diffraction · 3 distinct chains · 19% helix, 39% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AMHC class I antigenprotein27527% helix, 37% strandQ9MYA2
BBeta-2-microglobulinprotein1000% helix, 49% strandP61769
PKgppaaltl peptideprotein90% helix, 0% strand—

Ligands and binding sites

  • CO · Cobalt (II) ion · metal · chains B
  • CL · Chloride ion · ion · 2 copies · chains B

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
16500.700.7852empty
2670.410.8016empty
31200.400.7528empty
4730.360.7715empty
5530.260.7312empty

Interfaces

2 interfaces between chains.

  • A–B · 1365 Ų buried · 22 hydrogen bonds · protein-protein
  • A–P · 795 Ų buried · 14 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 disulfide (disulfide).

Compared structures

  • 3KYN · Crystal structure of HLA-G presenting KGPPAALTL 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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