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Crystal structure of the HLA-B8-A66-flr, mutant A66 of the HLA B8

Analyse Crystal structure of the HLA-B8-A66-flr, mutant A66 of the HLA B8 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3SKO
Type
protein
Length
382 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
HLA class I histocompatibility antigen, B-8 alpha chain; Beta-2-microglobulin…
UniProt
P30460, P61769, Q3KST2
Ligands
NA
Pockets
5 · best druggability 0.66

Structure

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

ChainMoleculeTypeResiduesSecondary structureUniProt
AHLA class I histocompatibility antigen, B-8 alpha chainprotein27328% helix, 39% strandP30460
BBeta-2-microglobulinprotein1000% helix, 49% strandP61769
CEpstein-barr nuclear antigen 3protein90% helix, 0% strandQ3KST2

Ligands and binding sites

  • NA · Sodium ion · metal · chains A

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
15780.660.7658empty
2600.400.8117empty
3770.380.7819empty
4750.330.7416empty
5580.310.7515empty

Interfaces

2 interfaces between chains.

  • A–B · 1375 Ų buried · 19 hydrogen bonds · protein-protein
  • A–C · 994 Ų buried · 20 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 disulfide (disulfide).

Compared structures

  • 3SKO · Crystal structure of the HLA-B8-A66-FLR, mutant A66 of the HLA B8 · 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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