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Crystal structure of the tapbpr-MHC I peptide editing complex

Analyse Crystal structure of the tapbpr-MHC I peptide editing complex in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5OPI
Type
protein
Length
709 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
H-2 class I histocompatibility antigen, D-B alpha chain; Beta-2-microglobulin; Tap…
UniProt
P01899, P61769, Q53GH5
Pockets
8 · best druggability 0.76

Structure

x-ray diffraction · 3 distinct chains · 13% helix, 45% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AH-2 class I histocompatibility antigen, D-B alpha chainprotein27827% helix, 41% strandP01899
BBeta-2-microglobulinprotein990% helix, 60% strandP61769
CTap binding protein-like variantprotein3325% helix, 44% strandQ53GH5

Pockets

8 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110050.760.7993empty
21810.730.8934empty
32270.700.8638empty
46660.670.7663empty
52120.560.7931empty

Interfaces

3 interfaces between chains.

  • A–C · 1675 Ų buried · 27 hydrogen bonds · protein-protein
  • A–B · 1282 Ų buried · 17 hydrogen bonds · protein-protein
  • B–C · 605 Ų buried · 7 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 disulfide (disulfide).

Compared structures

  • 5OPI · Crystal structure of the TAPBPR-MHC I peptide editing complex · 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 0.95

Analyse

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