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Mch class I H-2KB molecule complexed with PBM1 peptide

Analyse Mch class I H-2KB molecule complexed with PBM1 peptide in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1NAN
Type
protein
Length
770 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
H-2 class I histocompatibility antigen, K-B alpha chain; Beta-2-microglobulin; PBM1…
UniProt
P01901, P01887
Pockets
9 · best druggability 0.67

Structure

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

ChainMoleculeTypeResiduesSecondary structureUniProt
H, LH-2 class I histocompatibility antigen, K-B alpha chainprotein27826% helix, 39% strandP01901
P, IBeta-2-microglobulinprotein990% helix, 49% strandP01887
M, QPBM1 peptideprotein80% helix, 0% strand—

Pockets

9 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16990.670.7560empty
25630.630.7552empty
31730.500.7836empty
41310.470.7829empty
5610.450.8318empty

Interfaces

5 interfaces between chains.

  • H–P · 1292 Ų buried · 22 hydrogen bonds · protein-protein
  • L–I · 1257 Ų buried · 23 hydrogen bonds · protein-protein
  • L–Q · 932 Ų buried · 19 hydrogen bonds · protein-protein
  • H–M · 888 Ų buried · 18 hydrogen bonds · protein-protein
  • H–L · 180 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 disulfide (disulfide).

Compared structures

  • 1NAN · Mch class I H-2KB molecule complexed with PBM1 peptide · the same entry in another collection · chain Q against Q, TM-score 1.00
  • P01887 · AlphaFold monomer V2.0 prediction for beta-2-microglobulin (P01887) · a predicted model of the same protein · chain I against A, TM-score 0.99

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