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Crystal structure of murine class I H-2DB complexed with peptide GP33 (C9M/K1S)

Analyse Crystal structure of murine class I H-2DB complexed with peptide GP33 (C9M/K1S) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1FFP
Type
protein
Length
764 residues
Chains
6
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 beta…
UniProt
P01899, P01887
Pockets
6 · best druggability 0.64

Structure

x-ray diffraction · 3 distinct chains · 20% helix, 40% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, DH-2 class I histocompatibility antigen, D-B, alpha chainprotein27328% helix, 38% strandP01899
B, EBeta-2 microglobulin beta chainprotein1000% helix, 49% strandP01887
C, FSynthetic peptide with sequence ser-ala-val-tyr- asn-phe-ala-thr-metprotein90% helix, 0% strand—

Pockets

6 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16150.640.7550empty
25440.630.7547empty
3780.400.7825empty
4570.400.8118empty
5580.310.7519empty

Interfaces

4 interfaces between chains.

  • A–B · 1393 Ų buried · 22 hydrogen bonds · protein-protein
  • D–E · 1380 Ų buried · 22 hydrogen bonds · protein-protein
  • A–C · 904 Ų buried · 29 hydrogen bonds · protein-protein
  • D–F · 893 Ų buried · 28 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 disulfide (disulfide).

Compared structures

  • 1FFP · Crystal structure of murine class I H-2DB complexed with peptide GP33 (C9M/K1S) · the same entry in another collection · chain F against F, TM-score 1.00
  • P01887 · AlphaFold monomer V2.0 prediction for beta-2-microglobulin (P01887) · a predicted model of the same protein · chain E against A, TM-score 0.98

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