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Crystal structure of the class I MHC molecule H-2KWM7 with a single self peptide vndiferi

Analyse Crystal structure of the class I MHC molecule H-2KWM7 with a single self… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3FOL
Type
protein
Length
382 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
MHC; Beta-2-microglobulin; 8 residue synthetic peptide
UniProt
P01887
Pockets
4 · best druggability 0.65

Structure

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

ChainMoleculeTypeResiduesSecondary structureUniProt
AMHCprotein27426% helix, 39% strand—
BBeta-2-microglobulinprotein1000% helix, 48% strandP01887
P8 residue synthetic peptideprotein80% helix, 0% strand—

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15980.650.7649empty
2780.320.7417empty
3510.290.7517empty
4520.280.7515empty

Interfaces

2 interfaces between chains.

  • A–B · 1445 Ų buried · 17 hydrogen bonds · protein-protein
  • A–P · 879 Ų buried · 19 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 disulfide (disulfide).

Compared structures

  • 3FOL · Crystal structure of the Class I MHC Molecule H-2Kwm7 with a Single Self Peptide VNDIFERI · the same entry in another collection · chain A against A, TM-score 1.00
  • P01887 · AlphaFold monomer V2.0 prediction for beta-2-microglobulin (P01887) · a predicted model of the same protein · chain B against A, TM-score 0.96

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