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Crystal structure of the Class I MHC Molecule H-2Kwm7 with a Single Self Peptide VNDIFEAI

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
3FON
Type
protein
Length
764 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.03
Source
Mus musculus; SYNTHETIC CONSTRUCT
Molecule
MHC; Beta-2-microglobulin; Peptide
UniProt
P01887
Pockets
8 · best druggability 0.66

Structure

x-ray diffraction · resolution 2.03 · 3 distinct chains · 20% helix, 42% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CMHCprotein27428% helix, 41% strand—
B, DBeta-2-microglobulinprotein1000% helix, 49% strandP01887
P, EPeptideprotein80% helix, 0% strand—

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16630.660.7560empty
26010.640.7557empty
31510.440.7527empty
41300.430.7626empty
51270.390.7422empty

Interfaces

5 interfaces between chains.

  • A–B · 1357 Ų buried · 21 hydrogen bonds · protein-protein
  • C–D · 1350 Ų buried · 20 hydrogen bonds · protein-protein
  • A–P · 836 Ų buried · 28 hydrogen bonds · protein-protein
  • C–E · 834 Ų buried · 26 hydrogen bonds · protein-protein
  • A–C · 196 Ų buried · 5 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 disulfide (disulfide).

Compared structures

  • 3FON · Crystal structure of the class I MHC molecule H-2KWM7 with a single self peptide vndifeai · the same entry in another collection · chain P against P, 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 0.98

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