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Single chain trimer HLA-A*02:01 (H98L, Y108C) with HPV.16 E7 peptide YMLDLQPETTDL

Analyse Single chain trimer HLA-A*02:01 (H98L, Y108C) with HPV.16 E7 peptide… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7SR3
Type
protein
Length
933 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.49
Source
Homo sapiens; Human papillomavirus type 16; Lama glama; Pongo pygmaeus
Molecule
Protein E7 peptide,Beta-2-microglobulin,MHC class I antigen chimera; Vhh
UniProt
P03129, P16213, A0A678ZGP6
Pockets
8 · best druggability 0.65

Structure

x-ray diffraction · resolution 2.49 · 4 distinct chains · 17% helix, 41% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AProtein E7 peptide,Beta-2-microglobulin,MHC class I antigen chimeraprotein35621% helix, 38% strandP03129, P16213, A0A678ZGP6
BVhhprotein1125% helix, 49% strand—
CProtein E7 peptide,Beta-2-microglobulin,MHC class I antigen chimeraprotein35220% helix, 39% strandP03129, P16213, A0A678ZGP6
DVhhprotein1138% helix, 50% strand—

Pockets

8 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15620.650.7653empty
24840.650.7745empty
33540.570.7649empty
43180.550.7546empty
51970.520.7730empty

Interfaces

3 interfaces between chains.

  • C–D · 917 Ų buried · 19 hydrogen bonds · protein-protein
  • A–B · 879 Ų buried · 17 hydrogen bonds · protein-protein
  • A–C · 191 Ų buried · 1 hydrogen bond · protein-protein

Modifications

Observed in the structure: 10 disulfide (disulfide).

Compared structures

  • P16213 · AlphaFold monomer V2.0 prediction for beta-2-microglobulin (P16213) · a predicted model of the same protein · chain C against A, TM-score 0.28

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