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Complex of a B21 chicken MHC class I molecule and a 11MER chicken peptide

Analyse Complex of a B21 chicken MHC class I molecule and a 11MER chicken peptide in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5AD0
Type
protein
Length
378 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
MHC class I alpha chain 2; Beta-2-microglobulin; 11MER peptide
UniProt
Q95601, P21611
Ligands
CA
Pockets
1 · best druggability 0.66

Structure

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

ChainMoleculeTypeResiduesSecondary structureUniProt
AMHC class I alpha chain 2protein26927% helix, 41% strandQ95601
BBeta-2-microglobulinprotein980% helix, 51% strandP21611
C11MER peptideprotein1136% helix, 0% strand—

Ligands and binding sites

  • CA · Calcium ion · metal · chains C
  • EDO · 1,2-ethanediol · additive · 2 copies · chains A, C

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14860.660.7850empty

Interfaces

2 interfaces between chains.

  • A–B · 1635 Ų buried · 16 hydrogen bonds · protein-protein
  • A–C · 915 Ų buried · 18 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 disulfide (disulfide).

Compared structures

  • 5AD0 · Complex of a B21 chicken MHC class I molecule and a 11MER chicken peptide · the same entry in another collection · chain A against A, TM-score 1.00
  • P21611 · AlphaFold monomer V2.0 prediction for beta-2-microglobulin (P21611) · a predicted model of the same protein · chain B against A, TM-score 0.96

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