Structure of HLA-A*1101 in complex with a hepatitis B peptide homologue

Acta Crystallogr Sect F Struct Biol Cryst Commun. 2006 Dec 1;62(Pt 12):1179-84. doi: 10.1107/S1744309106044228. Epub 2006 Nov 4.

Abstract

A high-resolution structure of the human MHC-I molecule HLA-A*1101 is presented in which it forms a complex with a sequence homologue of a peptide that occurs naturally in hepatitis B virus DNA polymerase. The sequence of the bound peptide is AIMPARFYPK, while that of the corresponding natural peptide is LIMPARFYPK. The peptide does not make efficient use of the middle E pocket for binding, which leads to a rather superficial and exposed binding mode for the central peptide residues. Despite this, the peptide binds with high affinity (IC50 of 31 nM).

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Crystallization
  • DNA-Directed DNA Polymerase / chemistry*
  • HLA-A Antigens / chemistry*
  • HLA-A11 Antigen
  • Hepatitis B virus / chemistry
  • Humans
  • Hydrogen Bonding
  • Oligopeptides / chemistry*
  • Peptide Fragments / chemistry*
  • Protein Binding
  • Protein Conformation

Substances

  • HLA-A Antigens
  • HLA-A*11:01 antigen
  • HLA-A11 Antigen
  • Oligopeptides
  • Peptide Fragments
  • alanyl-isoleucyl-methionyl-prolyl-alanyl-arginyl-phenylalanyl-tyrosyl-prolyl-lysine
  • DNA-Directed DNA Polymerase

Associated data

  • PDB/2HN7
  • PDB/R2HN7SF