Protein-DNA and protein-hormone interactions in prealbumin: a model of the thyroid hormone nuclear receptor?

Nature. 1977 Jul 14;268(5616):115-20. doi: 10.1038/268115a0.

Abstract

High resolution X-ray analysis of the hormone-binding protein prealbumin has shown that it has a structural complementarity to double-helical DNA. The proposed binding site is composed of two symmetry-related beta-sheets containing a pair of helically disposed arms, which can interact with the bases in the wide groove of DNA. A palindromic target sequence is indicated by the symmetry of the protein. The two identical thyroid hormone binding sites on prealbumin are located in a channel that runs completely through the molecule. These two structural features suggest prealbumin as a model for the thyroid hormone nuclear receptor, providing a number of detailed predictions of its properties.

MeSH terms

  • Amino Acid Sequence
  • Binding Sites
  • Cell Nucleus / metabolism
  • Crystallography
  • DNA / metabolism*
  • Models, Molecular
  • Nucleic Acid Conformation
  • Prealbumin / metabolism*
  • Protein Binding
  • Protein Conformation
  • Receptors, Cell Surface / metabolism*
  • Serum Albumin / metabolism*
  • Thyroid Hormones / metabolism*
  • Thyroxine / metabolism

Substances

  • Prealbumin
  • Receptors, Cell Surface
  • Serum Albumin
  • Thyroid Hormones
  • DNA
  • Thyroxine