Human DBI (endozepine): relationship to a homologous membrane associated protein (MA-DBI)

Neuropharmacology. 1991 Dec;30(12B):1373-80. doi: 10.1016/s0028-3908(11)80004-3.

Abstract

Human endozepine, an 86 amino acid polypeptide, was originally isolated from human brain tissue as a putative ligand of the benzodiazepine receptor. Complete amino acid sequencing of the human and bovine proteins revealed significant homology with the partial sequence of diazepam binding inhibitor (DBI), a protein from rat brain. Both endozepine and DBI have been shown to elicit behavioral effects, suggesting that they function as pharmacologically-active ligands of the GABA (gamma-aminobutyric acid) receptor complex. Subsequent cDNA cloning of human and bovine endozepine, rat DBI and human DBI has shown that these proteins are encoded by the same gene. A related cDNA, encoding a transmembrane protein of 533 amino acids with a domain homologous to DBI, has also been cloned from bovine brain.

Publication types

  • Comparative Study
  • Review

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Cattle
  • Diazepam Binding Inhibitor
  • Humans
  • Membrane Proteins / genetics*
  • Models, Structural
  • Molecular Sequence Data
  • Neuropeptides / genetics*
  • Protein Conformation
  • Sequence Homology, Nucleic Acid

Substances

  • Diazepam Binding Inhibitor
  • Membrane Proteins
  • Neuropeptides

Associated data

  • GENBANK/M67516
  • GENBANK/S61932
  • GENBANK/S61935
  • GENBANK/S70258
  • GENBANK/S70261
  • GENBANK/S70262
  • GENBANK/S80107
  • GENBANK/X57453
  • GENBANK/X57454
  • GENBANK/X57455