Adenylyl cyclase amino acid sequence: possible channel- or transporter-like structure

Science. 1989 Jun 30;244(4912):1558-64. doi: 10.1126/science.2472670.

Abstract

Complementary DNA's that encode an adenylyl cyclase were isolated from a bovine brain library. Most of the deduced amino acid sequence of 1134 residues is divisible into two alternating sets of hydrophobic and hydrophilic domains. Each of the two large hydrophobic domains appears to contain six transmembrane spans. Each of the two large hydrophilic domains contains a sequence that is homologous to a single cytoplasmic domain of several guanylyl cyclases; these sequences may represent nucleotide binding sites. An unexpected topographical resemblance between adenylyl cyclase and various plasma membrane channels and transporters was observed. This structural complexity suggests possible, unappreciated functions for this important enzyme.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenylyl Cyclases* / genetics
  • Adenylyl Cyclases* / isolation & purification
  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Brain / enzymology
  • Carrier Proteins*
  • Cattle
  • Cell Line
  • Cloning, Molecular
  • DNA / genetics
  • Electrophoresis, Polyacrylamide Gel
  • Ion Channels*
  • Membrane Proteins
  • Molecular Sequence Data
  • Nucleic Acid Hybridization
  • Protein Conformation
  • Transfection

Substances

  • Carrier Proteins
  • Ion Channels
  • Membrane Proteins
  • DNA
  • Adenylyl Cyclases

Associated data

  • GENBANK/M25579