A novel superfamily of nucleoside triphosphate-binding motif containing proteins which are probably involved in duplex unwinding in DNA and RNA replication and recombination

FEBS Lett. 1988 Aug 1;235(1-2):16-24. doi: 10.1016/0014-5793(88)81226-2.

Abstract

A statistically significant similarity was demonstrated between the amino acid sequences of 4 Escherichia coli helicases and helicase subunits, a family of non-structural proteins of eukaryotic positive-strand RNA viruses and 2 herpesvirus proteins all of which contain an NTP-binding sequence motif. Based on sequence analysis and secondary structure predictions, a generalized structural model for the ATP-binding core is proposed. It is suggested that all these proteins constitute a superfamily of helicases (or helicase subunits) involved in NTP-dependent duplex unwinding during DNA and RNA replication and recombination.

Publication types

  • Comparative Study
  • Review

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Amino Acid Sequence
  • Bacterial Proteins
  • Binding Sites
  • Biological Evolution
  • DNA Helicases / metabolism*
  • DNA Replication
  • DNA, Viral / metabolism*
  • Escherichia coli / enzymology*
  • Molecular Sequence Data
  • Protein Conformation
  • RNA, Viral / metabolism*
  • Viral Proteins / metabolism

Substances

  • Bacterial Proteins
  • DNA, Viral
  • RNA, Viral
  • Viral Proteins
  • Adenosine Triphosphate
  • DNA Helicases

Associated data

  • GENBANK/UNKNOWN