Sequence and crystallization of Escherichia coli dethiobiotin synthetase, the penultimate enzyme of biotin biosynthesis

J Mol Biol. 1994 Jan 14;235(2):774-6. doi: 10.1006/jmbi.1994.1030.

Abstract

The enzyme dethiobiotin synthetase (EC 6.3.3.3) has been cloned and over-expressed in Escherichia coli in such a way that milligram quantities are available. The purified enzyme has been subjected to a number of physical and chemical studies, sequenced and most notably it has been crystallized in a form that is suitable for X-ray structure determination. The cell dimensions are a = 72.8 A, b = 49.2 A, c = 61.4 A, beta = 106.2 degrees. The systematic absences are consistent with the monoclinic space group C2 with one polypeptide chain in the asymmetric unit.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • Biotin / biosynthesis
  • Carbon-Nitrogen Ligases*
  • Crystallization
  • Escherichia coli / enzymology*
  • Escherichia coli / genetics
  • Genes, Bacterial / genetics
  • Ligases / chemistry*
  • Ligases / genetics
  • Molecular Sequence Data

Substances

  • Biotin
  • Ligases
  • Carbon-Nitrogen Ligases
  • dethiobiotin synthetase

Associated data

  • GENBANK/S68059