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Characterization of four orthologs of stringent starvation protein A.

Abstract
Orthologous proteins can be beneficial for X-ray crystallographic studies when a protein from an organism of choice fails to crystallize or the crystals are not suitable for structure determination. Their amino-acid sequences should be similar enough that they will share the same fold, but different enough so that they may crystallize under alternative conditions and diffract to higher resolution. This multi-species approach was employed to obtain diffraction-quality crystals of the RNA polymerase (RNAP) associated stringent starvation protein A (SspA). Although Escherichia coli SspA could be crystallized, the crystals failed to diffract well enough for structure determination. Therefore, SspA proteins from Yersinia pestis, Vibrio cholerae and Pseudomonas aeruginosa were cloned, expressed, purified and subjected to crystallization trials. The V. cholerae SspA protein failed to crystallize under any conditions tested and the P. aeruginosa SspA protein did not form crystals suitable for data collection. On the other hand, Y. pestis SspA crystallized readily and the crystals diffracted to 2.0 A.
AuthorsMichelle Andrykovitch, Karen M Routzahn, Mi Li, Yijun Gu, David S Waugh, Xinhua Ji
JournalActa crystallographica. Section D, Biological crystallography (Acta Crystallogr D Biol Crystallogr) Vol. 59 Issue Pt 5 Pg. 881-6 (May 2003) ISSN: 0907-4449 [Print] United States
PMID12777805 (Publication Type: Journal Article)
Chemical References
  • Bacterial Proteins
  • Escherichia coli Proteins
  • Recombinant Proteins
  • SspA protein, E coli
Topics
  • Amino Acid Sequence
  • Bacterial Proteins (biosynthesis, chemistry, genetics)
  • Cloning, Molecular
  • Crystallization
  • Escherichia coli (chemistry, genetics)
  • Escherichia coli Proteins (biosynthesis, chemistry, genetics)
  • Molecular Sequence Data
  • Pseudomonas aeruginosa (chemistry, genetics)
  • Recombinant Proteins (biosynthesis, chemistry, genetics)
  • Sequence Alignment
  • Sequence Homology, Amino Acid
  • Vibrio cholerae (chemistry, genetics)
  • X-Ray Diffraction
  • Yersinia pestis (chemistry, genetics)

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