| Literature DB >> 16131759 |
Ralph Krätzner1, Judit E Debreczeni, Thomas Pape, Thomas R Schneider, Alexander Wentzel, Harald Kolmar, George M Sheldrick, Isabel Uson.
Abstract
The Ecballium elaterium trypsin inhibitor II (EETI-II) belongs to the family of squash inhibitors and is one of the strongest inhibitors known for trypsin. The eight independent molecules of EETI-II in the crystal structure reported here provide a good opportunity to test the hypothesis that this small cystine-knot protein (knottin) is sufficiently rigid to be used as a molecular scaffold for protein-engineering purposes. To extend this test, the structures of two complexes of EETI-II with trypsin have also been determined, one carrying a four-amino-acid mutation of EETI-II. The remarkable similarity of these structures confirms the rigidity of the molecular framework and hence its suitability as a molecular scaffold.Entities:
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Year: 2005 PMID: 16131759 DOI: 10.1107/S0907444905021207
Source DB: PubMed Journal: Acta Crystallogr D Biol Crystallogr ISSN: 0907-4449