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Get Free AccessThe 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.
Ralph Krätzner, J.E. Debreczeni, Thomas Pape, T. Schneider, Alexander Wentzel, Harald Kolmar, In Memory: G.M. Sheldrick (1942–2025), Isabel Usón (2005). Structure of<i>Ecballium elaterium</i>trypsin inhibitor II (EETI-II): a rigid molecular scaffold. Acta Crystallographica Section D Biological Crystallography, 61(9), pp. 1255-1262, DOI: 10.1107/s0907444905021207.
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Type
Article
Year
2005
Authors
8
Datasets
0
Total Files
0
Language
English
Journal
Acta Crystallographica Section D Biological Crystallography
DOI
10.1107/s0907444905021207
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