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StructureFunction Studies of the Plant Cyclotides: The Role of a Circular Protein Backbone

Authors :
Craik, David J.
Barry, Daniel G.
Clark, Richard J.
Daly, Norelle L.
Sando, Lillian
Source :
Toxin Reviews; 2003, Vol. 22 Issue: 4 p555-576, 22p
Publication Year :
2003

Abstract

The traditional idea of proteins as linear chains of amino acids is being challenged with the discovery of miniproteins that contain a circular backbone. The cyclotide family is the largest group of circular proteins and is characterized by an amidecircularized protein backbone and six conserved cysteine residues. These conserved cysteines are paired to form a knotted network of disulfide bonds. The combination of the circular backbone and a cystine knot, known as the cyclic cystine knot CCK motif, confers exceptional stability upon the cyclotides. This review discusses the role of the circular backbone based on studies of both the oxidative folding of kalata B1, the prototypical cyclotide, and a comparison of the structure and activity of kalata B1 and its acyclic permutants.

Details

Language :
English
ISSN :
15569543 and 15569551
Volume :
22
Issue :
4
Database :
Supplemental Index
Journal :
Toxin Reviews
Publication Type :
Periodical
Accession number :
ejs11278296
Full Text :
https://doi.org/10.1081/TXR-120026914