| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 2050266 | FEBS Letters | 2009 | 6 Pages | 
Abstract
												Naturally split DnaE intein from Nostoc punctiforme (Npu) has robust protein trans-splicing activity and high tolerance of sequence variations at the splicing junctions. We determined the solution structure of a single chain variant of NpuDnaE intein by NMR spectroscopy. Based on the NMR structure and the backbone dynamics of the single chain NpuDnaE intein, we designed a functional split variant of the NpuDnaE intein having a short C-terminal half (C-intein) composed of six residues. In vivo and in vitro protein ligation of model proteins by the newly designed split intein were demonstrated.
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											Authors
												Jesper S. Oeemig, A. Sesilja Aranko, Janica Djupsjöbacka, Kimmo Heinämäki, Hideo Iwaï, 
											