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. 2015 Feb 8;43(4):2424–2432. doi: 10.1093/nar/gkv096

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© The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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Figure 3. — Architecture of the pre-TS cleavage Mos1 paired-end complex. (A) Sequence of the DNA substrate used in crystallisation of the pre-TS cleavage Mos1 PEC, with the flanking TA underlined. The NTS had a 5′ phosphate (indicated by a bold P), mimicking the strand cleavage product. (B) Schematic of the pre-TS cleavage Mos1 PEC, with conserved amino acid motifs indicated on monomer A (orange). The circle and DAD motif (magenta), indicate the active site of the mutant D249A Mos1 transposase. (C) Orthogonal views of the pre-TS cleavage PEC crystal structure. Transferred strands are coloured in a darker shade than non-transferred strands.