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. 2014 Sep 8;7:430. doi: 10.1186/1756-3305-7-430

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© Garcia et al.; licensee BioMed Central Ltd. 2014

This article is published under license to BioMed Central Ltd. 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 use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Phylogenetic analysis of the DAP-36 immunosuppressant proteins from hard ticks. Phylogram resulting from the alignment of 15 full-length protein sequences from the sialotranscriptomes of A. triste (At-17164, At-17166, At-9070, At-98384 and At-17165), A. parvum (Ap-16029, Ap-15676, Ap-10830, Ap-8059, Ap-12208 and Ap-20449) and A. cajennense (Ac-67048, Ac-58724, Ac-104824 and Ac-58982) as well as sequences from other hard ticks previously deposited in the NCBI protein database, including A. maculatum (Am-3467, Am-2059, Am-8781 and Am-0397), A. variegatum (Av-4090 and Av-3456), Ixodes ricinus (Ir-0457, Ir-8919, Ir-8705 and Ir-8701) and Dermacentor andersoni (Da-3605). The database access numbers used in this analysis are listed in Additional file 5: AF5. The neighbor-joining method with 1,000 bootstrap replicates was used for analysis in MEGA 5.05 software. Brackets highlight branches with more than 75% bootstrap support. The bar at bottom indicates 20% amino acid divergence.