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. 2018 Dec 29;18:1299. doi: 10.1186/s12885-018-5142-7

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© The Author(s). 2018

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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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Fig. 1 — Interaction of ligands that stabilize the KRas4B-PDE6δ molecular complex in silico. The interprotein surface of interaction marked with gray color was used for the accomplishment of docking, being this the region with greater contact between KRas4B GTPase (pink and yellow) and PDE6δ (blue). The compounds D14 (black) and C22 (aqua) were identified in the same inter-protein interactions sites. (Molecular Operating Environment (MOE), 2014.09)