| Literature DB >> 33746549 |
Kotaro Koiwai1, Kana Morohashi2, Kazue Inaba1,2, Kana Ebihara2, Hirotatsu Kojima3, Takayoshi Okabe3, Ryunosuke Yoshino4, Takatsugu Hirokawa5,6,7, Taiki Nampo8, Yuuta Fujikawa8, Hideshi Inoue8, Fumiaki Yumoto1, Toshiya Senda1,9,10, Ryusuke Niwa1,2,11.
Abstract
Insect growth regulators (IGRs) can be developed by elucidating the molecular mechanisms of insect-specific biological events. Because insect molting, and metamorphosis are controlled by ecdysteroids, their biosynthetic pathways can serve as targets for IGR development. The glutathione S-transferase Noppera-bo (Nobo), which is conserved in dipteran and lepidopteran species, plays an essential role in ecdysteroid biosynthesis. Our previous study using 17β-estradiol as a molecular probe revealed that Asp113 of Drosophila melanogaster Nobo (DmNobo) is essential for its biological function. However, to develop IGRs with a greater Nobo inhibitory activity than 17β-estradiol, further structural information is warranted. Here, we report five novel non-steroidal DmNobo inhibitors. Analysis of crystal structures of complexes revealed that DmNobo binds these inhibitors in an Asp113-independent manner. Among amino acid residues at the substrate-recognition site, conformation of conserved Phe39 was dynamically altered upon inhibitor binding. Therefore, these inhibitors can serve as seed compounds for IGR development. © Pesticide Science Society of Japan 2021. This is an open access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) License (https://creativecommons.org/licenses/by-nc-nd/4.0/).Entities:
Keywords: ecdysone; ecdysteroid; glutathione S-transferase; insect growth regulator; structure–activity relationship
Year: 2021 PMID: 33746549 PMCID: PMC7953034 DOI: 10.1584/jpestics.D20-072
Source DB: PubMed Journal: J Pestic Sci ISSN: 1348-589X Impact factor: 2.529