7MLC
PYL10 bound to the ABA pan-antagonist 4a
7MLC の概要
エントリーDOI | 10.2210/pdb7mlc/pdb |
分子名称 | Abscisic acid receptor PYL10, GLYCEROL, 1-{2-[3,5-dicyclopropyl-4-(4-{[(quinoxaline-2-carbonyl)amino]methyl}-1H-1,2,3-triazol-1-yl)phenyl]acetamido}cyclohexane-1-carboxylic acid, ... (4 entities in total) |
機能のキーワード | pyr/pyl/rcar, pyl10, hormone receptor, plant protein, plant protein-antagonist complex, plant protein/antagonist |
由来する生物種 | Arabidopsis thaliana (Mouse-ear cress) |
タンパク質・核酸の鎖数 | 1 |
化学式量合計 | 18433.08 |
構造登録者 | Peterson, F.C.,Vaidya, A.S.,Volkman, B.F.,Cutler, S.R. (登録日: 2021-04-28, 公開日: 2021-09-29, 最終更新日: 2024-11-20) |
主引用文献 | Vaidya, A.S.,Peterson, F.C.,Eckhardt, J.,Xing, Z.,Park, S.Y.,Dejonghe, W.,Takeuchi, J.,Pri-Tal, O.,Faria, J.,Elzinga, D.,Volkman, B.F.,Todoroki, Y.,Mosquna, A.,Okamoto, M.,Cutler, S.R. Click-to-lead design of a picomolar ABA receptor antagonist with potent activity in vivo. Proc.Natl.Acad.Sci.USA, 118:-, 2021 Cited by PubMed Abstract: Abscisic acid (ABA) is a key plant hormone that mediates both plant biotic and abiotic stress responses and many other developmental processes. ABA receptor antagonists are useful for dissecting and manipulating ABA's physiological roles in vivo. We set out to design antagonists that block receptor-PP2C interactions by modifying the agonist opabactin (OP), a synthetically accessible, high-affinity scaffold. Click chemistry was used to create an ∼4,000-member library of C4-diversified opabactin derivatives that were screened for receptor antagonism in vitro. This revealed a peptidotriazole motif shared among hits, which we optimized to yield antabactin (ANT), a pan-receptor antagonist. An X-ray crystal structure of an ANT-PYL10 complex (1.86 Å) reveals that ANT's peptidotriazole headgroup is positioned to sterically block receptor-PP2C interactions in the 4' tunnel and stabilizes a noncanonical closed-gate receptor conformer that partially opens to accommodate ANT binding. To facilitate binding-affinity studies using fluorescence polarization, we synthesized TAMRA-ANT. Equilibrium dissociation constants for TAMRA-ANT binding to receptors range from ∼400 to 1,700 pM. ANT displays improved activity in vivo and disrupts ABA-mediated processes in multiple species. ANT is able to accelerate seed germination in , tomato, and barley, suggesting that it could be useful as a germination stimulant in species where endogenous ABA signaling limits seed germination. Thus, click-based diversification of a synthetic agonist scaffold allowed us to rapidly develop a high-affinity probe of ABA-receptor function for dissecting and manipulating ABA signaling. PubMed: 34531324DOI: 10.1073/pnas.2108281118 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.77 Å) |
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