Crystal structure of DRIK1, a stress-responsive receptor-like pseudokinase, reveals the molecular basis for the absence of ATP binding

Abstract Background Plants reprogram metabolism and development to rapidly adapt to biotic and abiotic stress. Protein kinases play a significant role in this process by phosphorylating protein substrates that activate or inactivate signaling cascades that regulate cellular and metabolic adaptations...

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Main Authors: Bruno Aquino, Viviane C. H. da Silva, Katlin B. Massirer, Paulo Arruda
Format: Article
Language:English
Published: BMC 2020-04-01
Series:BMC Plant Biology
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12870-020-2328-3
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spelling doaj-6269aeed46384b9887869649bafdbd942020-11-25T02:02:14ZengBMCBMC Plant Biology1471-22292020-04-0120111510.1186/s12870-020-2328-3Crystal structure of DRIK1, a stress-responsive receptor-like pseudokinase, reveals the molecular basis for the absence of ATP bindingBruno Aquino0Viviane C. H. da Silva1Katlin B. Massirer2Paulo Arruda3Structural Genomics Consortium, Universidade Estadual de Campinas – UNICAMPStructural Genomics Consortium, Universidade Estadual de Campinas – UNICAMPStructural Genomics Consortium, Universidade Estadual de Campinas – UNICAMPStructural Genomics Consortium, Universidade Estadual de Campinas – UNICAMPAbstract Background Plants reprogram metabolism and development to rapidly adapt to biotic and abiotic stress. Protein kinases play a significant role in this process by phosphorylating protein substrates that activate or inactivate signaling cascades that regulate cellular and metabolic adaptations. Despite their importance in plant biology, a notably small fraction of the plant kinomes has been studied to date. Results In this report, we describe ZmDRIK1, a stress-responsive receptor-like pseudokinase whose expression is downregulated under water restriction. We show the structural features and molecular basis of the absence of ATP binding exhibited by ZmDRIK1. The ZmDRIK1 kinase domain lacks conserved amino acids that are essential for phosphorylation activity. The crystal structure of the ZmDRIK1 kinase domain revealed the presence of a spine formed by the side chain of the triad Leu240, Tyr363, and Leu375 that occludes the ATP binding pocket. Although ZmDRIK1 is unable to bind nucleotides, it does bind the small molecule ENMD-2076 which, in a cocrystal structure, revealed the potential to serve as a ZmDRIK1 inhibitor. Conclusion ZmDRIK1 is a novel receptor-like pseudokinase responsive to biotic and abiotic stress. The absence of ATP binding and consequently, the absence of phosphorylation activity, was proven by the crystal structure of the apo form of the protein kinase domain. The expression profiling of the gene encoding ZmDRIK1 suggests this kinase may play a role in downregulating the expression of stress responsive genes that are not necessary under normal conditions. Under biotic and abiotic stress, ZmDRIK1 is down-regulated to release the expression of these stress-responsive genes.http://link.springer.com/article/10.1186/s12870-020-2328-3Protein kinasePseudokinaseDrought stressBiotic stressAbiotic stress
collection DOAJ
language English
format Article
sources DOAJ
author Bruno Aquino
Viviane C. H. da Silva
Katlin B. Massirer
Paulo Arruda
spellingShingle Bruno Aquino
Viviane C. H. da Silva
Katlin B. Massirer
Paulo Arruda
Crystal structure of DRIK1, a stress-responsive receptor-like pseudokinase, reveals the molecular basis for the absence of ATP binding
BMC Plant Biology
Protein kinase
Pseudokinase
Drought stress
Biotic stress
Abiotic stress
author_facet Bruno Aquino
Viviane C. H. da Silva
Katlin B. Massirer
Paulo Arruda
author_sort Bruno Aquino
title Crystal structure of DRIK1, a stress-responsive receptor-like pseudokinase, reveals the molecular basis for the absence of ATP binding
title_short Crystal structure of DRIK1, a stress-responsive receptor-like pseudokinase, reveals the molecular basis for the absence of ATP binding
title_full Crystal structure of DRIK1, a stress-responsive receptor-like pseudokinase, reveals the molecular basis for the absence of ATP binding
title_fullStr Crystal structure of DRIK1, a stress-responsive receptor-like pseudokinase, reveals the molecular basis for the absence of ATP binding
title_full_unstemmed Crystal structure of DRIK1, a stress-responsive receptor-like pseudokinase, reveals the molecular basis for the absence of ATP binding
title_sort crystal structure of drik1, a stress-responsive receptor-like pseudokinase, reveals the molecular basis for the absence of atp binding
publisher BMC
series BMC Plant Biology
issn 1471-2229
publishDate 2020-04-01
description Abstract Background Plants reprogram metabolism and development to rapidly adapt to biotic and abiotic stress. Protein kinases play a significant role in this process by phosphorylating protein substrates that activate or inactivate signaling cascades that regulate cellular and metabolic adaptations. Despite their importance in plant biology, a notably small fraction of the plant kinomes has been studied to date. Results In this report, we describe ZmDRIK1, a stress-responsive receptor-like pseudokinase whose expression is downregulated under water restriction. We show the structural features and molecular basis of the absence of ATP binding exhibited by ZmDRIK1. The ZmDRIK1 kinase domain lacks conserved amino acids that are essential for phosphorylation activity. The crystal structure of the ZmDRIK1 kinase domain revealed the presence of a spine formed by the side chain of the triad Leu240, Tyr363, and Leu375 that occludes the ATP binding pocket. Although ZmDRIK1 is unable to bind nucleotides, it does bind the small molecule ENMD-2076 which, in a cocrystal structure, revealed the potential to serve as a ZmDRIK1 inhibitor. Conclusion ZmDRIK1 is a novel receptor-like pseudokinase responsive to biotic and abiotic stress. The absence of ATP binding and consequently, the absence of phosphorylation activity, was proven by the crystal structure of the apo form of the protein kinase domain. The expression profiling of the gene encoding ZmDRIK1 suggests this kinase may play a role in downregulating the expression of stress responsive genes that are not necessary under normal conditions. Under biotic and abiotic stress, ZmDRIK1 is down-regulated to release the expression of these stress-responsive genes.
topic Protein kinase
Pseudokinase
Drought stress
Biotic stress
Abiotic stress
url http://link.springer.com/article/10.1186/s12870-020-2328-3
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