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A Bacterial Tyrosine Phosphatase Inhibits Plant Pattern Recognition Receptor Activation
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1 of the 25 references listed on this page is in the Retraction Watch database as retracted (export 2026-10-28): 10.1073/pnas.0915064107 (notice 2016-06-20).
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/j.cell.2006.03.037openalex-snapshot
Perception of the Bacterial PAMP EF-Tu by the Receptor EFR Restricts Agrobacterium-Mediated Transformation
inferredcites →https://doi.org/10.1016/j.cell.2010.06.011openalex-snapshot
Cell Signaling by Receptor Tyrosine Kinases
inferredcites →https://doi.org/10.1016/j.chom.2010.03.007openalex-snapshot
Receptor-like Cytoplasmic Kinases Integrate Signaling from Multiple Plant Immune Receptors and Are Targeted by a Pseudomonas syringae Effector
inferredcites →https://doi.org/10.1016/j.pbi.2012.03.004openalex-snapshot
Plant–bacterial pathogen interactions mediated by type III effectors
inferredcites →https://doi.org/10.1016/j.pbi.2012.05.002openalex-snapshot
Non-arginine-aspartate (non-RD) kinases are associated with innate immune receptors that recognize conserved microbial signatures
inferredcites →https://doi.org/10.1016/j.tplants.2013.10.003openalex-snapshot
Two for all: receptor-associated kinases SOBIR1 and BAK1
inferredcites →https://doi.org/10.1038/emboj.2009.262openalex-snapshot
Control of the pattern‐recognition receptor EFR by an ER protein complex in plant immunity
inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03588.xopenalex-snapshot
The Pseudomonas syringae type III‐secreted protein HopPtoD2 possesses protein tyrosine phosphatase activity and suppresses programmed cell death in plants
inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03616.xopenalex-snapshot
A translocated protein tyrosine phosphatase of Pseudomonas syringae pv. tomato DC3000 modulates plant defence response to infection
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00343.xopenalex-snapshot
Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.0810249106openalex-snapshot
Tyrosine phosphorylation of the BRI1 receptor kinase emerges as a component of brassinosteroid signaling in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0909705107openalex-snapshot
A receptor-like cytoplasmic kinase, BIK1, associates with a flagellin receptor complex to initiate plant innate immunity
inferredcites →https://doi.org/10.1073/pnas.0915064107openalex-snapshot
RETRACTED: Autophosphorylation of Tyr-610 in the receptor kinase BAK1 plays a role in brassinosteroid signaling and basal defense gene expression
inferredcites →https://doi.org/10.1073/pnas.1109921108openalex-snapshot
Brassinosteroids inhibit pathogen-associated molecular pattern–triggered immune signaling independent of the receptor kinase BAK1
inferredcites →https://doi.org/10.1073/pnas.1318817111openalex-snapshot
Tyrosine phosphorylation of protein kinase complex BAK1/BIK1 mediates Arabidopsis innate immunity
inferredcites →https://doi.org/10.1073/pnas.181141598openalex-snapshot
Receptor-like kinases from Arabidopsis form a monophyletic gene family related to animal receptor kinases
inferredcites →https://doi.org/10.1093/bioinformatics/btq054openalex-snapshot
Skyline: an open source document editor for creating and analyzing targeted proteomics experiments
inferredcites →https://doi.org/10.1101/gad.2001911openalex-snapshot
Tyrosine phosphorylation controls brassinosteroid receptor activation by triggering membrane release of its kinase inhibitor
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02617.xopenalex-snapshot
Gateway‐compatible vectors for plant functional genomics and proteomics
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03262.xopenalex-snapshot
The Pseudomonas syringae type III effector tyrosine phosphatase HopAO1 suppresses innate immunity in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1574-6976.2011.00271.xopenalex-snapshot
Functional domains and motifs of bacterial type III effector proteins and their roles in infection
inferredcites →https://doi.org/10.1146/annurev.arplant.57.032905.105346openalex-snapshot
A Renaissance of Elicitors: Perception of Microbe-Associated Molecular Patterns and Danger Signals by Pattern-Recognition Receptors
inferredcites →https://doi.org/10.1371/journal.pgen.1002046openalex-snapshot
Phosphorylation-Dependent Differential Regulation of Plant Growth, Cell Death, and Innate Immunity by the Regulatory Receptor-Like Kinase BAK1
inferredcites →https://doi.org/10.1371/journal.ppat.1002132openalex-snapshot
Dynamic Evolution of Pathogenicity Revealed by Sequencing and Comparative Genomics of 19 Pseudomonas syringae Isolates
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.3155959openalex-extracted
A Tyrosine Phosphorylation Cycle of a Plant Receptor Ser/Thr Kinase Controls the on and Off of Chitin Signaling
inferred← citeshttps://doi.org/10.2139/ssrn.4847325openalex-extracted
Soybean Phr1-Regulated Low Phosphorus-Responsive Gmralf22 Increases Uptake of Phosphate Via Stimulating Gmpts Expression
inferred← citeshttps://doi.org/10.1002/1873-3468.13071openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9780470015902.a0023736openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/bies.202400171openalex-snapshot
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Highly flexible infection programs in a specialized wheat pathogen
inferred← citeshttps://doi.org/10.1002/iub.1398openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/wsbm.1592openalex-snapshot
Pathogenesis mechanisms of phytopathogen effectors
inferred← citeshttps://doi.org/10.1007/978-1-0716-5138-4_2openalex-snapshot
Identification of Phosphorylation and Protein Interactions of Plant Pattern Recognition Receptors Through Immunoprecipitation
inferred← citeshttps://doi.org/10.1007/978-1-4939-2540-7_14openalex-snapshot
Designing Climate-Smart Future Crops Employing Signal Transduction Components
inferred← citeshttps://doi.org/10.1007/978-1-4939-2648-0_10openalex-snapshot
Phosphopeptide Immuno-Affinity Enrichment to Enhance Detection of Tyrosine Phosphorylation in Plants
inferred← citeshttps://doi.org/10.1007/978-1-4939-3115-6_11openalex-snapshot
Immunoprecipitation of Plasma Membrane Receptor-Like Kinases for Identification of Phosphorylation Sites and Associated Proteins
inferred← citeshttps://doi.org/10.1007/978-1-4939-6859-6_11openalex-snapshot
Analysis of PAMP-Triggered ROS Burst in Plant Immunity
inferred← citeshttps://doi.org/10.1007/978-3-030-48733-1_15openalex-snapshot
Protein Phosphatase Mediated Responses in Plant Host-Pathogen Interactions
inferred← citeshttps://doi.org/10.1007/978-3-031-87035-4_1openalex-snapshot
Microbiome Engineering of the Mango Rhizosphere: A Sustainable Solution for Climate-Resilient Production and Way Forward
inferred← citeshttps://doi.org/10.1007/s11295-020-01481-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12298-024-01452-7openalex-snapshot
Pattern-Triggered Immunity and Effector-Triggered Immunity: crosstalk and cooperation of PRR and NLR-mediated plant defense pathways during host–pathogen interactions
inferred← citeshttps://doi.org/10.1007/s13258-019-00801-1openalex-snapshot
Pattern recognition receptors and their interactions with bacterial type III effectors in plants
inferred← citeshttps://doi.org/10.1016/b978-0-12-812689-9.00010-8openalex-snapshot
Metabolic Responses of Plants Upon Different Plant–Pathogen Interactions
inferred← citeshttps://doi.org/10.1016/b978-0-323-90568-8.00005-5openalex-snapshot
Microbial elicitors: Positive and negative modulators of plant defense
inferred← citeshttps://doi.org/10.1016/b978-0-323-90594-7.00014-4openalex-snapshot
Role of receptor-like kinases in plant-pathogen interaction
inferred← citeshttps://doi.org/10.1016/b978-0-444-63987-5.00006-2openalex-snapshot
Innate Immunity Engaged or Disengaged in Plant-Microbe Interactions ☆
inferred← citeshttps://doi.org/10.1016/bs.enz.2016.09.003openalex-snapshot
Receptor-Like Kinases and Regulation of Plant Innate Immunity
inferred← citeshttps://doi.org/10.1016/j.bbrc.2015.06.006openalex-snapshot
PopW activates PAMP-triggered immunity in controlling tomato bacterial spot disease
inferred← citeshttps://doi.org/10.1016/j.cell.2020.07.020openalex-snapshot
A Defense Pathway Linking Plasma Membrane and Chloroplasts and Co-opted by Pathogens
inferred← citeshttps://doi.org/10.1016/j.cell.2024.04.040openalex-snapshot
Peptide REF1 is a local wound signal promoting plant regeneration
inferred← citeshttps://doi.org/10.1016/j.chom.2016.09.007openalex-snapshot
Activation-Dependent Destruction of a Co-receptor by a Pseudomonas syringae Effector Dampens Plant Immunity
inferred← citeshttps://doi.org/10.1016/j.chom.2017.12.005openalex-snapshot
A Tyrosine Phosphorylation Cycle Regulates Fungal Activation of a Plant Receptor Ser/Thr Kinase
inferred← citeshttps://doi.org/10.1016/j.copbio.2025.103420openalex-snapshot
A guide to designing cell-surface receptors in plants
inferred← citeshttps://doi.org/10.1016/j.cropd.2024.100077openalex-snapshot
Decoding post-translational modification for understanding stress tolerance in plant
inferred← citeshttps://doi.org/10.1016/j.devcel.2024.11.005openalex-snapshot
Antagonistic systemin receptors integrate the activation and attenuation of systemic wound signaling in tomato
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2023.124834openalex-snapshot
Comparative transcriptome analysis reveals the core molecular network in pattern-triggered immunity in Sorghum bicolor
inferred← citeshttps://doi.org/10.1016/j.jplph.2018.10.025openalex-snapshot
An Arabidopsis thaliana leucine-rich repeat protein harbors an adenylyl cyclase catalytic center and affects responses to pathogens
inferred← citeshttps://doi.org/10.1016/j.mib.2014.10.009openalex-snapshot
Targeting of plant pattern recognition receptor-triggered immunity by bacterial type-III secretion system effectors
inferred← citeshttps://doi.org/10.1016/j.molcel.2021.07.029openalex-snapshot
Molecular mechanisms of early plant pattern-triggered immune signaling
inferred← citeshttps://doi.org/10.1016/j.molp.2014.12.022openalex-snapshot
Signaling Mechanisms in Pattern-Triggered Immunity (PTI)
inferred← citeshttps://doi.org/10.1016/j.molp.2026.04.012openalex-snapshot
Receptor-like protein kinases in plants: Post-translational regulation and functional effects
inferred← citeshttps://doi.org/10.1016/j.pbi.2015.12.005openalex-snapshot
Organ-specific regulation of growth-defense tradeoffs by plants
inferred← citeshttps://doi.org/10.1016/j.pbi.2017.04.007openalex-snapshot
A look at plant immunity through the window of the multitasking coreceptor BAK1
inferred← citeshttps://doi.org/10.1016/j.pbi.2017.05.004openalex-snapshot
Post-translational regulation of plant immunity
inferred← citeshttps://doi.org/10.1016/j.pbi.2018.07.008openalex-snapshot
Regulation of pattern recognition receptor signalling by phosphorylation and ubiquitination
inferred← citeshttps://doi.org/10.1016/j.pbi.2021.102051openalex-snapshot
More than an on-and-off switch: Post-translational modifications of plant pattern recognition receptor complexes
inferred← citeshttps://doi.org/10.1016/j.pestbp.2023.105728openalex-snapshot
Separation of anti-TMV active components and modes of action of Omphalia lapidescens
inferred← citeshttps://doi.org/10.1016/j.plantsci.2024.112211openalex-snapshot
Soybean PHR1-regulated low phosphorus-responsive GmRALF22 promotes phosphate uptake by stimulating the expression of GmPTs
inferred← citeshttps://doi.org/10.1016/j.tplants.2015.02.005openalex-snapshot
Importance of tyrosine phosphorylation in receptor kinase complexes
inferred← citeshttps://doi.org/10.1016/j.tplants.2019.04.009openalex-snapshot
Plant Immunity: Thinking Outside and Inside the Box
inferred← citeshttps://doi.org/10.1016/j.xplc.2025.101383openalex-snapshot
Flagellin sensing, signaling, and immune responses in plants
inferred← citeshttps://doi.org/10.1021/acs.jproteome.5c00185openalex-snapshot
Integrated Single-Tip IMAC-HILIC Enables Simultaneous Analysis of Plant Phosphoproteomics and N-Glycoproteomics
inferred← citeshttps://doi.org/10.1038/ncomms10311openalex-snapshot
A Phytophthora infestans RXLR effector targets plant PP1c isoforms that promote late blight disease
inferred← citeshttps://doi.org/10.1038/nri.2016.77openalex-snapshot
Regulation of pattern recognition receptor signalling in plants
inferred← citeshttps://doi.org/10.1038/s41438-020-00410-0openalex-snapshot
Perception of unrelated microbe-associated molecular patterns triggers conserved yet variable physiological and transcriptional changes in Brassica rapa ssp. pekinensis
inferred← citeshttps://doi.org/10.1038/s41467-017-02195-8openalex-snapshot
A 1-phytase type III effector interferes with plant hormone signaling
inferred← citeshttps://doi.org/10.1038/s41467-018-06943-2openalex-snapshot
Identification and characterization of a large family of superbinding bacterial SH2 domains
inferred← citeshttps://doi.org/10.1038/s41467-024-48313-1openalex-snapshot
Receptor-like cytoplasmic kinases of different subfamilies differentially regulate SOBIR1/BAK1-mediated immune responses in Nicotiana benthamiana
inferred← citeshttps://doi.org/10.1038/s41579-022-00710-3openalex-snapshot
Evasion of plant immunity by microbial pathogens
inferred← citeshttps://doi.org/10.1038/s41586-018-0471-xopenalex-snapshot
Phosphocode-dependent functional dichotomy of a common co-receptor in plant signalling
inferred← citeshttps://doi.org/10.1038/s41586-020-2032-3openalex-snapshot
Hydrogen peroxide sensor HPCA1 is an LRR receptor kinase in Arabidopsis
inferred← citeshttps://doi.org/10.1042/bcj20160238openalex-snapshot
Plant cell wall signalling and receptor-like kinases
inferred← citeshttps://doi.org/10.1042/bcj20210202openalex-snapshot
Importance of tyrosine phosphorylation for transmembrane signaling in plants
inferred← citeshttps://doi.org/10.1042/ebc20210088openalex-snapshot
What’s new in protein kinase/phosphatase signalling in the control of plant immunity?
inferred← citeshttps://doi.org/10.1073/pnas.1614468114openalex-snapshot
Arabidopsis glycosylphosphatidylinositol-anchored protein LLG1 associates with and modulates FLS2 to regulate innate immunity
inferred← citeshttps://doi.org/10.1073/pnas.2108242118openalex-snapshot
Activation loop phosphorylation of a non-RD receptor kinase initiates plant innate immune signaling
inferred← citeshttps://doi.org/10.1080/13102818.2025.2512720openalex-snapshot
Antibacterial potential of Piper nigrum L. essential oil targeting FtsZ, GyrB, murA, and PTP proteins: in silico study
inferred← citeshttps://doi.org/10.1080/15592324.2018.1435228openalex-snapshot
Autophosphorylation site Y428 is essential for the in vivo activation of CERK1
inferred← citeshttps://doi.org/10.1080/15592324.2025.2552895openalex-snapshot
Genome-wide identification and expression analysis of NPR1- like genes in pearl millet under diverse biotic and abiotic stresses and phytohormone treatments
inferred← citeshttps://doi.org/10.1093/femsre/fuw003openalex-snapshot
Exploring the diversity of protein modifications: special bacterial phosphorylation systems
inferred← citeshttps://doi.org/10.1093/femsre/fuw026openalex-snapshot
Behind the lines–actions of bacterial type III effector proteins in plant cells
inferred← citeshttps://doi.org/10.1093/jxb/erab225openalex-snapshot
Open stomata 1 exhibits dual serine/threonine and tyrosine kinase activity in regulating abscisic acid signaling
inferred← citeshttps://doi.org/10.1093/jxb/erae358openalex-snapshot
Post-translational modifications control the signal at the crossroads of plant–pathogen interactions
inferred← citeshttps://doi.org/10.1093/pcp/pcw150openalex-snapshot
Autophosphorylation of Specific Threonine and Tyrosine Residues in Arabidopsis CERK1 is Essential for the Activation of Chitin-Induced Immune Signaling
inferred← citeshttps://doi.org/10.1093/pcp/pcz096openalex-snapshot
AtCERK1 Phosphorylation Site S493 Contributes to the Transphosphorylation of Downstream Components for Chitin-Induced Immune Signaling
inferred← citeshttps://doi.org/10.1093/plcell/koac041openalex-snapshot
Thirty years of resistance: Zig-zag through the plant immune system
inferred← citeshttps://doi.org/10.1093/plcell/koac154openalex-snapshot
Ustilaginoidea virens secretes a family of phosphatases that stabilize the negative immune regulator OsMPK6 and suppress plant immunity
inferred← citeshttps://doi.org/10.1094/mpmi-07-20-0173-cropenalex-snapshot
Receptors in the Induction of the Plant Innate Immunity
inferred← citeshttps://doi.org/10.1094/mpmi-08-17-0203-fiopenalex-snapshot
The Bacterial Effector AvrPto Targets the Regulatory Coreceptor SOBIR1 and Suppresses Defense Signaling Mediated by the Receptor-Like Protein Cf-4
inferred← citeshttps://doi.org/10.1094/mpmi-10-20-0271-ropenalex-snapshot
AKSF1 Isolated From the Rice-Virulent Strain Acidovorax avenae K1 Is a Novel Effector That Suppresses PAMP-Triggered Immunity in Rice
inferred← citeshttps://doi.org/10.1098/rstb.2018.0310openalex-snapshot
Early signalling mechanisms underlying receptor kinase-mediated immunity in plants
inferred← citeshttps://doi.org/10.1101/053504openalex-snapshot
The proteasome acts as a hub for local and systemic plant immunity in Arabidopsis thaliana and constitutes a virulence target of Pseudomonas syringae type-III effector proteins
inferred← citeshttps://doi.org/10.1101/2021.04.07.438767openalex-snapshot
Combinatorial interactions between viral proteins expand the functional landscape of the viral proteome
inferred← citeshttps://doi.org/10.1101/2021.10.08.463713openalex-snapshot
Stimulus-specific processing of the plasma membrane receptor-like kinase FERONIA in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1101/2022.03.30.486374openalex-snapshot
The Structural and Biochemical Basis for FER Receptor Kinase Early Signaling Initiation in Arabidopsis
inferred← citeshttps://doi.org/10.1101/2023.08.23.554490openalex-snapshot
Allosteric activation of the co-receptor BAK1 by the EFR receptor kinase initiates immune signaling
inferred← citeshttps://doi.org/10.1101/2024.05.29.596424openalex-snapshot
Soybean PHR1-regulated low phosphorus-responsive GmRALF22 increases uptake of phosphate via stimulating GmPT s expression
inferred← citeshttps://doi.org/10.1104/pp.16.00808openalex-snapshot
The Proteasome Acts as a Hub for Plant Immunity and Is Targeted by Pseudomonas Type III Effectors
inferred← citeshttps://doi.org/10.1104/pp.19.00913openalex-snapshot
H2Bub1 Regulates RbohD-Dependent Hydrogen Peroxide Signal Pathway in the Defense Responses to Verticillium dahliae Toxins
inferred← citeshttps://doi.org/10.1104/pp.19.01299openalex-snapshot
Surface Sensor Systems in Plant Immunity
inferred← citeshttps://doi.org/10.1105/tpc.16.00891openalex-snapshot
Receptor Kinases in Plant-Pathogen Interactions: More Than Pattern Recognition
inferred← citeshttps://doi.org/10.1105/tpc.17.01000openalex-snapshot
The Receptor-Like Cytoplasmic Kinase STRK1 Phosphorylates and Activates CatC, Thereby Regulating H 2 O 2 Homeostasis and Improving Salt Tolerance in Rice
inferred← citeshttps://doi.org/10.1111/febs.13613openalex-snapshot
Making sense of plant autoimmunity and ‘negative regulators’
inferred← citeshttps://doi.org/10.1111/febs.16549openalex-snapshot
The emerging frontier of plant immunity's core hubs
inferred← citeshttps://doi.org/10.1111/jipb.13747openalex-snapshot
SERKs serve as co‐receptors for SYR1 to trigger systemin‐mediated defense responses in tomato
inferred← citeshttps://doi.org/10.1111/jipb.70306openalex-snapshot
Decoding MAPK cascades in plant immunity: Activation, regulation, integration, and pathogen manipulation
inferred← citeshttps://doi.org/10.1111/mpp.12767openalex-snapshot
Kinase activity of SOBIR1 and BAK1 is required for immune signalling
inferred← citeshttps://doi.org/10.1111/mpp.13447openalex-snapshot
Functional screening of the Arabidopsis 2C protein phosphatases family identifies PP2C15 as a negative regulator of plant immunity by targeting BRI1 ‐associated receptor kinase 1
inferred← citeshttps://doi.org/10.1111/mpp.70322openalex-snapshot
Beneath the Bark: Molecular Determinants of Adaptation and Infection in Bacterial Pathogens of Woody Hosts
inferred← citeshttps://doi.org/10.1111/nph.13194openalex-snapshot
A snapshot of molecular plant–microbe interaction research
inferred← citeshttps://doi.org/10.1111/ppa.12983openalex-snapshot
Post‐translational modifications in effectors and plant proteins involved in host–pathogen conflicts
inferred← citeshttps://doi.org/10.1111/tpj.13808openalex-snapshot
Pattern recognition receptors and signaling in plant–microbe interactions
inferred← citeshttps://doi.org/10.1111/tpj.14093openalex-snapshot
Tyrosine phosphorylation of a receptor‐like cytoplasmic kinase, BSR1, plays a crucial role in resistance to multiple pathogens in rice
inferred← citeshttps://doi.org/10.1111/tpj.15056openalex-snapshot
Agromonas: a rapid disease assay for Pseudomonas syringae growth in agroinfiltrated leaves
inferred← citeshttps://doi.org/10.1111/tpj.16479openalex-snapshot
Ralstonia solanacearum effector RipAK suppresses homodimerization of the host transcription factor ERF098 to enhance susceptibility and the sensitivity of pepper plants to dehydration
inferred← citeshttps://doi.org/10.1128/jvi.00300-17openalex-snapshot
Mimic Phosphorylation of a βC1 Protein Encoded by TYLCCNB Impairs Its Functions as a Viral Suppressor of RNA Silencing and a Symptom Determinant
inferred← citeshttps://doi.org/10.1146/annurev-phyto-011325-012824openalex-snapshot
Extracellular Antagonists: Offense and Counter-Defense in the Apoplast
inferred← citeshttps://doi.org/10.1146/annurev-phyto-021621-121935openalex-snapshot
Diversity, Evolution, and Function of Pseudomonas syringae Effectoromes
inferred← citeshttps://doi.org/10.1146/annurev-phyto-080614-120347openalex-snapshot
A Moving View: Subcellular Trafficking Processes in Pattern Recognition Receptor–Triggered Plant Immunity
inferred← citeshttps://doi.org/10.1146/annurev-phyto-080615-100204openalex-snapshot
Plant-Pathogen Effectors: Cellular Probes Interfering with Plant Defenses in Spatial and Temporal Manners
inferred← citeshttps://doi.org/10.11575/prism/26416openalex-snapshot
Identification and Characterization of a Novel Tyrosine Phosphatase in Plants
inferred← citeshttps://doi.org/10.11606/d.17.2018.tde-17042018-143059openalex-snapshot
O papel de uma serina/treonina fosfatase do tipo eucariótico na virulência de Chromobacterium violaceum
inferred← citeshttps://doi.org/10.1177/1753425917738885openalex-snapshot
Plant immunity and symbiosis signaling mediated by LysM receptors
inferred← citeshttps://doi.org/10.1186/preaccept-1479195265134573openalex-snapshot
Transcriptomic analysis reveals tomato genes whose expression is induced specifically during effector-triggered immunity and identifies the Epk1 protein kinase which is required for the host response to three bacterial effector proteins
inferred← citeshttps://doi.org/10.1186/s12864-019-6409-3openalex-snapshot
Network analysis exposes core functions in major lifestyles of fungal and oomycete plant pathogens
inferred← citeshttps://doi.org/10.1186/s12864-026-12935-0openalex-snapshot
Comprehensive in silico characterization of proteins associated with light responses, transport, and stress-related processes in the gametophyte of the fern Dryopteris affinis ssp. affinis
inferred← citeshttps://doi.org/10.1186/s12870-026-09617-0openalex-snapshot
The divergent V2 protein encoded by parsley yellow leaf curl virus is a suppressor of transcriptional and post-transcriptional gene silencing and a potential symptom determinant
inferred← citeshttps://doi.org/10.1186/s12985-026-03309-9openalex-snapshot
Characterization of the C4 protein encoded by parsley yellow leaf curl virus
inferred← citeshttps://doi.org/10.1186/s13007-019-0515-8openalex-snapshot
Proteomics: a powerful tool to study plant responses to biotic stress
inferred← citeshttps://doi.org/10.1360/tb-2023-0788openalex-snapshot
Research advances of phytopathogen effectors
inferred← citeshttps://doi.org/10.1371/journal.pone.0116152openalex-snapshot
Immunomodulation by the Pseudomonas syringae HopZ Type III Effector Family in Arabidopsis
inferred← citeshttps://doi.org/10.1371/journal.pone.0147203openalex-snapshot
Analysis of Phosphorylation of the Receptor-Like Protein Kinase HAESA during Arabidopsis Floral Abscission
inferred← citeshttps://doi.org/10.1371/journal.ppat.1004602openalex-snapshot
The Phylogenetically-Related Pattern Recognition Receptors EFR and XA21 Recruit Similar Immune Signaling Components in Monocots and Dicots
inferred← citeshttps://doi.org/10.1371/journal.ppat.1004809openalex-snapshot
Transgenic Expression of the Dicotyledonous Pattern Recognition Receptor EFR in Rice Leads to Ligand-Dependent Activation of Defense Responses
inferred← citeshttps://doi.org/10.1371/journal.ppat.1005811openalex-snapshot
The Arabidopsis Protein Phosphatase PP2C38 Negatively Regulates the Central Immune Kinase BIK1
inferred← citeshttps://doi.org/10.1371/journal.ppat.1010909openalex-snapshot
Combinatorial interactions between viral proteins expand the potential functional landscape of the tomato yellow leaf curl virus proteome
inferred← citeshttps://doi.org/10.15252/embj.201591807openalex-snapshot
Danger peptide receptor signaling in plants ensures basal immunity upon pathogen‐induced depletion of BAK1
inferred← citeshttps://doi.org/10.15252/embj.2019102856openalex-snapshot
Tyrosine phosphorylation of the lectin receptor‐like kinase LORE regulates plant immunity
inferred← citeshttps://doi.org/10.15252/embj.2021109102openalex-snapshot
Plant immunity suppression via PHR1‐RALF‐FERONIA shapes the root microbiome to alleviate phosphate starvation
inferred← citeshttps://doi.org/10.18154/rwth-conv-145365openalex-snapshot
Molecular aspects of Arabidopsis nonhost resistance to Phakopsora pachyrhizi
inferred← citeshttps://doi.org/10.18174/454717openalex-snapshot
SOBIR1-containing immune complexes at the plant cell surface: partners and signalling
inferred← citeshttps://doi.org/10.18174/504639openalex-snapshot
Regulation and activation of SOBIR1-containing receptor complexes involved in plant immune signalling
inferred← citeshttps://doi.org/10.18174/566633openalex-snapshot
Activation and signal transduction of SOBIR1/BAK1-containing immune complexes present at the plant cell surface
inferred← citeshttps://doi.org/10.21285/2227-2925-2020-10-3-424-438openalex-snapshot
Evolution of views on plant immunity: from Flor’s “gene-for-gene” theory to the “zig-zag model” developed by Jones and Dangl
inferred← citeshttps://doi.org/10.2210/pdb6e8k/pdbopenalex-snapshot
Legionella Longbeachae LeSH (Llo2327) bound to the human interleukin-2 receptor beta pTyr387 peptide
inferred← citeshttps://doi.org/10.3389/fgene.2019.00162openalex-snapshot
Commentary: Leucine-rich Repeat Receptor-Like Gene Screen Reveals that Nicotiana RXEG1 Regulates Glycoside Hydrolase 12 MAMP Detection
inferred← citeshttps://doi.org/10.3389/fgene.2020.00469openalex-snapshot
Wheat Encodes Small, Secreted Proteins That Contribute to Resistance to Septoria Tritici Blotch
inferred← citeshttps://doi.org/10.3389/fmicb.2014.00320openalex-snapshot
Killing two birds with one stone: trans-kingdom suppression of PAMP/MAMP-induced immunity by T3E from enteropathogenic bacteria
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1305899openalex-snapshot
The Pseudomonas syringae pv. tomato DC3000 effector HopD1 interferes with cellular dynamics associated with the function of the plant immune protein AtNHR2B
inferred← citeshttps://doi.org/10.3389/fpls.2014.00671openalex-snapshot
Improving crop disease resistance: lessons from research on Arabidopsis and tomato
inferred← citeshttps://doi.org/10.3389/fpls.2015.00200openalex-snapshot
Unmasking host and microbial strategies in the Agrobacterium-plant defense tango
inferred← citeshttps://doi.org/10.3389/fpls.2017.00622openalex-snapshot
Both Light-Induced SA Accumulation and ETI Mediators Contribute to the Cell Death Regulated by BAK1 and BKK1
inferred← citeshttps://doi.org/10.3389/fpls.2017.00680openalex-snapshot
Suppression of Plant Immune Responses by the Pseudomonas savastanoi pv. savastanoi NCPPB 3335 Type III Effector Tyrosine Phosphatases HopAO1 and HopAO2
inferred← citeshttps://doi.org/10.3389/fpls.2017.01273openalex-snapshot
Tyrosine-610 in the Receptor Kinase BAK1 Does Not Play a Major Role in Brassinosteroid Signaling or Innate Immunity
inferred← citeshttps://doi.org/10.3389/fpls.2017.01687openalex-snapshot
Convergent Evolution of Pathogen Effectors toward Reactive Oxygen Species Signaling Networks in Plants
inferred← citeshttps://doi.org/10.3389/fpls.2019.00936openalex-snapshot
Tomato Dynamin Related Protein 2A Associates With LeEIX2 and Enhances PRR Mediated Defense by Modulating Receptor Trafficking
inferred← citeshttps://doi.org/10.3389/fpls.2020.00049openalex-snapshot
The Rice Xa3 Gene Confers Resistance to Xanthomonas oryzae pv. oryzae in the Model Rice Kitaake Genetic Background
inferred← citeshttps://doi.org/10.3389/fpls.2022.872901openalex-snapshot
Large-Scale Protein and Phosphoprotein Profiling to Explore Potato Resistance Mechanisms to Spongospora subterranea Infection
inferred← citeshttps://doi.org/10.3389/fpls.2023.1201805openalex-snapshot
Ligand recognition and signal transduction by lectin receptor-like kinases in plant immunity
inferred← citeshttps://doi.org/10.3389/fpls.2023.1224308openalex-snapshot
The genetic structure and demographic history revealed by whole-genome resequencing provide insights into conservation of critically endangered Artocarpus nanchuanensis
inferred← citeshttps://doi.org/10.3389/fpls.2025.1753391openalex-snapshot
Tomato activates ethylene signaling to maintain pathogenesis-related genes expression for conferring bacterial wilt resistance
inferred← citeshttps://doi.org/10.3390/biom11081122openalex-snapshot
Understanding and Exploiting Post-Translational Modifications for Plant Disease Resistance
inferred← citeshttps://doi.org/10.3390/cimb46120831openalex-snapshot
Transcriptome Analysis Provides Insights into the Safe Overwintering of Local Peach Flower Buds
inferred← citeshttps://doi.org/10.3390/ijms150610424openalex-snapshot
Alternative Splicing in Plant Immunity
inferred← citeshttps://doi.org/10.3390/ijms20112807openalex-snapshot
Post-Translational Modifications of Proteins Have Versatile Roles in Regulating Plant Immune Responses
inferred← citeshttps://doi.org/10.3390/ijms20235974openalex-snapshot
Genome-Wide Identification and Analysis of the NPR1-Like Gene Family in Bread Wheat and Its Relatives
inferred← citeshttps://doi.org/10.3390/ijms21124340openalex-snapshot
Regulation of Three Key Kinases of Brassinosteroid Signaling Pathway
inferred← citeshttps://doi.org/10.3390/ijms23126603openalex-snapshot
Importance of Tyrosine Phosphorylation in Hormone-Regulated Plant Growth and Development
inferred← citeshttps://doi.org/10.3390/ijms23137450openalex-snapshot
Silencing GmBIR1 in Soybean Results in Activated Defense Responses
inferred← citeshttps://doi.org/10.3390/ijms232214168openalex-snapshot
The Gain-of-Function Mutation, OsSpl26, Positively Regulates Plant Immunity in Rice
inferred← citeshttps://doi.org/10.3390/ijms24054597openalex-snapshot
dCas9-BE3 and dCas12a-BE3 Systems Mediated Base Editing in Kiwifruit Canker Causal Agent Pseudomonas syringae pv. actinidiae
inferred← citeshttps://doi.org/10.3390/jof9050574openalex-snapshot
Identification and Characterization of Novel Candidate Effector Proteins from Magnaporthe oryzae
inferred← citeshttps://doi.org/10.3390/microorganisms9051029openalex-snapshot
What the Wild Things Do: Mechanisms of Plant Host Manipulation by Bacterial Type III-Secreted Effector Proteins
inferred← citeshttps://doi.org/10.3390/plants14101515openalex-snapshot
Role of Tyrosine Phosphorylation in PEP1 Receptor 1(PEPR1) in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3390/plants15091395openalex-snapshot
Refractory Behavior in Plant Cells—Calcium Signaling Induced by Biotic Stress
inferred← citeshttps://doi.org/10.3390/v14122804openalex-snapshot
The V2 Protein from the Geminivirus Tomato Yellow Leaf Curl Virus Largely Associates to the Endoplasmic Reticulum and Promotes the Accumulation of the Viral C4 Protein in a Silencing Suppression-Independent Manner
inferred← citeshttps://doi.org/10.3410/f.727416872.793566961openalex-snapshot
Faculty Opinions recommendation of Receptor Kinases in Plant-Pathogen Interactions: More Than Pattern Recognition.
inferred← citeshttps://doi.org/10.3410/f.733934026.793551928openalex-snapshot
Faculty Opinions recommendation of Phosphocode-dependent functional dichotomy of a common co-receptor in plant signalling.
inferred← citeshttps://doi.org/10.3934/molsci.2017.3.370openalex-snapshot
Plant signaling pathways activating defence response and interfering mechanisms by pathogen effectors, protein decoys and bodyguards
inferred← citeshttps://doi.org/10.5010/jpb.2015.42.4.277openalex-snapshot
Tyrosine phosphorylation as a signaling component for plant improvement
inferred← citeshttps://doi.org/10.5010/jpb.2018.45.4.315openalex-snapshot
Expression and phosphorylation analysis of soluble proteins and membrane-localised receptor-like kinases from Arabidopsis thaliana in Escherichia coli
inferred← citeshttps://doi.org/10.53846/goediss-8211openalex-snapshot
Two cysteine-rich receptor-like protein kinases, CRK7 and CRK43, are required for CERK1-4 dependent cell death responses in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.64898/2026.02.19.706752openalex-snapshot
Alternative splicing expands the functional portfolio of a plant virus to control the viral cycle
inferred← citeshttps://doi.org/10.70675/0896c1f9ze4f4z4cbbzab44z3badf9cc47a1openalex-snapshot
La phosphorylation de l'effecteur PopP2 de Ralstonia solanacearum par des MAPKs immunitaires potentialise ses fonctions de virulence et limite sa reconnaissance chez Arabidopsis
inferred← citeshttps://doi.org/10.70675/1cd04e39zd1cfz46afz8061z25c9bc0c6579openalex-snapshot
Structure génétique des populations de Xanthomonas oryzae pv. oryzae, diversité du Talome et évaluation de la résistance de variétés élites de riz au Burkina Faso
inferred← citeshttps://doi.org/10.70675/33c41b11z195dz471cz83a8z54f4ddc477e5openalex-snapshot
Towards a global interactomic map between the Ralstonia solanacearum species complex core type III effectors and the tomato proteome
inferred← citeshttps://doi.org/10.70675/ea895fa4z89fbz4d1cz988ez37dd2b534c60openalex-snapshot
Effects of the Xanthomonas campestris pv campestris type III effectors on Arabidopsis physiology
inferred← citeshttps://doi.org/10.7287/peerj.6074v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Four tyrosine residues of the rice immune receptor XA21 are not required for interaction with the co-receptor OsSERK2 or resistance to Xanthomonas oryzae pv. oryzae (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.6074v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Four tyrosine residues of the rice immune receptor XA21 are not required for interaction with the co-receptor OsSERK2 or resistance to Xanthomonas oryzae pv. oryzae (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.6074v0.1/reviews/3openalex-snapshot
Peer Review #3 of "Four tyrosine residues of the rice immune receptor XA21 are not required for interaction with the co-receptor OsSERK2 or resistance to Xanthomonas oryzae pv. oryzae (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.6074v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Four tyrosine residues of the rice immune receptor XA21 are not required for interaction with the co-receptor OsSERK2 or resistance to Xanthomonas oryzae pv. oryzae (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.6074v0.2/reviews/3openalex-snapshot
Peer Review #3 of "Four tyrosine residues of the rice immune receptor XA21 are not required for interaction with the co-receptor OsSERK2 or resistance to Xanthomonas oryzae pv. oryzae (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.7346v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Pangenomic type III effector database of the plant pathogenic Ralstonia spp. (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.7346v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Pangenomic type III effector database of the plant pathogenic Ralstonia spp. (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.7346v0.1/reviews/3openalex-snapshot
Peer Review #3 of "Pangenomic type III effector database of the plant pathogenic Ralstonia spp. (v0.1)"
inferred← citeshttps://doi.org/10.7554/elife.16793openalex-snapshot
Pathogenic shifts in endogenous microbiota impede tissue regeneration via distinct activation of TAK1/MKK/p38
inferred← citeshttps://doi.org/10.7554/elife.92110openalex-snapshot
Allosteric activation of the co-receptor BAK1 by the EFR receptor kinase initiates immune signaling
inferred← citeshttps://doi.org/10.7554/elife.92110.1openalex-snapshot
Allosteric activation of the co-receptor BAK1 by the EFR receptor kinase initiates immune signaling
inferred← citeshttps://doi.org/10.7554/elife.92110.1.sa0openalex-snapshot
Reviewer #3 (Public Review): Allosteric activation of the co-receptor BAK1 by the EFR receptor kinase initiates immune signaling
inferred← citeshttps://doi.org/10.7554/elife.92110.1.sa1openalex-snapshot
Reviewer #2 (Public Review): Allosteric activation of the co-receptor BAK1 by the EFR receptor kinase initiates immune signaling
inferred← citeshttps://doi.org/10.7554/elife.92110.1.sa2openalex-snapshot
Reviewer #1 (Public Review): Allosteric activation of the co-receptor BAK1 by the EFR receptor kinase initiates immune signaling
inferred← citeshttps://doi.org/10.7554/elife.92110.1.sa3openalex-snapshot
eLife Assessment: Allosteric activation of the co-receptor BAK1 by the EFR receptor kinase initiates immune signaling
inferred← citeshttps://doi.org/10.7554/elife.92110.2openalex-snapshot
Allosteric activation of the co-receptor BAK1 by the EFR receptor kinase initiates immune signaling
inferred← citeshttps://doi.org/10.7554/elife.92110.3openalex-snapshot
Allosteric activation of the co-receptor BAK1 by the EFR receptor kinase initiates immune signaling
inferred← citeshttps://doi.org/10.7554/elife.92110.4openalex-snapshot
Allosteric activation of the co-receptor BAK1 by the EFR receptor kinase initiates immune signaling
inferred← citeshttps://doi.org/10.7717/peerj.6074openalex-snapshot
Four tyrosine residues of the rice immune receptor XA21 are not required for interaction with the co-receptor OsSERK2 or resistance to Xanthomonas oryzae pv. oryzae
inferred← citeshttps://doi.org/10.7717/peerj.7346openalex-snapshot
Pangenomic type III effector database of the plant pathogenic Ralstonia spp.
Editorial review for independent work. ICSAC — the Institute for Complexity
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