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Members of the GH3 Family of Proteins Conjugate 2,4-D and Dicamba with Aspartate and Glutamate
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/j.1537-2197.1937.tb09119.xopenalex-snapshot
ON THE NATURE OF INHIBITIONS CAUSED BY AUXIN
inferredcites →https://doi.org/10.1006/abio.1976.9999openalex-snapshot
A Rapid and Sensitive Method for the Quantitation of Microgram Quantities of Protein Utilizing the Principle of Protein-Dye Binding
inferredcites →https://doi.org/10.1007/s00344-007-9027-2openalex-snapshot
The Auxin Conjugate Hydrolase Family of Medicago truncatula and Their Expression During the Interaction with Two Symbionts
inferredcites →https://doi.org/10.1007/s00425-006-0462-2openalex-snapshot
Arabidopsis thaliana GH3.9 influences primary root growth
inferredcites →https://doi.org/10.1007/s00438-011-0672-6openalex-snapshot
Genome-wide investigation and expression analysis suggest diverse roles of auxin-responsive GH3 genes during development and response to different stimuli in tomato (Solanum lycopersicum)
inferredcites →https://doi.org/10.1007/s10142-005-0142-5openalex-snapshot
The auxin-responsive GH3 gene family in rice (Oryza sativa)
inferredcites →https://doi.org/10.1007/s11103-005-6505-4openalex-snapshot
A GH3-like gene, CcGH3, isolated from Capsicum chinense L. fruit is regulated by auxin and ethylene*
inferredcites →https://doi.org/10.1007/s11103-011-9776-yopenalex-snapshot
Evolutionary history of the GH3 family of acyl adenylases in rosids
inferredcites →https://doi.org/10.1007/s11105-010-0266-1openalex-snapshot
Truncation of Medicago truncatula Auxin Conjugate Hydrolases Alters Substrate Specificity
inferredcites →https://doi.org/10.1016/b978-1-4832-2734-4.50017-6openalex-snapshot
Evolutionary Divergence and Convergence in Proteins
inferredcites →https://doi.org/10.1016/j.bbrc.2011.05.055openalex-snapshot
OsJAR1 and OsJAR2 are jasmonyl-l-isoleucine synthases involved in wound- and pathogen-induced jasmonic acid signalling
inferredcites →https://doi.org/10.1016/j.gene.2005.12.014openalex-snapshot
The GH3 family in plants: Genome wide analysis in rice and evolutionary history based on EST analysis
inferredcites →https://doi.org/10.1016/j.gene.2011.05.033openalex-snapshot
Two GH3 genes from longan are differentially regulated during fruit growth and development
inferredcites →https://doi.org/10.1016/j.jplph.2003.12.010openalex-snapshot
Loss of GH3 function does not affect phytochrome-mediated development in a moss, Physcomitrella patens
inferredcites →https://doi.org/10.1016/j.pestbp.2007.04.002openalex-snapshot
Recent developments in auxin biology and new opportunities for auxinic herbicide research
inferredcites →https://doi.org/10.1021/jf60188a058openalex-snapshot
Metabolism of 2,4-dichlorophenoxyacetic acid. V. Identification of metabolites in soybean callus tissue cultures
inferredcites →https://doi.org/10.1021/jf60192a040openalex-snapshot
Metabolism of 2,4-dichlorophenoxyacetic acid. VI. Biological properties of amino acid conjugates
inferredcites →https://doi.org/10.1023/a:1015207114117openalex-snapshot
Auxin-responsive gene expression: genes, promoters and regulatory factors
inferredcites →https://doi.org/10.1073/pnas.1612635113openalex-snapshot
Arabidopsis thaliana GH3.5 acyl acid amido synthetase mediates metabolic crosstalk in auxin and salicylic acid homeostasis
inferredcites →https://doi.org/10.1074/jbc.m110.146431openalex-snapshot
Kinetic Basis for the Conjugation of Auxin by a GH3 Family Indole-acetic Acid-Amido Synthetase
inferredcites →https://doi.org/10.1074/jbc.m111955200openalex-snapshot
Characterization of a Family of IAA-Amino Acid Conjugate Hydrolases from Arabidopsis
inferredcites →https://doi.org/10.1074/jbc.m113.499228openalex-snapshot
The Amidohydrolases IAR3 and ILL6 Contribute to Jasmonoyl-Isoleucine Hormone Turnover and Generate 12-Hydroxyjasmonic Acid Upon Wounding in Arabidopsis Leaves
inferredcites →https://doi.org/10.1074/jbc.m500597200openalex-snapshot
A Three-component Dicamba O-Demethylase from Pseudomonas maltophilia, Strain DI-6
inferredcites →https://doi.org/10.1074/jbc.m806662200openalex-snapshot
Arabidopsis GH3.12 (PBS3) Conjugates Amino Acids to 4-Substituted Benzoates and Is Inhibited by Salicylate
inferredcites →https://doi.org/10.1093/jxb/erq412openalex-snapshot
Auxin conjugates: their role for plant development and in the evolution of land plants
inferredcites →https://doi.org/10.1093/jxb/err134openalex-snapshot
Acyl substrate preferences of an IAA-amido synthetase account for variations in grape (Vitis vinifera L.) berry ripening caused by different auxinic compounds indicating the importance of auxin conjugation in plant development
inferredcites →https://doi.org/10.1093/jxb/erv521openalex-snapshot
Hormone crosstalk in wound stress response: wound-inducible amidohydrolases can simultaneously regulate jasmonate and auxin homeostasis in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/molbev/mst197openalex-snapshot
MEGA6: Molecular Evolutionary Genetics Analysis Version 6.0
inferredcites →https://doi.org/10.1093/mp/ssr109openalex-snapshot
Cellular Auxin Homeostasis: Gatekeeping Is Housekeeping
inferredcites →https://doi.org/10.1093/nar/gkh340openalex-snapshot
MUSCLE: multiple sequence alignment with high accuracy and high throughput
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040454openalex-snapshot
The neighbor-joining method: a new method for reconstructing phylogenetic trees.
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a078709openalex-snapshot
IAA Metabolism in Embryogenic and Non-Embryogenic Carrot Cells
inferredcites →https://doi.org/10.1093/pcp/pcp101openalex-snapshot
Auxin Amidohydrolases from Brassica rapa Cleave the Alanine Conjugate of Indolepropionic Acid as a Preferable Substrate: A Biochemical and Modeling Approach
inferredcites →https://doi.org/10.1104/pp.100.1.63openalex-snapshot
Analysis of Indole-3-Acetic Acid Metabolites from Dalbergia dolichopetala by High Performance Liquid Chromatography-Mass Spectrometry
inferredcites →https://doi.org/10.1104/pp.104.039677openalex-snapshot
A Family of Auxin-Conjugate Hydrolases That Contributes to Free Indole-3-Acetic Acid Levels during Arabidopsis Germination
inferredcites →https://doi.org/10.1104/pp.109.138529openalex-snapshot
The Tryptophan Conjugates of Jasmonic and Indole-3-Acetic Acids Are Endogenous Auxin Inhibitors
inferredcites →https://doi.org/10.1104/pp.114.247205openalex-snapshot
Broad 4-Hydroxyphenylpyruvate Dioxygenase Inhibitor Herbicide Tolerance in Soybean with an Optimized Enzyme and Expression Cassette
inferredcites →https://doi.org/10.1104/pp.118.1.285openalex-snapshot
Metabolism of Indole-3-Acetic Acid in Arabidopsis1
inferredcites →https://doi.org/10.1104/pp.50.1.80openalex-snapshot
The Relative Amounts and Identification of Some 2,4-Dichlorophenoxyacetic Acid Metabolites Isolated from Soybean Cotyledon Callus Cultures
inferredcites →https://doi.org/10.1105/tpc.000885openalex-snapshot
Jasmonate Response Locus JAR1 and Several Related Arabidopsis Genes Encode Enzymes of the Firefly Luciferase Superfamily That Show Activity on Jasmonic, Salicylic, and Indole-3-Acetic Acids in an Assay for Adenylation
inferredcites →https://doi.org/10.1105/tpc.104.023549openalex-snapshot
The Oxylipin Signal Jasmonic Acid Is Activated by an Enzyme That Conjugates It to Isoleucine in Arabidopsis[W]
inferredcites →https://doi.org/10.1105/tpc.104.026690openalex-snapshot
Characterization of an Arabidopsis Enzyme Family That Conjugates Amino Acids to Indole-3-Acetic Acid
inferredcites →https://doi.org/10.1105/tpc.11.3.365openalex-snapshot
IAR3 Encodes an Auxin Conjugate Hydrolase from Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.112.102921openalex-snapshot
Crystal Structure of an Indole-3-Acetic Acid Amido Synthetase from Grapevine Involved in Auxin Homeostasis
inferredcites →https://doi.org/10.1111/j.1469-8137.2006.01677.xopenalex-snapshot
The auxin‐inducible GH3 homologue Pp‐GH3.16 is downregulated in Pinus pinaster root systems on ectomycorrhizal symbiosis establishment
inferredcites →https://doi.org/10.1111/j.1469-8137.2008.02677.xopenalex-snapshot
Moss ( Physcomitrella patens ) GH3 proteins act in auxin homeostasis
inferredcites →https://doi.org/10.1111/j.1742-4658.2009.07033.xopenalex-snapshot
Transcript profiling reveals diverse roles of auxin‐responsive genes during reproductive development and abiotic stress in rice
inferredcites →https://doi.org/10.1126/science.1096770openalex-snapshot
Discovery and Directed Evolution of a Glyphosate Tolerance Gene
inferredcites →https://doi.org/10.1126/science.1221863openalex-snapshot
Structural Basis for Prereceptor Modulation of Plant Hormones by GH3 Proteins
inferredcites →https://doi.org/10.1126/science.7792599openalex-snapshot
ILR1, an Amidohydrolase That Releases Active Indole-3-Acetic Acid from Conjugates
inferredcites →https://doi.org/10.1242/dev.086363openalex-snapshot
Auxin metabolism and homeostasis during plant development
inferredcites →https://doi.org/10.3389/fpls.2014.00789openalex-snapshot
Genome-wide analysis and expression profiling suggest diverse roles of GH3 genes during development and abiotic stress responses in legumes
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.113039zenodo-depositor-declared
The GH3 amidosynthetases family and their role in metabolic crosstalk modulation of plant signaling compounds
inferred← citeshttps://doi.org/10.1002/pld3.70105openalex-snapshot
Determination of the Mechanisms of MCPA Resistance in Amaranthus powellii
inferred← citeshttps://doi.org/10.1002/ps.8913openalex-snapshot
Auxin‐mimic herbicides dilema: Their benefits and limitations
inferred← citeshttps://doi.org/10.1007/s11240-020-01995-zopenalex-snapshot
Pretreatment free of 2,4-dichlorophenoxyacetic acid improves the differentiation of sugarcane somatic embryos by affecting the hormonal balance and the accumulation of reserves
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2020.124250openalex-snapshot
Auxin metabolic network regulates the plant response to metalloids stress
inferred← citeshttps://doi.org/10.1016/j.jprot.2021.104434openalex-snapshot
Mitochondrial proteomics reveals new insights into embryogenic competence acquisition in Carica papaya L. callus
inferred← citeshttps://doi.org/10.1016/j.jprot.2026.105602openalex-snapshot
Early regulatory networks driving somatic embryogenesis in Saccharum spp. L. revealed by time-resolved proteomics
inferred← citeshttps://doi.org/10.1016/j.pbi.2022.102194openalex-snapshot
Connecting primary and specialized metabolism: Amino acid conjugation of phytohormones by GRETCHEN HAGEN 3 (GH3) acyl acid amido synthetases
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114332openalex-snapshot
Biochemical and proteomic approaches to investigating effects of IAA-aspartate in pea (Pisum sativum L.) seedlings during osmotic shock
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.108210openalex-snapshot
Auxin homeostasis in plant responses to heavy metal stress
inferred← citeshttps://doi.org/10.1021/acs.jafc.2c05908openalex-snapshot
Identification of a Novel 2,4- D Metabolic Detoxification Pathway in 2,4- D -Resistant Waterhemp (Amaranthus tuberculatus)
inferred← citeshttps://doi.org/10.1021/acsomega.5c06484openalex-snapshot
Biotransformation of Pesticides across Biological Systems: Molecular Mechanisms, Omics Insights, and Biotechnological Advances for Environmental Sustainability
inferred← citeshttps://doi.org/10.1038/s41598-024-57506-zopenalex-snapshot
THOUSAND-GRAIN WEIGHT 6, which is an IAA-glucose hydrolase, preferentially recognizes the structure of the indole ring
inferred← citeshttps://doi.org/10.1093/pcp/pcaa098openalex-snapshot
An Evolutionarily Primitive and Distinct Auxin Metabolism in the Lycophyte Selaginella moellendorffii
inferred← citeshttps://doi.org/10.1101/cshperspect.a040048openalex-snapshot
On the Evolutionary Origins of Land Plant Auxin Biology
inferred← citeshttps://doi.org/10.1101/cshperspect.a040105openalex-snapshot
Chemical Biology in Auxin Research
inferred← citeshttps://doi.org/10.1111/tpj.15724openalex-snapshot
AtGH3 .10 is another jasmonic acid‐amido synthetase in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1186/s12864-020-07345-9openalex-snapshot
Genome-wide identification of GH3 genes in Brassica oleracea and identification of a promoter region for anther-specific expression of a GH3 gene
inferred← citeshttps://doi.org/10.3389/fpls.2021.735514openalex-snapshot
Early “Rootprints” of Plant Terrestrialization: Selaginella Root Development Sheds Light on Root Evolution in Vascular Plants
inferred← citeshttps://doi.org/10.3390/agronomy14061198openalex-snapshot
Comparative Gene Expression following 2,4-D Treatment in Two Red Clover (Trifolium pratense L.) Populations with Differential Tolerance to the Herbicide
inferred← citeshttps://doi.org/10.3390/biom11081153openalex-snapshot
Two Auxinic Herbicides Affect Brassica napus Plant Hormone Levels and Induce Molecular Changes in Transcription
inferred← citeshttps://doi.org/10.3390/plants10102034openalex-snapshot
Genome-Wide Analysis, Modeling, and Identification of Amino Acid Binding Motifs Suggest the Involvement of GH3 Genes during Somatic Embryogenesis of Coffea canephora
inferred← citeshttps://doi.org/10.3390/plants12223891openalex-snapshot
Time-Dependent Proteomic Signatures Associated with Embryogenic Callus Induction in Carica papaya L.
inferred← citeshttps://doi.org/10.5511/plantbiotechnology.19.0805bopenalex-snapshot
Anise-cultured cells abolish 2,4-dichlorophenoxyacetic acid in culture medium
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