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Crystal Structure of an Indole-3-Acetic Acid Amido Synthetase from Grapevine Involved in Auxin Homeostasis
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Fast, efficient generation of high‐quality atomic charges. AM1‐BCC model: II. Parameterization and validation
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Asparagine and glutamine: using hydrogen atom contacts in the choice of side-chain amide orientation 1 1Edited by J. Thornton
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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/s10725-008-9313-4openalex-snapshot
Research progresses on GH3s, one family of primary auxin-responsive genes
inferredcites →https://doi.org/10.1007/s11103-011-9776-yopenalex-snapshot
Evolutionary history of the GH3 family of acyl adenylases in rosids
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Truncation of Medicago truncatula Auxin Conjugate Hydrolases Alters Substrate Specificity
inferredcites →https://doi.org/10.1016/j.ab.2009.04.027openalex-snapshot
A liquid chromatography–tandem mass spectrometry-based assay for indole-3-acetic acid–amido synthetase
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
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Inference of Macromolecular Assemblies from Crystalline State
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Acyl-Adenylate Motif of the Acyl-Adenylate/Thioester-Forming Enzyme Superfamily: A Site-Directed Mutagenesis Study with the Pseudomonas sp. Strain CBS3 4-Chlorobenzoate:Coenzyme A Ligase
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inferredcites →https://doi.org/10.1046/j.1365-313x.2001.00957.xopenalex-snapshot
DFL1, an auxin-responsive GH3 gene homologue, negatively regulates shoot cell elongation and lateral root formation, and positively regulates the light response of hypocotyl length
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01973.xopenalex-snapshot
ydk1‐D , an auxin‐responsive GH3 mutant that is involved in hypocotyl and root elongation
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
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Characterization of a Family of IAA-Amino Acid Conjugate Hydrolases from Arabidopsis
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Auxin conjugates: their role for plant development and in the evolution of land plants
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Auxin Amidohydrolases from Brassica rapa Cleave the Alanine Conjugate of Indolepropionic Acid as a Preferable Substrate: A Biochemical and Modeling Approach
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inferredcites →https://doi.org/10.1104/pp.109.138529openalex-snapshot
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Altered Architecture and Enhanced Drought Tolerance in Rice via the Down-Regulation of Indole-3-Acetic Acid by TLD1/OsGH3.13 Activation
inferredcites →https://doi.org/10.1104/pp.110.163774openalex-snapshot
Manipulating Broad-Spectrum Disease Resistance by Suppressing Pathogen-Induced Auxin Accumulation in Rice
inferredcites →https://doi.org/10.1104/pp.114.4.1385openalex-snapshot
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Metabolism of Indole-3-Acetic Acid in Arabidopsis1
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inferredcites →https://doi.org/10.1105/tpc.104.026690openalex-snapshot
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Activation of the Indole-3-Acetic Acid–Amido Synthetase GH3-8 Suppresses Expansin Expression and Promotes Salicylate- and Jasmonate-Independent Basal Immunity in Rice
inferredcites →https://doi.org/10.1105/tpc.111.095190openalex-snapshot
The Conjugated Auxin Indole-3-Acetic Acid–Aspartic Acid Promotes Plant Disease Development
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Phaser crystallographic software
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Features and development of Coot
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Refinement of Macromolecular Structures by the Maximum-Likelihood Method
inferredcites →https://doi.org/10.1111/j.1399-3054.1989.tb02068.xopenalex-snapshot
IAA‐induced adventitious root formation in greenwood cuttings of Populus tremula and formation of 2‐indolone‐3‐acetylaspartic acid, a new metabolite of exogeneously applied indole‐3‐acetic acid
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.1755-0238.2010.00110.xopenalex-snapshot
Auxin treatment of pre-veraison grape (Vitis vinifera L.) berries both delays ripening and increases the synchronicity of sugar accumulation
inferredcites →https://doi.org/10.1126/science.1221863openalex-snapshot
Structural Basis for Prereceptor Modulation of Plant Hormones by GH3 Proteins
inferredcites →https://doi.org/10.1371/journal.pone.0037632openalex-snapshot
A Novel Tool for Studying Auxin-Metabolism: The Inhibition of Grapevine Indole-3-Acetic Acid-Amido Synthetases by a Reaction Intermediate Analogue
inferredcites →https://doi.org/10.4161/psb.5.12.13941openalex-snapshot
Modulating plant hormones by enzyme action
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Recent advances in auxin biosynthesis and homeostasis
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Preference of Arabidopsis thaliana GH3.5 acyl amido synthetase for growth versus defense hormone acyl substrates is dictated by concentration of amino acid substrate aspartate
inferred← citeshttps://doi.org/10.1016/j.plaphy.2016.05.031openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tplants.2019.05.006openalex-snapshot
Auxin Metabolism Controls Developmental Decisions in Land Plants
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inferred← citeshttps://doi.org/10.6084/m9.figshare.13535746openalex-snapshot
Additional file 1 of 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/10.6084/m9.figshare.13535752openalex-snapshot
Additional file 2 of 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/10.6084/m9.figshare.13535758openalex-snapshot
Additional file 3 of 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/10.6084/m9.figshare.13535761openalex-snapshot
Additional file 4 of 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/10.6084/m9.figshare.13535767openalex-snapshot
Additional file 5 of 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/10.6084/m9.figshare.13535773openalex-snapshot
Additional file 7 of 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/10.6084/m9.figshare.13535776openalex-snapshot
Additional file 8 of 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/10.6084/m9.figshare.20226994openalex-snapshot
Additional file 10 of Integrated transcriptome and hormonal analysis of naphthalene acetic acid-induced adventitious root formation of tea cuttings (Camellia sinensis)
inferred← citeshttps://doi.org/10.6084/m9.figshare.20226997openalex-snapshot
Additional file 1 of Integrated transcriptome and hormonal analysis of naphthalene acetic acid-induced adventitious root formation of tea cuttings (Camellia sinensis)
inferred← citeshttps://doi.org/10.6084/m9.figshare.20227003openalex-snapshot
Additional file 2 of Integrated transcriptome and hormonal analysis of naphthalene acetic acid-induced adventitious root formation of tea cuttings (Camellia sinensis)
inferred← citeshttps://doi.org/10.6084/m9.figshare.20227006openalex-snapshot
Additional file 3 of Integrated transcriptome and hormonal analysis of naphthalene acetic acid-induced adventitious root formation of tea cuttings (Camellia sinensis)
inferred← citeshttps://doi.org/10.6084/m9.figshare.20227009openalex-snapshot
Additional file 4 of Integrated transcriptome and hormonal analysis of naphthalene acetic acid-induced adventitious root formation of tea cuttings (Camellia sinensis)
inferred← citeshttps://doi.org/10.6084/m9.figshare.20227012openalex-snapshot
Additional file 5 of Integrated transcriptome and hormonal analysis of naphthalene acetic acid-induced adventitious root formation of tea cuttings (Camellia sinensis)
inferred← citeshttps://doi.org/10.6084/m9.figshare.20227015openalex-snapshot
Additional file 6 of Integrated transcriptome and hormonal analysis of naphthalene acetic acid-induced adventitious root formation of tea cuttings (Camellia sinensis)
inferred← citeshttps://doi.org/10.6084/m9.figshare.20227018openalex-snapshot
Additional file 7 of Integrated transcriptome and hormonal analysis of naphthalene acetic acid-induced adventitious root formation of tea cuttings (Camellia sinensis)
inferred← citeshttps://doi.org/10.6084/m9.figshare.20227021openalex-snapshot
Additional file 8 of Integrated transcriptome and hormonal analysis of naphthalene acetic acid-induced adventitious root formation of tea cuttings (Camellia sinensis)
inferred← citeshttps://doi.org/10.6084/m9.figshare.20227024openalex-snapshot
Additional file 9 of Integrated transcriptome and hormonal analysis of naphthalene acetic acid-induced adventitious root formation of tea cuttings (Camellia sinensis)
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