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Aspartate-Derived Amino Acid Biosynthesis inArabidopsis thaliana
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1521-3803(199808)42:03/04<125::aid-food125>3.3.co;2-1openalex-snapshot
Genetic engineering for high methionine grain legumes
inferredcites →https://doi.org/10.1006/abbi.1999.1481openalex-snapshot
Identification of the Gene Encoding Homoserine Kinase from Arabidopsis thaliana and Characterization of the Recombinant Enzyme Derived from the Gene
inferredcites →https://doi.org/10.1006/jmbi.1996.0580openalex-snapshot
Rational Molecular Design and Genetic Engineering of Herbicide Resistant Crops by Structure Modeling and Site-directed Mutagenesis of Acetohydroxyacid Synthase
inferredcites →https://doi.org/10.1006/jmbi.1999.2828openalex-snapshot
Structure of Aspartate-β-semialdehyde Dehydrogenase from Escherichia coli, a Key Enzyme in the Aspartate Family of Amino Acid Biosynthesis
inferredcites →https://doi.org/10.1006/jmbi.1999.2935openalex-snapshot
The crystal structure of cystathionine γ-synthase from Nicotiana tabacum reveals its substrate and reaction specificity
inferredcites →https://doi.org/10.1006/prep.2001.1539openalex-snapshot
Overproduction, Purification, and Characterization of Recombinant Bifunctional Threonine-Sensitive Aspartate Kinase-Homoserine Dehydrogenase from Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/3-540-45989-8_3openalex-snapshot
Biotechnological Manufacture of Lysine
inferredcites →https://doi.org/10.1007/3-540-45989-8_5openalex-snapshot
Economic Aspects of Amino Acids Production
inferredcites →https://doi.org/10.1007/bf00014439openalex-snapshot
Molecular analysis of the aspartate kinase-homoserine dehydrogenase gene from Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/bf00020213openalex-snapshot
Lysine and threonine metabolism are subject to complex patterns of regulation in Arabidopsis
inferredcites →https://doi.org/10.1007/bf00041177openalex-snapshot
Cloning of an Arabidopsis thaliana cDNA encoding cystathionine ?-lyase by functional complementation in Escherichia coli
inferredcites →https://doi.org/10.1007/bf00041395openalex-snapshot
Cloning and analysis of the gene for cystathionine ?-synthase from Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/bf00043882openalex-snapshot
Isolation of a poplar and anArabidopsis thaliana dihydrodipicolinate synthase cDNA clone
inferredcites →https://doi.org/10.1007/bf00193218openalex-snapshot
A double mutant allele, csr1-4, of Arabidopsis thaliana encodes an acetolactate synthase with altered kinetics
inferredcites →https://doi.org/10.1007/bf00197040openalex-snapshot
Effect of four classes of herbicides on growth and acetolactate-synthase activity in several variants of Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/bf00279993openalex-snapshot
Multiple resistance to sulfonylureas and imidazolinones conferred by an acetohydroxyacid synthase gene with separate mutations for selective resistance
inferredcites →https://doi.org/10.1007/bf00280315openalex-snapshot
Intragenic recombination in the CSR1 locus of Arabidopsis
inferredcites →https://doi.org/10.1007/bf00331020openalex-snapshot
Sulfonylurea-resistant mutants of Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/bf01089041openalex-snapshot
A valine-resistant mutant ofArabidopsis thaliana displays an acetolactate synthase with altered feedback control
inferredcites →https://doi.org/10.1007/s00239-002-2340-2openalex-snapshot
Molecular Evolution of the Lysine Biosynthetic Pathways
inferredcites →https://doi.org/10.1007/s11103-004-0500-zopenalex-snapshot
A site-directed mutagenesis interrogation of the carboxy-terminal end of Arabidopsis thaliana threonine dehydratase/deaminase reveals a synergistic interaction between two effector-binding sites and contributes to the development of a novel selectable marker
inferredcites →https://doi.org/10.1007/s11103-004-7533-1openalex-snapshot
The mitochondrial branched-chain aminotransferase (AtBCAT-1) is capable to initiate degradation of leucine, isoleucine and valine in almost all tissues in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/0014-5793(96)00633-3openalex-snapshot
Characterization of an Arabidopsis thaliana cDNA encoding an S‐adenosylmethionine‐sensitive threonine synthase Threonine synthase from higher plants
inferredcites →https://doi.org/10.1016/0031-9422(83)80129-0openalex-snapshot
Feedback inhibition of homoserine kinase from radish leaves
inferredcites →https://doi.org/10.1016/0304-4211(78)90237-7openalex-snapshot
Biosynthesis of threonine from homoserine in pea seedlings: I. Homoserine kinase.
inferredcites →https://doi.org/10.1016/0378-1119(89)90510-6openalex-snapshot
Structure and expression analyses of the S-adenosylmethionine synthetase gene family in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/j.bbagen.2004.09.008openalex-snapshot
Biosynthesis of lysine in plants: evidence for a variant of the known bacterial pathways
inferredcites →https://doi.org/10.1016/j.gene.2005.05.028openalex-snapshot
Evolutionary plasticity of methionine biosynthesis
inferredcites →https://doi.org/10.1016/j.jbiotec.2006.10.015openalex-snapshot
Improving the nutritive value of tubers: Elevation of cysteine and glutathione contents in the potato cultivar White Lady by marker-free transformation
inferredcites →https://doi.org/10.1016/s0014-5793(00)02303-6openalex-snapshot
Arabidopsis loss‐of‐function mutant in the lysine pathway points out complex regulation mechanisms
inferredcites →https://doi.org/10.1016/s0014-5793(02)02253-6openalex-snapshot
Regulatory interactions in Arabidopsis thaliana acetohydroxyacid synthase
inferredcites →https://doi.org/10.1016/s0021-9258(17)37089-8openalex-snapshot
Cloning and molecular characterization of three genes, including two genes encoding serine hydroxymethyltransferases, whose inactivation is required to render yeast auxotrophic for glycine.
inferredcites →https://doi.org/10.1016/s0021-9258(18)38087-6openalex-snapshot
L-threonine dehydrogenase from Escherichia coli. Identification of an active site cysteine residue and metal ion studies.
inferredcites →https://doi.org/10.1016/s0168-9452(99)00188-0openalex-snapshot
Repression of cystathionine γ-synthase in Arabidopsis thaliana produces partial methionine auxotrophy and developmental abnormalities
inferredcites →https://doi.org/10.1016/s0176-1617(11)82049-3openalex-snapshot
Threonine Accumulation in a Mutant of Arabidopsis thaliana (L.) Heynh. with an Altered Aspartate Kinase
inferredcites →https://doi.org/10.1016/s0378-1097(97)00096-7openalex-snapshot
Identification of GLY1 as a threonine aldolase: a key enzyme in glycine biosynthesis
inferredcites →https://doi.org/10.1016/s0764-4469(00)01242-7openalex-snapshot
Mechanisms to account for maintenance of the soluble methionine pool in transgenic Arabidopsis plants expressing antisense cystathionine γ-synthase cDNA
inferredcites →https://doi.org/10.1016/s1360-1385(02)02227-6openalex-snapshot
Cystathionine γ-synthase and threonine synthase operate in concert to regulate carbon flow towards methionine in plants
inferredcites →https://doi.org/10.1021/bi001625copenalex-snapshot
Evidence for Two Distinct Effector-Binding Sites in Threonine Deaminase by Site-Directed Mutagenesis, Kinetic, and Binding Experiments
inferredcites →https://doi.org/10.1021/bi002775qopenalex-snapshot
Identification of the Regulatory Subunit of Arabidopsis thaliana Acetohydroxyacid Synthase and Reconstitution with Its Catalytic Subunit
inferredcites →https://doi.org/10.1021/bi0262348openalex-snapshot
Biochemical and Mass Spectrometric Evidence for Quaternary Structure Modifications of Plant Threonine Deaminase Induced by Isoleucine
inferredcites →https://doi.org/10.1021/bi980068fopenalex-snapshot
Allosteric Activation of Arabidopsis Threonine Synthase by S-Adenosylmethionine
inferredcites →https://doi.org/10.1021/ja01524a039openalex-snapshot
S-Adenosylmethionine: The Relation of Configuration at the Sulfonium Center to Enzymatic Reactivity1
inferredcites →https://doi.org/10.1023/a:1005808923191openalex-snapshot
Lysine-ketoglutarate reductase and saccharopine dehydrogenase from Arabidopsis thaliana: nucleotide sequence and characterization
inferredcites →https://doi.org/10.1023/a:1005849228945openalex-snapshot
Cloning and expression of an Arabidopsis thaliana cDNA encoding a monofunctional aspartate kinase homologous to the lysine-sensitive enzyme of Escherichia coli
inferredcites →https://doi.org/10.1023/a:1005863128558openalex-snapshot
Molecular characterization of an Arabidopsis thaliana cDNA coding for a monofunctional aspartate kinase
inferredcites →https://doi.org/10.1023/a:1006132428623openalex-snapshot
The Arabidopsis thaliana dhdps gene encoding dihydrodipicolinate synthase, key enzyme of lysine biosynthesis, is expressed in a cell-specific manner
inferredcites →https://doi.org/10.1023/a:1021134621488openalex-snapshot
Transcriptional and biochemical regulation of a novel Arabidopsis thaliana bifunctional aspartate kinase-homoserine dehydrogenase gene isolated by functional complementation of a yeast hom6 mutant
inferredcites →https://doi.org/10.1023/a:1022265825402openalex-snapshot
A Mutant of Arabidopsis thaliana lpar;L.) Heynh. with Modified Control of Aspartate Kinase by Threonine
inferredcites →https://doi.org/10.1038/287357a0openalex-snapshot
S-adenosylmethionine—a novel regulator of aspartate kinase
inferredcites →https://doi.org/10.1038/nbt0695-577openalex-snapshot
Transgenic Canola and Soybean Seeds with Increased Lysine
inferredcites →https://doi.org/10.1042/bj3200383openalex-snapshot
Purification and properties of cystathionine β-lyase from Arabidopsis thaliana overexpressed in Escherichia coli
inferredcites →https://doi.org/10.1042/bj3270161openalex-snapshot
Expression, purification and characterization of Arabidopsis thaliana acetohydroxyacid synthase
inferredcites →https://doi.org/10.1042/bj3310639openalex-snapshot
Cystathionine γ-synthase from Arabidopsis thaliana: purification and biochemical characterization of the recombinant enzyme overexpressed in Escherichia coli
inferredcites →https://doi.org/10.1042/bj3330765openalex-snapshot
Herbicide-resistant forms of Arabidopsis thaliana acetohydroxyacid synthase: characterization of the catalytic properties and sensitivity to inhibitors of four defined mutants
inferredcites →https://doi.org/10.1042/bst0320597openalex-snapshot
Autoregulation of the gene for cystathionine γ-synthase in Arabidopsis: post-transcriptional regulation induced by S-adenosylmethionine
inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00668.xopenalex-snapshot
Functional rescue of a bacterial dapA auxotroph with a plant cDNA library selects for mutant clones encoding a feedback‐insensitive dihydrodipicolinate synthase
inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00770.xopenalex-snapshot
A novel composite locus of Arabidopsis encoding two polypeptides with metabolically related but distinct functions in lysine catabolism
inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00884.xopenalex-snapshot
Identification of an Arabidopsis thaliana mutant accumulating threonine resulting from mutation in a new dihydrodipicolinate synthase gene
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.00988.xopenalex-snapshot
The S ‐methylmethionine cycle in angiosperms: ubiquity, antiquity and activity
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01221.xopenalex-snapshot
High free‐methionine and decreased lignin content result from a mutation in the Arabidopsis S‐adenosyl‐L‐methionine synthetase 3 gene
inferredcites →https://doi.org/10.1046/j.1432-1033.2003.03851.xopenalex-snapshot
A kinetic model of the branch‐point between the methionine and threonine biosynthesis pathways in Arabidopsis thaliana
inferredcites →https://doi.org/10.1046/j.1432-1327.1999.00487.xopenalex-snapshot
Characterization of recombinant Arabidopsis thaliana threonine synthase
inferredcites →https://doi.org/10.1073/pnas.0508701103openalex-snapshot
Herbicide-binding sites revealed in the structure of plant acetohydroxyacid synthase
inferredcites →https://doi.org/10.1073/pnas.0606195103openalex-snapshot
Methionine catabolism in Arabidopsis cells is initiated by a γ-cleavage process and leads to S -methylcysteine and isoleucine syntheses
inferredcites →https://doi.org/10.1073/pnas.1831512100openalex-snapshot
S-adenosyl- l -methionine is an effector in the posttranscriptional autoregulation of the cystathionine γ-synthase gene in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.91.7.2577openalex-snapshot
Lysine synthesis and catabolism are coordinately regulated during tobacco seed development.
inferredcites →https://doi.org/10.1074/jbc.m001116200openalex-snapshot
Characterization and Functional Expression of cDNAs Encoding Methionine-sensitive and -insensitive Homocysteine S-Methyltransferases from Arabidopsis
inferredcites →https://doi.org/10.1074/jbc.m204645200openalex-snapshot
Identification of a Short Highly Conserved Amino Acid Sequence as the Functional Region Required for Posttranscriptional Autoregulation of the Cystathionine γ-Synthase Gene in Arabidopsis
inferredcites →https://doi.org/10.1074/jbc.m205466200openalex-snapshot
The Activity of the Arabidopsis Bifunctional Lysine-ketoglutarate Reductase/Saccharopine Dehydrogenase Enzyme of Lysine Catabolism Is Regulated by Functional Interaction between Its Two Enzyme Domains
inferredcites →https://doi.org/10.1074/jbc.m207379200openalex-snapshot
Mechanism of Control of Arabidopsis thaliana Aspartate Kinase-Homoserine Dehydrogenase by Threonine
inferredcites →https://doi.org/10.1074/jbc.m313250200openalex-snapshot
Methionine Metabolism in Plants
inferredcites →https://doi.org/10.1074/jbc.m407380200openalex-snapshot
Lipid Utilization, Gluconeogenesis, and Seedling Growth in Arabidopsis Mutants Lacking the Glyoxylate Cycle Enzyme Malate Synthase
inferredcites →https://doi.org/10.1074/jbc.m509324200openalex-snapshot
Identification of Six Novel Allosteric Effectors of Arabidopsis thaliana Aspartate Kinase-Homoserine Dehydrogenase Isoforms
inferredcites →https://doi.org/10.1074/jbc.m511635200openalex-snapshot
Differential Inhibition of Arabidopsis Methionine Adenosyltransferases by Protein S-Nitrosylation
inferredcites →https://doi.org/10.1074/jbc.m610029200openalex-snapshot
Recognition of Age-damaged (R,S)-Adenosyl-L-methionine by Two Methyltransferases in the Yeast Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1093/jxb/eri031openalex-snapshot
Regulation of lysine catabolism in Arabidopsis through concertedly regulated synthesis of the two distinct gene products of the composite AtLKR/SDH locus
inferredcites →https://doi.org/10.1093/molbev/msg169openalex-snapshot
In Vivo Analysis of Various Substrates Utilized by Cystathionine -Synthase and O-Acetylhomoserine Sulfhydrylase in Methionine Biosynthesis
inferredcites →https://doi.org/10.1093/nar/18.8.2188openalex-snapshot
Nucleotide sequence of a mutant acetolactate synthase gene from an imidazolinone-resistantArabidopsis thalianavar. Columbia
inferredcites →https://doi.org/10.1093/nar/30.1.276openalex-snapshot
The Pfam Protein Families Database
inferredcites →https://doi.org/10.1093/oxfordjournals.jhered.a111307openalex-snapshot
Isolation and Genetic Analysis of a Triazolopyrimidine-Resistant Mutant of Arabidopsis
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a029444openalex-snapshot
Characterization of an Arabidopsis thaliana Mutant that Has a Defect in ABA Accumulation: ABA-Dependent and ABA-Independent Accumulation of Free Amino Acids during Dehydration
inferredcites →https://doi.org/10.1093/pcp/pce146openalex-snapshot
The First Exon Coding Region of Cystathionine γ-Synthase Gene is Necessary and Sufficient for Downregulation of its own mRNA Accumulation in Transgenic Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/pcp/pcg114openalex-snapshot
Decay Kinetics of Autogenously Regulated CGS1 mRNA That Codes for Cystathionine γ-Synthase in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/pcp/pcl055openalex-snapshot
Functional Characterization of a Methionine -Lyase in Arabidopsis and its Implication in an Alternative to the Reverse Trans-sulfuration Pathway
inferredcites →https://doi.org/10.1093/pcp/pcn005openalex-snapshot
Ribosome Stacking Defines CGS1 mRNA Degradation Sites During Nascent Peptide-Mediated Translation Arrest
inferredcites →https://doi.org/10.1093/pcp/pcn028openalex-snapshot
Nascent Peptide-Mediated Translation Elongation Arrest of Arabidopsis thaliana CGS1 mRNA Occurs Autonomously
inferredcites →https://doi.org/10.1101/gad.1317105openalex-snapshot
Nascent peptide-mediated translation elongation arrest coupled with mRNA degradation in the CGS1 gene of Arabidopsis
inferredcites →https://doi.org/10.1104/pp.001602openalex-snapshot
The Branched-Chain Amino Acid Transaminase Gene Family in Arabidopsis Encodes Plastid and Mitochondrial Proteins
inferredcites →https://doi.org/10.1104/pp.001693openalex-snapshot
An Essential Role ofS-Adenosyl- l -Methionine: l -MethionineS-Methyltransferase in Selenium Volatilization by Plants. Methylation of Selenomethionine to Selenium-Methyl- l -Selenium- Methionine, the Precursor of Volatile Selenium
inferredcites →https://doi.org/10.1104/pp.005660openalex-snapshot
The Bifunctional LKR/SDH Locus of Plants Also Encodes a Highly Active Monofunctional Lysine-Ketoglutarate Reductase Using a Polyadenylation Signal Located within an Intron,
inferredcites →https://doi.org/10.1104/pp.010438openalex-snapshot
Antisense Inhibition of Threonine Synthase Leads to High Methionine Content in Transgenic Potato Plants
inferredcites →https://doi.org/10.1104/pp.010819openalex-snapshot
The N-Terminal Region of Arabidopsis Cystathionine γ-Synthase Plays an Important Regulatory Role in Methionine Metabolism
inferredcites →https://doi.org/10.1104/pp.101801openalex-snapshot
Constitutive Overexpression of Cystathionine γ-Synthase in Arabidopsis Leads to Accumulation of Soluble Methionine andS-Methylmethionine
inferredcites →https://doi.org/10.1104/pp.102.010397openalex-snapshot
Ethylmethanesulfonate Saturation Mutagenesis in Arabidopsis to Determine Frequency of Herbicide Resistance
inferredcites →https://doi.org/10.1104/pp.102.018846openalex-snapshot
Insertional Inactivation of the Methionine S-Methyltransferase Gene Eliminates the S-Methylmethionine Cycle and Increases the Methylation Ratio
inferredcites →https://doi.org/10.1104/pp.103.026294openalex-snapshot
Synthesis of the Arabidopsis Bifunctional Lysine-Ketoglutarate Reductase/Saccharopine Dehydrogenase Enzyme of Lysine Catabolism Is Concertedly Regulated by Metabolic and Stress-Associated Signals
inferredcites →https://doi.org/10.1104/pp.103.037168openalex-snapshot
Lysine Metabolism Is Concurrently Regulated by Synthesis and Catabolism in Both Reproductive and Vegetative Tissues
inferredcites →https://doi.org/10.1104/pp.104.058719openalex-snapshot
Proteomic Identification of S -Nitrosylated Proteins in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.104.3.881openalex-snapshot
Isolation of an Arabidopsis thaliana Mutant, mto1, That Overaccumulates Soluble Methionine (Temporal and Spatial Patterns of Soluble Methionine Accumulation)
inferredcites →https://doi.org/10.1104/pp.105.072629openalex-snapshot
An ll -Diaminopimelate Aminotransferase Defines a Novel Variant of the Lysine Biosynthesis Pathway in Plants
inferredcites →https://doi.org/10.1104/pp.106.4.1257openalex-snapshot
Inhibition of Threonine Dehydratase Is Herbicidal
inferredcites →https://doi.org/10.1104/pp.107.105379openalex-snapshot
Regulation of One-Carbon Metabolism in Arabidopsis: The N-Terminal Regulatory Domain of Cystathionine γ-Synthase Is Cleaved in Response to Folate Starvation
inferredcites →https://doi.org/10.1104/pp.107.111609openalex-snapshot
Arabidopsis Branched-Chain Aminotransferase 3 Functions in Both Amino Acid and Glucosinolate Biosynthesis
inferredcites →https://doi.org/10.1104/pp.107.115220openalex-snapshot
New Connections across Pathways and Cellular Processes: Industrialized Mutant Screening Reveals Novel Associations between Diverse Phenotypes in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.108.115733openalex-snapshot
Principal Transcriptional Programs Regulating Plant Amino Acid Metabolism in Response to Abiotic Stresses
inferredcites →https://doi.org/10.1104/pp.123.1.101openalex-snapshot
Mutation in the Threonine Synthase Gene Results in an Over-Accumulation of Soluble Methionine in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.126.4.1539openalex-snapshot
A T-DNA Insertion Knockout of the Bifunctional Lysine-Ketoglutarate Reductase/Saccharopine Dehydrogenase Gene Elevates Lysine Levels in Arabidopsis Seeds
inferredcites →https://doi.org/10.1104/pp.82.2.607openalex-snapshot
Inhibition by Ethylene of Polyamine Biosynthetic Enzymes Enhanced Lysine Decarboxylase Activity and Cadaverine Accumulation in Pea Seedlings
inferredcites →https://doi.org/10.1104/pp.90.4.1577openalex-snapshot
Aspartokinase of Lemna paucicostata Hegelm. 6746
inferredcites →https://doi.org/10.1104/pp.92.4.1081openalex-snapshot
A Mutation Causing Imidazolinone Resistance Maps to the Csr1 Locus of Arabidopsis thaliana
inferredcites →https://doi.org/10.1104/pp.97.3.1044openalex-snapshot
Molecular Basis of Imidazolinone Herbicide Resistance in Arabidopsis thaliana var Columbia
inferredcites →https://doi.org/10.1105/tpc.009647openalex-snapshot
Increased Lysine Synthesis Coupled with a Knockout of Its Catabolism Synergistically Boosts Lysine Content and Also Transregulates the Metabolism of Other Amino Acids in Arabidopsis Seeds
inferredcites →https://doi.org/10.1105/tpc.019372openalex-snapshot
Divergent Roles in Arabidopsis thaliana Development and Defense of Two Homologous Genes, ABERRANT GROWTH AND DEATH2 and AGD2-LIKE DEFENSE RESPONSE PROTEIN1, Encoding Novel Aminotransferases
inferredcites →https://doi.org/10.1105/tpc.1.1.81openalex-snapshot
Strong cellular preference in the expression of a housekeeping gene of Arabidopsis thaliana encoding S-adenosylmethionine synthetase.
inferredcites →https://doi.org/10.1105/tpc.105.039339openalex-snapshot
BRANCHED-CHAIN AMINOTRANSFERASE4 Is Part of the Chain Elongation Pathway in the Biosynthesis of Methionine-Derived Glucosinolates in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.105.040451openalex-snapshot
A Novel Organization of ACT Domains in Allosteric Enzymes Revealed by the Crystal Structure of Arabidopsis Aspartate Kinase
inferredcites →https://doi.org/10.1105/tpc.106.044958openalex-snapshot
Two Arabidopsis Threonine Aldolases Are Nonredundant and Compete with Threonine Deaminase for a Common Substrate Pool
inferredcites →https://doi.org/10.1105/tpc.11.8.1485openalex-snapshot
S-Methylmethionine Plays a Major Role in Phloem Sulfur Transport and Is Synthesized by a Novel Type of Methyltransferase
inferredcites →https://doi.org/10.1105/tpc.7.7.899openalex-snapshot
Regulation of Lysine and Threonine Synthesis
inferredcites →https://doi.org/10.1110/ps.44301openalex-snapshot
Crystal structure of threonine synthase from Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02140.xopenalex-snapshot
Application of a high‐throughput HPLC‐MS/MS assay to Arabidopsis mutant screening; evidence that threonine aldolase plays a role in seed nutritional quality
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02329.xopenalex-snapshot
Methionine and threonine synthesis are limited by homoserine availability and not the activity of homoserine kinase in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02661.xopenalex-snapshot
An in vivo internal deletion in the N‐terminus region of Arabidopsis cystathionine γ ‐synthase results in CGS expression that is insensitive to methionine
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03184.xopenalex-snapshot
Lysine enhances methionine content by modulating the expression of S‐adenosylmethionine synthase
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03419.xopenalex-snapshot
Reduced activity of Arabidopsis thaliana HMT2, a methionine biosynthetic enzyme, increases seed methionine content
inferredcites →https://doi.org/10.1111/j.1399-3054.2006.00800.xopenalex-snapshot
Branched‐chain amino acid metabolism in higher plants
inferredcites →https://doi.org/10.1111/j.1467-7652.2007.00290.xopenalex-snapshot
Modifying lysine biosynthesis and catabolism in corn with a single bifunctional expression/silencing transgene cassette
inferredcites →https://doi.org/10.1111/j.1574-6968.1997.tb10349.xopenalex-snapshot
Identification of Saccharomyces cerevisiae GLY1 as a threonine aldolase: a key enzyme in glycine biosynthesis
inferredcites →https://doi.org/10.1111/j.1742-4658.2006.05573.xopenalex-snapshot
Allosteric monofunctional aspartate kinases from Arabidopsis
inferredcites →https://doi.org/10.1126/science.285.5426.372openalex-snapshot
Gene Discovery and Product Development for Grain Quality Traits
inferredcites →https://doi.org/10.1126/science.286.5443.1371openalex-snapshot
Evidence for Autoregulation of Cystathionine γ-Synthase mRNA Stability in Arabidopsis
inferredcites →https://doi.org/10.1146/annurev.arplant.53.091401.110929openalex-snapshot
N EW I NSIGHTS INTO THE R EGULATION AND F UNCTIONAL S IGNIFICANCE OF L YSINE M ETABOLISM IN P LANTS
inferredcites →https://doi.org/10.1146/annurev.bi.44.070175.002251openalex-snapshot
Biological Methylation: Selected Aspects
inferredcites →https://doi.org/10.1146/annurev.ento.43.1.17openalex-snapshot
Nutritional Interactions in Insect-Microbial Symbioses: Aphids and Their Symbiotic BacteriaBuchnera
inferredcites →https://doi.org/10.1186/1471-2091-3-19openalex-snapshot
Molecular cloning and tissue distribution of mammalian L-threonine 3-dehydrogenases
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inferredcites →https://doi.org/10.2135/cropsci1978.0011183x001800030029xopenalex-snapshot
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Additional file 1 of Integrative physiological, metabolomic, and transcriptomic analysis reveals the drought responses of two apple rootstock cultivars
inferred← citeshttps://doi.org/10.6084/m9.figshare.26697974openalex-snapshot
Additional file 2 of Integrative physiological, metabolomic, and transcriptomic analysis reveals the drought responses of two apple rootstock cultivars
inferred← citeshttps://doi.org/10.6084/m9.figshare.26697977openalex-snapshot
Additional file 3 of Integrative physiological, metabolomic, and transcriptomic analysis reveals the drought responses of two apple rootstock cultivars
inferred← citeshttps://doi.org/10.6084/m9.figshare.26697980openalex-snapshot
Additional file 4 of Integrative physiological, metabolomic, and transcriptomic analysis reveals the drought responses of two apple rootstock cultivars
inferred← citeshttps://doi.org/10.6084/m9.figshare.26697983openalex-snapshot
Additional file 5 of Integrative physiological, metabolomic, and transcriptomic analysis reveals the drought responses of two apple rootstock cultivars
inferred← citeshttps://doi.org/10.6084/m9.figshare.26697986openalex-snapshot
Additional file 6 of Integrative physiological, metabolomic, and transcriptomic analysis reveals the drought responses of two apple rootstock cultivars
inferred← citeshttps://doi.org/10.6084/m9.figshare.26697989openalex-snapshot
Additional file 7 of Integrative physiological, metabolomic, and transcriptomic analysis reveals the drought responses of two apple rootstock cultivars
inferred← citeshttps://doi.org/10.6084/m9.figshare.26697992openalex-snapshot
Additional file 8 of Integrative physiological, metabolomic, and transcriptomic analysis reveals the drought responses of two apple rootstock cultivars
inferred← citeshttps://doi.org/10.6084/m9.figshare.26697995openalex-snapshot
Additional file 9 of Integrative physiological, metabolomic, and transcriptomic analysis reveals the drought responses of two apple rootstock cultivars
inferred← citeshttps://doi.org/10.6084/m9.figshare.26697998openalex-snapshot
Additional file 10 of Integrative physiological, metabolomic, and transcriptomic analysis reveals the drought responses of two apple rootstock cultivars
inferred← citeshttps://doi.org/10.6084/m9.figshare.26698001openalex-snapshot
Additional file 11 of Integrative physiological, metabolomic, and transcriptomic analysis reveals the drought responses of two apple rootstock cultivars
inferred← citeshttps://doi.org/10.6084/m9.figshare.26698004openalex-snapshot
Additional file 12 of Integrative physiological, metabolomic, and transcriptomic analysis reveals the drought responses of two apple rootstock cultivars
inferred← citeshttps://doi.org/10.6084/m9.figshare.26698007openalex-snapshot
Additional file 13 of Integrative physiological, metabolomic, and transcriptomic analysis reveals the drought responses of two apple rootstock cultivars
inferred← citeshttps://doi.org/10.6084/m9.figshare.26698010openalex-snapshot
Additional file 14 of Integrative physiological, metabolomic, and transcriptomic analysis reveals the drought responses of two apple rootstock cultivars
inferred← citeshttps://doi.org/10.6084/m9.figshare.26698013openalex-snapshot
Additional file 15 of Integrative physiological, metabolomic, and transcriptomic analysis reveals the drought responses of two apple rootstock cultivars
inferred← citeshttps://doi.org/10.70675/736b1d6fz82d8z405bzb340zbcaa21303873openalex-snapshot
Physiological and molecular characterization of the mitigation of nitrogen deficiency stress by the arbuscular mycorrhizal fungus Rhizophagus irregularis associated with Maize (Zea mays L.)
inferred← citeshttps://doi.org/10.70675/77a3d2e1z37a8z48b5zb653z23c6eaf0b9f1openalex-snapshot
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inferred← citeshttps://doi.org/10.7287/peerj.12343v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Genome-wide association study and population structure analysis of seed-bound amino acids and total protein in watermelon (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.12343v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Genome-wide association study and population structure analysis of seed-bound amino acids and total protein in watermelon (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.12343v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Genome-wide association study and population structure analysis of seed-bound amino acids and total protein in watermelon (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.12343openalex-snapshot
Genome-wide association study and population structure analysis of seed-bound amino acids and total protein in watermelon
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