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amino acid metabolism

23075 relationships annotated with this phrase. Showing first 500 of 23075.
Source entity Relationship Target entity Species
DEGs overlapping with CHH-DMRs demonstrated additional connections to protein turnover, carbohydrate, lipid and amino acid metabolism, self-incompatibility system and regulation of gene expression Fragaria vesca
amino acid metabolism is strongly linked to microbial growth and development
Arabidopsis thaliana accessions measured for total amino acid content Arabidopsis thaliana
significant changes in profile of free amino acids could impact final proteinogenic amino acid composition Glycine max
AtME2 events show more pronounced effect on aspartate family amino acids reduction Glycine max
shaded Posidonia australis leaves were correlated with amino acids (l-pyroglutamate, l-aspartate, l-threonine, serine) Posidonia australis
Halodule uninervis T5 samples under 'Combined' treatment were correlated with pyroglutamate (amino acid) Halodule uninervis
repartitioning of carbon from aspartate to pyruvate family was more pronounced in AtME2 events Glycine max
enhanced total seed lipid levels affects free amino acids Glycine max
heating during marine heatwave under future warming conditions caused increase in l-isoleucine Posidonia australis
proportion of pyruvate-derived and phosphorylated intermediate-derived amino acids had increased at the expense of aspartate family in both AtME2 and AtME4 by R6 Glycine max
sulfide treatment increased amino acid content in plants under NPC Arabidopsis thaliana
branched-chain amino acid degradation is part of d-ESR (diatom common environmental stress response) Thalassiosira pseudonana
osers1 mutant had 2.44 times the level of Glu compared with wild type Oryza sativa
cluster 3 is significantly enriched in amino acids Arabidopsis thaliana
C3 scion glutamate (Glu) concentration is reduced when supplied by C4 stock Flaveria robusta; Flaveria bidentis
branched-chain amino acid leucine was elevated significantly by R7 in AtME4 events Glycine max
plants with suppressed photorespiration show decrease in amino acid content Arabidopsis thaliana
sulfide treatment had enhancement effect on Gly : Ser ratio Arabidopsis thaliana
increased leucine in the AtME4 events indicated available pyruvate supplies inside the plastid Glycine max
Halodule uninervis leaves harvested after 6 wk of shade (T4) were correlated with amino acids (l-valine, l-alanine, l-proline) Halodule uninervis
amino acid levels were altered seed composition Glycine max
AtME2 events maintained elevated level of alanine Glycine max
aspartate has been identified as metabolic hub in plants
Ala:glyoxylate aminotransferase3 (AGT3, AT2G38400) was significantly up-regulated by submergence stress in Arabidopsis Arabidopsis thaliana
enhancing organellar malic enzyme impacted amino acid distributions Glycine max
NR-reverse amino acid metabolism categories covers Serine (Ser) biosynthesis Chlamydomonas reinhardtii
serine (Ser) concentration in C3/C3 homografts shows reversed allocation pattern compared to C4/C4 homografts Flaveria robusta
complex, photosynthesis type-dependent interplay of shoot and root is involved in Ser homeostasis Flaveria
regulation of Ser homeostasis is potentially under the control of stock tissue Flaveria
(AOX1A, ATAOX1A, AtHSR3, HSR3, AT3G22370) mutants treated with antimycin A show no significant changes in levels of alanine
depression of aspartate levels led to overall depression of entire aspartate family Glycine max
exogenous sulfide increases amino acid content Arabidopsis thaliana
amino acids (l-alanine, l-valine, l-isoleucine, l-proline) were significantly higher in Halodule uninervis leaves kept under 'Shade' and 'Combined' treatments Halodule uninervis
increases in pyruvate-derived and decreases in aspartate-derived amino acids were maintained to maturity Glycine max
amino acid aspartate significantly increased in Posidonia australis leaves exposed to 'Shade' treatment Posidonia australis
aspartate family of free amino acids accounted for over 58% of total free amino acids in WT at R5 Glycine max
Posidonia australis leaves collected after 3-wk exposure to +1.5°C under light deprivation (T2) were correlated with amino acid l-proline Posidonia australis
phosphorylated intermediate family comprised 17.5% of total free amino acids in WT at R5 Glycine max
T3 samples of Posidonia australis during the first week of simulated MHW showed largest variation driven by amino acids (l-isoleucine, l-alanine, l-valine, phenylalanine, putrescine) Posidonia australis
relative abundance of the 'amino acid metabolism' module increases in acidic soils
Gly : Ser ratio decreases dramatically in plants under nonphotorespiration Arabidopsis thaliana
increases in alanine accounted for largest proportional change in AtME2 Glycine max
Plants cosilenced for both aminotransferases showed clearly increased levels of both threonine (approximately 2-fold) and isoleucine (approximately 3-fold) Nicotiana benthamiana
Amino acids in Haberlea rhodopensis leaves increase in abundance during extended darkness Haberlea rhodopensis
methionine (Met) concentration was reduced by about 8- to 30-fold in transgenic plants Hordeum vulgare
cytosol- and mitochondria-localized GluRS, OsERS1 affects amino acid-derived metabolism Oryza sativa
key amino acids accumulated in leaves during DP conditions darkened plant (DP) leaves Arabidopsis thaliana
glutamate family comprised 21% of total free amino acids in WT at R5 Glycine max
(IDH-I, IDH1, AT4G35260) mutant shows altered levels of Asp
Asp family pathway has metabolic connection with tricarboxylic acid cycle Arabidopsis thaliana
E. coli K12 strain cannot grow in medium with glutamate as sole carbon and nitrogen source Escherichia coli
barley leaves infected with B. graminis showed highly increased Gln-Glu ratio Hordeum vulgare
aspartate aminotransferase (AAT, ATAAT, MEE17, PAT, AT2G22250) catalyzes reversible transamination between glutamate and oxaloacetate
high spermidine (Spd) content exhibits strong effects on amino acid metabolism Solanum lycopersicum
Cluster 3 metabolites increase in abundance in entire plant darkening (DP) conditions but not in IDL or control conditions Arabidopsis thaliana
many amino acids in DP leaves accumulated 20- to 100-fold in DP when compared with light samples Arabidopsis thaliana
Arg and (TRP, AT3G56390) in IDL samples at 6-day darkening at T1 show 20% enrichment while pool of these metabolites was not detectable in light samples Arabidopsis thaliana
(CAT2, AT4G35090) mutant shows increased glycine Arabidopsis thaliana
Plants silenced for NbAsp5 or NbAsp5/NbPAT showed dramatically increased lysine levels Nicotiana benthamiana
tryptophan (Trp) belongs to aromatic amino acids higher plants
serine (Ser) concentration allocation pattern in C3 species Flaveria robusta is reversed compared to C4 species Flaveria robusta
branched-chain amino acids (BCAAs) (valine (Val), leucine (Leu), and isoleucine (Ile)) and proline (Pro) were significantly higher in cold-treated and dehydration-treated plants compared with untreated plants Oryza sativa
proline accumulation affected by general mechanisms coordinating amino acid and nitrogen metabolism pathways Arabidopsis thaliana
plant prokaryotic-type AATs displayed aspartate aminotransferase (AAT, ATAAT, MEE17, PAT, AT2G22250) activity
11 groups of interactions are related to amino acid metabolism (27%), mETC/ATP synthesis (13%), signaling (11%), lipid metabolism (5%), nitrogen metabolism (3%), and stress (19%) Arabidopsis thaliana
(ATGRX4, GRX4, GRXS15, AT3G15660) knockdown mutant showed decreased contents of Phe, Lys, Ser, β-Ala, Pro Arabidopsis thaliana
Thr concentrations under control conditions were significantly higher in transgenic plants than in wild-type plants Hordeum vulgare
different amino acid metabolic pathways have been well elucidated amino acid metabolic pathways
HFL2 rice line showed same phenomenon as HFL1 rice Oryza sativa
branched-chained amino acid aminotransferases not upregulated during developmental leaf senescence (DLS) Hordeum vulgare
peroxisomal processes include metabolism of the branched-chain amino acids
increased catabolic activity after (TOR, AT1G50030) repression leads to increased accumulation of amino acids Arabidopsis thaliana
cluster 3 metabolites in individual leaf darkening (IDL) remain quite low Arabidopsis thaliana
scion-stock allocation of Ser in interspecies grafts was rather C4-like Flaveria
pyrroline-5-carboxylate dehydrogenase produces glutamate with concomitant generation of NADH Jatropha curcas
NI correlation analysis revealed two groups of amino acids that correlated strongly to each other
γ-zein deletion in hemizygous state increased lysine in Quality Protein Maize (QPM) Zea mays
aromatic amino acids (particularly tryptophan and phenylalanine) and glutamine levels are significantly lower in leaves of SlNAP2-KD and dKD plants Solanum lycopersicum
amino acid accumulation in DP leaves confirmed considerable accumulation of amino acids in DP, particularly those with high N:C ratio and Gln Arabidopsis thaliana
peroxisomal β-hydroxyisobutyryl-CoA hydrolase is needed for valine catabolism Arabidopsis thaliana
branched chain amino acids (isoleucine and valine), glycine, serine, lysine, aspartate, and glutamate are downregulated in SlNAP2-OX plants Solanum lycopersicum
branched chain amino acids (isoleucine and valine), glycine, serine, lysine, aspartate, and glutamate are upregulated in SlNAP2-KD plants Solanum lycopersicum
two MAT mutants in Saccharomyces cerevisiae display opposite phenotypes to excess ethionine added in growth medium Saccharomyces cerevisiae
(ATRAPTOR1B, RAPTOR1, RAPTOR1B, AT3G08850) lines show increased levels of aliphatic amino acids (Ala, Ile, Leu, (REM11, VAL, AT5G60140) ) Arabidopsis thaliana
altered sink/source relationships would naturally lead to accumulation of specific amino acid groups, likely compartmentalized in vacuoles Arabidopsis thaliana
methylacrylyl–CoA is toxic, reacting rapidly with glutathione
In high nitrate, Glu/Asn levels remained higher in gin2-1 in contrast to Ler
glutathionylated proteins identified in vivo and in vitro in photosynthetic organisms participate in diverse biological processes such as photosynthesis, oxidative stress responses, protein folding, amino acid metabolism, ATP metabolism
Crocus sativus (ALDH5F1, ENF1, SSADH, SSADH1, AT1G79440) (CsALDH5F1) oxidizes succinic semialdehydes Crocus sativus
loss of function of OsERS1 may cause accumulation of free Glu not used for protein synthesis in anther Oryza sativa
osers1 mutant had increased levels of Glu family members including Gln, α-ketoglutarate (α-KG), His, and Arg Oryza sativa
free Lys content in mature seeds of TDC3-overexpressed rice increased dramatically mature seeds Oryza sativa
mitochondria house amino acid biosynthesis
steady state levels of free amino acids (FAAs) may be driven by general cell metabolism
FADH is transferred to quinone acceptor Jatropha curcas
glutamate (Glu) is synthesized in plastids
threonine (Thr) is major fuel source for S-adenosylmethionine (SAM)
amino acid metabolism is better understood through findings in HFL rice Oryza sativa
cluster 3 metabolites in entire plant darkening (DP) increase substantially throughout time course, reaching maximum levels at D6 Arabidopsis thaliana
Asn (asparagine) in DP leaves represented 40-fold accumulation compared with illuminated leaves Arabidopsis thaliana
NR-specific amino acid metabolism categories covers more biosynthesis of aromatic amino acids and Asp family amino acids Chlamydomonas reinhardtii
opaque2 (o2) mutant shows increased lysine level Zea mays
(AtSAMS3, MAT4, MTO3, SAMS3, AT3G17390) mutant shows increased level of methionine (Met) Arabidopsis thaliana
osers1 mutant had increased levels of Leu, Ser, and Asp families derived from pyruvate, phosphoglycerate, and OAA Oryza sativa
γ-zein deletion further increased lysine in Quality Protein Maize (QPM) Zea mays
aromatic amino acids (particularly tryptophan and phenylalanine) and glutamine levels are greater in SlNAP2-OX plants Solanum lycopersicum
glycine were relatively quantified using GC–TOF–MS (gas chromatography–time-of-flight mass spectrometry)
the Shahdara accession instead accumulates higher levels of Leu, Ile, and other amino acids Arabidopsis thaliana
Plants silenced for both NbAsp5 and NbPAT showed concomitant increase in free glutamate levels (approximately 5-fold) Nicotiana benthamiana
PATs are competent to function as PATs and AATs in petunia petunia
Cys and Gly require Ser for their synthesis
(AOX1A, ATAOX1A, AtHSR3, HSR3, AT3G22370) mutants display increased levels of isoleucine
N. benthamiana (AAT, ATAAT, MEE17, PAT, AT2G22250) gene family includes five genes encoding eukaryotic-type aspartate aminotransferases (NbAsp1–NbAsp5) Nicotiana benthamiana
γ-Aminobutyric acid (GABA) in Haberlea rhodopensis leaves decreases in darkness Haberlea rhodopensis
O-acetyl-Ser (OAS) is a Ser derivative
thioredoxin (Trx) involved in amino acid metabolic pathway higher plants
serine were relatively quantified using GC–TOF–MS (gas chromatography–time-of-flight mass spectrometry)
(AOX1A, ATAOX1A, AtHSR3, HSR3, AT3G22370) mutants treated with antimycin A show no significant changes in levels of valine
Thr has been suggested to have regulatory role within network of amino acid metabolism Arabidopsis thaliana
amidase mutant showed decreased levels of amino acids (Phe, Ser, β-Ala, Gly, Glu) Arabidopsis thaliana
none of the mutants displayed significantly altered levels of total amino acids Arabidopsis thaliana
Serine (Ser) in Haberlea rhodopensis leaves decreases in abundance following long-term darkness Haberlea rhodopensis
amino acid metabolism categories are affected in different aspects in NR-reverse and NR-specific data sets Chlamydomonas reinhardtii
γ-aminobutyrate was found to have most pronounced bootstrapped value for PC3 Solanum lycopersicum
VIGS resulted in altered amino acid profiles Nicotiana benthamiana
threonine (Thr) is major fuel source for acetyl-CoA
osers1 mutant had increased expression of genes encoding Glu dehydrogenase (GDH1, AT5G18170) Oryza sativa
loss of function of OsERS1 results in changes in amino acids and their derived metabolic pathways Oryza sativa
IDH4 transgenic line shows significantly reduced level of β-alanine Solanum lycopersicum
C- and S1-group AtbZIPs are involved in (AT-POX, ATPDH, ATPOX, ERD5, PDH1, PRO1, PRODH, AT3G30775) gene activation Arabidopsis thaliana
amino acid import or synthesis rate determines amino acid levels Arabidopsis thaliana
enzymes involved in amino acid metabolism undergo evolutionary protein relocations
loss of function of OsERS1 results in accumulation of free Glu Oryza sativa
almost all amino acids (apart from Asp, Gly, and Pro) were accumulated in entire plant darkening (DP) leaves Arabidopsis thaliana
C3/C4 grafted plants resemble C4/C4 homografts Flaveria robusta; Flaveria bidentis
ammonia provided by photorespiration or protein degradation could be metabolized by cytosolic glutamate dehydrogenase Solanum lycopersicum
(IDH-I, IDH1, AT4G35260) transgenic line shows significantly reduced level of proline Solanum lycopersicum
transcriptional regulation requires further investigation
amino acids levels depend on relative rates of synthesis and utilization Arabidopsis thaliana
P35S:myc:PDX1.3 stunted plants show massive increase in glycine content Arabidopsis thaliana
P35S:myc:PDX1.3 stunted plants show significantly increased ornithine content Arabidopsis thaliana
γ-Aminobutyrate high bootstrap value for PC3 might be attributed to pathways separating Nr mutant from tomato cv M82 Solanum lycopersicum
amidase is related to amino acid metabolism
(ATRAPTOR1B, RAPTOR1, RAPTOR1B, AT3G08850) up-regulates proteins involved in amino acid metabolism Arabidopsis thaliana
gin2-1 mutant did not influence amino acid levels in response to (GLC, AT1G65450)
pyruvate and shikimate rescued NRT2.1 expression and increased levels of amino acids derived from them but did not lower Asp, Gln/His, and Glu/Asn levels
526 signals 140 of which received putative annotations revealing components involved in amino acid, organic acid, and sugar metabolism
C4/C3 grafts accumulated comparable amounts of Ser in scions and stocks Flaveria bidentis; Flaveria robusta
signals, transport processes, and mechanisms driving the interplay of shoot and root in Ser homeostasis remain to be elucidated Flaveria
red-light-regulated metabolites participate in cysteine metabolism Arabidopsis thaliana
quadruple mutants with growth phenotype accumulate serine
sulfur is central element in methionine
Pre-treatment with Phe caused increase in Tryptophan (Trp) levels following infection Chrysanthemum morifolium
potato plants exhibiting overexpression of phosphoenolpyruvate carboxylase (PEPC) display elevated glutamate:glutamine ratio Solanum tuberosum
aspartate and alanine amino transferase reactions are quantitatively important in amino acid metabolism
P35S:myc:PDX2 plants show reduced glutamine content Arabidopsis thaliana
K+ -modulated metabolites participate in amino acid metabolism Arabidopsis thaliana
heterodimerization between GLDP proteins and InLYP1-mediated degradation of (AtGLDP2, GLDP2, AT2G26080) may together provide more physiological flexibility to fine-tune the rate of cellular glycine metabolism Arabidopsis thaliana
C β -S lyase activity is involved in amino acid metabolism
ectopic (ATPDX1, ATPDX1.3, PDX1, PDX1.3, RSR4, AT5G01410) expression triggers glycine accumulation Arabidopsis thaliana
P35S:myc:PDX lines show general increase in proline content Arabidopsis thaliana
IDH transgenic tomato plants show unaltered level of total amino acid levels in leaves Solanum lycopersicum
GDH (NAD) was assayed as described in Gibon et al. (2004) assay protocol
A9:u-ATP9 and AP3:u-ATP9 transgenic lines show increased expression of Bifunctional aspartate kinase/homoserine dehydrogenase (AK-HSDH, AK-HSDH II, AT4G19710) Arabidopsis thaliana
LOC_Os03g53650 involved in amino acid metabolism Oryza sativa
(IDH-I, IDH1, AT4G35260) transgenic line shows significantly increased level of tyramine Solanum lycopersicum
nutrient ion stresses lead to perturbations in composition of overall amino acid pool
phenylalanine (Phe) is aromatic amino acid
tyrosine (Tyr) is aromatic amino acid
re-illumination leads to simultaneous decrease in glutamate and aspartate
dominant product of lysine catabolic pathway is glutamate
AATs catalyze transamination of aspartate and α-ketoglutarate to glutamate and oxaloacetate
red-light-regulated metabolites participate in glutamate metabolism Arabidopsis thaliana
hyperspectral sensors can predict free amino acid content
similar shifts were observed for amino acid metabolism
glycine shows increase of up to 65-fold in (PCK2, PEPCK, AT5G65690) mutant compared to wild-type Arabidopsis thaliana
β-alanine was strongly increased in P35S:myc:PDX1.3 stunted plants Arabidopsis thaliana
vitB6 has long-recognized role in metabolism
snp_06_7615114 associated with ornithine Oryza sativa
SAR-DEFICIENT4 (SARD4, AT5G52810) displays enzyme characteristics similar to CRYM Arabidopsis thaliana
protein catabolism obtains amino acids Arabidopsis thaliana
red-light-regulated metabolites participate in aspartate metabolism Arabidopsis thaliana
zero sulphate roots results in asparagine comprising 85±2% of total free amino acids white clover
Two spots (6 and 86) were found to be similar to cysteine synthase Chinese fir
cysteine is first reduced by sulphur-containing compound
fructose, galactose, citric acid, and malic acid had negative correlations with serine, glutamic acid, threonine, and isoleucine
asparagine accumulation may be restricted to physiologically active subcellular compartments Medicago truncatula
biomass does not correlate with thiol contents
threonine synthase shows largest deviation of calculated in vivo catalytic rates and median reported plant-specific in vitro values kinetic parameters Arabidopsis thaliana
(ATB2, AtbZIP11, BZIP11, GBF6, AT4G34590) affects amino acids' metabolism by regulating expression of PROLINE DEHYDROGENASE2 (ProDH2) Arabidopsis thaliana
red-light-regulated metabolites participate in arginine metabolism Arabidopsis thaliana
glycine and glutamine showed dramatic change in abundance
2-oxoglutarate provided by cytosolic isocitrate dehydrogenase could be metabolized by cytosolic glutamate dehydrogenase Solanum lycopersicum
(IDH-I, IDH1, AT4G35260) transgenic line shows significantly reduced level of β-alanine Solanum lycopersicum
group 2 quadruple mutants Q2;1, Q3;1, and Q3;2 display perturbed amino acid content Arabidopsis thaliana
Arabidopsis (ATPAL1, PAL1, AT2G37040) and (ATPAL2, PAL2, AT3G53260) double mutant possesses increased tryptophan (Trp) levels Arabidopsis thaliana
transient decrease in sugars after single night leads to rapid and reversible decrease of all minor amino acids
upregulation of components involved in translation or protein folding appears to be contradictory to increased pool of amino acids Arabidopsis thaliana
transformation with AroG* results in overproduction of phenylalanine Arabidopsis thaliana; Solanum lycopersicum; Petunia hybrida
biomass correlates with changes in amino acid contents
P35S:myc:PDX2 plants show reduced arginine content Arabidopsis thaliana
(ATPDX1, ATPDX1.3, PDX1, PDX1.3, RSR4, AT5G01410) overexpressor lines show unchanged or increased β-alanine content Arabidopsis thaliana
sucrose provides carbon skeletons for glutamine biosynthesis
proline did not demonstrate strong correlation coefficients to other amino acids
many mutations could be expected to destroy enzymatic function of the protein
red-light-regulated metabolites participate in proline metabolism Arabidopsis thaliana
CpAlaAT2 is orthologous to AtAlaAT2 Cucurbita pepo; Arabidopsis thaliana
(AtGLDP2, GLDP2, AT2G26080) plays overall negative role in degrading glycine Arabidopsis thaliana
five gene categories containing differentially expressed genes (DEGs) in the 'Amino acid synthesis' section of the mapman database were significantly lower at 71 days after sprouting (71 DAS) than at 80 days after sprouting (80 DAS) in the lateral root (LR) Aconitum kusnezoffii
both (ACS, AT5G36880) homologs in the moss Physcomitrella patens exhibit C β -S lyase activity Physcomitrella patens
aspartic acid is UP9-dependent up-regulated metabolite during S-deficit
aspartate and alanine accumulate to high levels in leaves
P35S:myc:PDX2 plants show reduced β-alanine content Arabidopsis thaliana
PLP-dependent l-amino acid decarboxylases have been shown to exhibit distinct substrate and mechanistic selectivity
mur9-1 mutant and eto1-1 mutant show dramatic increases in γ-aminobutyric acid Arabidopsis thaliana
changes of several amino acids in IDH mutant have been published for mutant of amidase interactor IDH
(AOX1A, ATAOX1A, AtHSR3, HSR3, AT3G22370) mutants treated with antimycin A display significant relative increase in γ-amino butyric acid (GABA)
phenylalanine shows high levels at 26 days after anthesis (DAA) Triticum aestivum
amino acid metabolism proteins are upregulated at 26 days after anthesis (DAA) Triticum aestivum
disturbance of mineral nutrient metabolism leads to alterations of amino acid pools Arabidopsis thaliana
ASPARTATE AMINOTRANSFERASE2 (AAT2, ASP2, AT5G19550) encodes cytosolically targeted Aspartate Aminotransferase (AAT, ATAAT, MEE17, PAT, AT2G22250) enzyme Arabidopsis thaliana
red-light-regulated metabolites participate in amino acid metabolism Arabidopsis thaliana
proteomic data showed increase in several amino acid biosynthetic proteins Arabidopsis thaliana
increase in seed FAA levels may have originated from amino acid synthesis Arabidopsis thaliana
Os03g38540 is probably encoding amino acid transferase Oryza sativa
ZmAlaAT1 gene is involved in Ala (alanine) metabolism Zea mays
two regulatory ACT domains have also been found in other enzymes involved in amino acid metabolism Arabidopsis thaliana
Q3;1 mutant shows overall increase in amino acid concentrations
sucrose addition to C-starved seedlings decreases levels of minor amino acids Arabidopsis thaliana
GmSPX5 overexpression does not significantly affect amino acid concentrations in nodules Glycine max
aminomethyltransferase is highly abundant at 26 days after anthesis (DAA) Triticum aestivum
water deficit (PEG) increases proline content Medicago truncatula
asparagine accumulation may be restricted to mitochondria Medicago truncatula
drought causes decrease in glutamic acid (Glu) levels
cysteine level was similar in all plant lines tested Nicotiana tabacum
methylglyoxal (MG) is formed by oxidation of aminoacetone during threonine biosynthesis
BCAAs following initial increase at D1 decreased in abundance at D2 and later increased again at R1 Craterostigma plantagineum
IDH4 transgenic line shows significantly reduced level of proline Solanum lycopersicum
full nitrate starvation leads to general decrease in amino acids
amino acid transferase is upregulated at 26 days after anthesis (DAA) Triticum aestivum
glycine levels are higher in SUL under drought stress than under well-watered conditions Solanum tuberosum subsp. tuberosum
alanine aminotransferase catalyses transamination reactions
synthesis of amino acids in the lateral root (LR) was gradually inhibited throughout the growing season Aconitum kusnezoffii
genes in cluster CBS were enriched in amino acid metabolism Oryza sativa
drought increases levels of pyroglutamate
tyrosine shows high levels at 26 days after anthesis (DAA) Triticum aestivum
azidohomoalanine (Aha) induces methionine metabolism Arabidopsis thaliana
serine contents positive correlation observed for transcript level of phosphoserine phosphatase 1 Craterostigma plantagineum
Q2;1 mutant shows overall increase in amino acid concentrations
quadruple mutants with growth phenotype accumulate glycine
(ATB2, AtbZIP11, BZIP11, GBF6, AT4G34590) affects amino acids' metabolism by regulating expression of ASPARAGINE SYNTHETASE1 (ASN1, AT-ASN1, DIN6, AT3G47340) Arabidopsis thaliana
glutamate is increased in P35S:myc:PDX1.3 stunted plants Arabidopsis thaliana
A9:u-ATP9 and AP3:u-ATP9 transgenic lines show increased expression of Serine O-acetyltransferase (ATSERAT3;2, SERAT3;2, AT4G35640) Arabidopsis thaliana
aspartate, asparagine, glutamate, and glutamine are typically the most abundant in plants plants
isoleucine, methionine, phenylalanine, tryptophan, tyrosine and valine demonstrated strong negative correlations to proline and aspartate
down-regulated genes in (PXY, TDR, AT5G61480) mutant are related to amino acid transport and metabolism Oryza sativa
Sullu cultivar accumulates higher levels of proline
tryptophan and phenylalanine increased further when desiccated and remained elevated during rehydration Craterostigma plantagineum
zero sulphate treatment results in 4-times higher amino acid concentration in roots white clover
tyrosine is amino acid Brunfelsia
pavement cells seemed to accumulate amino acids to higher extent Arabidopsis thaliana
Delta-1-pyrroline-5-carboxylate dehydrogenase (ALDH12A1, ATP5CDH, P5CDH, AT5G62530) was down-regulated berry flesh at véraison Vitis vinifera
proline, tryptophan, and methionine degradation enzyme genes were down-regulated in SS2613
Pro (proline) content is much higher in line F2 compared with lines (B73, CHL6, CNX, CNX1, SIR4, AT5G20990) and Io Zea mays
ZmAspAT1.2 gene is involved in Asp (aspartate) metabolism Zea mays
2-oxoglutarate can be produced from amino acid transamination
above-mentioned metabolites displayed significantly increased levels in trichomes and pavement cells
N -methyl- L -proline (MP) showed significant increases in leaves of both clones in response to drought treatment
asparagine 3 is higher in upper section of the internode Helianthus annuus
SUL maintains more balanced composition of amino acids Solanum tuberosum subsp. tuberosum
–S plants showed elevated levels of Asn (asparagine)
sugar starvation leads to increased levels of Asn Arabidopsis thaliana
amino acids are strongly intercorrelated network module
S-adenosylmethionine (SAM) synthase catalyses attachment of an adenosyl residue to methionine
plastids are involved in amino acid biosynthesis
five asparagine synthetase-related genes showed >3-fold increases in transcription Glycine max
leucine is highly accumulated at 26 days after anthesis (DAA) Triticum aestivum
Met is involved in numerous biochemical processes
integrative analysis of transcriptome, proteome and metabolite data was performed with emphasis on amino acid metabolism Craterostigma plantagineum
maize roots have been used to uncover differences in spatial localization of free amino acids in different maize genotypes Zea mays
amino acid degradation-related gene expression was more strongly repressed in Sullu than in SS2613
glutamate is product and substrate for glutamate dehydrogenase (GDH)
cysteine (Cys) is used as sulphur donor for methionine synthesis
ZmGln1-4 gene is involved in Gln (glutamine) metabolism Zea mays
HPLC coupled with fluorescence detection was used to investigate changes of main amino acid components during development of strawberry fruits
water deficit (PEG) increases asparagine content Medicago truncatula
(ADT4, AT3G44720) (arogenate dehydratase 4) is gene regulated by both nNOS transgene and NO donor (SNP) treatment Arabidopsis thaliana
heating in Experiment 3 resulted in increases in relative concentrations of glutamate
asparagine synthetase (AS) mediates asparagine biosynthesis
LAO1 and LAO2 (periplasmic L-amino acid oxidases) catalyse deamination of all L-amino acids Chlamydomonas
methionine peaks at 12 days after anthesis (DAA) Triticum aestivum
tryptophan decarboxylase is PLP-dependent enzyme
glutamate dehydrogenase (GDH) main role is thought to recycle glutamate
exogenous ABA triggers increase in content of total free amino acids Medicago truncatula
isoleucine is synthesized from threonine by threonine deaminase
NaTD (threonine deaminase) transcript levels in control plants were somewhat higher in NaGSNOR-VIGS plants compared with those in EV plants Nicotiana attenuata
pyruvate,orthophosphate dikinase (PPDK, AT4G15530) functions in pathway that generates phloem transported amino acid glutamine
threonine deaminase (NaTD) converts Thr to Ile Nicotiana attenuata
total free amino acids in gapcp1gapcp2 increased as compared with control plants Arabidopsis thaliana
genetic manipulation can increase transcript abundance for genes encoding aspartate amino transferase (AspAT) Zea mays
SlAREB1 most probably regulates expression of enzyme-encoding genes involved in primary amino acid metabolic pathways
folates play a central role in biosynthesis and metabolism of amino acids
Ser was highly accumulated in response to fluoranthene and tebuconazole Lolium perenne
transgenic tobacco plants overexpressing P5CS were shown to have increased proline production Nicotiana tabacum
ZmAspAT1.2 transcript is higher in line (B73, CHL6, CNX, CNX1, SIR4, AT5G20990) compared with the other two lines Zea mays
ZmAlaAT2 mRNA is higher in line Io Zea mays
changes in proline content were not significant in SS2613
breeding can increase transcript abundance for genes encoding alanine amino transferase (AlaAT) Zea mays
GDH activity and ZmAspAT2.1, ZmAspAT1.2, and ZmAlaAT1 mRNAs belong to cluster containing traits related to yield in line (B73, CHL6, CNX, CNX1, SIR4, AT5G20990) Zea mays
turnover of excess free amino acid causes smaller free amino acid pools in mature seeds
amino acids identified were evidently more highly abundant in pavement cells Arabidopsis thaliana
ornithine also increased in response to drought
phenylalanine is amino acid Brunfelsia
proline degradation remained unchanged in Sullu
Regent presents constitutive accumulation of alanine Vitis vinifera
alanine aminotransferase 2 (ALAAT2, AT1G72330) has a role in alanine metabolism
ZmAlaAT1 mRNA is higher in line (B73, CHL6, CNX, CNX1, SIR4, AT5G20990) compared with the two other lines Zea mays
galactose had negative correlations with glycine, histidine, arginine, and methionine
cytosolic and chloroplastic isoforms of glutamine synthetase ( (GPP2, GS1, AT5G57440) and (ATGSL1, GLN2, GS2, AT5G35630) ) cooperate with glutamate synthase (GOGAT)
severe S limitation can result in up to 30 times more Asn accumulation in the grain
glutamine is amino acid metabolite Vitis vinifera
valine is amino acid metabolite Vitis vinifera
GABAT1-1 knockout mutant possesses increased leaf glutamine concentration Arabidopsis thaliana
Glu and glutamine (GLN) usually are principal amino acids present in foliar tissue
alanine was present at lower levels of -5-fold in salt-treated Clipper leaves after 5 weeks Hordeum vulgare
accumulation of phenylalanine at the expense of glutamine suggests change in resource partitioning among the free amino acid pool Eucalyptus globulus
asparagine concentration in xylem sap and nodules showed significant shifts between vegetative growth and pod formation stages
combination of higher Km and increased feedback sensitivity may cause temporal impaired synthesis of branched chain amino acids during active plant growth Lolium rigidum
alanine accumulation in diseased leaves may result from availability of GABA and pyruvic acid Vitis vinifera
tobacco leaves supplied with 30 mM glutamine exhibits elevated glutamate content Nicotiana tabacum
ABA (10 μM) treatment transiently increases asparagine content Medicago truncatula
serine supply could be related to changes in amino acid pools Arabidopsis thaliana
water deficit (PEG) increases alanine content Medicago truncatula
drought treatment decreased glutamic acid content in nodules Medicago sativa
branched-chain amino acids (BCAAs) are essential amino acids for food and feed Solanum lycopersicum
leguminous hairy vetch (Vicia villosa Roth) (HV) mulch significantly stimulates accumulation of asparagine Solanum lycopersicum
glutamate is higher in upper section of the internode Helianthus annuus
Each arrow in Fig. 6 represents a single enzymatic step Triticum aestivum
COR (coronatine) induces changes in amino acid content Nicotiana tabacum
increase in proline and proline analogues was linked to up-regulation of P5CS and down-regulation of proline dehydrogenase on day 28 after drought
ZmAspAT1.2 transcript is more marked in kernels than in the (COB, ATMG00220) Zea mays
AspAT1.3 mRNA is involved in Asp (aspartate) metabolism Zea mays
glutamate is regenerated as by-product of asparagine synthesis Medicago truncatula
glutamate degradation is catalysed by GDH-deaminating activity Medicago truncatula
synthesis of alanine may occur at the expense of amino acids glutamate and aspartate
specialized response of amino acid biosynthesis during senescence is distinct from response under abiotic stress
Atscp2-1 seedlings show increased levels of serine and glycine Arabidopsis thaliana
Atscp2-1 seedlings show decreased levels of β-alanine Arabidopsis thaliana
sugar starvation probably due to increase in expression of Asn synthase Arabidopsis thaliana
crude cell-free extracts of Arabidopsis leaves contain glyoxylate-dependent (GABA-T, HER1, POP2, AT3G22200) activity Arabidopsis thaliana
elevated GABA levels in GABAT1-1 knockout mutant provides evidence for inability of (GABA-T, HER1, POP2, AT3G22200) knockout plants to catabolize GABA Arabidopsis thaliana
β-Alanine and proline showed biggest increases of 20-fold and 117-fold respectively in Clipper roots after 3 weeks of salt exposure Hordeum vulgare
heat stress (HS) affects genes/gene families related to amino acid metabolism
asparagine synthetase catalyzes the transfer of the glutamine amide group to aspartate, and thus produces asparagine and glutamate
amino acid profiles of developing endosperm were very similar to those of mature endosperm Zea mays
nitrogen absorption into the berries is parallel with concentration of total free amino acids increase
primary metabolism sequences are distributed among amino acid metabolism Picea glauca
asparaginase (NSE) catalyzes hydrolysis of asparagine to aspartic acid and ammonium
synthesis of glutamate semialdehyde (GSA) from ornithine by ornithine-δ-aminotransferase (OAT) has conflicting data about the quantitative implication of in response to abiotic stress
NaHS treatment increases cysteine content Spinacia oleracea
glutamate is product of ammonia assimilation through reaction catalysed by glutamine synthetase (GS)
free proline is accumulated at high concentration in grape berries during ripening Vitis vinifera
proline and trigonelline contents were also increased in Sullu
free amino acids increased significantly in over-ripening stage Fragaria × ananassa
slight decrease in tyrosine and slight increase in phenylalanine in arodh-1 mutant leaf tissue suggests AroDH-1 has some leaf function Zea mays
mitochondrial activity in SUL is directed towards provision of carbon skeletons for amino acid biosynthesis Solanum tuberosum
hda101 down-regulation (AS33 line) causes reduction in level of asparagine Zea mays
Gly-Gly incubation for 4 h caused 46-fold increase in glycine in roots Hakea actites
other proline analogues also increased in Sullu
proline content significantly increased upon drought stress in cultivar Sullu
ZmAspAT2.1 mRNA is higher in line (B73, CHL6, CNX, CNX1, SIR4, AT5G20990) compared with the two other lines Zea mays
GS1a transgenic poplar leaves exhibits significantly enhanced glutamate content Populus trichocarpa
poplar GS1a transgenics display significantly enhanced glutamate levels in leaves Populus sp.
18 individual free amino acids increased over time time
extended nitrogen starvation caused later decrease in glutamate, glutamine, tryptophan, and tyrosine concentrations Arabidopsis thaliana
cluster B consisted of aromatic amino acids (Tyr and Phe) Lolium perenne
drought treatment decreased glutamic acid content in leaves Medicago sativa
drought treatment did not significantly affect serine content in nodules Medicago sativa
hda101 up-regulation (OE1 line) causes notable accumulation of gamma-aminobutyric acid (GABA) Zea mays
most amino acid pools in stressed Arabidopsis thaliana were shown to be regulated by transcription of catabolic enzymes, with biosynthetic enzymes remaining largely unresponsive Arabidopsis thaliana
glutamine helps plant cell to recycle ammonia ions liberated from phenylalanine through action of PAL
Asn synthase catalyzes formation of Asn through transfer of amide group from Gln to Asp Arabidopsis thaliana
genotype affects aspartate content Solanum lycopersicum
asparagine and homoserine were at lower levels of -9-fold and -25-fold respectively in Clipper roots after 5 weeks of salt stress Hordeum vulgare
(AGT, AGT1, SGAT, AT2G13360) and GGAT overexpression increases enzyme activities
leguminous hairy vetch (Vicia villosa Roth) (HV) mulch significantly stimulates accumulation of glutamine Solanum lycopersicum
aspartic acid levels decline to non-detectable in both lines under drought conditions Solanum tuberosum subsp. tuberosum
free amino acids in grain showed ∼3-fold reductions by 14 dpa amino acid content
Gly-Gly incubation for 15 h caused 25-fold increase in glycine in roots Hakea actites
INO-rolB-transformed fruits had higher concentrations of serine, β-alanine, and asparagine Solanum lycopersicum
phenylalanine increase in arodh-1 may also reflect a general increase of all free amino acids except tyrosine in arodh-1 Zea mays
arodh-1 mutant displays slight decrease in tyrosine in leaf tissue Zea mays
increase in amino acid levels in mutants is due to loss of gene function Arabidopsis thaliana
pgl3-1 mutant shoots show significantly lower total abundance of amino acids Arabidopsis thaliana
low R/FR ratio increases levels of pyroglutamate in the lower section Helianthus annuus
parasite's xylem sap containing significantly more glutamine, alanine, valine, and γ-aminobutyric acid compared with that of its host Rhinanthus minor; Vicia faba
Pro (proline) was the exception to general pattern of amino acid regulation under abiotic stress
threonine is amino acid metabolite Vitis vinifera
free amino acid pool in developing soybean seeds contains asparagine at 33% to 49% Glycine max
amino acids in Clipper leaves after 3 weeks of salt stress were at 2-65-fold higher concentrations in salt-treated Clipper leaves Hordeum vulgare
β-alanine, asparagine, aspartate, GABA, glutamte, glutamine, glycine, homoserine, proline, putrescine, serine, threonine, and valine were at 2-65-fold higher concentrations in salt-treated Clipper leaves Hordeum vulgare
(AGT, AGT1, SGAT, AT2G13360) catalyses conversion of glyoxylate into glycine
elevated [CO2] decreased amino acid content in leaves
high functional connectivity within pathways of amino acid metabolism is supported by changes in metabolites in transgenic lines Solanum lycopersicum
modifications in transcript abundance of genes involved in amino acid metabolism are limited in Arabidopsis roots Arabidopsis thaliana
arginine (Arg) concentration increases significantly in response to 13 d water cycle Theobroma cacao
hypoxic stress increased ammonium incorporation into alanine Medicago truncatula
energy formed by malate-Asp shuttle might be necessary for amino acid metabolism in Hoya carnosa Hoya carnosa
methionine is amino acid metabolite Vitis vinifera
alanine (Ala) concentration increases in DIS 219b-colonized seedlings compared with non-colonized seedlings Theobroma cacao
inducible Ala aminotransferase degrades alanine (Ala)
hda101 down-regulation (AS33 line) causes reduction in level of valine Zea mays
alanine aminotransferase catalyses reversible transfer of amino group from glutamate to pyruvate
cysteine synthase and isovaleryl-CoA dehydrogenase are associated with amino acid metabolism Arabidopsis thaliana
AK107064 is probably encoding amino acid transferase Oryza sativa
hypoxic stress resulted in up-regulation of mitochondrial alanine aminotransferase (mAlaAT) gene expression Medicago truncatula
Atscp2-1 seedlings show decreased levels of aspartate Arabidopsis thaliana
Atscp2-1 seedlings had decreased levels of Asp, Glu, and Gln Arabidopsis thaliana
19 amino acids remained constant in soluble pool of root tissue over incubation period Hakea actites
methionine synthesized simultaneously with cysteine about 20% incorporated into proteins
glutamate (Glu) and arginine (Arg) can function as Pro precursors
(AT-POX, ATPDH, ATPOX, ERD5, PDH1, PRO1, PRODH, AT3G30775) /proline oxidase shows opposite fold change in sucrose-inducible gene expression Arabidopsis thaliana
protein degradation was unlikely to drive changes in amino acid pools
changes in Asn and BCAA metabolism were important features of the chemical stress responses Lolium perenne
arginine occurs in soluble form
cysteine is at low level in (ATPUMP1, ATUCP1, PUMP1, UCP, UCP1, AT3G54110) mutant compared with wild-type Arabidopsis thaliana
genes associated with amino acid metabolism showed statistical differences for (GPP2, GS1, AT5G57440) (GLT1, AT5G53460) (AS1, ATMYB91, ATPHAN, LL2, MYB91, AT2G37630) AK, TS, TD, TSB, AROD, and PAL Solanum lycopersicum
heating in Experiment 3 resulted in increases in relative concentrations of threonine
cluster B metabolites increased in the leaf across all chemical stressors in at least one exposure condition Lolium perenne
genes involved in catabolism include genes involved in amino acid catabolism
up-regulated genes are mostly associated with amino acid metabolism Solanum chacoense
reduction of tyrosine in the protein-bound endosperm fraction of arodh-1 is only minor Zea mays
(AOAT1, GGAT1, GGT1, AT1G23310) gene encodes alanine-2-oxoglutarate aminotransferase 1 Arabidopsis thaliana
AK expression was significantly up-regulated in SlAREB1 overexpression lines Solanum lycopersicum
Overexpression of SlCDF3 in Arabidopsis significantly induced the accumulation of L-proline Arabidopsis thaliana
heating in Experiment 3 resulted in increases in relative concentrations of aspartate
alanine accumulated as major amino acid instead of asparagine Medicago truncatula
glutamic acid is not detectable in NOJ under drought conditions Solanum tuberosum subsp. tuberosum
At (GABA-T, HER1, POP2, AT3G22200) utilizes GABA Arabidopsis thaliana
alanine, asparagine, homoserine, isoleucine, leucine, putrescine, serine, threonine, tyrosine, and valine were present at -2 to -10-fold lower levels in Clipper roots after 24 hours salt stress Hordeum vulgare
mto140 / arodh-1 seeds shows elevated lysine phenotype Zea mays
tyrosine and phenylalanine in developing endosperm were reduced to a greater extent than in mature endosperm Zea mays
o5 and o9 both showed an even more pronounced general increase in leaf free amino acids Zea mays
total amino acid content typically decreases when N is limiting Arabidopsis thaliana
strong decrease in pyruvate levels could contribute to large decrease in alanine during light period Arabidopsis thaliana
3h of N resupply causes significant increases in amino acids β-alanine, glycine, serine, homoserine, cysteine, valine, and acetylserine Arabidopsis thaliana
glutamine abundance increased in the overexpressing lines compared with the WT Arabidopsis thaliana
specific effects of chemical stressors occur in association with trans-regulation of global amino acid metabolism Lolium perenne
Asn was positively correlated with Ser Lolium perenne
reversible transfer of amino group from glutamate to pyruvate forms 2-oxoglutarate and alanine
leucine (Leu) concentration increases significantly in response to 13 d water cycle Theobroma cacao
amino acids in Clipper roots after 24 hours salt stress showed decreases in levels of most amino acids Hordeum vulgare
glutamate and glutamine can be converted to GABA (γ-aminobutyric acid) Hordeum vulgare
volatile organic compounds (VOCs) primarily consist of amino acid derivatives
Asn (asparagine) content is higher in line Io Zea mays
tryptophan is amino acid Brunfelsia
short-term exposure to high level of Hydrogen sulphide (H2S) increases cysteine content in shoot Brassica oleracea
free amino acids decreased gradually before red-ripening stage Fragaria × ananassa
changes in amino acid pattern were more similar between (UMAMIT11, AT2G40900) and 14, both clade III UmamiTs Arabidopsis thaliana
tryptophan is (TRP, AT3G56390)
total amino acid content does not increase in response to DIS 219b colonization Theobroma cacao
β-alanine, alanine, GABA, glycine, proline, and putrescine were all above those of control plants by 3 weeks of salt exposure in Clipper roots Hordeum vulgare
amino acids show differences in transgenic parthenocarpic fruits Solanum lycopersicum
synthesis of alanine occurs concomitantly with accumulation of 4-aminobutyrate or GABA
all plant tissues limited in protein synthesis when grown in adequate N supply accumulate Asn
COR (coronatine) decreases aspartate Nicotiana tabacum
GABA was at 43-fold level in salt-treated Clipper leaves after 5 weeks Hordeum vulgare
(THA1, AT1G08630) mutant has 50% decrease in Gly content Arabidopsis thaliana
down-regulated genes are overrepresented in amino acid synthesis pathway Rorippa amphibia; Rorippa sylvestris
shaded Posidonia australis leaves exposed to 1 and 2 wk of simulated MHW (+5.5°C; T3, T4) and to 1 wk of 'MHW recovery' at +1.5°C (T5) clustered together and were correlated with L-aspartate Posidonia australis
phenylalanine, glutamic acid, methionine and asparagine were all significantly higher in leaves receiving both Shade and Combined treatments relative to Control plants Posidonia australis
genes related to cell wall function, nucleotide metabolism, amino acid metabolism, and protein translation are activated in both micropylar and chalazal endosperm (MCE) and radicle (RAD) Arabidopsis thaliana
heating during marine heatwave under future warming conditions caused increase in L-valine Posidonia australis
free amino acid content changed gradually resting cell formation Thalassiosira pseudonana
SlAREB1 overexpression lines accumulated greater amounts of amino acids from glutamate family Solanum lycopersicum
threonine (Thr) is amino acid that cannot be synthesized de novo by monogastric animals
pathways of amino acid metabolism are displayed in major pathway groups Triticum aestivum
methylglyoxal is breakdown product of threonine and acetone
sulfide treatment enhancement of Gly : Ser ratio reaches even higher ratio than plants with active photorespiration Arabidopsis thaliana
large increase in alanine at R6 for all events including WT was followed by drop in WT alanine levels beginning at R7 Glycine max
several pyruvate-derived amino acids (l-alanine, l-isoleucine, l-valine) accumulated in leaves of tropical Halophila uninervis exposed to both Shade and Combined treatments at T4 Halophila uninervis
OsMPS over-expression line OE6–2 accumulates significantly higher levels of Phe Oryza sativa
OsMPS over-expression line OE6–2 accumulates significantly higher levels of Thr Oryza sativa
(ATPUMP1, ATUCP1, PUMP1, UCP, UCP1, AT3G54110) and (AOX1A, ATAOX1A, AtHSR3, HSR3, AT3G22370) mutants show significant increase in asparagine levels Arabidopsis thaliana
OsMPS knockdown line KD4–5 shows down-regulated levels of γ-aminobutyric acid (GABA) Oryza sativa
Ser is substrate for synthesis of glutathione Pisum sativum
proline is the main free amino acid in pollen of several species
enhanced cysteine biosynthesis in pOsGPX1::astol1 transgenic plants may increase biosynthesis of methionine Oryza sativa
(ATPUMP1, ATUCP1, PUMP1, UCP, UCP1, AT3G54110) mutant Arabidopsis thaliana under 1000 μmol quanta m−2 s−1 saturating irradiance has significantly decreased glycine content compared with wild-type Arabidopsis thaliana
glutamine/glutamate ratio was not altered in present study Arabidopsis thaliana
heating in Experiment 3 resulted in increases in relative concentrations of leucine
(AtBCAT7, BCAT7, AT1G50090) expression was down-regulated in SlAREB1 overexpression lines at red ripe stage Solanum lycopersicum
asparagine is synthesized by transfer of amide group from glutamine
germinated wild-type pollen differs from germinating (ATPROT1, PROT1, AT2G39890) pollen Arabidopsis thaliana
glutamic acid levels are higher in SUL under drought stress than under well-watered conditions Solanum tuberosum subsp. tuberosum
elevated Gly levels in mls-2 seedlings is, to some extent, related to increased (THA1, AT1G08630) activity Arabidopsis thaliana
attachment of an adenosyl residue to methionine results in formation of S-adenosylmethionine (SAM)
(ATPUMP1, ATUCP1, PUMP1, UCP, UCP1, AT3G54110) mutant Arabidopsis thaliana under 1000 μmol quanta m−2 s−1 saturating irradiance has similar cysteine content compared with wild-type Arabidopsis thaliana
22% increase in lysine in developing arodh-1 endosperm was less pronounced than in mature endosperm Zea mays