D-Glutamic acid (BioDeep_00000014484)
Secondary id: BioDeep_00001867999
human metabolite PANOMIX_OTCML-2023 blood metabolite
代谢物信息卡片
delta-2-Aminopentanedioic acid
化学式: C5H9NO4 (147.0531554)
中文名称: D-谷氨酸
谱图信息:
最多检出来源 Homo sapiens(blood) 0.52%
分子结构信息
SMILES: C(=O)(CC[C@H](C(=O)O)N)O
InChI: InChI=1S/C5H9NO4/c6-3(5(9)10)1-2-4(7)8/h3H,1-2,6H2,(H,7,8)(H,9,10)/t3-/m1/s1
描述信息
There are two forms of glutamic acid found in nature: L-glutamic acid and D-glutamic acid. D-glutamic acid, is not endogenously produced in higher mammals. It is found naturally primarily in the cell walls of certain bacteria. D-glutamate is also present in certain foods e.g., soybeans and also arises from the turnover of the intestinal tract microflora, whose cell walls contain significant D-glutamate. Unlike other D-amino acids, D-glutamate is not oxidized by the D-amino acid oxidases, and therefore this detoxification pathway is not available for handling D-glutamate. Likewise, D-glutamic acid, when ingested, largely escapes most deamination reactions (unlike the L-counterpart). Free D-glutamate is found in mammalian tissue at surprisingly high levels, with D-glutamate accounting for 9\\% of the total glutamate present in liver. D-glutamate is the most potent natural inhibitor of glutathione synthesis identified to date and this may account for its localization to the liver, since circulating D-glutamate may alter redox stabiity (PMID 11158923). Certain eels are known to use D-glutamic acid as a phermone for chemical communication. D-Glutamic acid has been found to be a metabolite of Lactobacillus (PMID: 22754309).
There are two forms of glutamic acid found in nature: L-glutamic acid and D-glutamic acid. D-glutamic acid, is not endogenously produced in higher mammals. It is found naturally primarily in the cell walls of certain bacteria. D-glutamate is also present in certain foods e.g., soybeans and also arises from the turnover of the intestinal tract microflora, whose cell walls contain significant D-glutamate. Unlike other D-amino acids, D-glutamate is not oxidized by the D-amino acid oxidases, and therefore this detoxification pathway is not available for handling D-glutamate. Likewise, D-glutamic acid, when ingested, largely escapes most deamination reactions (unlike the L-counterpart). Free D-glutamate is found in mammalian tissue at surprisingly high levels, with D-glutamate accounting for 9\\% of the total glutamate present in liver. D-glutamate is the most potent natural inhibitor of glutathione synthesis identified to date and this may account for its localization to the liver, since circulating D-glutamate may alter redox stabiity (PMID 11158923). Certain eels are known to use D-glutamic acid as a phermone for chemical communication. [HMDB]
D018377 - Neurotransmitter Agents > D018846 - Excitatory Amino Acids
KEIO_ID G005
同义名列表
45 个代谢物同义名
delta-2-Aminopentanedioic acid; (2R)-2-Aminopentanedioic acid; (R)-2-Aminopentanedioic acid; delta-2-Aminopentanedioate; D-2-Aminopentanedioic acid; delta-2-Aminoglutaric acid; (2R)-2-Aminopentanedioate; Glutamic Acid, (D)-Isomer; (R)-2-Aminopentanedioate; D-2-Aminoglutaric acid; D-2-Aminopentanedioate; delta-2-Aminoglutarate; delta-Glutaminic acid; L-Glutamate, Aluminum; delta-Glutaminsaeure; Aluminum L Glutamate; Glutamate, Potassium; Aluminum L-Glutamate; Glutamic acid D-form; delta-Glutamic acid; R-(-)-Glutamic acid; Potassium Glutamate; D(-)-Glutamic acid; D-2-Aminoglutarate; delta-Glutaminate; D-Glutaminic acid; Lopac-gamma-2128; D-Glutaminsaeure; Glutamate D-form; L-glutamic acid; R-(-)-Glutamate; delta-Glutamate; L Glutamic Acid; D-Glutamic acid; D-Glutaminate; Glutamic Acid; Lopac-g-2128; L Glutamate; Tocris-0217; L-glutamate; D Glutamate; D-Glutamate; glutamate; D-Glu; DGL
数据库引用编号
32 个数据库交叉引用编号
- ChEBI: CHEBI:53375
- ChEBI: CHEBI:15966
- KEGG: C00217
- PubChem: 23327
- HMDB: HMDB0003339
- DrugBank: DB02517
- ChEMBL: CHEMBL76232
- Wikipedia: Glutamic acid
- MeSH: Glutamic Acid
- MetaCyc: D-GLT
- KNApSAcK: C00019577
- foodb: FDB023148
- chemspider: 21814
- CAS: 11070-68-1
- CAS: 6893-26-1
- CAS: 138-16-9
- MoNA: KO002920
- MoNA: KO000820
- MoNA: KO002921
- MoNA: KO002922
- MoNA: KO000821
- MoNA: KO000822
- MoNA: KO000823
- MoNA: KO000819
- MoNA: KO002919
- MoNA: KO002923
- PubChem: 3517
- PDB-CCD: DGL
- PDB-CCD: FGA
- 3DMET: B01192
- NIKKAJI: J9.214B
- RefMet: D-Glutamic acid
分类词条
相关代谢途径
Reactome(0)
PlantCyc(0)
代谢反应
224 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(1)
- peptidoglycan biosynthesis I:
ATP + D-glutamate + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + H+ + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate + phosphate
Plant Reactome(216)
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Carbohydrate metabolism:
ATP + beta-D-glucose ⟶ ADP + H+ + beta-D-glucose-6-phosphate - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Carbohydrate metabolism:
H2O + alpha,alpha-trehalose ⟶ beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Carbohydrate metabolism:
ATP + beta-D-glucose ⟶ ADP + H+ + beta-D-glucose-6-phosphate - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
L-Glu + imidazole acetol-phosphate ⟶ 2OG + L-histidinol-phosphate - Carbohydrate metabolism:
ATP + Glycerol ⟶ ADP + G3P - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
ATP + CoA + propionate ⟶ AMP + PPi + PROP-CoA - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + L-Ala + UDP-N-acetylmuramate ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanine - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Carbohydrate metabolism:
Suc ⟶ 1-kestose + beta-D-glucose - Peptidoglycan biosynthesis I:
ATP + D-Glu + UDP-N-acetylmuramoyl-L-alanine ⟶ ADP + Pi + UDP-N-acetylmuramoyl-L-alanyl-D-glutamate
INOH(0)
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(6)
- D-Glutamine and D-Glutamate Metabolism:
L-Glutamine + Water ⟶ Ammonia + L-Glutamic acid - Peptidoglycan Biosynthesis I:
Adenosine triphosphate + L-Alanine + UDP-N-acetyl- -D-muramate ⟶ Adenosine diphosphate + Hydrogen Ion + Phosphate + UDP-N-acetylmuramoyl-L-alanine - Peptidoglycan Biosynthesis II:
Adenosine triphosphate + L-Alanine + UDP-N-acetyl- -D-muramate ⟶ Adenosine diphosphate + Hydrogen Ion + Phosphate + UDP-N-Acetylmuramyl-L-Ala - D-Glutamine and D-Glutamate Metabolism:
L-Glutamine + Water ⟶ Ammonia + L-Glutamic acid - Peptidoglycan Biosynthesis I:
Adenosine triphosphate + L-Alanine + UDP-N-acetyl- -D-muramate ⟶ Adenosine diphosphate + Hydrogen Ion + Phosphate + UDP-N-acetylmuramoyl-L-alanine - Peptidoglycan Biosynthesis II:
Adenosine triphosphate + L-Alanine + UDP-N-acetyl- -D-muramate ⟶ Adenosine diphosphate + Hydrogen Ion + Phosphate + UDP-N-Acetylmuramyl-L-Ala
PharmGKB(0)
2 个相关的物种来源信息
- 9606 Homo sapiens: -
- 569774 金线莲: -
在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有：
- PubMed: 来源于PubMed文献库中的文献信息，我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表，这个列表按照代谢物同时出现的文献数量降序排序，取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
- NCBI Taxonomy: 通过文献数据挖掘，得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序，取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
- Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
- Chemical Reaction: 在化学反应过程中，存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。
点击图上的相关代谢物的名称，可以跳转到相关代谢物的信息页面。
文献列表
- Jingbin Chen, Yali Liu, Yonggui Song, Huihui Liang, Genhua Zhu, Bike Zhang, Liangliang Liao, Jian Luo, Ming Yang, Dan Su. Neuro-stimulating effect of Citri Reticulata Pericarpium Viride essential oil through regulating Glu/NMDAR on olfactory bulb to improve anxiety-like behavior.
Journal of ethnopharmacology.
2024 Sep; 331(?):118332. doi:
10.1016/j.jep.2024.118332. [PMID: 38735421] - Parham Khoshbakht Marvi, Syed Rahin Ahmed, Poushali Das, Raja Ghosh, Seshasai Srinivasan, Amin Reza Rajabzadeh. Prunella vulgaris-phytosynthesized platinum nanoparticles: Insights into nanozymatic activity for H2O2 and glutamate detection and antioxidant capacity.
Talanta.
2024 Jul; 274(?):125998. doi:
10.1016/j.talanta.2024.125998. [PMID: 38574541] - Cheng-Wei Lu, Tzu-Yu Lin, Kuan-Ming Chiu, Ming-Yi Lee, Su-Jane Wang. Gypenoside XVII Reduces Synaptic Glutamate Release and Protects against Excitotoxic Injury in Rats.
Biomolecules.
2024 May; 14(5):. doi:
10.3390/biom14050589. [PMID: 38785996] - Giulia Leni, Gabriele Rocchetti, Terenzio Bertuzzi, Alessio Abate, Alessandra Scansani, Federico Froldi, Aldo Prandini. Volatile compounds, gamma-glutamyl-peptides and free amino acids as biomarkers of long-ripened protected designation of origin Coppa Piacentina.
Food chemistry.
2024 May; 440(?):138225. doi:
10.1016/j.foodchem.2023.138225. [PMID: 38134826] - Tenghan Ling, Aiping Yin, Yan Cao, Jiali Li, Hengxi Li, Ying Zhou, Xiaobing Guo, Jinghui Li, Ruilin Zhang, Haiying Wu, Ping Li. Purinergic Astrocyte Signaling Driven by TNF-α After Cannabidiol Administration Restores Normal Synaptic Remodeling Following Traumatic Brain Injury.
Neuroscience.
2024 May; 545(?):31-46. doi:
10.1016/j.neuroscience.2024.03.002. [PMID: 38460903] - Stanislav Jabinski, Wesley D M Rangel, Marek Kopáček, Veronika Jílková, Jan Jansa, Travis B Meador. Constraining activity and growth substrate of fungal decomposers via assimilation patterns of inorganic carbon and water into lipid biomarkers.
Applied and environmental microbiology.
2024 Apr; 90(4):e0206523. doi:
10.1128/aem.02065-23. [PMID: 38527003] - Jinpeng Li, Xingbei Liu, Shumin Chang, Wei Chu, Jingchen Lin, Hui Zhou, Zhuoran Hu, Mancang Zhang, Mingming Xin, Yingyin Yao, Weilong Guo, Xiaodong Xie, Huiru Peng, Zhongfu Ni, Qixin Sun, Yu Long, Zhaorong Hu. The potassium transporter TaNHX2 interacts with TaGAD1 to promote drought tolerance via modulating stomatal aperture in wheat.
Science advances.
2024 Apr; 10(15):eadk4027. doi:
10.1126/sciadv.adk4027. [PMID: 38608020] - František Sedlák, Aleš Kvasnička, Barbora Marešová, Radana Brumarová, Dana Dobešová, Kateřina Dostálová, Karolína Šrámková, Martin Pehr, Pavel Šácha, David Friedecký, Jan Konvalinka. Parallel Metabolomics and Lipidomics of a PSMA/GCPII Deficient Mouse Model Reveal Alteration of NAAG Levels and Brain Lipid Composition.
ACS chemical neuroscience.
2024 Apr; 15(7):1342-1355. doi:
10.1021/acschemneuro.3c00494. [PMID: 38377674] - Giuseppe Forlani, Giuseppe Sabbioni, Simone Barera, Dietmar Funck. A complex array of factors regulate the activity of Arabidopsis thaliana δ1 -pyrroline-5-carboxylate synthetase isoenzymes to ensure their specific role in plant cell metabolism.
Plant, cell & environment.
2024 Apr; 47(4):1348-1362. doi:
10.1111/pce.14817. [PMID: 38223941] - Lei Zhang, Xin Yue Bai, Ke Yao Sun, Xuan Li, Zhao Qi Zhang, Yi Ding Liu, Yang Xiang, Xiao Long Liu. A New Perspective in the Treatment of Ischemic Stroke: Ferroptosis.
Neurochemical research.
2024 Apr; 49(4):815-833. doi:
10.1007/s11064-023-04096-3. [PMID: 38170383] - Raul Sanchez-Muñoz. Highway to cell: Unravelling the main player in Arabidopsis chloroplast glutamate export.
The Plant cell.
2024 Mar; 36(4):805-806. doi:
10.1093/plcell/koad322. [PMID: 38134387] - Samantha Vivia The, James P Santiago, Clara Pappenberger, Ulrich Z Hammes, Mechthild Tegeder. UMAMIT44 is a key player in glutamate export from Arabidopsis chloroplasts.
The Plant cell.
2024 Mar; 36(4):1119-1139. doi:
10.1093/plcell/koad310. [PMID: 38092462] - Siyu Zhang, Dong Wang, Yawen Ding, Fuyang Song, Yong Li, Jin Zeng, Yujiong Wang. Injury of Macrophages Induced by Clostridium perfringens Type C Exotoxins.
International journal of molecular sciences.
2024 Mar; 25(7):. doi:
10.3390/ijms25073718. [PMID: 38612529] - Hongqian Zhang, Xue Gao, Qian Sun, Xiaoxue Dong, Zongwei Zhu, Chuanxu Yang. Incorporation of poly(γ-glutamic acid) in lipid nanoparticles for enhanced mRNA delivery efficiency in vitro and in vivo.
Acta biomaterialia.
2024 Mar; 177(?):361-376. doi:
10.1016/j.actbio.2024.02.004. [PMID: 38342193] - Namita Nabar, Tamara G Dacoba, Gil Covarrubias, Denisse Romero-Cruz, Paula T Hammond. Electrostatic adsorption of polyanions onto lipid nanoparticles controls uptake, trafficking, and transfection of RNA and DNA therapies.
Proceedings of the National Academy of Sciences of the United States of America.
2024 Mar; 121(11):e2307809121. doi:
10.1073/pnas.2307809121. [PMID: 38437543] - Ju-Bin Kang, Hyun-Kyoung Son, Dong-Ju Park, Yeung-Bae Jin, Fawad-Ali Shah, Phil-Ok Koh. Modulation of thioredoxin by chlorogenic acid in an ischemic stroke model and glutamate-exposed neurons.
Neuroscience letters.
2024 Mar; 825(?):137701. doi:
10.1016/j.neulet.2024.137701. [PMID: 38395190] - Yueruxin Jin, Canying Li, Shuran Zhang, Jiaqi Liu, Miao Wang, Yan Guo, Hengping Xu, Yonghong Ge. Sucrose, cell wall, and polyamine metabolisms involve in preserving postharvest quality of 'Zaosu' pear fruit by L-glutamate treatment.
Plant physiology and biochemistry : PPB.
2024 Mar; 208(?):108455. doi:
10.1016/j.plaphy.2024.108455. [PMID: 38428157] - Li Ren. The mechanistic basis for the rapid antidepressant-like effects of ketamine: From neural circuits to molecular pathways.
Progress in neuro-psychopharmacology & biological psychiatry.
2024 Feb; 129(?):110910. doi:
10.1016/j.pnpbp.2023.110910. [PMID: 38061484] - Sarathadevi Rajendran, Patrick Silcock, Phil Bremer. Volatile Organic Compounds (VOCs) Produced by Levilactobacillus brevis WLP672 Fermentation in Defined Media Supplemented with Different Amino Acids.
Molecules (Basel, Switzerland).
2024 Feb; 29(4):. doi:
10.3390/molecules29040753. [PMID: 38398505] - Yangxia Han, Manchang Kou, Kaijun Quan, Juanjuan Wang, Haixia Zhang, Hirotaka Ihara, Makoto Takafuji, Hongdeng Qiu. Enantioselective Glutamic Acid Discrimination and Nanobiological Imaging by Chiral Fluorescent Silicon Nanoparticles.
Analytical chemistry.
2024 02; 96(5):2173-2182. doi:
10.1021/acs.analchem.3c05150. [PMID: 38261544] - Ji-Yun Kang, Ji-Yeon Gu, Dong-Cheol Baek, Chang-Gue Son, Jin-Seok Lee. A Capsicum annuum L. seed extract exerts anti-neuroexcitotoxicity in HT22 hippocampal neurons.
Food & function.
2024 Feb; ?(?):. doi:
10.1039/d3fo04501c. [PMID: 38305768] - Yoichiro Kasuga, Ailing Hu, Zenji Kawakami, Masahiro Tabuchi, Takuji Yamaguchi, Hiroyuki Kobayashi, Shigaku Ikeda. Suppressive effect of Yokukansan on glutamate released from canine keratinocytes.
Open veterinary journal.
2024 Feb; 14(2):683-691. doi:
10.5455/ovj.2024.v14.i2.8. [PMID: 38549576] - Delin Yan, Lei Huang, Zhiqing Mei, Han Bao, Yaman Xie, Cunyi Yang, Xiangyang Gao. Untargeted metabolomics revealed the effect of soybean metabolites on poly(γ-glutamic acid) production in fermented natto and its metabolic pathway.
Journal of the science of food and agriculture.
2024 Feb; 104(3):1298-1307. doi:
10.1002/jsfa.13011. [PMID: 37782527] - Xi Zhang, Hong Zheng, Zhitao Ni, Yuyin Shen, Die Wang, Wenqing Li, Liangcai Zhao, Chen Li, Hongchang Gao. Fibroblast growth factor 21 alleviates diabetes-induced cognitive decline.
Cerebral cortex (New York, N.Y. : 1991).
2024 01; 34(2):. doi:
10.1093/cercor/bhad502. [PMID: 38220573] - Xiaorui Xing, Qin Sun, Ruwen Wang, Yibing Wang, Ru Wang. Impacts of glutamate, an exercise-responsive metabolite on insulin signaling.
Life sciences.
2024 Jan; ?(?):122471. doi:
10.1016/j.lfs.2024.122471. [PMID: 38301875] - Ruyan Gao, Tahir Ali, Zizhen Liu, Axiang Li, Liangliang Hao, Liufang He, Xiaoming Yu, Shupeng Li. Ceftriaxone averts neuroinflammation and relieves depressive-like behaviors via GLT-1/TrkB signaling.
Biochemical and biophysical research communications.
2024 Jan; 701(?):149550. doi:
10.1016/j.bbrc.2024.149550. [PMID: 38310688] - Tzu-Kang Lin, Kun-Chieh Yeh, Ming-Shang Pai, Pei-Wen Hsieh, Su-Jane Wang. Ursolic acid inhibits the synaptic release of glutamate and prevents glutamate excitotoxicity in rats.
European journal of pharmacology.
2024 Jan; 963(?):176280. doi:
10.1016/j.ejphar.2023.176280. [PMID: 38113967] - Huizhen Sun, Shanshan Wei, Yanchun Gong, Kaizhi Ding, Shan Tang, Wei Sun, Chunhua Yuan, Liping Huang, Zhibing Liu, Chong Chen, Lihua Yao. Neuroprotective effects of cordycepin inhibit glutamate-induced apoptosis in hippocampal neurons.
Cell stress & chaperones.
2024 Jan; ?(?):. doi:
10.1016/j.cstres.2024.01.001. [PMID: 38219840] - Shreya Banerjee, Rakesh Sarkar, Arpita Mukherjee, Suvrotoa Mitra, Animesh Gope, Mamta Chawla-Sarkar. Rotavirus-induced lncRNA SLC7A11-AS1 promotes ferroptosis by targeting cystine/glutamate antiporter xCT (SLC7A11) to facilitate virus infection.
Virus research.
2024 01; 339(?):199261. doi:
10.1016/j.virusres.2023.199261. [PMID: 37923170] - Lenka Vlasatikova, Michal Zeman, Magdalena Crhanova, Jitka Matiasovicova, Daniela Karasova, Marcela Faldynova, Hana Prikrylova, Alena Sebkova, Ivan Rychlik. Colonization of chickens with competitive exclusion products results in extensive differences in metabolite composition in cecal digesta.
Poultry science.
2024 Jan; 103(1):103217. doi:
10.1016/j.psj.2023.103217. [PMID: 37980752] - Anqi Ge, Qi He, Da Zhao, Yuwei Li, Junpeng Chen, Ying Deng, Wang Xiang, Hongqiao Fan, Shiting Wu, Yan Li, Lifang Liu, Yue Wang. Mechanism of ferroptosis in breast cancer and research progress of natural compounds regulating ferroptosis.
Journal of cellular and molecular medicine.
2024 01; 28(1):e18044. doi:
10.1111/jcmm.18044. [PMID: 38140764] - Mengran Wang, Tingting Xuan, Haining Li, Jing An, Tianhui Hao, Jiang Cheng. Protective effect of FXN overexpression on ferroptosis in L-Glu-induced SH-SY5Y cells.
Acta histochemica.
2024 Jan; 126(1):152135. doi:
10.1016/j.acthis.2024.152135. [PMID: 38266318] - Xin Jin, Hangyi Wu, Jie Yu, Yanni Cao, Lanyi Zhang, Zhenhai Zhang, Huixia Lv. Glutamate affects self-assembly, protein corona, and anti-4 T1 tumor effects of melittin/vitamin E-succinic acid-(glutamate)n nanoparticles.
Journal of controlled release : official journal of the Controlled Release Society.
2024 Jan; 365(?):802-817. doi:
10.1016/j.jconrel.2023.12.013. [PMID: 38092255] - Danuta Jantas, Piotr Warszyński, Władysław Lasoń. Carnosic Acid Shows Higher Neuroprotective Efficiency than Edaravone or Ebselen in In Vitro Models of Neuronal Cell Damage.
Molecules (Basel, Switzerland).
2023 Dec; 29(1):. doi:
10.3390/molecules29010119. [PMID: 38202702] - Kim-Teng Lee, Hong-Sheng Liao, Ming-Hsiun Hsieh. Glutamine Metabolism, Sensing and Signaling in Plants.
Plant & cell physiology.
2023 Dec; 64(12):1466-1481. doi:
10.1093/pcp/pcad054. [PMID: 37243703] - M Oqal, E Qnais, A Alqudah, O Gammoh. Analgesic effect of the flavonoid herbacetin in nociception animal models.
European review for medical and pharmacological sciences.
2023 Dec; 27(23):11236-11248. doi:
10.26355/eurrev_202312_34563. [PMID: 38095373] - Jiang-Ping Wei, Zi-Xuan Zhao, Jing Zeng, Fang-Hong Shang, Lei Hua, Yong Yang, Xiao-Mei Zhang. [Yigong Powder regulates CXCL12/CXCR4 signaling to reduce glutamate release and prevent cognitive decline in mouse model of aging].
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica.
2023 Dec; 48(23):6483-6491. doi:
10.19540/j.cnki.cjcmm.20230811.702. [PMID: 38212005] - Wanli You, Jinglin Zhang, Xueyin Ru, Feng Xu, Zhengguo Wu, Peng Jin, Yonghua Zheng, Shifeng Cao. CmCML11 interacts with CmCAMTA5 to enhance γ-aminobutyric acid (GABA) accumulation by regulating GABA shunt in fresh-cut cantaloupe.
Plant physiology and biochemistry : PPB.
2023 Nov; 206(?):108217. doi:
10.1016/j.plaphy.2023.108217. [PMID: 38039581] - Hongxing Tang, Kejun He, Kun Zhao, Chen Zheng, Weichi Wu, Weilin Jin, Lixuan Yang, Baoshu Xie. Protective effects of Hinokitiol on neuronal ferroptosis by activating the KEAP1/NRF-2/HO-1 pathway in traumatic brain injury.
Journal of neurotrauma.
2023 Nov; ?(?):. doi:
10.1089/neu.2023.0150. [PMID: 37962273] - Yung-Chih Kuo, Sheng-Yuan Lin, Sourav De, Rajendiran Rajesh. Regeneration of Pancreatic Cells Using Optimized Nanoparticles and l-Glutamic Acid-Gelatin Scaffolds with Controlled Topography and Grafted Activin A/BMP4.
ACS biomaterials science & engineering.
2023 11; 9(11):6208-6224. doi:
10.1021/acsbiomaterials.3c00791. [PMID: 37882705] - Bo Jing, Wenjuan Shi, Lu Liu, Ying Wang. Poly-γ-glutamic acid improved biological nitrogen fixation, water-nitrogen productivity, and nitrate residue in cotton/soybean intercropping.
Journal of the science of food and agriculture.
2023 Nov; 103(14):7284-7292. doi:
10.1002/jsfa.12814. [PMID: 37378640] - Danni Xie, Caiyou Song, Tao Qin, Zhenwei Zhai, Jie Cai, Jingyi Dai, Tao Sun, Ying Xu. Moschus ameliorates glutamate-induced cellular damage by regulating autophagy and apoptosis pathway.
Scientific reports.
2023 10; 13(1):18586. doi:
10.1038/s41598-023-45878-7. [PMID: 37903904] - Chen Han, Haiying Bao. Therapeutic effects and mechanisms of Inonotus hispidus extract and active monomer compounds in a rat mammary gland hyperplasia model.
Journal of ethnopharmacology.
2023 Oct; 319(Pt 2):117274. doi:
10.1016/j.jep.2023.117274. [PMID: 37797875] - Sherrye T Glaser, Kalani Jayanetti, Saida Oubraim, Andrew Hillowe, Elena Frank, Jason Jong, Liqun Wang, Hehe Wang, Iwao Ojima, Samir Haj-Dahmane, Martin Kaczocha. Fatty acid binding proteins are novel modulators of synaptic epoxyeicosatrienoic acid signaling in the brain.
Scientific reports.
2023 Sep; 13(1):15234. doi:
10.1038/s41598-023-42504-4. [PMID: 37709856] - Yi Lu, Xin Gao, Shadi A D Mohammed, Tianyu Wang, Jiaqi Fu, Yu Wang, Yang Nan, Fang Lu, Shumin Liu. Efficacy and mechanism study of Baichanting compound, a combination of Acanthopanax senticosus (Rupr. and Maxim.) Harms, Paeonia lactiflora Pall and Uncaria rhynchophylla (Miq.) Miq. ex Havil, on Parkinson's disease based on metagenomics and metabolomics.
Journal of ethnopharmacology.
2023 Sep; ?(?):117182. doi:
10.1016/j.jep.2023.117182. [PMID: 37714224] - Cosimo Taiti, Giacomo Di Matteo, Mattia Spano, Vittorio Vinciguerra, Elisa Masi, Luisa Mannina, Stefania Garzoli. Metabolomic Approach Based on Analytical Techniques for the Detection of Secondary Metabolites from Humulus lupulus L. Dried Leaves.
International journal of molecular sciences.
2023 Sep; 24(18):. doi:
10.3390/ijms241813732. [PMID: 37762036] - Huiting Yang, Xiaohong Gu, Huihui Chen, Qingfei Zeng, Zhigang Mao, You Ge. Omics techniques reveal the toxicity mechanisms of three antiepileptic drugs to juvenile zebrafish (Danio rerio) brain and liver.
Aquatic toxicology (Amsterdam, Netherlands).
2023 Sep; 262(?):106668. doi:
10.1016/j.aquatox.2023.106668. [PMID: 37659109] - Aditya Kumar, Ankush Prasad, Michaela Sedlářová, Pavel Pospíšil. Malondialdehyde enhances PsbP protein release during heat stress in Arabidopsis.
Plant physiology and biochemistry : PPB.
2023 Sep; 202(?):107984. doi:
10.1016/j.plaphy.2023.107984. [PMID: 37669610] - Pinghui Wei, Guoge Han, Meiqin He, Yan Wang. Retinal Neurotransmitter Alteration in Response to Dopamine D2 Receptor Antagonist from Myopic Guinea Pigs.
ACS chemical neuroscience.
2023 Aug; ?(?):. doi:
10.1021/acschemneuro.3c00099. [PMID: 37647579] - Zhaolong Pan, Jan-Lars Van den Bossche, Eva Rodriguez-Aznar, Pauline Janssen, Olaya Lara, Gamze Ates, Ann Massie, Diedert Luc De Paep, Isabelle Houbracken, Marco Mambretti, Ilse Rooman. Pancreatic acinar cell fate relies on system xC- to prevent ferroptosis during stress.
Cell death & disease.
2023 08; 14(8):536. doi:
10.1038/s41419-023-06063-w. [PMID: 37604805] - S B Caine, S Plant, K Furbish, M Yerton, E Smaragdi, B Niclou, J M Lorusso, J Y Chang, C Bitter, A Basu, S Miller, C-Y Huang, R Komson, D Liu, S Behar, M Thomsen. Sprague Dawley rats from different vendors vary in the modulation of prepulse inhibition of startle (PPI) by dopamine, acetylcholine, and glutamate drugs.
Psychopharmacology.
2023 Aug; ?(?):. doi:
10.1007/s00213-023-06444-1. [PMID: 37580441] - Mohammad Keimasi, Kowsar Salehifard, Sayyed Jafar Hoseini, Fariba Esmaeili, Noushin Mirshah Jafar Esfahani, Mohammadreza Amirsadri, Mohammadjavad Keimasi, Majid Moradmand, Mohammad Reza Mofid. Purified Native Protein Extracted from the Venom of Agelena orientalis Attenuates Memory Defects in the Rat Model of Glutamate-Induced Excitotoxicity.
The protein journal.
2023 Aug; ?(?):. doi:
10.1007/s10930-023-10140-6. [PMID: 37531037] - Yang Liu, Amei Tang, Ming Liu, Changjun Xu, Feng Cao, Changfu Yang. Tuberostemonine may enhance the function of the SLC7A11/glutamate antiporter to restrain the ferroptosis to alleviate pulmonary fibrosis.
Journal of ethnopharmacology.
2023 Aug; 318(Pt B):116983. doi:
10.1016/j.jep.2023.116983. [PMID: 37532076] - P A Perez-Corredor, P Oluwatomilayo-Ojo, J A Gutierrez-Vargas, G P Cardona-Gómez. Obesity induces extracellular vesicle release from the endothelium as a contributor to brain damage after cerebral ischemia in rats.
Nutritional neuroscience.
2023 Aug; 26(8):680-695. doi:
10.1080/1028415x.2022.2078173. [PMID: 36039918] - Tanya Denne, Lila C Winfrey, Cindy Moore, Chase Whitner, Theresa D'Silva, Amala Soumyanath, Lynne Shinto, Amie Hiller, Charles K Meshul. Recovery of motor function is associated with rescue of glutamate biomarkers in the striatum and motor cortex following treatment with Mucuna pruriens in a murine model of Parkinsons disease.
Molecular and cellular neurosciences.
2023 Jul; 126(?):103883. doi:
10.1016/j.mcn.2023.103883. [PMID: 37527694] - Mauricio Tavares Jacques, Viviane de Souza, Flávio Augusto Rocha Barbosa, Rômulo Faria Santos Canto, Samantha Cristiane Lopes, Rui Daniel Prediger, Antônio Luiz Braga, Michael Aschner, Marcelo Farina. Novel Probucol Analogue, 4,4'-Diselanediylbis (2,6-Di-tert-Butylphenol), Prevents Oxidative Glutamate Neurotoxicity In Vitro and Confers Neuroprotection in a Rodent Model of Ischemic Stroke.
ACS chemical neuroscience.
2023 Jul; ?(?):. doi:
10.1021/acschemneuro.3c00138. [PMID: 37499207] - Ramóna Pap, Edina Pandur, Gergely Jánosa, Katalin Sipos, Ferenc Rómeó Fritz, Tamás Nagy, Attila Agócs, József Deli. Protective Effects of 3'-Epilutein and 3'-Oxolutein against Glutamate-Induced Neuronal Damage.
International journal of molecular sciences.
2023 Jul; 24(15):. doi:
10.3390/ijms241512008. [PMID: 37569384] - Marta Grzechowiak, Joanna Sliwiak, Mariusz Jaskolski, Milosz Ruszkowski. Structural and functional studies of Arabidopsis thaliana glutamate dehydrogenase isoform 2 demonstrate enzyme dynamics and identify its calcium binding site.
Plant physiology and biochemistry : PPB.
2023 Jul; 201(?):107895. doi:
10.1016/j.plaphy.2023.107895. [PMID: 37478728] - Namho Kim, Ji Hye Lee, Yeonho Song, Jeong-Hyung Lee, George C Schatz, Hyonseok Hwang. Molecular Dynamics Simulation Study of the Protonation State Dependence of Glutamic Acid Transport through a Cyclic Peptide Nanotube.
The journal of physical chemistry. B.
2023 07; 127(27):6061-6072. doi:
10.1021/acs.jpcb.3c02285. [PMID: 37369069] - Pradeep K Anand, Jagdeep Kaur. Rv3539 (PPE63) of Mycobacterium Tuberculosis Promotes Survival of Mycobacterium Smegmatis in Human Macrophages Cell Line via Cell Wall Modulation of Bacteria and Altering Host's Immune Response.
Current microbiology.
2023 Jul; 80(8):267. doi:
10.1007/s00284-023-03360-7. [PMID: 37401981] - Yaron Caspi, Chrysoula K Pantazopoulou, Jeanine J Prompers, Corné M J Pieterse, Hilleke Hulshoff Pol, Kaisa Kajala. Why did glutamate, GABA, and melatonin become intercellular signalling molecules in plants?.
eLife.
2023 Jun; 12(?):. doi:
10.7554/elife.83361. [PMID: 37338964] - Chunni Chen, Linlin Yang, Mengru Li, Li Gao, Xuemei Qin, Guanhua Du, Yuzhi Zhou. Study on the targeted regulation of Scutellaria baicalensis leaf on glutamine-glutamate metabolism and glutathione synthesis in the liver of D-gal ageing rats.
The Journal of pharmacy and pharmacology.
2023 Jun; ?(?):. doi:
10.1093/jpp/rgad050. [PMID: 37329511] - Xin Zhang, Weijie Xue, Changbo Zhang, Changrong Wang, Yongchun Huang, Yanting Wang, Liangcai Peng, Zhongqi Liu. Cadmium pollution leads to selectivity loss of glutamate receptor channels for permeation of Ca2+/Mn2+/Fe2+/Zn2+ over Cd2+ in rice plant.
Journal of hazardous materials.
2023 06; 452(?):131342. doi:
10.1016/j.jhazmat.2023.131342. [PMID: 37023578] - Sheikh Azimullah, Mohamed Fizur Nagoor Meeran, Khatija Ayoob, Seenipandi Arunachalam, Shreesh Ojha, Rami Beiram. Tannic Acid Mitigates Rotenone-Induced Dopaminergic Neurodegeneration by Inhibiting Inflammation, Oxidative Stress, Apoptosis, and Glutamate Toxicity in Rats.
International journal of molecular sciences.
2023 Jun; 24(12):. doi:
10.3390/ijms24129876. [PMID: 37373023] - Jannatul Fardus, Shahadat Hossain, Md Mahfuzur Rob, Masayuki Fujita. ʟ-glutamic acid modulates antioxidant defense systems and nutrient homeostasis in lentil (Lens culinaris Medik.) under copper toxicity.
Environmental science and pollution research international.
2023 Jun; ?(?):. doi:
10.1007/s11356-023-27993-0. [PMID: 37270757] - Kasumi Takeuchi, Masayo Ogiso, Tomohiro Morohoshi, Shigemi Seo. Glutamate Positively Regulates Chitinase Activity and the Biocontrol Efficacy of Pseudomonas protegens.
Molecular plant-microbe interactions : MPMI.
2023 Jun; 36(6):323-333. doi:
10.1094/mpmi-09-22-0178-r. [PMID: 36749296] - Fei Kang, Qilin Lv, Jingbiao Fan, Yun Zhang, Yuling Song, Xueqin Ren, Shuwen Hu. Ameliorative effect of calcium poly(aspartic acid) (PASP-Ca) and calcium poly-γ-glutamic acid (γ-PGA-Ca) on soil acidity in different horizons.
Environmental science and pollution research international.
2023 Jun; 30(30):75681-75693. doi:
10.1007/s11356-023-27713-8. [PMID: 37222895] - Rafael Short Ferreira, Paulo Roberto Ribeiro, Juliana Helena Castro E Silva, Juliana Bender Hoppe, Monique Marylin Alves de Almeida, Beatriz Correia de Lima Ferreira, Gustavo Borges Andrade, Suzana Braga de Souza, Luzimar Gonzaga Ferdandez, Maria de Fátima Dias Costa, Christianne Gazzana Salbego, Andrea Domenico Rivera, Aline Longoni, Adriano Martimbianco de Assis, Francesca Pieropan, José Cláudio Fonseca Moreira, Silvia Lima Costa, Arthur Morgan Butt, Victor Diogenes Amaral da Silva. Amburana cearensis seed extract stimulates astrocyte glutamate homeostatic mechanisms in hippocampal brain slices and protects oligodendrocytes against ischemia.
BMC complementary medicine and therapies.
2023 May; 23(1):154. doi:
10.1186/s12906-023-03959-0. [PMID: 37170258] - Cheng-Wei Lu, Tzu-Yu Lin, Pei-Wen Hsieh, Kuan-Ming Chiu, Ming-Yi Lee, Su-Jane Wang. Cynarin, a caffeoylquinic acid derivative in artichoke, inhibits exocytotic glutamate release from rat cortical nerve terminals (synaptosomes).
Neurochemistry international.
2023 May; 167(?):105537. doi:
10.1016/j.neuint.2023.105537. [PMID: 37164158] - Anchalee Prasansuklab, Suporn Sukjamnong, Atsadang Theerasri, Valerie W Hu, Tewarit Sarachana, Tewin Tencomnao. Transcriptomic analysis of glutamate-induced HT22 neurotoxicity as a model for screening anti-Alzheimer's drugs.
Scientific reports.
2023 05; 13(1):7225. doi:
10.1038/s41598-023-34183-y. [PMID: 37142620] - Xiaonan Zhang, Mengxue Xia, Yingjie Wu, Fang Zhang. Branched-Chain Amino Acids Metabolism and Their Roles in Retinopathy: From Relevance to Mechanism.
Nutrients.
2023 Apr; 15(9):. doi:
10.3390/nu15092161. [PMID: 37432261] - Wu Li, Zifei Yan, Nan Zhang, Zhiyong Zhang, Xiaohong Xiang. Novel role of PE_PGRS47 in the alteration of mycobacterial cell wall integrity and drug resistance.
Archives of microbiology.
2023 Apr; 205(5):174. doi:
10.1007/s00203-023-03515-x. [PMID: 37022460] - M V Kustova, I I Prokofiev, V N Perfilova, E A Muzyko, V E Zavadskaya, S V Varlamova, A S Kucheryavenko, I N Tyurenkov, O S Vasilyeva. The role of iNOS inhibition in the mechanism of the cardioprotective effect of new GABA and glutamic acid derivatives in the model of acute alcoholic myocardial injury in rats.
Biomeditsinskaia khimiia.
2023 Apr; 69(2):112-124. doi:
10.18097/pbmc20236902112. [PMID: 37132493] - Pei-Shin Gu, Kuan-Wen Su, Kuo-Wei Yeh, Jing-Long Huang, Fu-Sung Lo, Chih-Yung Chiu. Metabolomics Analysis Reveals Molecular Signatures of Metabolic Complexity in Children with Hypercholesterolemia.
Nutrients.
2023 Mar; 15(7):. doi:
10.3390/nu15071726. [PMID: 37049565] - Ritesh Kumar, Gayatri Tripathi, Isha Goyal, Jaydeep Sharma, Ruchi Tiwari, Rinchuila Shimphrui, Neelam K Sarkar, Anil Grover. Insights into genomic variations in rice Hsp100 genes across diverse rice accessions.
Planta.
2023 Mar; 257(5):91. doi:
10.1007/s00425-023-04123-1. [PMID: 36995438] - Matteo Grenzi, Stefano Buratti, Ambra Selene Parmagnani, Ilaria Abdel Aziz, Iwona Bernacka-Wojcik, Francesca Resentini, Jan Šimura, Fabrizio Gandolfo Doccula, Andrea Alfieri, Laura Luoni, Karin Ljung, Maria Cristina Bonza, Eleni Stavrinidou, Alex Costa. Long-distance turgor pressure changes induce local activation of plant glutamate receptor-like channels.
Current biology : CB.
2023 03; 33(6):1019-1035.e8. doi:
10.1016/j.cub.2023.01.042. [PMID: 36796359] - Deirdre H McLachlan. Plant physiology: Untangling the roles of glutamate and turgor pressure.
Current biology : CB.
2023 03; 33(6):R221-R223. doi:
10.1016/j.cub.2023.02.026. [PMID: 36977382] - Wei Shen, Yanlin Tao, Fang Zheng, Houyuan Zhou, Hui Wu, Hailian Shi, Fei Huang, Xiaojun Wu. The alteration of gut microbiota in venlafaxine-ameliorated chronic unpredictable mild stress-induced depression in mice.
Behavioural brain research.
2023 Mar; 446(?):114399. doi:
10.1016/j.bbr.2023.114399. [PMID: 36963638] - Canying Li, Chenyang Zhang, Jiaxin Liu, Linhong Qu, Yonghong Ge. l-Glutamate maintains the quality of apple fruit by mediating carotenoid, sorbitol and sucrose metabolisms.
Journal of the science of food and agriculture.
2023 Mar; ?(?):. doi:
10.1002/jsfa.12566. [PMID: 36944028] - Xin Tang, Jingyu Wen, Li Mu, Ziwei Gao, Jingxian Weng, Xiaokang Li, Xiangang Hu. Regulation of arsenite toxicity in lettuce by pyrite and glutamic acid and the related mechanism.
The Science of the total environment.
2023 Mar; 877(?):162928. doi:
10.1016/j.scitotenv.2023.162928. [PMID: 36934948] - Fanrong Zeng, Muhammad Mudassir Nazir, Temoor Ahmed, Muhammad Noman, Shafaqat Ali, Muhammad Rizwan, Mohammad Shah Alam, Jonas Lwalaba Wa Lwalaba, Guoping Zhang. Calcium and L-glutamate present the opposite role in managing arsenic in barley.
Environmental pollution (Barking, Essex : 1987).
2023 Mar; 321(?):121141. doi:
10.1016/j.envpol.2023.121141. [PMID: 36702433] - José Miguel Valderrama-Martín, Francisco Ortigosa, Juan Carlos Aledo, Concepción Ávila, Francisco M Cánovas, Rafael A Cañas. Pine has two glutamine synthetase paralogs, GS1b.1 and GS1b.2, exhibiting distinct biochemical properties.
The Plant journal : for cell and molecular biology.
2023 03; 113(6):1330-1347. doi:
10.1111/tpj.16113. [PMID: 36658761] - Dawei Chen, Yating Liang, Jiaojiao Liang, Feifei Shen, Yue Cheng, Hengxian Qu, Yunchao Wa, Congcong Guo, Ruixia Gu, Jianya Qian, Xia Chen, Chenchen Zhang, Chengran Guan. Beneficial effects of Lactobacillus rhamnosus hsryfm 1301 fermented milk on rats with nonalcoholic fatty liver disease.
Journal of dairy science.
2023 Mar; 106(3):1533-1548. doi:
10.3168/jds.2022-22383. [PMID: 36710180] - Xiaojuan Sun, Hongbo Deng, Tengyun Shu, Min Xu, Lihua Su, Haizhou Li. Study on Chemical Constituents of Panax notoginseng Leaves.
Molecules (Basel, Switzerland).
2023 Feb; 28(5):. doi:
10.3390/molecules28052194. [PMID: 36903439] - Aifang Cheng, Yan Zhang, Jin Sun, Duli Huang, Jordy Evan Sulaiman, Xin Huang, Long Wu, Wenkang Ye, Chuanhai Wu, Hei-Ning Lam, Yusheng Shi, Pei-Yuan Qian. Pterosin sesquiterpenoids from Pteris laeta Wall. ex Ettingsh. Protect cells from glutamate excitotoxicity by modulating mitochondrial signals.
Journal of ethnopharmacology.
2023 Feb; ?(?):116308. doi:
10.1016/j.jep.2023.116308. [PMID: 36822346] - Lucas Matheus Gonçalves de Oliveira, Rodrigo Barreto Carreira, Juciele Valeria Ribeiro de Oliveira, Ravena Pereira do Nascimento, Cleide Dos Santos Souza, Emiliano Trias, Victor Diogenes Amaral da Silva, Silvia Lima Costa. Impact of Plant-Derived Compounds on Amyotrophic Lateral Sclerosis.
Neurotoxicity research.
2023 Feb; ?(?):. doi:
10.1007/s12640-022-00632-1. [PMID: 36800114] - Baskar Selvaraj, Tam Thi Le, Dae Won Kim, Bo Hyun Jung, Ki-Yeon Yoo, Hong Ryul Ahn, Phuong Thien Thuong, Thi Thu Thuy Tran, Ae Nim Pae, Sang Hoon Jung, Jae Wook Lee. Neuroprotective Effects of Ethanol Extract of Polyscias fruticosa (EEPF) against Glutamate-Mediated Neuronal Toxicity in HT22 Cells.
International journal of molecular sciences.
2023 Feb; 24(4):. doi:
10.3390/ijms24043969. [PMID: 36835378] - Pipeng Xing, Haowen Luo, Zhenzhen He, Longxin He, Hua Zhao, Xiangru Tang, Meiyang Duan. Trans-Zeatin induce regulation the biosynthesis of 2-acetyl-1-pyrroline in fragrant rice (Oryza sativa L.) seedlings.
BMC plant biology.
2023 Feb; 23(1):88. doi:
10.1186/s12870-023-04106-0. [PMID: 36765297] - Kohei Oda, Alexander Wlodawer. Overview of the Properties of Glutamic Peptidases That Are Present in Plant and Bacterial Pathogens and Play a Role in Celiac Disease and Cancer.
Biochemistry.
2023 Feb; 62(3):672-694. doi:
10.1021/acs.biochem.2c00622. [PMID: 36705990] - Hedan Li, Daqing Xu, Xin Tan, Danyang Huang, Yu Huang, Guihong Zhao, Xiaoqing Hu, Xiaoyuan Wang. The role of trehalose biosynthesis on mycolate composition and L-glutamate production in Corynebacterium glutamicum.
Microbiological research.
2023 Feb; 267(?):127260. doi:
10.1016/j.micres.2022.127260. [PMID: 36463830] - Ola E Mohamed, Dalaal M Abdallah, Ahmed M Fayez, Reem A Mohamed, Hanan S El-Abhar. Morin post-treatment surpassed calpeptin in ameliorating 3-NP-induced cortical neurotoxicity via modulation of glutamate/calpain axis, Kidins220, and BDNF/TrkB/AKT/CREB trajectory.
International immunopharmacology.
2023 Feb; 116(?):109771. doi:
10.1016/j.intimp.2023.109771. [PMID: 36736222] - Bao Gong, Can-Hong Wang, Yu-Lan Wu, Yang-Yang Liu, Jian-He Wei. [Anxiolytic and antidepressant effects of agarwood inhalation and its mechanism].
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica.
2023 Feb; 48(4):1023-1031. doi:
10.19540/j.cnki.cjcmm.20221027.401. [PMID: 36872273] - Chongxi Liu, Zhiyan Wang, Yin Chen, Yijun Yan, Lei Li, Yong-Jiang Wang, Lu Bai, Shanshan Li, Yanyan Zhang, Xiangjing Wang, Sheng-Xiong Huang, Wensheng Xiang. Guvermectin Biosynthesis Revealing the Key Role of a Phosphoribohydrolase and Structural Insight into the Active Glutamate of a Noncanonical Adenine Phosphoribosyltransferase.
ACS chemical biology.
2023 01; 18(1):102-111. doi:
10.1021/acschembio.2c00739. [PMID: 36623177] - Yu Wang, Weidong Duan, Chao Lv, Zhuangzhuang Wei, Yanping Zhu, Qi Yang, Ying Liu, Zhenguo Shen, Yan Xia, Kun Duan, Lingtong Quan. Citric Acid and Poly-glutamic Acid Promote the Phytoextraction of Cadmium and Lead in Solanum nigrum L. Grown in Compound Cd-Pb Contaminated Soils.
Bulletin of environmental contamination and toxicology.
2023 Jan; 110(1):37. doi:
10.1007/s00128-022-03682-5. [PMID: 36607448] - Toshihiko Tsuruda, Riichiro Yoshida. l-Glutamate activates salicylic acid signaling to promote stomatal closure and PR1 expression in Arabidopsis.
Physiologia plantarum.
2023 Jan; 175(1):e13858. doi:
10.1111/ppl.13858. [PMID: 36658465] - Yunan Hu, Mingxia Li, Yongjun Hu, Defu Han, Jian Wei, Tao Zhang, Jixun Guo, Lianxuan Shi. Wild soybean salt tolerance metabolic model: Assessment of storage protein mobilization in cotyledons and C/N balance in the hypocotyl/root axis.
Physiologia plantarum.
2023 Jan; 175(1):e13863. doi:
10.1111/ppl.13863. [PMID: 36688582] - Xiao-Hong Li, Jie-Jun Fu, Xiao-Juan Shi, Yun-Na Zhang, Min Shao, Shao-Jie Yue, Chen Li, Zi-Qiang Luo. Sp1 mediated the inhibitory effect of glutamate on pulmonary surfactant synthesis.
PloS one.
2023; 18(8):e0289530. doi:
10.1371/journal.pone.0289530. [PMID: 37556489] - Kanako Takahashi, Luying Chen, Misa Sayama, Mian Wu, Mariko Kato Hayashi, Tomohiko Irie, Tomohiko Ohwada, Kaoru Sato. Leucine 434 is essential for docosahexaenoic acid-induced augmentation of L-glutamate transporter current.
The Journal of biological chemistry.
2023 01; 299(1):102793. doi:
10.1016/j.jbc.2022.102793. [PMID: 36509140] - Qili Wang, Shunping Han, Yongqin Zhu, Guowei Wang, Danfei Chen. Poly-γ-glutamic acid coating polymeric nanoparticles enhance renal drug distribution and cellular uptake for diabetic nephropathy therapy.
Journal of drug targeting.
2023 01; 31(1):89-99. doi:
10.1080/1061186x.2022.2106488. [PMID: 35880399]