D-Alanine (BioDeep_00000014410)

Secondary id: BioDeep_00000399983, BioDeep_00000404106

human metabolite PANOMIX_OTCML-2023 Endogenous blood metabolite BioNovoGene_Lab2019 natural product

代谢物信息卡片

D-alpha-Aminopropionic acid

化学式: C3H7NO2 (89.0477)
中文名称: D-丙氨酸
谱图信息: 最多检出来源 Homo sapiens(plant) 24.53%

Reviewed

Last reviewed on 2024-09-13.

Cite this Page

D-Alanine. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China. https://query.biodeep.cn/s/d-alanine (retrieved 2024-12-22) (BioDeep RN: BioDeep_00000014410). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

分子结构信息

SMILES: C(=O)([C@@H](C)N)O
InChI: InChI=1S/C3H7NO2/c1-2(4)3(5)6/h2H,4H2,1H3,(H,5,6)/t2-/m1/s1

描述信息

Alanine is a nonessential amino acid made in the body from the conversion of the carbohydrate pyruvate or the breakdown of DNA and the dipeptides carnosine and anserine. It is highly concentrated in muscle and is one of the most important amino acids released by muscle, functioning as a major energy source. Plasma alanine is often decreased when the BCAA (Branched Chain Amino Acids) are deficient. This finding may relate to muscle metabolism. Alanine is highly concentrated in meat products and other high-protein foods like wheat germ and cottage cheese. Alanine is an important participant as well as regulator in glucose metabolism. Alanine levels parallel blood sugar levels in both diabetes and hypoglycemia, and alanine reduces both severe hypoglycemia and the ketosis of diabetes. It is an important amino acid for lymphocyte reproduction and immunity. Alanine therapy has helped dissolve kidney stones in experimental animals. Normal alanine metabolism, like that of other amino acids, is highly dependent upon enzymes that contain vitamin B6. Alanine, like GABA, taurine and glycine, is an inhibitory neurotransmitter in the brain. Alanine can be found in some Gram-positive bacteria (PMID:24752840).
Amino acids are one of the most important molecules in living organisms, and most of them have a chiral carbon at a -position. In the higher animals, a large part of the naturally occurring amino acids is the L-form, and the stereoisomers (D-amino acids) had been believed to be rare. However, several D-amino acids have been found in mammals including humans, and their distributions, functions and origins have gradually been clarified. The D-alanine (D-Ala) amounts have also been reported to change in the case of diseases. Proteins of the frontal lobe white and gray matter of human brains, both normal and Alzheimer subjects, contain D-alanine at concentrations between 0.50 and 1.28 mumol/g of wet tissue, 50-70-times lower than the concentration of L-alanine. D-Alanine have been detected in the sera of both normal subjects and patients with renal dysfunction, and their concentrations were higher in the patients than in the normal subjects. (PMID: 16141519, 1450921, 8535409, 1426150, 1933416) [HMDB]
KEIO_ID A011
D-Alanine is a weak GlyR (inhibitory glycine receptor) and PMBA agonist, with an EC50 of 9 mM for GlyR.
D-Alanine is a weak GlyR (inhibitory glycine receptor) and PMBA agonist, with an EC50 of 9 mM for GlyR.

同义名列表

30 个代谢物同义名

D-alpha-Aminopropionic acid; (2R)-2-aminopropanoic acid; (2R)-2-Aminopropionic acid; (R)-2-Aminopropionic acid; (R)-2-Aminopropanoic acid; D-Α-aminopropionic acid; D-alpha-Aminopropionate; D-a-Aminopropionic acid; D-2-Aminopropionic acid; (2R)-2-Aminopropanoate; (R)-2-Aminopropanoate; D-Α-aminopropionate; D-a-Aminopropionate; D-2-Aminopropionate; D(-)-alpha-Alanine; D-alpha-Alanine; D(-)-a -Alanine; D(-)-Α-alanine; D-(-)-Alanine; (R)-Alanine; D-a-Alanine; D-Α-alanine; D-Alanine; D-Alanin; Alanine; D-Ala; DAL; Ba 2776; D-Alanine; D-alanine

数据库引用编号

29 个数据库交叉引用编号

ChEBI: CHEBI:15570
KEGG: C00133
PubChem: 71080
HMDB: HMDB0001310
Metlin: METLIN58035
DrugBank: DB01786
ChEMBL: CHEMBL66693
Wikipedia: Alanine
MetaCyc: D-ALANINE
KNApSAcK: C00019654
foodb: FDB022546
chemspider: 64234
CAS: 338-69-2
MoNA: KO000019
MoNA: KO000020
MoNA: KO002052
MoNA: KO002048
MoNA: KO002049
MoNA: KO002050
MoNA: KO002051
PubChem: 3433
PDB-CCD: DAL
3DMET: B00036
NIKKAJI: J9.190A
RefMet: D-Alanine
medchemexpress: HY-41700
BioNovoGene_Lab2019: BioNovoGene_Lab2019-335
KNApSAcK: 15570
LOTUS: LTS0272178

分类词条

代谢反应

246 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(5)

peptidoglycan and lipid A precursor biosynthesis: ATP + UDP-N-acetylmuramate + ala ⟶ ADP + H⁺ + UDP-N-acetylmuramyl-L-Ala + phosphate
peptidoglycan biosynthesis I (meso-diaminopimelate containing): ATP + UDP-N-acetylmuramate + ala ⟶ ADP + H⁺ + UDP-N-acetylmuramyl-L-Ala + phosphate
superpathway of alanine biosynthesis: pyruvate + val ⟶ 2-oxoisovalerate + ala
UDP-N-acetylmuramoyl-pentapeptide biosynthesis III (meso-DAP-containing): ATP + UDP-N-acetylmuramate + ala ⟶ ADP + H⁺ + UDP-N-acetylmuramyl-L-Ala + phosphate
alanine biosynthesis I: pyruvate + val ⟶ 2-oxoisovalerate + ala

WikiPathways(2)

Metabolism overview: NH3 ⟶ Glutamic acid
Peptidoglycan cytoplasmic synthesis and recycling pathways: D-glucosamine-6-phosphate ⟶ Fructose-6-phosphate

Plant Reactome(231)

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: H2O + alpha,alpha-trehalose ⟶ beta-D-glucose
Peptidoglycan biosynthesis I: ATP + D-Ala ⟶ ADP + D-alanyl-D-alanine + Pi
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-Ala ⟶ ADP + D-alanyl-D-alanine + Pi
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-Ala ⟶ ADP + D-alanyl-D-alanine + Pi
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-Ala ⟶ ADP + D-alanyl-D-alanine + Pi
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: 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-Ala ⟶ ADP + D-alanyl-D-alanine + Pi
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: L-Glu + imidazole acetol-phosphate ⟶ 2OG + L-histidinol-phosphate
Carbohydrate metabolism: H2O + alpha,alpha-trehalose ⟶ beta-D-glucose
Peptidoglycan biosynthesis I: ATP + D-Ala ⟶ ADP + D-alanyl-D-alanine + Pi
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-Ala ⟶ ADP + D-alanyl-D-alanine + Pi
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(8)

D-Alanine Metabolism: L-Alanine ⟶ D-Alanine
L-Alanine Metabolism: L-Valine + Pyruvic acid ⟶ -Ketoisovaleric acid + L-Alanine
D-Alanine Metabolism: L-Alanine ⟶ D-Alanine
L-Alanine Metabolism: L-Valine + Pyruvic acid ⟶ -Ketoisovaleric acid + L-Alanine
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
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)

425 个相关的物种来源信息

3319 - Abies: LTS0272178
90345 - Abies balsamea: 10.1016/S0021-9673(01)97854-9
90345 - Abies balsamea: LTS0272178
13328 - Achillea: LTS0272178
13329 - Achillea millefolium: 10.1016/S0031-9422(00)90576-4
13329 - Achillea millefolium: LTS0272178
2012474 - Agaraceae: LTS0272178
5339 - Agaricaceae: LTS0272178
155619 - Agaricomycetes: LTS0272178
5340 - Agaricus: LTS0272178
56157 - Agaricus campestris: 10.1021/JF60199A047
56157 - Agaricus campestris: LTS0272178
4449 - Alismataceae: LTS0272178
4678 - Allium: LTS0272178
4682 - Allium sativum: 10.1016/0378-8741(96)01416-X
4682 - Allium sativum: LTS0272178
94326 - Alpinia: LTS0272178
94327 - Alpinia galanga: 10.1016/0305-1978(86)90092-X
94327 - Alpinia galanga: LTS0272178
230707 - Alpinia purpurata: 10.1016/0305-1978(86)90092-X
230707 - Alpinia purpurata: LTS0272178
3563 - Amaranthaceae: LTS0272178
3564 - Amaranthus: LTS0272178
124765 - Amaranthus spinosus: 10.1079/9781780642635.0298
124765 - Amaranthus spinosus: LTS0272178
4668 - Amaryllidaceae: LTS0272178
31332 - Analipus: LTS0272178
4614 - Ananas: LTS0272178
4615 - Ananas comosus: 10.1016/0305-1978(86)90092-X
4615 - Ananas comosus: LTS0272178
4037 - Apiaceae: LTS0272178
4056 - Apocynaceae: LTS0272178
4454 - Araceae: LTS0272178
4050 - Araliaceae: LTS0272178
131254 - Archontophoenix: LTS0272178
180981 - Archontophoenix alexandrae: 10.1016/0305-1978(86)90092-X
180981 - Archontophoenix alexandrae: LTS0272178
115440 - Areca: LTS0272178
184783 - Areca catechu: 10.1016/0305-1978(86)90092-X
184783 - Areca catechu: LTS0272178
4710 - Arecaceae: LTS0272178
6660 - Artemia: LTS0272178
85549 - Artemia salina: 10.1021/JF60200A008
85549 - Artemia salina: LTS0272178
38009 - Artemiidae: LTS0272178
4219 - Artemisia: LTS0272178
72332 - Artemisia absinthium: 10.1007/BF00600846
72332 - Artemisia absinthium: LTS0272178
6656 - Arthropoda: LTS0272178
4890 - Ascomycota: LTS0272178
40552 - Asparagaceae: LTS0272178
1131492 - Aspergillaceae: LTS0272178
5052 - Aspergillus: 10.1271/BBB.57.935
5052 - Aspergillus: LTS0272178
4210 - Asteraceae: LTS0272178
7601 - Asterias: LTS0272178
7603 - Asterias forbesi: 10.1021/NP50028A028
7603 - Asterias forbesi: LTS0272178
7600 - Asteriidae: LTS0272178
7588 - Asteroidea: LTS0272178
20400 - Astragalus: LTS0272178
20414 - Astragalus hamosus: 10.1021/NP50075A009
20414 - Astragalus hamosus: LTS0272178
2 - Bacteria: LTS0272178
5204 - Basidiomycota: LTS0272178
7091 - Bombyx Mori L.: -
6658 - Branchiopoda: LTS0272178
3705 - Brassica: LTS0272178
3708 - Brassica napus: 10.1021/JF00011A007
3708 - Brassica napus: LTS0272178
3700 - Brassicaceae: LTS0272178
4613 - Bromeliaceae: LTS0272178
37796 - Buccinidae: LTS0272178
4269 - Byrsonima: LTS0272178
4270 - Byrsonima crassifolia: 10.3109/13880209509088143
4270 - Byrsonima crassifolia: LTS0272178
3593 - Cactaceae: LTS0272178
41495 - Calendula: LTS0272178
41496 - Calendula officinalis: 10.29296/25877313-2018-06-01
41496 - Calendula officinalis: LTS0272178
3481 - Cannabaceae: LTS0272178
3482 - Cannabis: LTS0272178
3483 - Cannabis sativa: 10.1021/NP50008A001
3483 - Cannabis sativa: LTS0272178
4200 - Caprifoliaceae: LTS0272178
1804623 - Chenopodiaceae: LTS0272178
3041 - Chlorophyta: LTS0272178
7711 - Chordata: LTS0272178
74098 - Coccophora: LTS0272178
74099 - Coccophora langsdorfii: 10.1271/BBB.59.2176
74099 - Coccophora langsdorfii: LTS0272178
13893 - Cocos: LTS0272178
13894 - Cocos nucifera: 10.1016/0305-1978(86)90092-X
13894 - Cocos nucifera: LTS0272178
41218 - Colchicaceae: LTS0272178
4743 - Commelina: LTS0272178
4740 - Commelinaceae: LTS0272178
2871 - Costaria: LTS0272178
2872 - Costaria costata: 10.1271/BBB.59.2176
2872 - Costaria costata: LTS0272178
28832 - Cucumaria: LTS0272178
36326 - Cucumaria frondosa: 10.1021/NP50028A028
36326 - Cucumaria frondosa: LTS0272178
36325 - Cucumariidae: LTS0272178
3660 - Cucurbita: LTS0272178
184136 - Cucurbita foetidissima: 10.1021/JF60216A022
184136 - Cucurbita foetidissima: LTS0272178
3650 - Cucurbitaceae: LTS0272178
3367 - Cupressaceae: LTS0272178
3394 - Cycadaceae: LTS0272178
3296 - Cycadopsida: LTS0272178
3395 - Cycas: LTS0272178
3397 - Cycas circinalis: 10.1055/S-2006-958002
3397 - Cycas circinalis: LTS0272178
4609 - Cyperaceae: LTS0272178
4610 - Cyperus: LTS0272178
1234190 - Cyperus aromaticus: 10.1016/0305-1978(86)90092-X
1234190 - Cyperus aromaticus: LTS0272178
4038 - Daucus: LTS0272178
4039 - Daucus carota: 10.1016/0008-6215(84)85339-2
4039 - Daucus carota: 10.1079/9781780642635.0298
4039 - Daucus carota: LTS0272178
37818 - Dendrobium: LTS0272178
51096 - Dendrobium crumenatum: 10.1016/0305-1978(86)90092-X
51096 - Dendrobium crumenatum: LTS0272178
42195 - Dieffenbachia: LTS0272178
4671 - Dioscoreaceae: LTS0272178
44615 - Discinaceae: LTS0272178
40129 - Donax: LTS0272178
96514 - Donax canniformis: 10.1016/0305-1978(86)90092-X
96514 - Donax canniformis: LTS0272178
210034 - Donax grandis: 10.1016/0305-1978(86)90092-X
210034 - Donax grandis: LTS0272178
147541 - Dothideomycetes: LTS0272178
72720 - Echinaster: LTS0272178
72721 - Echinaster sepositus: 10.1021/NP50028A028
72721 - Echinaster sepositus: LTS0272178
60576 - Echinasteridae: LTS0272178
7586 - Echinodermata: LTS0272178
2814 - Endocladiaceae: LTS0272178
543 - Enterobacteriaceae: LTS0272178
174214 - Epipremnum: LTS0272178
78380 - Epipremnum aureum: 10.1016/0305-1978(86)90092-X
78380 - Epipremnum aureum: LTS0272178
258264 - Epipremnum pinnatum: 10.1016/0305-1978(86)90092-X
258264 - Epipremnum pinnatum: LTS0272178
561 - Escherichia: LTS0272178
562 - Escherichia coli: LTS0272178
2759 - Eukaryota: LTS0272178
3990 - Euphorbia: LTS0272178
212836 - Euphorbia prostrata: 10.1016/S0031-9422(00)86537-1
212836 - Euphorbia prostrata: LTS0272178
3977 - Euphorbiaceae: LTS0272178
147545 - Eurotiomycetes: LTS0272178
3803 - Fabaceae: LTS0272178
38944 - Flammulina: LTS0272178
38945 - Flammulina velutipes: 10.1111/J.1365-2621.1987.TB13989.X
38945 - Flammulina velutipes: LTS0272178
2806 - Florideophyceae: LTS0272178
3746 - Fragaria: LTS0272178
3747 - Fragaria × ananassa: 10.1021/JF00023A036
4751 - Fungi: LTS0272178
1236 - Gammaproteobacteria: LTS0272178
5314 - Ganoderma: LTS0272178
5315 - Ganoderma lucidum: LTS0272178
6448 - Gastropoda: LTS0272178
3310 - Ginkgo: LTS0272178
3311 - Ginkgo biloba: 10.1016/S0731-7085(98)00094-6
3311 - Ginkgo biloba: LTS0272178
3309 - Ginkgoaceae: LTS0272178
29811 - Ginkgoopsida: LTS0272178
2823 - Gloiopeltis: LTS0272178
42017 - Gloiopeltis furcata: 10.1271/BBB.59.2176
42017 - Gloiopeltis furcata: LTS0272178
41219 - Gloriosa: LTS0272178
41220 - Gloriosa superba: 10.1016/0305-1978(86)90092-X
41220 - Gloriosa superba: LTS0272178
3846 - Glycine: LTS0272178
3847 - Glycine max: 10.1007/BF00576124
3847 - Glycine max: LTS0272178
33160 - Gyromitra: LTS0272178
33161 - Gyromitra esculenta: 10.1021/JF60199A047
33161 - Gyromitra esculenta: LTS0272178
7705 - Holothuroidea: LTS0272178
9604 - Hominidae: LTS0272178
9605 - Homo: LTS0272178
9606 - Homo sapiens: -
9606 - Homo sapiens: 10.1038/NBT.2488
9606 - Homo sapiens: LTS0272178
51023 - Hydrilla: LTS0272178
51024 - Hydrilla verticillata: 10.1016/0305-1978(86)90092-X
51024 - Hydrilla verticillata: LTS0272178
26319 - Hydrocharitaceae: LTS0272178
20685 - Indigofera: LTS0272178
520844 - Indigofera hendecaphylla: 10.1021/JF60189A002
520844 - Indigofera hendecaphylla: LTS0272178
539088 - Indigofera hirsuta: 10.1021/JF60189A002
539088 - Indigofera hirsuta: LTS0272178
3089969 - Indigofera pilosa: LTS0272178
138272 - Indigofera schimperi: 10.1021/JF60189A002
138272 - Indigofera schimperi: LTS0272178
304104 - Iochroma: LTS0272178
304105 - Iochroma fuchsioides: 10.1021/NP50078A017
304105 - Iochroma fuchsioides: LTS0272178
3995 - Jatropha: LTS0272178
454931 - Jatropha gossypiifolia: 10.1016/0031-9422(71)85055-0
454931 - Jatropha gossypiifolia: 10.1016/S0031-9422(00)80544-0
454931 - Jatropha gossypiifolia: LTS0272178
13100 - Juniperus: LTS0272178
114265 - Juniperus occidentalis: 10.1016/S0021-9673(01)97854-9
114265 - Juniperus occidentalis: LTS0272178
466205 - Juniperus scopulorum: 10.1016/S0021-9673(01)97854-9
466205 - Juniperus scopulorum: LTS0272178
4136 - Lamiaceae: LTS0272178
33636 - Laminariaceae: LTS0272178
3853 - Lathyrus: LTS0272178
3860 - Lathyrus sativus: 10.1016/0021-9673(94)00777-2
3860 - Lathyrus sativus: LTS0272178
147547 - Lecanoromycetes: LTS0272178
147548 - Leotiomycetes: LTS0272178
4447 - Liliopsida: LTS0272178
60583 - Luidia: LTS0272178
72670 - Luidia ciliaris: 10.1021/NP50028A028
72670 - Luidia ciliaris: LTS0272178
60582 - Luidiidae: LTS0272178
3398 - Magnoliopsida: LTS0272178
4268 - Malpighiaceae: LTS0272178
3629 - Malvaceae: LTS0272178
40674 - Mammalia: LTS0272178
4619 - Marantaceae: LTS0272178
7608 - Marthasterias: LTS0272178
7609 - Marthasterias glacialis: 10.1021/NP50028A028
7609 - Marthasterias glacialis: LTS0272178
33208 - Metazoa: LTS0272178
3537 - Mirabilis: LTS0272178
3538 - Mirabilis jalapa: 10.1079/9781780642635.0298
3538 - Mirabilis jalapa: LTS0272178
6447 - Mollusca: LTS0272178
63411 - Monostroma: LTS0272178
138667 - Monostroma nitidum: 10.1271/BBB.59.2176
138667 - Monostroma nitidum: LTS0272178
153902 - Monostromataceae: LTS0272178
3487 - Moraceae: LTS0272178
5193 - Morchella: LTS0272178
60347 - Morchella angusticeps: 10.1021/JF60199A047
60347 - Morchella angusticeps: LTS0272178
62754 - Morchella crassipes: 10.1021/JF60199A047
62754 - Morchella crassipes: LTS0272178
1579548 - Morchella deliciosa: 10.1021/JF60199A047
1579548 - Morchella deliciosa: LTS0272178
39407 - Morchella esculenta: 10.1021/JF60199A047
39407 - Morchella esculenta: LTS0272178
5192 - Morchellaceae: LTS0272178
168074 - Murdannia: LTS0272178
428249 - Murdannia nudiflora: 10.1016/0305-1978(86)90092-X
428249 - Murdannia nudiflora: LTS0272178
4640 - Musa: LTS0272178
89151 - Musa × paradisiaca: 10.1016/0305-1978(86)90092-X
4637 - Musaceae: LTS0272178
37240 - Myxotrichaceae: LTS0272178
78133 - Myxotrichum: 10.1016/0305-1978(86)90092-X
78133 - Myxotrichum: LTS0272178
57632 - Neptunea: LTS0272178
167137 - Neptunea antiqua: 10.1016/0041-0101(89)90038-X
167137 - Neptunea antiqua: LTS0272178
3536 - Nyctaginaceae: LTS0272178
2696291 - Ochrophyta: LTS0272178
42451 - Onchidiidae: LTS0272178
69681 - Onchidium: 10.1016/0305-1978(86)90092-X
69681 - Onchidium: LTS0272178
45173 - Oncidium: 10.1016/0305-1978(86)90092-X
45173 - Oncidium: LTS0272178
106975 - Opuntia: LTS0272178
371859 - Opuntia ficus-indica: 10.1055/S-1999-14037
371859 - Opuntia ficus-indica: LTS0272178
4747 - Orchidaceae: LTS0272178
4053 - Panax: LTS0272178
4054 - Panax ginseng: 10.1021/JF00093A051
4054 - Panax ginseng: LTS0272178
4724 - Pandanaceae: LTS0272178
4725 - Pandanus: LTS0272178
1165086 - Pandanus odorifer: 10.1016/0305-1978(86)90092-X
1165086 - Pandanus odorifer: LTS0272178
7688 - Parastichopus: LTS0272178
1497336 - Parastichopus regalis: 10.1021/NP50028A028
1497336 - Parastichopus regalis: LTS0272178
59064 - Peliosanthes: LTS0272178
148715 - Pentaclethra: LTS0272178
148716 - Pentaclethra macrophylla: 10.1007/BF02666050
148716 - Pentaclethra macrophylla: LTS0272178
147549 - Pezizomycetes: LTS0272178
2870 - Phaeophyceae: LTS0272178
862241 - Physalacriaceae: LTS0272178
3328 - Picea: LTS0272178
3330 - Picea glauca: 10.1016/S0021-9673(01)97854-9
3330 - Picea glauca: LTS0272178
3335 - Picea mariana: 10.1016/S0021-9673(01)97854-9
3335 - Picea mariana: LTS0272178
3331 - Picea pungens: 10.1016/S0021-9673(01)97854-9
3331 - Picea pungens: LTS0272178
3318 - Pinaceae: LTS0272178
58019 - Pinopsida: LTS0272178
3337 - Pinus: LTS0272178
3339 - Pinus contorta: 10.1016/S0021-9673(01)97854-9
3339 - Pinus contorta: LTS0272178
77912 - Pinus densiflora: 10.1248/YAKUSHI1947.107.4_279
77912 - Pinus densiflora: LTS0272178
55062 - Pinus ponderosa: 10.1016/S0021-9673(01)97854-9
55062 - Pinus ponderosa: 10.1034/J.1399-3054.1990.790104.X
55062 - Pinus ponderosa: LTS0272178
3887 - Pisum: LTS0272178
3888 - Pisum sativum: 10.1007/BF00574236
3888 - Pisum sativum: 10.1016/S0031-9422(00)85399-6
3888 - Pisum sativum: LTS0272178
104366 - Pleurotaceae: LTS0272178
5320 - Pleurotus: LTS0272178
5322 - Pleurotus ostreatus: 10.3136/NSKKK1962.32.338
5322 - Pleurotus ostreatus: LTS0272178
52847 - Plumeria: 10.1201/9780203022320.CH4
52847 - Plumeria: LTS0272178
5317 - Polyporaceae: LTS0272178
16367 - Pontederiaceae: LTS0272178
3754 - Prunus: LTS0272178
3758 - Prunus domestica: 10.1021/JF00017A016
3758 - Prunus domestica: LTS0272178
3356 - Pseudotsuga: LTS0272178
3357 - Pseudotsuga menziesii: 10.1016/S0021-9673(01)97854-9
3357 - Pseudotsuga menziesii: LTS0272178
3889 - Psophocarpus: LTS0272178
3891 - Psophocarpus tetragonolobus: 10.1111/J.1365-2621.1985.TB10514.X
3891 - Psophocarpus tetragonolobus: LTS0272178
31334 - Ralfsiaceae: LTS0272178
56479 - Ramalina: LTS0272178
157169 - Ramalina fraxinea: 10.5586/ASBP.1979.002
157169 - Ramalina fraxinea: LTS0272178
56478 - Ramalinaceae: LTS0272178
35162 - Rhodomela: LTS0272178
2803 - Rhodomelaceae: LTS0272178
2763 - Rhodophyta: LTS0272178
46332 - Rhynchospora: LTS0272178
906937 - Rhynchospora colorata: 10.1016/0305-1978(86)90092-X
906937 - Rhynchospora colorata: LTS0272178
2872799 - Ripariosida: LTS0272178
108447 - Ripariosida hermaphrodita: LTS0272178
3745 - Rosaceae: LTS0272178
24966 - Rubiaceae: LTS0272178
4450 - Sagittaria: LTS0272178
4451 - Sagittaria sagittifolia: 10.1016/0305-1978(86)90092-X
4451 - Sagittaria sagittifolia: LTS0272178
35974 - Santalum Album L\uff0e: -
3014 - Sargassaceae: LTS0272178
3015 - Sargassum: LTS0272178
3016 - Sargassum fulvellum: 10.1271/BBB.59.2176
3016 - Sargassum fulvellum: LTS0272178
127575 - Sargassum nigrifolium: 10.1271/BBB.59.2176
127575 - Sargassum nigrifolium: LTS0272178
27966 - Scytosiphon: LTS0272178
27967 - Scytosiphon lomentaria: 10.1271/BBB.59.2176
27967 - Scytosiphon lomentaria: LTS0272178
2891 - Scytosiphonaceae: LTS0272178
53922 - Senna: LTS0272178
346985 - Senna obtusifolia: 10.1021/JF00102A014
346985 - Senna obtusifolia: LTS0272178
77655 - Sida: LTS0272178
108447 - Sida hermaphrodita: 10.1007/BF00607552
4070 - Solanaceae: LTS0272178
35916 - Spermacoce: LTS0272178
2491924 - Spermacoce pusilla: 10.4268/CJCMM20120313
2491924 - Spermacoce pusilla: LTS0272178
27029 - Stangeria: LTS0272178
34343 - Stangeria eriopus: 10.1016/0378-8741(94)90005-1
34343 - Stangeria eriopus: LTS0272178
7687 - Stichopodidae: LTS0272178
35493 - Streptophyta: LTS0272178
137301 - Styphnolobium: LTS0272178
3897 - Styphnolobium japonicum: 10.1016/S0031-9422(00)83857-1
3897 - Styphnolobium japonicum: LTS0272178
46108 - Suaeda: LTS0272178
224153 - Suaeda aegyptiaca: 10.4197/SCI.16-1.4
224153 - Suaeda aegyptiaca: LTS0272178
1735025 - Suaeda nudiflora: 10.1002/JPS.3030350906
1735025 - Suaeda nudiflora: LTS0272178
44981 - Tacca: LTS0272178
2487666 - Tacca cristata: 10.1016/0305-1978(86)90092-X
2487666 - Tacca cristata: LTS0272178
167567 - Tacca integrifolia: 10.1016/0305-1978(86)90092-X
167567 - Tacca integrifolia: LTS0272178
1898022 - Taccaceae: LTS0272178
56538 - Telekia: LTS0272178
56539 - Telekia speciosa: 10.1007/BF00633415
56539 - Telekia speciosa: LTS0272178
49990 - Thymus: LTS0272178
2019959 - Thymus transcaucasicus: 10.1007/BF00575075
2019959 - Thymus transcaucasicus: LTS0272178
58023 - Tracheophyta: LTS0272178
4741 - Tradescantia: LTS0272178
428268 - Tradescantia spathacea: 10.1016/0305-1978(86)90092-X
428268 - Tradescantia spathacea: LTS0272178
709071 - Treculia: LTS0272178
709072 - Treculia africana: 10.1007/BF02666050
709072 - Treculia africana: LTS0272178
28568 - Trichocomaceae: LTS0272178
3677 - Trichosanthes Kirilowii Maxim: -
3358 - Tsuga: LTS0272178
3359 - Tsuga heterophylla: 10.1016/S0021-9673(01)97854-9
3359 - Tsuga heterophylla: LTS0272178
3118 - Ulva: LTS0272178
63659 - Ulva compressa: 10.1271/BBB.59.2176
63659 - Ulva compressa: LTS0272178
3116 - Ulva intestinalis: 10.1271/BBB.59.2176
3116 - Ulva intestinalis: LTS0272178
3120 - Ulva pertusa: 10.1271/BBB.59.2176
3120 - Ulva pertusa: LTS0272178
3114 - Ulvaceae: LTS0272178
33103 - Ulvophyceae: LTS0272178
19952 - Valeriana: LTS0272178
19953 - Valeriana officinalis: 10.1055/S-2006-959538
19953 - Valeriana officinalis: LTS0272178
19944 - Valerianaceae: LTS0272178
44607 - Verpa: LTS0272178
44609 - Verpa bohemica: 10.1021/JF60199A047
44609 - Verpa bohemica: LTS0272178
33090 - Viridiplantae: LTS0272178
3298 - Zamiaceae: LTS0272178
4642 - Zingiberaceae: LTS0272178

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。

亚细胞结构定位		关联基因列表

文献列表

Kimberly N Karin, Mohammed A Mustafa, Justin L Poklis, Belle Buzzi, Joel E Schlosburg, Linda Parker, M Imad Damaj, Aron H Lichtman. N-oleoyl alanine attenuates nicotine reward and spontaneous nicotine withdrawal in mice. Drug and alcohol dependence. 2024 Jun; 259(?):111276. doi: 10.1016/j.drugalcdep.2024.111276. [PMID: 38676968]
Elisa de Lazzari, Eugenia B Negredo, Pere Domingo, Juan M Tiraboschi, Esteve Ribera, Nadia Abdulghani, Verònica Alba, Salvador Fernández-Arroyo, Consuelo Viladés, Joaquim Peraire, Jose M Gatell, Jose L Blanco, Francesc Vidal, Anna Rull, Esteban Martinez. Multiomics plasma effects of switching from triple antiretroviral regimens to dolutegravir plus lamivudine. The Journal of antimicrobial chemotherapy. 2024 May; 79(5):1133-1141. doi: 10.1093/jac/dkae083. [PMID: 38546974]
Dathan M Byonanebye, Mark N Polizzotto, Fernando Maltez, Andri Rauch, Katharina Grabmeier-Pfistershammer, Ferdinand Wit, Stéphane De Wit, Antonella Castagna, Antonella d'Arminio Monforte, Cristina Mussini, Jan-Christian Wasmuth, Eric Fontas, Irene Abela, Mario Sarcletti, Loveleen Bansi-Matharu, Nadine Jaschinski, Lars Peters, Sean R Hosein, Vani Vannappagari, Cal Cohen, Emiliano Bissio, Amanda Mocroft, Matthew Law, Lene Ryom, Kathy Petoumenos. Associations between change in BMI and the risk of hypertension and dyslipidaemia in people receiving integrase strand-transfer inhibitors, tenofovir alafenamide, or both compared with other contemporary antiretroviral regimens: a multicentre, prospective observational study from the RESPOND consortium cohorts. The lancet. HIV. 2024 May; 11(5):e321-e332. doi: 10.1016/s2352-3018(23)00328-4. [PMID: 38621392]
Setu Bazie Tagele, Emma W Gachomo. Evaluating the effects of mefenoxam on taxonomic and functional dynamics of nontarget fungal communities during carrot cultivation. Scientific reports. 2024 04; 14(1):9867. doi: 10.1038/s41598-024-59587-2. [PMID: 38684826]
Xiaogang Li, Zhuoling An, Aimin Yao, Rui Li, Suhan Zhang, Songlin Yu, Liangkun Ma, Yanping Liu. Targeted metabolomics profiling in pregnancy associated with vitamin D deficiency. BMC pregnancy and childbirth. 2024 Apr; 24(1):295. doi: 10.1186/s12884-024-06454-7. [PMID: 38643102]
Wenbo Sun, Dan Xu, YanXing Yang, Linfei Wen, Hanjiang Yu, Yaowen Xing, Xiaopeng Song, Huan Li, Haibo Xu. Improved Detection of Target Metabolites in Brain Tumors with Intermediate TE, High SNR, and High Bandwidth Spin-Echo Sequence at 5T. AJNR. American journal of neuroradiology. 2024 Apr; 45(4):461-467. doi: 10.3174/ajnr.a8150. [PMID: 38453417]
Jen-Yu Hsu, Hsin-Yun Sun, Ling-Ya Chen, Sui-Yuan Chang, Yu-Chung Chuang, Yu-Shan Huang, Yi-Ching Su, Wen-Chun Liu, Chien-Ching Hung. Weight and metabolic changes among virally suppressed people with HIV who switched to co-formulated bictegravir/emtricitabine/tenofovir alafenamide. Journal of global antimicrobial resistance. 2024 Mar; 36(?):426-435. doi: 10.1016/j.jgar.2023.10.012. [PMID: 37923129]
Jee Hoon Park, Rachel E Reviello, Patrick J Loll. Crystal structure of vancomycin bound to the resistance determinant D-alanine-D-serine. IUCrJ. 2024 Mar; ?(?):. doi: 10.1107/s2052252524000289. [PMID: 38277167]
Al Zahraa G Al Ashmawy, Gehan F Balata. Formulation and in vitro characterization of nanoemulsions containing remdesivir or licorice extract: A potential subcutaneous injection for coronavirus treatment. Colloids and surfaces. B, Biointerfaces. 2024 Feb; 234(?):113703. doi: 10.1016/j.colsurfb.2023.113703. [PMID: 38096607]
Hyeyeon Hong, Won-Mook Choi, Danbi Lee, Ju Hyun Shim, Kang Mo Kim, Young-Suk Lim, Han Chu Lee, Jonggi Choi. Cardiovascular risk in chronic hepatitis B patients treated with tenofovir disoproxil fumarate or tenofovir alafenamide. Clinical and molecular hepatology. 2024 Jan; 30(1):49-63. doi: 10.3350/cmh.2023.0328. [PMID: 37981763]
Wan-Chen Wu, I-Hsuan Chen, Pei-Yu Hou, Lan-Hui Wang, Ching-Hsiu Tsai, Chi-Ping Cheng. The phosphorylation of the movement protein TGBp1 regulates the accumulation of the Bamboo mosaic virus. The Journal of general virology. 2024 01; 105(1):. doi: 10.1099/jgv.0.001945. [PMID: 38189334]
Nisreen A Al-Quraan, Nezar H Samarah, Ayah A Tanash. Effect of drought stress on wheat (Triticum durum) growth and metabolism: insight from GABA shunt, reactive oxygen species and dehydrin genes expression. Functional plant biology : FPB. 2024 01; 51(1):NULL. doi: 10.1071/fp22177. [PMID: 36346967]
Yi Shen, Yi-Qi Sun, He-Ming Li, Quan-Long Zhang, Qi-Ming Zhao, Jin-Long Xu, Lu-Ping Qin, Qiao-Yan Zhang. [UPLC-Q-TOF-MS-based metabolomics reveals mechanism of Morinda officinalis iridoid glycosides in treating rheumatoid arthritis and bone loss]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2024 Jan; 49(2):453-460. doi: 10.19540/j.cnki.cjcmm.20230914.705. [PMID: 38403321]
Jing Wu, Shaoqian Deng, Xinyue Yu, Yanlin Wu, Xiaoyi Hua, Zunjian Zhang, Yin Huang. Identify production area, growth mode, species, and grade of Astragali Radix using metabolomics "big data" and machine learning. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2024 Jan; 123(?):155201. doi: 10.1016/j.phymed.2023.155201. [PMID: 37976693]
Scott K Fung, Calvin Q Pan, Grace Lai-Hung Wong, Wai-Kay Seto, Sang Hoon Ahn, Chi-Yi Chen, Hie-Won L Hann, Maciej S Jablkowski, Yoon Jun Kim, Cihan Yurdaydin, Cheng-Yuan Peng, Tuan Nguyen, Hiroshi Yatsuhashi, John F Flaherty, Leland J Yee, Frida Abramov, Hongyuan Wang, Dzhamal Abdurakhmanov, Young-Suk Lim, Maria Buti. Atherosclerotic cardiovascular disease risk profile of patients with chronic hepatitis B treated with tenofovir alafenamide or tenofovir disoproxil fumarate for 96 weeks. Alimentary pharmacology & therapeutics. 2024 Jan; 59(2):217-229. doi: 10.1111/apt.17764. [PMID: 37905449]
Pin-Nan Cheng, I-Cher Feng, Jyh-Jou Chen, Hsing-Tao Kuo, Pei-Lun Lee, Ming-Lung Yu, Yen-Cheng Chiu, Hung-Chih Chiu, Shih-Chieh Chien, Pei-Jer Chen, Chun-Jen Liu. Body weight increase and metabolic derangements after tenofovir disoproxil fumarate switch to tenofovir alafenamide in patients with chronic hepatitis B. Alimentary pharmacology & therapeutics. 2024 Jan; 59(2):230-238. doi: 10.1111/apt.17765. [PMID: 37845815]
Suvi E Laamanen, Aino-Maija Eloranta, Eero A Haapala, Taisa Sallinen, Ursula Schwab, Timo A Lakka. Associations of diet quality and food consumption with serum biomarkers for lipid and amino acid metabolism in Finnish children: the PANIC study. European journal of nutrition. 2023 Dec; ?(?):. doi: 10.1007/s00394-023-03293-8. [PMID: 38127151]
Lin Gan, Xiaoxin Xie, Yanhua Fu, Yebing Song, Chunli Song, Tingting Ren, Hai Long. Efficacy and safety of bictegravir/emtricitabine/tenofovir alafenamide fumarate for adult patients with human immunodeficiency virus-1 in China: a retrospective real-world cohort study. Expert review of anti-infective therapy. 2023 Dec; ?(?):1-7. doi: 10.1080/14787210.2023.2292544. [PMID: 38058002]
Geeisy Angela Cid, Davide Francioli, Steffen Kolb, Yudelsy Antonia Tandron Moya, Nicolaus von Wirén, Mohammad-Reza Hajirezaei. Elucidating the systemic response of wheat plants under waterlogging based on transcriptomic and metabolic approaches. Journal of experimental botany. 2023 Nov; ?(?):. doi: 10.1093/jxb/erad453. [PMID: 38014629]
D Wilkinson, I J Gallagher, A McNelly, D E Bear, N Hart, H E Montgomery, A Le Guennec, M R Conte, T Francis, S D R Harridge, P J Atherton, Z A Puthucheary. The metabolic effects of intermittent versus continuous feeding in critically ill patients. Scientific reports. 2023 11; 13(1):19508. doi: 10.1038/s41598-023-46490-5. [PMID: 37945671]
Wenjie Li, Wei Wang. Decoding the genetic links between serum lipidomic profile, amino acid biomarkers, and programmed cell death protein-1/programmed cell death-ligand-1. Cancer immunology, immunotherapy : CII. 2023 Oct; 72(10):3395-3399. doi: 10.1007/s00262-023-03501-8. [PMID: 37498324]
Jie Chen, Shao Bai Huang, Xue Wang, Li Zhen Huang, Cheng Gao, Xin-Yuan Huang, Fang-Jie Zhao. IAR4 mutation enhances cadmium toxicity by disturbing auxin homeostasis in Arabidopsis thaliana. Journal of experimental botany. 2023 Sep; ?(?):. doi: 10.1093/jxb/erad366. [PMID: 37721748]
Nicole Canon, Catherine H Schein, Werner Braun, Surendra S Negi, Xueni Chen, Michael D Kulis, Edwin H Kim, Vidya Pathy, Marina Pozzoli, Weimin Liu, Stephen C Dreskin. Alanine Scanning of the Unstructured Region of Ara h 2 and of a Related Mimotope Reveals Critical Amino Acids for IgE Binding. Molecular nutrition & food research. 2023 Sep; ?(?):e2300134. doi: 10.1002/mnfr.202300134. [PMID: 37706599]
Juan Moreno-Vedia, Dídac Llop, Ricardo Rodríguez-Calvo, Núria Plana, Núria Amigó, Roser Rosales, Yaiza Esteban, Josefa Girona, Lluís Masana, Daiana Ibarretxe. Serum branch-chained amino acids are increased in type 2 diabetes and associated with atherosclerotic cardiovascular disease. Cardiovascular diabetology. 2023 Sep; 22(1):249. doi: 10.1186/s12933-023-01958-6. [PMID: 37710233]
Xi Meng, Guoqi Yu, Tingyu Luo, Ruiyuan Zhang, Jun Zhang, Yongjie Liu. Transcriptomics integrated with metabolomics reveals perfluorobutane sulfonate (PFBS) exposure effect during pregnancy and lactation on lipid metabolism in rat offspring. Chemosphere. 2023 Sep; 341(?):140120. doi: 10.1016/j.chemosphere.2023.140120. [PMID: 37696479]
Hong Wang, Jinyang Wang, Mouliang Xiao, Tida Ge, Anna Gunina, Davey L Jones. The fate of amino acid and peptide as affected by soil depth and fertilization regime in subtropical paddies. The Science of the total environment. 2023 Sep; 889(?):164245. doi: 10.1016/j.scitotenv.2023.164245. [PMID: 37211099]
Xin Huang, Jie V Zhao. The associations of genetically predicted plasma alanine with coronary artery disease (CAD) and CAD risk factors: a Mendelian randomization study. The American journal of clinical nutrition. 2023 Aug; ?(?):. doi: 10.1016/j.ajcnut.2023.08.011. [PMID: 37640107]
Yan Lu, Peng Xiang, Shuqing Zhang, Zhiguo Lu, Zhidong Zhou, Yunlong Yin, Jianfeng Hua, Qin Shi, Wanwen Yu, Chaoguang Yu. Physiological and transcriptional regulation in Taxodium hybrid 'Zhongshanshan' leaves in acclimation to prolonged partial submergence. Planta. 2023 Aug; 258(3):66. doi: 10.1007/s00425-023-04225-w. [PMID: 37592053]
Eui Gwon Hwang, Eun-Ae Jung, Jeong-Ju Yoo, Sang Gyune Kim, Young Seok Kim. Risk of dyslipidemia in chronic hepatitis B patients taking tenofovir alafenamide: a systematic review and meta-analysis. Hepatology international. 2023 Aug; 17(4):860-869. doi: 10.1007/s12072-023-10528-7. [PMID: 37099248]
Victor Silva da Fonsêca, Valeria de Cassia Goncalves, Mario Augusto Izidoro, Antônio-Carlos Guimarães de Almeida, Fernando Luiz Affonso Fonseca, Fulvio Alexandre Scorza, Josef Finsterer, Carla Alessandra Scorza. Parkinson's Disease and the Heart: Studying Cardiac Metabolism in the 6-Hydroxydopamine Model. International journal of molecular sciences. 2023 Jul; 24(15):. doi: 10.3390/ijms241512202. [PMID: 37569578]
Marcus V Marin, Juliana S Baggio, Youngjae Oh, Hyeondae Han, Saket Chandra, Nan-Yi Wang, Seonghee Lee, Natalia A Peres. Identification of sequence mutations in Phytophthora cactorum genome associated with mefenoxam resistance and development of a molecular assay for the mutant detection in strawberry (F. × ananassa). Scientific reports. 2023 05; 13(1):7385. doi: 10.1038/s41598-023-34271-z. [PMID: 37149656]
Marta Mendes Costa, Alda Pereira Da Silva, Carolina Santos, Joana Ferreira, Mário Rui Mascarenhas, Manuel Bicho, Ana Paula Barbosa. Influence of the TAS2R38 Gene Single Nucleotide Polymorphisms in Metabolism and Anthropometry in Thyroid Dysfunction. Nutrients. 2023 May; 15(9):. doi: 10.3390/nu15092214. [PMID: 37432370]
Charlie Guittin, Faïza Maçna, Adeline Barreau, Xavier Poitou, Jean-Marie Sablayrolles, Jean-Roch Mouret, Vincent Farines. The aromatic profile of wine distillates from Ugni blanc grape musts is influenced by the nitrogen nutrition (organic vs. inorganic) of Saccharomyces cerevisiae. Food microbiology. 2023 May; 111(?):104193. doi: 10.1016/j.fm.2022.104193. [PMID: 36681397]
Yan Huang, Yezi Kong, Bingyu Shen, Bowen Li, Juan J Loor, Panpan Tan, Bo Wei, Linshan Mei, Zixin Zhang, Chenxu Zhao, Xiaoyan Zhu, Simeng Qi, Jianguo Wang. Untargeted metabolomics and lipidomics to assess plasma metabolite changes in dairy goats with subclinical hyperketonemia. Journal of dairy science. 2023 Apr; ?(?):. doi: 10.3168/jds.2022-22812. [PMID: 37028962]
Parisa Mansouri Rad, Leila Rahbarnia, Azam Safary, Azizeh ShadiDizaji, Zahra Maani. The Synthetic Antimicrobial Peptide Derived From Melittin Displays Low Toxicity and Anti-infectious Properties. Probiotics and antimicrobial proteins. 2023 Mar; ?(?):. doi: 10.1007/s12602-023-10066-6. [PMID: 36988897]
Courtney R Green, Roberto Bonelli, Brendan R E Ansell, Simone Tzaridis, Michal K Handzlik, Grace H McGregor, Barbara Hart, Jennifer Trombley, Mary M Reilly, Paul S Bernstein, Catherine Egan, Marcus Fruttiger, Martina Wallace, Melanie Bahlo, Martin Friedlander, Christian M Metallo, Marin L Gantner. Divergent amino acid and sphingolipid metabolism in patients with inherited neuro-retinal disease. Molecular metabolism. 2023 Mar; ?(?):101716. doi: 10.1016/j.molmet.2023.101716. [PMID: 36997154]
Zhenyu Zou, Meiyun Lin, Peihua Shen, Yi Guan. Alanine-Dependent TCA Cycle Promotion Restores the Zhongshengmycin-Susceptibility in Xanthomonas oryzae. International journal of molecular sciences. 2023 Feb; 24(3):. doi: 10.3390/ijms24033004. [PMID: 36769324]
Nathalie Lacrampe, Sophie Colombié, Doriane Dumont, Philippe Nicot, François Lecompte, Raphaël Lugan. Nitrogen-mediated metabolic patterns of susceptibility to Botrytis cinerea infection in tomato (Solanum lycopersicum) stems. Planta. 2023 Jan; 257(2):41. doi: 10.1007/s00425-022-04065-0. [PMID: 36680621]
Feng Huang, Tong Zhang, Bin Li, Shaosong Wang, Chang Xu, Caihua Huang, Donghai Lin. NMR-based metabolomic analysis for the effects of moxibustion on imiquimod-induced psoriatic mice. Journal of ethnopharmacology. 2023 Jan; 300(?):115626. doi: 10.1016/j.jep.2022.115626. [PMID: 36049653]
Ying He, Bang Cheng, Bing-Jian Guo, Zheng Huang, Jing-Hua Qin, Qian-Yi Wang, Lin-Lin Feng, Yun-Yuan Nong, Dan Zhu, Hong-Wei Guo, Zhi-Heng Su. Metabonomics and 16S rRNA gene sequencing to study the therapeutic mechanism of Danggui Sini decoction on collagen-induced rheumatoid arthritis rats with Cold Bi syndrome. Journal of pharmaceutical and biomedical analysis. 2023 Jan; 222(?):115109. doi: 10.1016/j.jpba.2022.115109. [PMID: 36270097]
Biao Jiang, Changmei Long, Yu Xu, Lizhen Han. Molecular mechanism of Tsukamurella tyrosinosolvens strain P9 in response to root exudates of peanut. Archives of microbiology. 2023 Jan; 205(1):48. doi: 10.1007/s00203-022-03387-7. [PMID: 36595098]
Jolanta Bugajska, Joanna Berska, Małgorzata Wójcik, Krystyna Sztefko. Amino acid profile in overweight and obese prepubertal children - can simple biochemical tests help in the early prevention of associated comorbidities?. Frontiers in endocrinology. 2023; 14(?):1274011. doi: 10.3389/fendo.2023.1274011. [PMID: 37964971]
Nicola Squillace, Elena Ricci, Paolo Maggi, Lucia Taramasso, Barbara Menzaghi, Giuseppe Vittorio De Socio, Stefania Piconi, Benedetto Maurizio Celesia, Giancarlo Orofino, Eleonora Sarchi, Giovanni Francesco Pellicanò, Filomena Simeone, Laura Valsecchi, Alessandra Bandera, Giovanni Cenderello, Letizia Attala, Goffredo Angioni, Katia Falasca, Antonio Cascio, Olivia Bargiacchi, Antonio Di Biagio, Paolo Bonfanti. Real-life safety of Emtricitabine/Tenofovir Alafenamide/Bictegravir. PloS one. 2023; 18(8):e0289132. doi: 10.1371/journal.pone.0289132. [PMID: 37556481]
M S Sadak, B A Bakry, T M Abdel-Razik, R S Hanafy. Amino acids foliar application for maximizing growth, productivity and quality of peanut grown under sandy soil. Brazilian journal of biology = Revista brasleira de biologia. 2023; 83(?):e256338. doi: 10.1590/1519-6984.256338. [PMID: 36753149]
Mozhgan Hashemi, Ahmad Moieni, Mohammad Sadegh Sabet. Improving the isolated microspore culture in eggplant (Solanum melongena L.) with amino acid nutrition. PloS one. 2023; 18(6):e0286809. doi: 10.1371/journal.pone.0286809. [PMID: 37289731]
Kai-Yin Lo, Yi-Fang Tsai, Chun-Hua Hsu, Chia-Yin Lee. Functional Characterization and Structural Modeling of a Novel Glycine Oxidase from Variovorax paradoxus Iso1. Applied and environmental microbiology. 2022 12; 88(23):e0107722. doi: 10.1128/aem.01077-22. [PMID: 36377957]
Ifeanyi J Ezeonwumelu, Abduljalil M Mode, Umar F Magaji, Nnamdi A Nzoniwu, Muhamad H Tangaza, Fatima I Tanimu, Shamsudeen U Dandare. Coadministration of L-alanine and L-glutamine ameliorate blood glucose levels, biochemical indices and histological features in alloxan-induced diabetic rats. Journal of food biochemistry. 2022 12; 46(12):e14420. doi: 10.1111/jfbc.14420. [PMID: 36125865]
Seung-Cheol Lee, Fernando Arias-Mendoza, Sanjeev Chawla, Kavindra Nath, Jerry D Glickson. In-phase simultaneous spectral editing of lactate and alanine with suppression of J-coupled lipids by the modified selective multiple quantum coherence sequences. Magnetic resonance imaging. 2022 12; 94(?):127-143. doi: 10.1016/j.mri.2022.08.020. [PMID: 36089181]
Arif Sarowar, Carla S Coffin, Scott Fung, Alexander Wong, Karen Doucette, David Truong, Brian Conway, Sarah Haylock-Jacobs, Alnoor Ramji, Bettina E Hansen, Harry L A Janssen, Curtis Cooper. Brief Report: Effect of Antiretroviral Switch From Tenofovir Disoproxil fumarate to Tenofovir Alafenamide on Alanine Aminotransferase, Lipid Profiles, and Renal Function in HIV/HBV-Coinfected Individuals in a Nationwide Canadian Study. Journal of acquired immune deficiency syndromes (1999). 2022 12; 91(4):368-372. doi: 10.1097/qai.0000000000003079. [PMID: 36288543]
Qing-Qi Chang, Long Chen, Ya-Fang Liao, Chun-Lu Yuan, Dan-Dan Zhang. [Mechanism of timosaponin AⅢ in regulation of metabolism against glioblastoma growth]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2022 Dec; 47(24):6679-6686. doi: 10.19540/j.cnki.cjcmm.20220728.401. [PMID: 36604918]
Hussain Ahmad, Xinrui Zhao, Nisar Ahmad, Abbas Khan, Yuexin Jin, Jie Du, Xuewei Zheng, Li Zeng, Yanan Ouyang, Pengfei Yang, Meng Chen, Xiaoxue Li, Zhe Yang, Zhongmin Tian. Benincasa hispida extracts positively regulated high salt-induced hypertension in Dahl salt-sensitive rats: Impact on biochemical profile and metabolic patterns. Journal of food biochemistry. 2022 12; 46(12):e14497. doi: 10.1111/jfbc.14497. [PMID: 36314446]
Qiding Peng, Daoyong Yang, Ting Yang, Yongchao Cheng, Yufan Yang, Dehui Xi. Construction of full-length cDNA infectious clones of Chilli veinal mottle virus. Virus research. 2022 12; 322(?):198948. doi: 10.1016/j.virusres.2022.198948. [PMID: 36181976]
L A Kovalchuk, V A Mishchenko, L V Chernaya, V P Snit'ko, V N Bolshakov. Assessment of Seasonal Variability of the Spectrum of Free Amino Acids in the Blood Plasma of the Boreal Bat Species (Myotis dasycneme Boie, 1825) of the Ural Fauna. Doklady. Biochemistry and biophysics. 2022 Dec; 507(1):268-272. doi: 10.1134/s1607672922060060. [PMID: 36786984]
Linhao Xu, Jinping Cheng, Hua Jiang. Mutation of histone H3 serine 28 to alanine influences H3K27me3-mediated gene silencing in Arabidopsis thaliana. Plant physiology. 2022 11; 190(4):2417-2429. doi: 10.1093/plphys/kiac409. [PMID: 36053193]
Zhehua Zhang, Deying Chen, Jiong Yu, Xiaoling Su, Lanjuan Li. Metabolic perturbations in human hepatocytes induced by bis (2-ethylhexyl)-2,3,4,5-tetrabromophthalate exposure: Insights from high-coverage quantitative metabolomics. Analytical biochemistry. 2022 11; 657(?):114887. doi: 10.1016/j.ab.2022.114887. [PMID: 36150471]
Hongzhao Yuan, Zhen He, Xiangbi Chen, Tida Ge, Liping Zhang, Jiurong Wang. Rapid, sensitive analysis method for determining the nitrogen stable isotope ratio of total free amino acids in soil. Rapid communications in mass spectrometry : RCM. 2022 Nov; 36(21):e9390. doi: 10.1002/rcm.9390. [PMID: 36056455]
Can Si, Danqi Zeng, Zhenming Yu, Jaime A Teixeira da Silva, Jun Duan, Chunmei He, Jianxia Zhang. Transcriptomic and metabolomic analyses reveal the main metabolites in Dendrobium officinale leaves during the harvesting period. Plant physiology and biochemistry : PPB. 2022 Nov; 190(?):24-34. doi: 10.1016/j.plaphy.2022.08.026. [PMID: 36088784]
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Sher Ali, Gul Badshah, Umar Ali, Muhammad Siddique Afridi, Anwar Shamim, Ajmir Khan, Frederico Luiz Felipe Soares, Leociley Rocha Alencar Menezes, Vanessa Theodoro Rezende, Andersson Barison, Carlos Augusto Fernandes de Oliveira, Fernando Gustavo Tonin. Leaf tissue metabolomics fingerprinting of Citronella gongonha Mart. by 1H HR-MAS NMR. Scientific reports. 2022 10; 12(1):17624. doi: 10.1038/s41598-022-22708-w. [PMID: 36271238]
Julia M T Ledderose, Jorge A Benitez, Amanda J Roberts, Rachel Reed, Willem Bintig, Matthew E Larkum, Robert N S Sachdev, Frank Furnari, Britta J Eickholt. The impact of phosphorylated PTEN at threonine 366 on cortical connectivity and behaviour. Brain : a journal of neurology. 2022 10; 145(10):3608-3621. doi: 10.1093/brain/awac188. [PMID: 35603900]
Gopal Peddinti, Hannu Hotti, Teemu H Teeri, Heiko Rischer. De novo transcriptome assembly of Conium maculatum L. to identify candidate genes for coniine biosynthesis. Scientific reports. 2022 10; 12(1):17562. doi: 10.1038/s41598-022-21728-w. [PMID: 36266299]
Eric Amenyogbe, Jun Luo, Wei-Jie Fu, Emmanuel Delwin Abarike, Zhong-Liang Wang, Jian-Sheng Huang, Christian Larbi Ayisi, Gang Chen. Effects of autochthonous strains mixture on gut microbiota and metabolic profile in cobia (Rachycentron canadum). Scientific reports. 2022 10; 12(1):17410. doi: 10.1038/s41598-022-19663-x. [PMID: 36258024]
Michael Noden, Jeremy Goodyear, Scott D Taylor. Effect of Lipid Length and Cationic Residues on the Antibacterial and Hemolytic Activities of Paenibacterin. ACS infectious diseases. 2022 10; 8(10):2073-2083. doi: 10.1021/acsinfecdis.2c00157. [PMID: 36083849]
Youjun Zhang, Alisdair R Fernie. Metabolite profiling of Arabidopsis mutants of lower glycolysis. Scientific data. 2022 10; 9(1):614. doi: 10.1038/s41597-022-01673-z. [PMID: 36220829]
Aradhana Mishra, Arpita Bhattacharya, Priyanka Chauhan, Shipra Pandey, Ashish Dwivedi. Phenotype microarray analysis reveals the biotransformation of Fusarium oxysporum f.sp. lycopersici influenced by Bacillus subtilis PBE-8 metabolites. FEMS microbiology ecology. 2022 10; 98(10):. doi: 10.1093/femsec/fiac102. [PMID: 36066920]
Chang Liu, Wenhao Jiang, Fangwei Yang, Yuliang Cheng, Yahui Guo, Weirong Yao, Yong Zhao, He Qian. The combination of microbiome and metabolome to analyze the cross-cooperation mechanism of Echinacea purpurea polysaccharide with the gut microbiota in vitro and in vivo. Food & function. 2022 Oct; 13(19):10069-10082. doi: 10.1039/d2fo02336a. [PMID: 36093868]
Danilo L Neves, Aiqin Wang, Japheth D Weems, Heather M Kelly, Daren S Mueller, Mark Farman, Carl A Bradley. Identification of Septoria glycines Isolates from Soybean with Resistance to Quinone Outside Inhibitor Fungicides. Plant disease. 2022 Oct; 106(10):2631-2637. doi: 10.1094/pdis-08-21-1836-re. [PMID: 35394334]
Zhiyuan Meng, Jiajia Cui, Li Liu, Chunmei Yang, Xin Bao, Jianjun Wang, Xiaojun Chen. Toxicity effects of chlorantraniliprole in zebrafish (Danio rerio) involving in liver function and metabolic phenotype. Pesticide biochemistry and physiology. 2022 Oct; 187(?):105194. doi: 10.1016/j.pestbp.2022.105194. [PMID: 36127066]
Antony Stalin, Ding Lin, Balakrishnan Senthamarai Kannan, Yue Feng, Yanjing Wang, Wei Zhao, Savarimuthu Ignacimuthu, Dong-Qing Wei, Yuan Chen. An in-silico approach to identify the potential hot spots in SARS-CoV-2 spike RBD to block the interaction with ACE2 receptor. Journal of biomolecular structure & dynamics. 2022 10; 40(16):7408-7423. doi: 10.1080/07391102.2021.1897682. [PMID: 33685364]
Thekla Cordes, Ramya S Kuna, Grace H McGregor, Sanika V Khare, Jivani Gengatharan, Thangaselvam Muthusamy, Christian M Metallo. 1-Deoxysphingolipid synthesis compromises anchorage-independent growth and plasma membrane endocytosis in cancer cells. Journal of lipid research. 2022 Oct; 63(10):100281. doi: 10.1016/j.jlr.2022.100281. [PMID: 36115594]
Yuan Kong, Chenyang Ji, Dong Guo, Rujian He, Meirong Zhao, Jun Fan. Triticonazole enantiomers induced enantioselective metabolic phenotypes in Fusarium graminearum and HepG2 cells. Environmental science and pollution research international. 2022 Oct; 29(50):75978-75988. doi: 10.1007/s11356-022-21137-6. [PMID: 35665887]
Liqin Sun, Yun He, Liumei Xu, Fang Zhao, Yang Zhou, Lukun Zhang, Qiaoli Peng, Haitao Zhang, Qiuyue Zhang, Tingzhi Cao, Ying Song, Siyuan Wang, Man Rao, Xinyun Jia, Xiaoning Liu, Jing Zhou, Bin Ju, Hui Wang, Jiaye Liu. Higher Risk of Dyslipidemia With Coformulated Elvitegravir, Cobicistat, Emtricitabine, and Tenofovir Alafenamide than Efavirenz, Lamivudine, and Tenofovir Disoproxil Fumarate Among Antiretroviral-Naive People Living With HIV in China. Journal of acquired immune deficiency syndromes (1999). 2022 10; 91(S1):S8-S15. doi: 10.1097/qai.0000000000003040. [PMID: 36094509]
William Liu, Sarah Yu, Bingfang Yan. Effect of alcohol exposure on the efficacy and safety of tenofovir alafenamide fumarate, a major medicine against human immunodeficiency virus. Biochemical pharmacology. 2022 10; 204(?):115224. doi: 10.1016/j.bcp.2022.115224. [PMID: 36007574]
Olayemi Osiyemi, Stéphane De Wit, Faïza Ajana, Fiona Bisshop, Joaquín Portilla, Jean Pierre Routy, Christoph Wyen, Mounir Ait-Khaled, Peter Leone, Keith A Pappa, Ruolan Wang, Jonathan Wright, Nisha George, Brian Wynne, Michael Aboud, Jean van Wyk, Kimberly Y Smith. Efficacy and Safety of Switching to Dolutegravir/Lamivudine Versus Continuing a Tenofovir Alafenamide-Based 3- or 4-Drug Regimen for Maintenance of Virologic Suppression in Adults Living With Human Immunodeficiency Virus Type 1: Results Through Week 144 From the Phase 3, Noninferiority TANGO Randomized Trial. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America. 2022 09; 75(6):975-986. doi: 10.1093/cid/ciac036. [PMID: 35079789]
Heming Sui, Shiqi Wang, Gang Liu, Fei Meng, Zubing Cao, Yunhai Zhang. Effects of Heat Stress on Motion Characteristics and Metabolomic Profiles of Boar Spermatozoa. Genes. 2022 09; 13(9):. doi: 10.3390/genes13091647. [PMID: 36140814]
Jun-Kyu Byun, John A Vu, Siou-Luan He, Jyan-Chyun Jang, Karin Musier-Forsyth. Plant-exclusive domain of trans-editing enzyme ProXp-ala confers dimerization and enhanced tRNA binding. The Journal of biological chemistry. 2022 09; 298(9):102255. doi: 10.1016/j.jbc.2022.102255. [PMID: 35835222]
Ling Gao, Qiang Gu, Hong Wang, Xingkong Ma, Feng Xue, Xing Zhang, Jiachun Ge, Tao Ding, Weijian Shen. [Determination of free amino acids in Eriocheir sinensis by ultra-high performance liquid chromatography-high resolution mass spectrometry]. Se pu = Chinese journal of chromatography. 2022 Sep; 40(9):825-832. doi: 10.3724/sp.j.1123.2022.03027. [PMID: 36156629]
Yali Wang, Haotian Wu, Siying Fei, Junzhe Zhang, Kun Hu. Characterizing the Mechanisms of Metalaxyl, Bronopol and Copper Sulfate against Saprolegnia parasitica Using Modern Transcriptomics. Genes. 2022 08; 13(9):. doi: 10.3390/genes13091524. [PMID: 36140692]
Natalia Krisanova, Natalia Pozdnyakova, Artem Pastukhov, Marina Dudarenko, Oleg Shatursky, Olena Gnatyuk, Uliana Afonina, Kyrylo Pyrshev, Galina Dovbeshko, Semen Yesylevskyy, Tatiana Borisova. Amphiphilic anti-SARS-CoV-2 drug remdesivir incorporates into the lipid bilayer and nerve terminal membranes influencing excitatory and inhibitory neurotransmission. Biochimica et biophysica acta. Biomembranes. 2022 08; 1864(8):183945. doi: 10.1016/j.bbamem.2022.183945. [PMID: 35461828]
Huoyong Jiang, Nengdang Jiang, Li Wang, Jingjing Guo, Kexin Chen, Yijun Dai. Characterization of nitrilases from Variovorax boronicumulans that functions in insecticide flonicamid degradation and β-cyano-L-alanine detoxification. Journal of applied microbiology. 2022 Aug; 133(2):311-322. doi: 10.1111/jam.15561. [PMID: 35365856]
Meng Jiang, Shang Dai, Yun-Chao Zheng, Rui-Qing Li, Yuan-Yuan Tan, Gang Pan, Ian Max Møller, Shi-Yong Song, Jian-Zhong Huang, Qing-Yao Shu. An alanine to valine mutation of glutamyl-tRNA reductase enhances 5-aminolevulinic acid synthesis in rice. TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik. 2022 Aug; 135(8):2817-2831. doi: 10.1007/s00122-022-04151-7. [PMID: 35779128]
Muhammad Nadeem-Ul-Haque, Anila Bashir, Humira Karim, Sadiq Noor Khan, Zafar Ali Shah, Almas Jabeen, Shaista Qayyum, A Ganesan, M Iqbal Choudhary, Farzana Shaheen. Synthesis of [1-8-NαC]-zanriorb A1, alanine-containing analogues, and their cytotoxic and anti-inflammatory activity. Journal of peptide science : an official publication of the European Peptide Society. 2022 Aug; 28(8):e3405. doi: 10.1002/psc.3405. [PMID: 35068012]
Amilcar Vargas, Pierce A Paul, Jonell Winger, Christine Susan Balk, Meredith Eyre, Bruce Clevinger, Sarah Noggle, Anne E Dorrance. Oxathiapiprolin Alone or Mixed with Metalaxyl Seed Treatment for Management of Soybean Seedling Diseases Caused by Species of Phytophthora, Phytopythium, and Pythium. Plant disease. 2022 Aug; 106(8):2127-2137. doi: 10.1094/pdis-09-21-1952-re. [PMID: 35133185]
Enhua Hao, Yini Li, Bing Guo, Xi Yang, Pengfei Lu, Haili Qiao. Key Residues Affecting Binding Affinity of Sirex noctilio Fabricius Odorant-Binding Protein (SnocOBP9) to Aggregation Pheromone. International journal of molecular sciences. 2022 Jul; 23(15):. doi: 10.3390/ijms23158456. [PMID: 35955589]
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Qianqian Zhang, Youmei Peng, Jiao Hou, Yanhong Chen, Bingjie Liu, Pinghu Zhang, Wenquan Yu, Junbiao Chang. An O-Benzyl Phosphonamidate Prodrug of Tenofovir for the Treatment of Hepatitis B Virus Infection. Journal of medicinal chemistry. 2022 07; 65(13):9493-9505. doi: 10.1021/acs.jmedchem.2c00869. [PMID: 35776695]
Ei Phyo Khaing, Victor Zhong, Sandeesha Kodru, Imre Vass, Julian J Eaton-Rye. Tyr244 of the D2 Protein Is Required for Correct Assembly and Operation of the Quinone-Iron-Bicarbonate Acceptor Complex of Photosystem II. Biochemistry. 2022 07; 61(13):1298-1312. doi: 10.1021/acs.biochem.2c00164. [PMID: 35699437]
Markus Fischer, Peter Müller, Holger A Scheidt, Meike Luck. Drug-Membrane Interactions: Effects of Virus-Specific RNA-Dependent RNA Polymerase Inhibitors Remdesivir and Favipiravir on the Structure of Lipid Bilayers. Biochemistry. 2022 Jul; 61(13):1392-1403. doi: 10.1021/acs.biochem.2c00042. [PMID: 35731976]
Meng Yuan, Wenjuan Hu, Yingying Feng, Yue Tong, Xin Wang, Bo Tan, Hui Xu, Jia Liu. Development and validation of an LC-MS/MS method for simultaneous determination of remdesivir and its hydrolyzed metabolite and nucleoside, and its application in a pharmacokinetic study of normal and diabetic nephropathy mice. Biomedical chromatography : BMC. 2022 Jul; 36(7):e5380. doi: 10.1002/bmc.5380. [PMID: 35373846]
Karen Liebrenz, Romina Frare, Cristina Gómez, Cecilia Pascuan, Silvina Brambilla, Diego Soldini, Vanina Maguire, Alejandro Carrio, Oscar Ruiz, Wayne McCormick, Gabriela Soto, Nicolás Ayub. Multiple ways to evade the bacteriostatic action of glyphosate in rhizobia include the mutation of the conserved serine 90 of the nitrogenase subunit NifH to alanine. Research in microbiology. 2022 Jul; 173(6-7):103952. doi: 10.1016/j.resmic.2022.103952. [PMID: 35436545]
Ling Yang, I-Hsin Lin, Lie-Chwen Lin, Jeffrey W Dalley, Tung-Hu Tsai. Biotransformation and transplacental transfer of the anti-viral remdesivir and predominant metabolite, GS-441524 in pregnant rats. EBioMedicine. 2022 Jul; 81(?):104095. doi: 10.1016/j.ebiom.2022.104095. [PMID: 35671622]
Jihye Lim, Won-Mook Choi, Ju Hyun Shim, Danbi Lee, Kang Mo Kim, Young-Suk Lim, Han Chu Lee, Jonggi Choi. Efficacy and safety of tenofovir alafenamide versus tenofovir disoproxil fumarate in treatment-naïve chronic hepatitis B. Liver international : official journal of the International Association for the Study of the Liver. 2022 07; 42(7):1517-1527. doi: 10.1111/liv.15261. [PMID: 35343041]
Eiichi Ogawa, Makoto Nakamuta, Toshimasa Koyanagi, Aritsune Ooho, Norihiro Furusyo, Eiji Kajiwara, Kazufumi Dohmen, Akira Kawano, Takeaki Satoh, Kazuhiro Takahashi, Koichi Azuma, Nobuyuki Yamashita, Naoki Yamashita, Rie Sugimoto, Hiromasa Amagase, Masami Kuniyoshi, Yasunori Ichiki, Chie Morita, Masaki Kato, Shinji Shimoda, Hideyuki Nomura, Jun Hayashi. Switching to tenofovir alafenamide for nucleos(t)ide analogue-experienced patients with chronic hepatitis B: Week 144 results from a real-world, multicentre cohort study. Alimentary pharmacology & therapeutics. 2022 Jun; ?(?):. doi: 10.1111/apt.17107. [PMID: 35735794]
Kai Juhani Kauppinen, Inka Aho, Jussi Sutinen. Switching from tenofovir alafenamide to tenofovir disoproxil fumarate improves lipid profile and protects from weight gain. AIDS (London, England). 2022 Jun; ?(?):. doi: 10.1097/qad.0000000000003245. [PMID: 35727143]
Mackenzie J Thompson, Jaimee A Domville, Claire H Edrington, Angelica Venes, Patrick M Giguère, John E Baenziger. Distinct functional roles for the M4 α-helix from each homologous subunit in the heteropentameric ligand-gated ion channel nAChR. The Journal of biological chemistry. 2022 Jun; 298(7):102104. doi: 10.1016/j.jbc.2022.102104. [PMID: 35679899]
Juliana González-Tobón, Richard Rabideau Childers, Alejandra Rodríguez, William Fry, Kevin L Myers, Jeremy R Thompson, Silvia Restrepo, Giovanna Danies. Searching for the Mechanism that Mediates Mefenoxam-Acquired Resistance in Phytophthora infestans and How It Is Regulated. Phytopathology. 2022 May; 112(5):1118-1133. doi: 10.1094/phyto-07-21-0280-r. [PMID: 34763530]
Shagufta Perveen, Abida Parveen, Muhammad Saeed, Rabia Arshad, Sara Zafar. Interactive effect of glycine, alanine, and calcium nitrate Ca(NO3)2 on wheat (Triticum aestivum L.) under lead (Pb) stress. Environmental science and pollution research international. 2022 May; 29(25):37954-37968. doi: 10.1007/s11356-021-17348-y. [PMID: 35075561]
Haining Huang, Chongkun Zuo, Yaqian Zhao, Shen Huang, Tongkai Wang, Min Zhu, Jia Li, Xiaorong Tao. Determination of key residues in tospoviral NSm required for Sw-5b recognition, their potential ability to overcome resistance, and the effective resistance provided by improved Sw-5b mutants. Molecular plant pathology. 2022 05; 23(5):622-633. doi: 10.1111/mpp.13182. [PMID: 34962031]
Joonho Jeong, Jung Woo Shin, Seok Won Jung, Eun Ji Park, Neung Hwa Park. Tenofovir alafenamide treatment may not worsen the lipid profile of chronic hepatitis B patients: A propensity score-matched analysis. Clinical and molecular hepatology. 2022 04; 28(2):254-264. doi: 10.3350/cmh.2021.0314. [PMID: 34959261]