関: uridyl transferase

WordNet

a salt of phosphoric acid (同)orthophosphate, inorganic_phosphate
carbonated drink with fruit syrup and a little phosphoric acid
a monosaccharide that contains six carbon atoms per molecule

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〈U〉リン酸塩 / 《複数形で》リン酸肥料

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1. 高リン血症の原因および治療の概要 overview of the causes and treatment of hyperphosphatemia
2. グルコース-6-リン酸脱水素酵素欠損症の診断および治療 diagnosis and treatment of glucose 6 phosphate dehydrogenase deficiency
3. 慢性腎疾患における高リン血症の治療 treatment of hyperphosphatemia in chronic kidney disease
4. グルコース-6-リン酸脱水素酵素欠損症の遺伝学および病態生理 genetics and pathophysiology of glucose 6 phosphate dehydrogenase deficiency
5. 低リン血症の評価および治療 evaluation and treatment of hypophosphatemia

English Journal

Structure-based virtual screening of novel inhibitors of the uridyltransferase activity of Xanthomonas oryzae pv. oryzae GlmU.

Min J, Lin D, Zhang Q, Zhang J, Yu Z.SourceState Key Laboratory of Agricultural Microbiology, National Engineering Research Centre of Microbial Pesticides, Huazhong Agricultural University, Wuhan 430070, PR China.
European journal of medicinal chemistry.Eur J Med Chem.2012 Jul;53:150-8. Epub 2012 Apr 4.
N-Acetylglucosamine-1-phosphate uridyltransferase (GlmU) catalyzes the formation of UDP-GlcNAc, a fundamental precursor in cell wall biosynthesis. GlmU represents an attractive target for new antibacterial agents. In this study, a theoretical three-dimensional (3D) structure of GlmU from Xanthomonas
PMID 22521370

Bifidobacterial enzymes involved in the metabolism of human milk oligosaccharides.

Kitaoka M.SourceNational Food Research Institute, National Agriculture and Food Research Organization, Tsukuba, Ibaraki, Japan. mkitaoka@affrc.go.jp
Advances in nutrition (Bethesda, Md.).Adv Nutr.2012 May 1;3(3):422S-9S. doi: 10.3945/an.111.001420.
Intestinal colonization of bifidobacteria is important for the health of infants. Human milk oligosaccharides (HMO) have been identified as growth factors for bifidobacteria. Recently, a bifidobacterial enzymatic system to metabolize HMO was identified. 1,3-β-Galactosyl-N-acetylhexosamine phosphory
PMID 22585921

Related Links

Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase

Galactosemia is a disorder of galactose metabolism that can result in life-threatening complications including feeding problems, failure to thrive, hepatocellular damage, bleeding, and sepsis in untreated infants. If a lactose/galactose ...

UDPglucose-hexose-1-phosphate uridylyltransferase ...

UDPglu·cose-hex·ose-1-phos·phate u·ri·dyl·yl·trans·fer·ase (glū'kōs-heks'ōs-fos'fāt ū'ri-dil'il-trans'fĕr-ās), An enzyme that catalyzes the reversible reaction of α-d-glucose 1-phosphate UDPgalactose to produce UDPglucose and α-d-galactose 1-phosphate.

★リンクテーブル★

リンク元	「UDPグルコース・ヘキソース-1-リン酸ウリジルトランスフェラーゼ」「uridyl transferase」
関連記事	「phosphate」「hexose」