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UDP-N-acteylglucosamine pyrophosphorylase 1

AgX, antigen X, AGX1, UDP-N-acetylglucosamine pyrophosphorylase
Top mentioned proteins: ACID, CAN, fibrillin-1, OUT, HAD
Papers on AgX
Silver(I) complexes with phthalazine and quinazoline as effective agents against pathogenic Pseudomonas aeruginosa strains.
Nikodinovic-Runic et al., Kragujevac, Serbia. In J Inorg Biochem, Feb 2016
Although different AgX salts reacted with phtz, only dinuclear silver(I) complexes of the general formula {[Ag(X-O)(phtz-N)]2(μ-phtz-N,N')2} were formed, X=NO3(-) (1), CF3SO3(-) (2) and ClO4(-) (3).
Two Chitin Biosynthesis Pathway Genes in Bactrocera dorsalis (Diptera: Tephritidae): Molecular Characteristics, Expression Patterns, and Roles in Larval-Pupal Transition.
Wang et al., Chongqing, China. In J Econ Entomol, Oct 2015
Glucose-6-phosphate isomerase (G6PI) and UDP-N-acetylglucosamine pyrophosphorylase (UAP), two key components in the chitin biosynthesis pathway, are critical for insect growth and metamorphosis.
Propionibacterium acnes catalase induces increased Th1 immune response in sarcoidosis patients.
Eishi et al., Tokyo, Japan. In Respir Investig, Jul 2015
RESULTS: MALDI-TOF/MS analysis identified propionyl-CoA carboxylase subunit beta, arginine deiminase (ADI), catalase (KAT), and UDP-N-acetylglucosamine pyrophosphorylase (UAP).
Identifying and assessing the impact of wine acid-related genes in yeast.
Bauer et al., Stellenbosch, South Africa. In Curr Genet, Jul 2015
Genes selected in this manner were ADH3, AAD6, SER33, ICL1, GLY1, SFC1, SER1, KGD1, AGX1, OSM1 and GPD2.
Heterologous Production of Hyaluronic Acid in an ε-Poly-L-Lysine Producer, Streptomyces albulus.
Yamanaka et al., Yokohama, Japan. In Appl Environ Microbiol, Jun 2015
The expression of the refactored hasA gene, along with genes coding for UDP-glucose dehydrogenase, UDP-N-acetylglucosamine pyrophosphorylase, and UDP-glucose pyrophosphorylase, which are involved in HA precursor sugar biosynthesis, resulted in efficient production of HA in the 2.0 MDa range, which is greater than typical bacterial HA, demonstrating that a sufficient amount of ATP was provided to support the biosynthesis of the precursor sugars, which in turn promoted HA production.
A new T-cell activation mode for suboptimal doses of antigen under the full activation of T cells with different specificity.
Yamamoto et al., Tokyo, Japan. In Eur J Immunol, Jun 2015
We investigated an activation mode of T cells (designated as "associator T cells") directed to a suboptimal dose of cognate antigen X in the presence of fully activated T cells (designated as "responder T cells") directed to an optimal dose of antigen Y.
Effect of charged amino acid side chain length on lateral cross-strand interactions between carboxylate- and guanidinium-containing residues in a β-hairpin.
Cheng et al., Taipei, Taiwan. In Amino Acids, May 2015
To investigate the effect of side chain length of guanidinium- and carboxylate-containing residues on lateral cross-strand ion pairing interactions at non-hydrogen-bonded positions, β-hairpin peptides containing Zbb-Agx (Zbb = Asp, Glu, Aad in increasing length; Agx = Agh, Arg, Agb, Agp in decreasing length) sequence patterns were studied by NMR methods.
Purification and biochemical characterisation of GlmU from Yersinia pestis.
Blanot et al., Orsay, France. In Arch Microbiol, Apr 2015
Previously, the gene encoding the bifunctional UDP-N-acetylglucosamine pyrophosphorylase/glucosamine-1-phosphate N-acetyltransferase enzyme GlmU was confirmed as an essential gene in Yersinia.
Effect of the urease-derived peptide Jaburetox on the central nervous system of Triatoma infestans (Insecta: Heteroptera).
Settembrini et al., Buenos Aires, Argentina. In Biochim Biophys Acta, Feb 2015
Combination of immunoprecipitation, two-dimensional electrophoresis and tandem mass spectrometry identified UDP-N-acetylglucosamine pyrophosphorylase (UDP-GlcNAcP) as a molecular target for Jbtx.
A common structural blueprint for plant UDP-sugar-producing pyrophosphorylases.
Wilczynska et al., Umeå, Sweden. In Biochem J, 2011
Plant pyrophosphorylases that are capable of producing UDP-sugars, key precursors for glycosylation reactions, include UDP-glucose pyrophosphorylases (A- and B-type), UDP-sugar pyrophosphorylase and UDP-N-acetylglucosamine pyrophosphorylase.
Molecular basis of antigen mimicry by an anti-idiotope.
Mariuzza et al., Rockville, United States. In Nature, 1995
It has been proposed that an anti-idiotypic antibody, anti-anti-X, may resemble the external antigen X and thus carry its 'internal image', but this idea is not unequivocally supported by the three-dimensional structures of anti-idiotopic antibodies, either because the structures of the external antigen or of the anti-idiotopic antibody were unknown, or because the anti-idiotopic antibodies showed no resemblance to the external antigens (reviewed in ref. 10).
Sex-steroid receptor mechanism related to neuronal aromatase and the stigmoid body.
Shinoda, Ōsaka, Japan. In Horm Behav, 1994
The stigmoid bodies, marked by placental aromatase-associated antigen X-P2 (PAX) antiserum, are also frequent in the sex-steroid targets of rat brains and intimately coexist with estrogen receptors in the mPO-AM of young females.
An aromatase-associated cytoplasmic inclusion, the "stigmoid body," in the rat brain: II. Ultrastructure (with a review of its history and nomenclature).
Osawa et al., Ōsaka, Japan. In J Comp Neurol, 1993
322:360-376, '92), were examined in the rat medial preoptic region, bed nucleus of the stria terminalis, medial amygdaloid nucleus, and arcuate nucleus by pre- and post-embedding marking with a polyclonal antibody against human placental antigen X-P2 (hPAX-P2) for immuno-electron microscopic analysis.
The human T cell receptor: analysis with cytotoxic T cell clones.
Schlossman et al., In Immunol Rev, 1982
One structure consists of the antigen-binding region (Tin-T3) which views antigen X in the context of a polymorphic region of an MHC molecule.
[Rheumatoid synovitis (problems of immunomorphology and immunopathogenesis)].
Makarova et al., In Arkh Patol, 1981
The immunopathogenesis of rheumatoid synovitis (RS) is assumed to be as follows: antigen X interacts with the organism of subjects genetically predisposed to rheumatoid arthritis (RA) as a result of which the immune response regulation is disturbed ("immunological discomfort") leading to changes in proliferation and differentiation of immunocompetent cells immunologically manifested by disturbed ratios of lymphocyte subpopulations and morphologically by immune inflammation of synovial membranes, i.e.
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