Chemoenzymatic Synthesis of Asymmetric Bisecting Bi-, Tri-, and Tetra-Antennary <i>N</i>-Glycans. [PDF]
J Am Chem SocGhotekar BK +4 more
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Polyamine Induction of Secondary Metabolite Biosynthetic Genes in Fungi Is Mediated by Global Regulator LaeA and α-NAC Transcriptional Coactivator: Connection to Epigenetic Modification of Histones. [PDF]
MoleculesMartín JF.
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Microbial community characterization in semi-hydroponic systems of Starbor kale (<i>Brassica oleracea</i> L.) grown under normal gravity and simulated microgravity. [PDF]
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Comprehensive annotation of the enzymes of Drosophila melanogaster. [PDF]
G3 (Bethesda)Garapati PV +6 more
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Biotransformation of Pesticides across Biological Systems: Molecular Mechanisms, Omics Insights, and Biotechnological Advances for Environmental Sustainability. [PDF]
ACS OmegaBasapuram G, Dutta A, Duttagupta S.
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▪ Abstract This review describes the three mammalian glutathione transferase (GST) families, namely cytosolic, mitochondrial, and microsomal GST, the latter now designated MAPEG. Besides detoxifying electrophilic xenobiotics, such as chemical carcinogens, environmental pollutants, and antitumor agents, these transferases inactivate endogenous α,β ...
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Glucosyl transferase activity of bovine galactosyl transferase
Biochimica et Biophysica Acta (BBA) - General Subjects, 1978Bovine galactosyl transferase was found to utilize UDPglucose as a substrate and elicit disaccharide biosynthesis with glucose and N-acetylglucosamine as acceptors. The relative rate of glucosyl transferase with N-acetylglucosamine as acceptor was 0.3%, the rate for N-acetyllactosamine biosynthesis.
P J, Andree, L J, Berliner
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The flavin isoalloxazine ring in electron transferases functions in a redox capacity, being able to take up electrons from a donor to subsequently deliver them to an acceptor. The main characteristics of these flavoproteins, including their unique ability to mediate obligatory processes of two-electron transfers with those involving single-electron ...
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Farnesyl Transferase Inhibitors
Cancer Investigation, 2007Substituted imidazoles and thiazoles having the formula are useful for inhibiting farnesyltransferase. Also disclosed are farnesyltransferase-inhibiting compositions and methods of inhibiting farnesyltransferase in a patient.
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