Chemoenzymatic synthesis of CMP-sialic acid derivatives by a one-pot two-enzyme system: comparison of substrate flexibility of three microbial CMP-sialic acid synthetases.
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One-pot three-enzyme chemoenzymatic approach to the synthesis of sialosides containing natural and non-natural functionalitiesStructure and Mechanism of the Lipooligosaccharide Sialyltransferase from Neisseria meningitidisA Sialyltransferase Mutant with Decreased Donor Hydrolysis and Reduced Sialidase Activities for Directly Sialylating Lewis xCharacterization of Receptor Binding Profiles of Influenza A Viruses Using An Ellipsometry-Based Label-Free Glycan Microarray Assay Platform.High-throughput substrate specificity studies of sialidases by using chemoenzymatically synthesized sialoside libraries.Efficient chemoenzymatic synthesis of biotinylated human serum albumin-sialoglycoside conjugates containing O-acetylated sialic acids.Advances in the biology and chemistry of sialic acids.Chemoenzymatic synthesis of GD3 oligosaccharides and other disialyl glycans containing natural and non-natural sialic acidsTools for Studying Glycans: Recent Advances in Chemoenzymatic Glycan LabelingLabeling glycans on living cells by a chemoenzymatic glycoengineering approachChemoenzymatic synthesis of α2-3-sialylated carbohydrate epitopes.Measurement of enzymatic activity and specificity of human and avian influenza neuraminidases from whole virus by glycoarray and MALDI-TOF mass spectrometry.Synthetic disialyl hexasaccharides protect neonatal rats from necrotizing enterocolitisChemoenzymatic synthesis of the sialyl Lewis X glycan and its derivatives.Exploration of sialic acid diversity and biology using sialoglycan microarrays.Chemoenzymatic synthesis of sialosides containing C7-modified sialic acids and their application in sialidase substrate specificity studies.Chemoenzymatic synthesis of C8-modified sialic acids and related α2-3- and α2-6-linked sialosides.A sialylated glycan microarray reveals novel interactions of modified sialic acids with proteins and viruses.One-pot bio-synthesis: N-acetyl-D-neuraminic acid production by a powerful engineered whole-cell catalystEfficient chemoenzymatic synthesis of novel galacto-N-biose derivatives and their sialylated formsDonor substrate promiscuity of bacterial β1-3-N-acetylglucosaminyltransferases and acceptor substrate flexibility of β1-4-galactosyltransferasesSequential One-Pot Multienzyme Chemoenzymatic Synthesis of Glycosphingolipid Glycans.Identification of the binding roles of terminal and internal glycan epitopes using enzymatically synthesized N-glycans containing tandem epitopes.Chemoenzymatic synthesis of α-dystroglycan core M1 O-mannose glycans.Converting Pasteurella multocidaα2-3-sialyltransferase 1 (PmST1) to a regioselective α2-6-sialyltransferase by saturation mutagenesis and regioselective screening.Sialic acid metabolism and sialyltransferases: natural functions and applications.Structural Basis for Sialoglycan Binding by the Streptococcus sanguinis SrpA Adhesin.Diversity in specificity, abundance, and composition of anti-Neu5Gc antibodies in normal humans: potential implications for diseaseMultifunctionality of Campylobacter jejuni sialyltransferase CstII: characterization of GD3/GT3 oligosaccharide synthase, GD3 oligosaccharide sialidase, and trans-sialidase activities.Pasteurella multocida sialic acid aldolase: a promising biocatalystParallel chemoenzymatic synthesis of sialosides containing a C5-diversified sialic acidSelective exo-enzymatic labeling of N-glycans on the surface of living cells by recombinant ST6Gal IToward automated oligosaccharide synthesis.Cell-Surface Glyco-Engineering by Exogenous Enzymatic Transfer using a Bi-Functional CMP-Neu5Ac Derivative.Cloning and characterization of a viral α2-3-sialyltransferase (vST3Gal-I) for the synthesis of sialyl Lewisx.Synthesis and In Vitro Anti-Influenza Virus Evaluation of Novel Sialic Acid (C-5 and C-9)-Pentacyclic Triterpene Derivatives.Efficient chemoenzymatic synthesis of sialyl Tn-antigens and derivatives.One-pot multienzyme (OPME) systems for chemoenzymatic synthesis of carbohydrates.The Hd0053 gene of Haemophilus ducreyi encodes an alpha2,3-sialyltransferase.A Chemical Biology Solution to Problems with Studying Biologically Important but Unstable 9-O-Acetyl Sialic Acids.
P2860
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P2860
Chemoenzymatic synthesis of CMP-sialic acid derivatives by a one-pot two-enzyme system: comparison of substrate flexibility of three microbial CMP-sialic acid synthetases.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
2004年學術文章
@zh-hant
name
Chemoenzymatic synthesis of CM ...... l CMP-sialic acid synthetases.
@en
Chemoenzymatic synthesis of CM ...... l CMP-sialic acid synthetases.
@nl
type
label
Chemoenzymatic synthesis of CM ...... l CMP-sialic acid synthetases.
@en
Chemoenzymatic synthesis of CM ...... l CMP-sialic acid synthetases.
@nl
prefLabel
Chemoenzymatic synthesis of CM ...... l CMP-sialic acid synthetases.
@en
Chemoenzymatic synthesis of CM ...... l CMP-sialic acid synthetases.
@nl
P2093
P1476
Chemoenzymatic synthesis of CM ...... l CMP-sialic acid synthetases.
@en
P2093
P304
P356
10.1016/J.BMC.2004.09.030
P407
P577
2004-12-01T00:00:00Z