论文信息 - Recognition of the acceptor β-d-Glc pNAc-(1 → 2)-α-d-Manp(1 → 6)-β-d-Glc p-OR by N-acetylglucosaminyltransferase-V: None of the hydroxyl groups on the Glc-residue are important - 字舞流文

Recognition of the acceptor β-d-Glc pNAc-(1 → 2)-α-d-Manp(1 → 6)-β-d-Glc p-OR by N-acetylglucosaminyltransferase-V: None of the hydroxyl groups on the Glc-residue are important

S. Crawley | O. Hindsgaul | T. Linker

[1] M. Blaszczyk-Thurin,et al. Evaluation of deoxygenated oligosaccharide acceptor analogs as specific inhibitors of glycosyltransferases. , 1991, The Journal of biological chemistry.

[2] M. Palcic,et al. Regulation of N-acetylglucosaminyltransferase V activity. Kinetic comparisons of parental, Rous sarcoma virus-transformed BHK, and L-phytohemagglutinin-resistant BHK cells using synthetic substrates and an inhibitory substrate analog. , 1990, The Journal of biological chemistry.

[3] S. Khan,et al. Synthesis of some oligosaccharides containing the O-(2-acetamido-2-deoxy-β-d-glucopyranosyl)-(1→2)-O-α-d-mannopyranosyl unit. Potential substrates for UDP-GlcNAc: α-d-mannopyranosyl-(1→6)-N-acetyl-β-d-glucosaminyl-transferase (GnT-V) , 1989 .

[4] M. Pierce,et al. Recognition of oligosaccharide substrates by N-acetyl-glucosaminyltransferase-V. , 1988, Carbohydrate research.

[5] R. Kerbel,et al. Beta 1-6 branching of Asn-linked oligosaccharides is directly associated with metastasis. , 1987, Science.

[6] O. Hindsgaul,et al. Substrates for the differentiation of the N-acetylglucosaminytransferases. Synthesis of βDGlcNAc(1 → 2)αDMan(1 → 6)βDMan and βDGlcNAc(1 → 2)αDMan(1 → 6) [αDMan(1 → 3)]βDMan glycosides , 1986 .

[7] H. Schachter,et al. Biosynthetic controls that determine the branching and microheterogeneity of protein-bound oligosaccharides. , 1986, Biochemistry and cell biology = Biochimie et biologie cellulaire.

[8] R. Cummings,et al. A mouse lymphoma cell line resistant to the leukoagglutinating lectin from Phaseolus vulgaris is deficient in UDP-GlcNAc: alpha-D-mannoside beta 1,6 N-acetylglucosaminyltransferase. , 1982, The Journal of biological chemistry.