Literature DB >> 964239

Structural determination of three glycoasparagines isolated from the urine of a patient with aspartylglycosaminuria.

A Lundblad, P K Masson, N E Nordén.   

Abstract

Three different glycoasparagines have been isolated from the urine of a patient with aspartylglycosaminuria and their structures determined using sugar, amino acid and methylation analysis, enzymic degradation and measurements of the optical rotations. The structures were 2-acetamido-1-N-(4'-L-aspartyl)-2-deoxy-beta-D-glucopyranosylamine (yield 135 mg/l) beta-D-galactopyranosyl-(1 leads to 4)-2-acetamido-1-N-(4'-L-aspartyl)-2-deoxy-beta-D-glucopyranosylamine (yield 35 mg/l), and alpha-D-mannopyranosyl-(1 leads to 6)-beta-D-mannopyranosyl-(1 leads to 4)-2-acetamido-2-deoxy-beta-D-glucopyranosyl-(1 leads to 4)-2-acetamido-1-N-(4'-L-aspartyl)-2-deoxy-beta-D-glucopyranosylamine (yield 30 mg/l). The first two compounds have previously been described, whereas the third compound is different from any of the glycoasparagines isolated before.

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Year:  1976        PMID: 964239     DOI: 10.1111/j.1432-1033.1976.tb10651.x

Source DB:  PubMed          Journal:  Eur J Biochem        ISSN: 0014-2956


  9 in total

1.  Isolation of a human hepatic 60 kDa aspartylglucosaminidase consisting of three non-identical polypeptides.

Authors:  M Baumann; L Peltonen; P Aula; N Kalkkinen
Journal:  Biochem J       Date:  1989-08-15       Impact factor: 3.857

2.  Urinary screening for disorders of heteroglycan metabolism. Results of 10 years experience with a comprehensive system.

Authors:  A C Sewell
Journal:  Klin Wochenschr       Date:  1988-01-15

3.  Metabolism of collagen in aspartylglycosaminuria: decreased synthesis by cultured fibroblasts.

Authors:  K Näntö-Salonen; R Penttinen
Journal:  J Inherit Metab Dis       Date:  1982       Impact factor: 4.982

Review 4.  Aspartylglycosaminuria: an inborn error of glycoprotein catabolism.

Authors:  C P Maury
Journal:  J Inherit Metab Dis       Date:  1982       Impact factor: 4.982

5.  Variation of urinary excretion of aspartylglucosamine and associated clinical findings in aspartyglucosaminuria.

Authors:  P Aula; K O Raivio; P Maury
Journal:  J Inherit Metab Dis       Date:  1980       Impact factor: 4.982

6.  Assignment of the structural gene encoding human aspartylglucosaminidase to the long arm of chromosome 4 (4q21----4qter).

Authors:  P Aula; K H Astrin; U Francke; R J Desnick
Journal:  Am J Hum Genet       Date:  1984-11       Impact factor: 11.025

7.  The core-specific lysosomal alpha(1-6)-mannosidase activity depends on aspartamidohydrolase activity.

Authors:  J F Haeuw; T Grard; C Alonso; G Strecker; J C Michalski
Journal:  Biochem J       Date:  1994-02-01       Impact factor: 3.857

8.  Urinary oligosaccharide excretion in disorders of glycolipid, glycoprotein and glycogen metabolism. A review of screening for differential diagnosis.

Authors:  A C Sewell
Journal:  Eur J Pediatr       Date:  1980-09       Impact factor: 3.183

9.  Characterization of four monosialo and a novel disialo Asn N-glycosides from the urine of a patient with aspartylglycosaminuria.

Authors:  F Irie; H Murakoshi; T Suzuki; Y Suzuki; K Kon; S Ando; K Yoshida; Y Hirabayashi
Journal:  Glycoconj J       Date:  1995-06       Impact factor: 2.916

  9 in total

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