Literature DB >> 189842

Genetic evidence for the common identity of glucose-6-phosphatase, pyrophosphate-glucose phosphotransferase, carbamyl phosphate-glucose phosphotransferase and inorganic pyrophosphatase.

P M Hefferan, R R Howell.   

Abstract

We demonstrate that glucose-6-phosphatase, pyrophosphate-glucose phosphotransferase, carbamyl phosphate-glucose phosphotransferase and inorganic pyrophosphatase activities are deficient in livers of patients with type I glycogen storage disease. This provides strong genetic evidence that these enzymatic activities reside in a single protein or share a common polypeptide chain.

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Year:  1977        PMID： 189842     DOI： 10.1016/0304-4165(77)90325-7

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN： 0006-3002


  4 in total

1.  Proceedings of a symposium on crystal-related arthropathies. 22 October and 23 October, 1982, Bristol Polytechnic, Bristol.

Authors: 
Journal:  Ann Rheum Dis       Date:  1983-08       Impact factor: 19.103

2.  Gluconeogenic enzymes in the human placenta.

Authors:  R Matalon; K Michals
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

Review 3.  Pathogenesis of chondrocalcinosis and pseudogout. Metabolism of inorganic pyrophosphate and production of calcium pyrophosphate dihydrate crystals.

Authors:  A Caswell; D F Guilland-Cumming; P R Hearn; M K McGuire; R G Russell
Journal:  Ann Rheum Dis       Date:  1983-08       Impact factor: 19.103

4.  ATP depletion, a possible role in the pathogenesis of hyperuricemia in glycogen storage disease type I.

Authors:  H L Greene; F A Wilson; P Hefferan; A B Terry; J R Moran; A E Slonim; T H Claus; I M Burr
Journal:  J Clin Invest       Date:  1978-08       Impact factor: 14.808
  4 in total

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