Literature DB >> 6500558

A unique electrophoretic slow-moving glucose 6-phosphate dehydrogenase variant (G6PD Asahikawa) with a markedly acidic pH optimum.

T Takizawa, H Fujii, S Takegawa, K Takahashi, A Hirono, T Morisaki, H Kanno, R Oka, H Yoshioka, S Miwa.   

Abstract

A new glucose 6-phosphate dehydrogenase (G6PD) variant associated with chronic nonspherocytic hemolytic anemia was discovered in Japan. The patient showed hemolytic crises after upper respiratory infections. The enzyme activity was about 3.8% of the normal. The partially purified enzyme revealed slow anodal electrophoretic mobility, high Km NADP, marked thermal-instability, and increased affinity for a substrate analogue (deamino-NADP). A particular characteristic of this enzyme was a biphasic pH curve with a greatly increased activity at low pH values. From these results, this variant was clearly different from hitherto observed G6PD variants, and was designated G6PD Asahikawa.

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Year:  1984        PMID: 6500558     DOI: 10.1007/bf00293876

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  16 in total

1.  [Glucose-6-phosphate dehydrogenase defect in Germany. II. Properties of the enzyme (type "Freiburg")].

Authors:  D Busch; K Boie
Journal:  Klin Wochenschr       Date:  1970-01-15

2.  Human glucose-6-phosphate dehydrogenase variants: a supplementary tabulation.

Authors:  E Beutler; A Yoshida
Journal:  Ann Hum Genet       Date:  1973-10       Impact factor: 1.670

3.  Human glucose-6-phosphate dehydrogenase variants.

Authors:  A Yoshida; E Beutler; A G Motulsky
Journal:  Bull World Health Organ       Date:  1971       Impact factor: 9.408

4.  New glucose-6-phosphate dehydrogenase variants observed in Israel and their association with congenital nonspherocytic hemolytic disease.

Authors:  B Ramot; I Ben-Bassat; M Shchory
Journal:  J Lab Clin Med       Date:  1969-12

5.  Biochemical variants of glucose-6-phosphate dehydrogenase giving rise to congenital nonspherocytic hemolytic disease.

Authors:  E Beutler; C K Mathai; J E Smith
Journal:  Blood       Date:  1968-02       Impact factor: 22.113

6.  G-6-PD variants: another up-date.

Authors:  A Yoshida; E Beutler
Journal:  Ann Hum Genet       Date:  1983-01       Impact factor: 1.670

7.  Four new electrophoretically slow-moving glucose 6-phosphate dehydrogenase variants associated with congenital nonspherocytic hemolytic anemia found in Japan: Gd(-) Kurume, Gd(-) Fukushima, Gd(-) Yamaguchi and Gd(-) Wakayama.

Authors:  S Miwa; H Fujii; T Nakatsuji; Y Ishida; E Oda; A Kaneto; M Motokawa; Y Ariga; S Fukuchi; S Sasai; K Hiraoka; H Kashii; T Kodama
Journal:  Am J Hematol       Date:  1978       Impact factor: 10.047

8.  Involvement of active oxygens released by activated leukocytes in hemolytic mechanism of G6PD deficient red cells.

Authors:  A Tomoda; H Suzuki; Y Fukuhara; Y Ueda; K Niho; Y Yoneyama; K Kakinuma
Journal:  Nihon Ketsueki Gakkai Zasshi       Date:  1984-02

9.  Sex-linkage of the glucose-6-phosphate dehydrogenase gene in Equidae.

Authors:  C K Mathai; S Ohno; E Beutler
Journal:  Nature       Date:  1966-04-02       Impact factor: 49.962

10.  Hemolytic anemia and G6PD deficiency.

Authors:  A Yoshida
Journal:  Science       Date:  1973-02-09       Impact factor: 47.728

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  2 in total

1.  Chronic nonspherocytic hemolytic anemia (CNSHA) and glucose 6 phosphate dehydrogenase (G6PD) deficiency in a patient with familial amyloidotic polyneuropathy (FAP). Molecular study of a new variant (G6PD Clinic) with markedly acidic pH optimum.

Authors:  J L Vives-Corrons; M A Pujades; J Petit; D Colomer; M Corbella; J L Aguilar i Bascompte; A Merino
Journal:  Hum Genet       Date:  1989-01       Impact factor: 4.132

2.  Three new G6PD variants, G6PD Adana, G6PD Samandağ, and G6PD Balcali in Cukurova, Turkey.

Authors:  K Aksoy; G T Yüregir; N Dikmen; I Unlükurt
Journal:  Hum Genet       Date:  1987-06       Impact factor: 4.132

  2 in total

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