Literature DB >> 11828

Hemoglobin Fannin-Lubbock [alpha2 beta 2 119 (GH2) Gly replaced by Asp]. A new hemoglobin variant at the alpha1 beta 1 contact.

W F Moo-Penn, K C Bechtel, M H Johnson, D L Jue, B L Therrell, B Y Morrison, R M Schmidt.   

Abstract

Hemoglobin Fannin-Lubbock was found in a 9-year-old Mexican-American female. The abnormal hemoglobin was detected as a fast-moving variant by electrophoresis on cellulose acetate at pH 8.4. Structural analysis indicated a substitution in the beta-chain of aspartic acid for glycine at position 119, a position involved in the alpha1beta1 contact of the hemoglobin tetramer. This contact between unlike chains is larger and undergoes a smaller shift during the process of oxygenation and deoxygenation that the alpha1beta2 contact (Perutz, M.F., Muirhead, H., Cox, J.M. and Goaman, L.C.G. (1968) Nature 219, 131-139). Mutations in this contact tend to cause slight or no changes in functional behavior. Apart from a mild anemia, the propositus did not exhibit any obvious clinical symptoms.

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Year:  1976        PMID: 11828     DOI: 10.1016/0005-2795(76)90142-2

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


  1 in total

1.  Identification of eleven human hemoglobin variants by high-performance liquid chromatography: additional data on functional properties and clinical expression.

Authors:  W A Schroeder; J B Shelton; J R Shelton; D Powars; S Friedman; J Baker; J Z Finklestein; B Miller; C S Johnson; J R Sharpsteen; L Sieger; E Kawaoka
Journal:  Biochem Genet       Date:  1982-02       Impact factor: 1.890

  1 in total

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