Literature DB >> 2272838

Hb Johnstown [beta 109 (G11) Val----Leu]: a new electrophoretically silent variant that causes erythrocytosis.

R T Jones1, H I Saiontz, C Head, D T Shih, V F Fairbanks.   

Abstract

A high oxygen affinity hemoglobin, previously undescribed, was found in a healthy, asymptomatic patient with mild erythrocytosis and left-shifted hemoglobin-O2 dissociation curve. The hemoglobin variant could not be distinguished from Hb A by any of several electrophoretic methods nor by ion exchange chromatography. It was separated and analyzed by reversed phase high performance liquid chromatography. Structural analysis revealed the substitution beta 109 (G11) Val----Leu. The variant was named Hb Johnstown. The amino acid substitution perhaps disrupts alpha 1 beta 1 contacts in the deoxyhemoglobin conformation, thus shifting the equilibrium towards the high affinity oxyhemoglobin conformation.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 2272838     DOI: 10.3109/03630269009046956

Source DB:  PubMed          Journal:  Hemoglobin        ISSN: 0363-0269            Impact factor:   0.849


  2 in total

1.  Genetic variations in the C epsilon mX domain of human membrane-bound IgE.

Authors:  Lei Wan; Jiun-Bo Chen; Hsih Hsin Chen; Janice Huang; Hui-Ming Yu; Shue-Fen Luo; Fuu Jen Tsai; Tse Wen Chang
Journal:  Immunogenetics       Date:  2010-03-24       Impact factor: 2.846

2.  Familial polycythemia caused by a novel mutation in the beta globin gene: essential role of P50 in evaluation of familial polycythemia.

Authors:  Neeraj Agarwal; Mariluz P Mojica-Henshaw; Elizabeth D Simmons; Dottie Hussey; Ching N Ou; Josef T Prchal
Journal:  Int J Med Sci       Date:  2007-10-04       Impact factor: 3.738

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.