Literature DB >> 3258831

The amino acid substitutions of human alpha 1-antitrypsin M3, X and Z.

J O Jeppsson1, C B Laurell.   

Abstract

alpha 1-Antitrypsin has been isolated from individuals with inherited genetic variants M3, X and Z. A fragmentation and peptide mapping system is described which together with amino acid and sequence analyses revealed the substitutions in M3 at 376 of Glu to Asp, in X at 204 of Glu to Lys and in the physiologically innocent Z a mutation at 213 of Val to Ala. The latter represents a second amino acid substitution in the Z protein.

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Year:  1988        PMID: 3258831     DOI: 10.1016/0014-5793(88)80843-3

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  3 in total

Review 1.  Molecular biology and respiratory disease. 7. The alpha 1 antitrypsin gene and chronic lung disease.

Authors:  N Kalsheker; K Morgan
Journal:  Thorax       Date:  1990-10       Impact factor: 9.139

2.  Characterisation of the alpha-1-antitrypsin M3 gene, a normal variant.

Authors:  A Graham; K Hayes; S Weidinger; C R Newton; A F Markham; N A Kalsheker
Journal:  Hum Genet       Date:  1990-08       Impact factor: 4.132

3.  Post-Transcriptional Regulation of Alpha One Antitrypsin by a Proteasome Inhibitor.

Authors:  Lang Rao; Yi Xu; Lucas Charles Reineke; Abhisek Bhattacharya; Alexey Tyryshkin; Jin Na Shin; N Tony Eissa
Journal:  Int J Mol Sci       Date:  2020-06-17       Impact factor: 5.923

  3 in total

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