Literature DB >> 2820795

Human protein S cDNA encodes Phe-16 and Tyr 222 in consensus sequences for the post-translational processing.

H K Ploos van Amstel1, A L van der Zanden, P H Reitsma, R M Bertina.   

Abstract

Partial cDNAs coding for human protein S were isolated from a pUC9 human liver cDNA library. Together, the overlapping clones span a (partial) 5'-non-coding region, and the complete protein S coding and 3'-untranslated regions. The derived amino acid sequence deviates at five positions from two previously reported protein S sequences. Two of these differences (Phe instead of Leu at position -16 and Tyr instead of Asp at position 222) are found in regions that are important for the post-translational modification of protein S, the gamma-carboxylation of glutamic acid and the hydroxylation of asparagine, respectively.

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Year:  1987        PMID: 2820795     DOI: 10.1016/0014-5793(87)80217-x

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


  4 in total

Review 1.  The interaction between complement component C4b-binding protein and the vitamin K-dependent protein S forms a link between blood coagulation and the complement system.

Authors:  M Hessing
Journal:  Biochem J       Date:  1991-08-01       Impact factor: 3.857

2.  A comprehensive list of cloned human DNA sequences.

Authors:  J Schmidtke; D N Cooper
Journal:  Nucleic Acids Res       Date:  1988       Impact factor: 16.971

3.  A target-specific approach for the identification of tyrosine-sulfated hemostatic proteins.

Authors:  Tzu-An Liu; Shin Yasuda; Frederick E Williams; Ming-Yih Liu; Masahito Suiko; Yoichi Sakakibara; Yuh-Shyong Yang; Ming-Cheh Liu
Journal:  Anal Biochem       Date:  2009-04-05       Impact factor: 3.365

4.  Three novel mutations in five unrelated subjects with hereditary protein S deficiency type I.

Authors:  P H Reitsma; H K Ploos van Amstel; R M Bertina
Journal:  J Clin Invest       Date:  1994-02       Impact factor: 14.808

  4 in total

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