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Human protein S cDNA encodes Phe-16 and Tyr 222 in consensus sequences for the post-translational processing.
Ploos van Amstel, H K; van der Zanden, A L; Reitsma, P H; Bertina, R M.
Affiliation
  • Ploos van Amstel HK; Dept of Hematology, Leiden University Hospital, The Netherlands.
FEBS Lett ; 222(1): 186-90, 1987 Sep 28.
Article in En | MEDLINE | ID: mdl-2820795
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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Collection: 01-internacional Database: MEDLINE Main subject: DNA / Glycoproteins / Protein Processing, Post-Translational Limits: Humans Language: En Journal: FEBS Lett Year: 1987 Document type: Article Affiliation country: Netherlands Country of publication: United kingdom
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: DNA / Glycoproteins / Protein Processing, Post-Translational Limits: Humans Language: En Journal: FEBS Lett Year: 1987 Document type: Article Affiliation country: Netherlands Country of publication: United kingdom