Literature DB >> 2345057

Thio-alpha-amino acids (S-acids) as a carboxyl component in peptide synthesis catalysed by papain.

N P Zapevalova.   

Abstract

Peptide synthesis catalysed by papain was studied using thio-alpha-amino acids (S-acids) as a carboxyl component. It was found, for example, that with Z-AlaSH (pK 2.70) the maximal yield of the peptide Z-AlaValNH2 was obtained at pH 8-8.5. A two-fold excess of Z-AlaSH furnished peptides with yields close to 100%. Thio-amino acids with bulky side groups, for example, Z-IleSH, Z-Asp(OBu')SH, gave peptides with a low yield. Papain interacts with Z-AlaSH better than do bromelain or ficin.

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Year:  1990        PMID: 2345057     DOI: 10.1111/j.1399-3011.1990.tb00060.x

Source DB:  PubMed          Journal:  Int J Pept Protein Res        ISSN: 0367-8377


  4 in total

1.  Dihydro-3-(triphenylphosphoranylidene)-2,5-thiophendione: A Convenient Synthon for the Preparation of Substituted 1,4-Thiazepin-5-ones and Piperidinones via the Intermediacy of Thioacids.

Authors:  David Crich; Md Yeajur Rahaman
Journal:  Tetrahedron       Date:  2010-08-14       Impact factor: 2.457

2.  Oligomerization of alpha-thioglutamic acid.

Authors:  M C Maurel; L E Orgel
Journal:  Orig Life Evol Biosph       Date:  2000-10       Impact factor: 1.950

3.  Reaction of thioacids with isocyanates and isothiocyanates: a convenient amide ligation process.

Authors:  David Crich; Kaname Sasaki
Journal:  Org Lett       Date:  2009-08-06       Impact factor: 6.005

4.  Solid-phase synthesis of peptidyl thioacids employing a 9-fluorenylmethyl thioester-based linker in conjunction with Boc chemistry.

Authors:  David Crich; Kasinath Sana
Journal:  J Org Chem       Date:  2009-10-02       Impact factor: 4.354

  4 in total

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