Enzymatic methyl esterification of synthetic tripeptides: structural requirements of the peptide substrate. Detection of the reaction products by fast-atom-bombardment mass spectrometry-Reference-Cited by-同舟云学术

Enzymatic methyl esterification of synthetic tripeptides: structural requirements of the peptide substrate. Detection of the reaction products by fast-atom-bombardment mass spectrometry

Published:1988-10 Issue:1 Volume:177 Page:233-239
ISSN:0014-2956
Container-title:European Journal of Biochemistry
language:en
Short-container-title:Eur J Biochem

Author:

GALLETTI Patrizia,INGROSSO Diego,MANNA Caterina,SICA Filomena,CAPASSO Sante,PUCCI Piero,MARINO Gennaro

Publisher

Wiley

Subject

Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1432-1033.1988.tb14367.x/fullpdf

Reference36 articles.

1. PROTEIN CARBOXYL METHYLTRANSFERASES: TWO DISTINCT CLASSES OF ENZYMES

2. 2. S. Clarke, R. T. Borchardt, C. R. Creveling, and P. M. Ueland (1986 ) inBiological methylation and drug design () pp.3 -14 , Humana Press, Clifton, NJ.

3. Stoichiometric methylation of porcine adrenocorticotropin by protein carboxyl methyltransferase requires deamidation of asparagine 25. Evidence for methylation at the alpha-carboxyl group of atypical L-isoaspartyl residues.

4. Synthetic peptide substrates for the erythrocyte protein carboxyl methyltransferase. Detection of a new site of methylation at isomerized L-aspartyl residues.

5. 5. S. Clarke, and J. Eaton (1985 ) inCellular and molecular aspects of ageing: the red cell as a model () pp.91 -98 , Alan R. Liss, New York.

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