| Literature DB >> 2387402 |
B Egestad1, M Estonius, O Danielsson, B Persson, E Cederlund, R Kaiser, B Holmquist, B Vallee, X Parés, J Jefferey.
Abstract
Peptide generation and fast atom bombardment mass spectrometry in combination with conventional chemical analysis was used to identify the blocking group and establish the N-terminal structure of six different proteins at the nanomole level. In this manner, the first terminal structures of three non-mammalian alcohol dehydrogenases were determined, demonstrating the presence of N-terminal acetylation in these piscine, amphibian, and avian enzymes. Similarly, two different yeast glucose-6-phosphate dehydrogenases and a minor variant of a human alcohol dehydrogenase were found to be acetylated. The exact end location of C-terminal structures was also established. Together, the analyses permit the definition of terminal regions and blocking groups, thus facilitating the delineation of remaining structures.Entities:
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Year: 1990 PMID: 2387402 DOI: 10.1016/0014-5793(90)81152-e
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124