Literature DB >> 2387402

Fast atom bombardment mass spectrometry and chemical analysis in determinations of acyl-blocked protein structures.

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.

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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


  1 in total

1.  Mutation of Arg-115 of human class III alcohol dehydrogenase: a binding site required for formaldehyde dehydrogenase activity and fatty acid activation.

Authors:  K Engeland; J O Höög; B Holmquist; M Estonius; H Jörnvall; B L Vallee
Journal:  Proc Natl Acad Sci U S A       Date:  1993-03-15       Impact factor: 11.205

  1 in total

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