| Literature DB >> 1977621 |
M Daly1, D Bruce, D J Perry, J Price, P L Harper, A O'Meara, R W Carrell.
Abstract
Antithrombin Dublin is an electrophoretically fast variant of antithrombin which has normal heparin affinity. Direct sequencing of amplified exon 2 revealed a Val----Glu substitution at position -3. N-terminal sequencing of antithrombin from two individuals, heterozygous for the Dublin mutation, showed the presence of a truncated antithrombin in which the N-terminal dipeptide is absent. We propose that the prepeptide mutation redirects signal peptidase cleavage to a site two amino acids downstream into the mature protein.Entities:
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Year: 1990 PMID: 1977621 DOI: 10.1016/0014-5793(90)81057-u
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124