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J. Biol. Chem., Vol. 268, Issue 5, 3052-3055, 02, 1993
F Ducancel, V Matre, C Dupont, E Lajeunesse, Z Wollberg, A Bdolah, E Kochva, JC Boulain and A Menez
Sarafotoxins (SRTXs) are 21-amino acid peptides structurally and
functionally similar to endothelins (ETs). To understand how SRTXs are
overproduced in venom glands of the snakes Atractaspis engaddensis and
hence used as toxins, we cloned cDNAs encoding SRTXs and elucidated their
nucleotide sequences. We predict that SRTX precursors are large
prepropolypeptide chains with an unusual "rosary-type" structure made of 12
successive similar stretches of 40 residues (39 in the first stretch). Each
stretch begins with a "spacer" of 19 invariant residues (18 in the first
stretch) immediately followed by the sequence of one SRTX isoform. Six
different isoforms are identified within a single precursor molecule.
Maturation of the precursor may require endopeptidases that cleave the
Leu-Cys bond and the Trp-Arg/Lys bond invariably found at the SRTX N and C
termini, respectively.
Cloning and sequence analysis of cDNAs encoding precursors of sarafotoxins. Evidence for an unusual "rosary-type" organization
Departement d'Ingenierie et d'Etudes des Proteines, C. E. Saclay, Gif sur Yvette, France.
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