Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/11262
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Type: Journal article
Title: Two isomeric a and b aspartyl dodecapeptides and their cyclic amino succinyl analogues from the Australian Green Tree Frog Litoria gilleni
Author: Waugh, R.
Steinborner, S.
Bowie, J.
Wallace, J.
Tyler, M.
Hu, P.
Gross, M.
Citation: Australian Journal of Chemistry: an international journal for chemical science, 1995; 48(12):1981-1987
Publisher: CSIRO
Issue Date: 1995
ISSN: 0004-9425
1445-0038
Abstract: <jats:p>Three related peptides, caeridins 1.1-1.3, have been isolated from the green tree frog Litoria gilleni. Caeridins 1.1 and 1.2 are dodecapeptides differing only in having α and β Asp at residue 4 [viz. Gly Leu Leu Asp Gly Leu Leu Gly Thr Leu Gly Leu (NH2)]. Caeridin 1.3 is the corresponding cyclic amino succinyl derivative derived formally by cyclization of Asp(4) and Gly (5). Hydrolysis of caeridin 1.3 yields caeridin 1.1 and 1.2 in the ratio 3:1. This constitutes a rare case of the isolation of three such related peptides from a natural system. </jats:p>
DOI: 10.1071/CH9951981
Description (link): http://www.publish.csiro.au/nid/51/paper/CH9951981.htm
Published version: http://dx.doi.org/10.1071/ch9951981
Appears in Collections:Aurora harvest 2
Biochemistry publications

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