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Molecular modelling of beta turns in a cyclic melanotropin.

作者信息

Chan N C, Branch S K, Moss S H, Pouton C W

机构信息

School of Pharmacy and Pharmacology, University of Bath, UK.

出版信息

J Pharm Pharmacol. 1996 Feb;48(2):218-22. doi: 10.1111/j.2042-7158.1996.tb07127.x.

DOI:10.1111/j.2042-7158.1996.tb07127.x
PMID:8935176
Abstract

Alpha-Melanocyte stimulating hormone (alpha-MSH) is a tridecapeptide which interacts with a family of G protein-coupled receptors, the melanocortin receptors, to cause its biological effects. We have modelled the low energy conformations of the alpha-MSH derivatives as part of a project to probe the receptor binding conformation of melanocortins, and also to design ligands for targeting cytotoxic drugs to MC1 receptors expressed by melanoma cells. Here we report a molecular dynamics study of beta turns in a cyclic lactam analogue [Nle4, Asp5, D-Phe7, Lys10]alpha-MSH. The data show that it is possible for a beta turn to exist in the ring portion of this molecule which contains the melanocortin conserved sequence - His-Phe-Arg-Trp-, even though the lowest energy conformers lack a beta turn.

摘要

相似文献

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