| Literature DB >> 6721829 |
T Ishida, M Kenmotsu, Y Mino, M Inoue, T Fujiwara, K Tomita, T Kimura, S Sakakibara.
Abstract
In order to investigate the structure-activity relationship of [Leu5]- and [Met5]enkephalins, [(4'-bromo)Phe4, Leu5]-, [(4'-bromo)Phe4, Met5]- and [Met5] enkephalins were synthesized and crystallized. The crystal structure of [(4'-bromo) Phe4, Leu5]- enkephalin was determined by X-ray diffraction method using the heavy atom method and refined to R = 0.092 by the least-squares method. The molecule in this crystal took essentially the same type I' beta-turn conformation found in [Leu5]enkephalin [Smith & Griffin (1978) Science 199, 1214-1216). On the other hand, the preliminary three-dimensional Patterson analyses showed that the most probable conformations of [(4'-bromo)Phe4,Met5]- and [Met5]enkephalins are both the dimeric extended forms. Based on these insights, the biologically active conformation of enkephalin was discussed in relation to the mu- and delta-receptors.Entities:
Mesh:
Substances:
Year: 1984 PMID: 6721829 PMCID: PMC1153395 DOI: 10.1042/bj2180677
Source DB: PubMed Journal: Biochem J ISSN: 0264-6021 Impact factor: 3.857