Conformational features responsible for binding of cyclic analogues of enkephalin to opioid receptors. I, Low-energy peptide backbone conformers of analogues containing Phe
Low-energy peptide backbone conformers were found by means of energy calculation for several cyclic analogues of enkephalin in an attempt to assess models for receptor-bound conformations for opioid receptors of the mu - and delta -types. The low-energy conformers obtained for these analogues were i...
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Veröffentlicht in: | International journal of peptide and protein research 1990, Vol.36 (1), p.67-78 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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