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
Hauptverfasser: NIKIFOROVICH, G. V, BALODIS, J, SHENDEROVICH, M. D, GOLBRAIKH, A. A
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Sprache:eng
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