A systematic survey has been made, using molecular mechanics, of the conformation of the ring entity of the enkephalin analogs, [~Cys~-~-Cys~]enkephalinamide and [D Cys2-~Cys5]enkephalinamide. These molecules are considerably more flexible than the analog Tyr-cyclo(Ny-DA,bu-Gly-Phe-Leu-), but the fa
Conformation of cyclic analogs of enkephalin. III. Effect of varying ring size
β Scribed by David Hall; Nicola Pavitt
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1985
- Tongue
- English
- Weight
- 513 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0006-3525
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β¦ Synopsis
Synopsis
A comparative study has been made using molecular mechanics of the ring entity of the active enkephalin analogs, Tyr-cyclo(-N'-D-XXX-Gly-Phe-Leu-), where XXX is variously A,pr, A,bu, and Orn. Several conformations are favored for all three, and the lower-energy models are compatible with a Gly3-Phe4 bend in the active form of enkephalin. Some difficulties in assuming standard geometries in conformational surveys are illustrated.
π SIMILAR VOLUMES
A systematic survey has been made, using molecular mechanics, of the conformation of cycle(-NY-Mabu-Gly-Ala-Ala-), where Mabu is (R)-a-methyl-y-arninobutyric acid. This molecule corresponds to the 14-membered ring of the conformationally restricted, biologically active, Leu-enkephalin analog, Tyr-~~