6533b82bfe1ef96bd128d760
RESEARCH PRODUCT
N‐[tert‐Butoxycarbonylglycyl‐(E)‐α,β‐dehydrophenylalanylglycylglycyl‐(E)‐α,β‐dehydrophenylalanyl]glycine
Maciej MakowskiTadeusz LisIwona MikołajczykMarek Lisowskisubject
chemistry.chemical_classificationResidue (chemistry)chemistryStereochemistryHydrogen bondGlycineGeneral Materials SciencePeptideTert-butoxyGeneral ChemistryCrystal structureCondensed Matter PhysicsAmino aciddescription
In the molecule of the title hexapeptide, Boc0–Gly1–ΔEPhe2–Gly3–Gly4–ΔEPhe5–Gly6–OH, C31H36N6O9, there are two overlapping β-turns, one of type II on the ΔEPhe2 (ΔEPhe is isomer E of the α,β-dehydrophenylalanine residue) and Gly3 residues and the second of type III′ on the Gly3 and Gly4 residues. All amino acids in the peptide are linked trans to each other. Three relatively strong intramolecular N—H⋯O hydrogen bonds stabilize the crystal structure. Two of them, of the 4→1 type, are responsible for two β-turns in the peptide.
year | journal | country | edition | language |
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2006-12-06 | Acta Crystallographica Section E-Structure Reports Online |