The crystal structure of Boc-Pro-Val-Gly-NH2, with a remark on the conformation of the valyl residues in peptides
Author:
Publisher
Wiley
Subject
Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-3011.1986.tb02766.x/fullpdf
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1. Solid state conformation of the C-terminal tripeptide of oxytocin, L-Pro-L-Leu-Gly-NH2.0.5H2O
2. The crystal structure of S-benzyl-L-cysteinyl-L-prolyl-L-leucylglycinamide and its selenium analog
3. The crystal and molecular structure of tert-butyloxycarbonyl-L-prolyl-L-prolylglycinamide
4. The structure of tert-butoxycarbonyl-L-prolyl-L-alanylglycinamide
5. Conformations moléculaires à l'état solide des deux diastéréoisomères de la N-isobutyrylprolylalanine-isopropylamide. Comparaison avec les conformations adoptées en solution
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1. Reengineering a type II β-turn as a potential helix nucleator. Part I. Crystal structure of Boc-Val-Pro-(D)Asp-Asp-Val-OMe monohydrate;The Journal of Peptide Research;2009-01-12
2. Observation of a mixed antiparallel and parallel β-sheet motif in the crystal structure of Boc-Ala-Ile-Aib-OMe;International Journal of Peptide and Protein Research;2009-01-12
3. Conformational versatility of the Nα-acylated tripeptide amide tail of oxytocin;International Journal of Peptide and Protein Research;2009-01-12
4. Conformational studies on polypeptide models of collagen. Poly(Gly-Pro-Val), poly(Gly-Pro-Met), poly(Gly-Val-Pro) and poly(Gly-Met-Pro);International Journal of Peptide and Protein Research;2009-01-12
5. Crystal Structure and Conformation of N-(t-Butoxycarbonyl)-L-Isoleucyl-L-Valine Methyl Ester (Boc-Ile-Val-OMe);Molecular Crystals and Liquid Crystals;2005-03-16
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