𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Conformational Preferences of Short Peptide Fragments

✍ Scribed by Yoshiyuki Hatakeyama; Tomohisa Sawada; Masaki Kawano; Makoto Fujita


Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
732 KB
Volume
121
Category
Article
ISSN
0044-8249

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Computational study of conformational pr
✍ Ho-Jin Lee; Jong Hyun Kim; Hee Jung Jung; Kun-Young Kim; Eun-Jung Kim; Young-San 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 351 KB 👁 1 views

## Abstract The effect of thioamide substitution on the conformational stability of an azaglycine‐containing peptide, For‐AzaGly‐NH~2~ (**1**), was investigated for the sake of finding possible applications by using __ab initio__ and DFT methods. As model compounds, For‐[ΨCSNH]‐AzaGly‐NH~2~ (**2**)

Solution conformational preferences of a
✍ Luca D. D'Andrea; Marco Mazzeo; Carla Isernia; Filomena Rossi; Michele Saviano; 📂 Article 📅 1997 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 158 KB 👁 1 views

The conformational behavior in solution of a cyclic peptide with sequence cyclo-(Pro 1 -Pro 2 -Dab 3 (cHexA)c[N g HCO]-Leu 4 c[NHCO]-Suc 5 -Gly 6 -) has been throughly investigated with the combined use of nmr and molecular dynamic techniques. The compound, which has been modeled to mimic the FK506

Two peptide fragments G55–I72 and K97–A1
✍ Min Wang; Lu Shan; Jinfeng Wang 📂 Article 📅 2006 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 823 KB

## Abstract Two synthetic peptides, SNaseα1 and SNaseα2, corresponding to residues G55–I72 and K97–A109, respectively, of staphylococcal nuclease (SNase), are adopted for detecting the role of helix α1 (E57–A69) and helix α2 (M98–Q106) in the initiation of folding of SNase. The helix‐forming tenden

Preferred conformations of peptides cont
✍ Claudio Toniolo; Gian Maria Bonora; Alfonso Bavoso; Ettore Benedetti; Benedetto 📂 Article 📅 1983 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 544 KB

The conformational preferences of linear peptides containing a,a-disubstituted a-amino acids, derived from the crystal structures of 28 compounds, are reviewed. In particular, the sensitivity of peptide conformation to the geometry of these unusual amino acids is underlined. We also consider possibl