Structure and conformation of peptides: N-benzyloxycarboyl-(γ-ethyl)-L-glutamyl-(γ-ethyl)-L-glutamic acid ethyl ester
✍ Scribed by Ettore Benedetti; Benedetto Di Blasio; Vincenzo Pavone; Carlo Pedone; Gabriel Germain; Murray Goodman
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1979
- Tongue
- English
- Weight
- 266 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0006-3525
No coin nor oath required. For personal study only.
✦ Synopsis
Synopsis
C Z ~H : ~~N ~O ~, orthorhombic, B212121; a = 39.432 (lo), b = 14.061 ( 5 ) , c = 4.850 (2) A, M = 494 a.m.u., Z = 4, Dm = 1.22 g cm-:', Dr = 1.22 g cm-3, R = 0.13 for 1205 observed reflections alter refinement with isotropic thermal factors. The urethane and amide bonds are in the trans configuration, as well as all the ester groups. The (c and $ angles of the L-glutamyl residues fall in the &structure region of the Ramachandran's plot; the molecule is rather flat with the amide plane almost parallel to the c axis along which two hydrogen bonds hold the molecules together to form long rows in a "parallel pleated-sheet'' fashion.
📜 SIMILAR VOLUMES
The yethyl-bglutamate NCA polymerization initiated by di-n-butyl and di-isopropyl amine was studied. The experimental kinetic curves show an autocatalytic portion with 2530% conversion, followed by a pseudo first-order region which extends up to at least 8590%. In this linear region, the reaction or