𝔖 Bobbio Scriptorium
✦   LIBER   ✦

NMR studies of the peptide group in dipeptides containing C-terminal glycine residue

✍ Scribed by M Sheinblatt


Publisher
Elsevier Science
Year
1972
Weight
324 KB
Volume
8
Category
Article
ISSN
0022-2364

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


1H and 13C nmr studies of cyclic and lin
✍ Marius Ptak; Annie Heitz; Michel Dreux πŸ“‚ Article πŸ“… 1978 πŸ› Wiley (John Wiley & Sons) 🌐 English βš– 995 KB

## Abstract The side‐chain conformations of D‐ orL‐ Thr, D‐ or L‐Ser, L‐Asp, and L‐ His residues in cyclic and linear dipeptides in D~2~O or in DMSO‐d~6~ are deduced from vicinal (^1^H,^1^H) and (^13^C, ^1^H) coupling constants. Vicinal (^13^C, ^13^C) coupling constants strongly depend on substitue

Stabilization of helical structure in tw
✍ James F. Collawn; Yvonne Paterson πŸ“‚ Article πŸ“… 1990 πŸ› Wiley (John Wiley & Sons) 🌐 English βš– 674 KB

The conformations of two 17-residue peptide analogues derived from the C-terminal sequence of pigeon cytochrome c (native sequence = KAERADLIAYLKQATAK) were examined in aqueous and lipid environments by CD spectroscopy. The two analogues, KKLLKKLIAYLKQATAK ( K peptide) and EELLEELIAYLKQATAK ( E pept

Kinetic study of the interaction of thre
✍ Subhasis Mallick; Subala Mondal; Arup Mandal; Biplab K. Bera; Parnajyoti Karmaka πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons 🌐 English βš– 200 KB

The kinetics of the interaction of three glycine-containing dipeptides, namely, glycine-L-leucine (Gly-Leu), glycine-L-isoleucine (Gly-Ile), and glycine-valine (Gly-Val) with [Pt(en)(H 2 O) 2 ](ClO 4 ) 2 has been studied spectrophotometrically as a function of [substrate complex], [dipeptides] and t

13C-NMR chemical shift tensor and hydrog
✍ Naoto Takeda; Shigeki Kuroki; Hiromichi Kurosu; Isao Ando πŸ“‚ Article πŸ“… 1999 πŸ› Wiley (John Wiley & Sons) 🌐 English βš– 149 KB πŸ‘ 2 views

C-nmr chemical shift tensor components are reported for a 13 C-labeled Gly 1 amide carbonyl carbon of a glycylglycine (Gly 1 Gly 2 ) single crystal, a GlyGly ⅐ HNO 3 single crystal and a GlyGly ⅐ HCl ⅐ H 2 O single crystal, for which the three-dimensional crystal structures have already been determi