𝔖 Bobbio Scriptorium
✦   LIBER   ✦

1H,13C and15N random coil NMR chemical shifts of the common amino acids. I. Investigations of nearest-neighbor effects

✍ Scribed by D. S. Wishart; C. G. Bigam; A. Holm; R. S. Hodges; B. D. Sykes

Publisher
Springer Netherlands
Year
1995
Tongue
English
Weight
32 KB
Volume
5
Category
Article
ISSN
0925-2738

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

13C isotope effects on 1H chemical shift
13C isotope effects on 1H chemical shifts: NMR spectral analysis of 13C-labelled D-glucose and some 13C-labelled amino acids
✍ Mika Tiainen; Hannu Maaheimo; Pasi Soininen; Reino Laatikainen 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 187 KB

## Abstract The one‐ and two‐bond ^13^C isotope shifts, typically −1.5 to −2.5 ppb and −0.7 ppb respectively, in non‐cyclic aliphatic systems and up to −4.4 ppb and −1.0 ppb in glucose cause effects that need to be taken into account in the adaptive NMR spectral library‐based quantification of the

Predominance of resonance over polar eff
Predominance of resonance over polar effects on 1H, 13C and 15N NMR substituent chemical shifts in N-arylglycines
✍ Ryszard Gawinecki; Erkki Kolehmainen; Zdzisław Kucybała; Borys Ośmiałowski; Reij 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 260 KB 👁 2 views

1H, 13C and 15N NMR spectra of the ring-substituted N-phenylglycines (1) and their ethyl esters (2) were measured in The chemical shift determinations and assignments are based on modern inverse 2D DMSO-d 6 . techniques (HMQC, HMBC). Dependences between chemical shifts and substituent constants sho

The impact of the π-electron conjugation
The impact of the π-electron conjugation on 15N, 13C and 1H NMR chemical shifts in push–pull benzothiazolium salts. Experimental and theoretical study
✍ Peter Hrobárik; Branislav Horváth; Ivica Sigmundová; Pavol Zahradník; Olga L. Ma 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 319 KB

## Abstract The ^15^N as well as ^13^C and ^1^H chemical shifts of eight __push–pull__ benzothiazolium iodides with various π‐conjugated chains between dimethylamino group and benzothiazolium moiety have been determined by NMR spectroscopy at the natural‐abundance level of all nuclei in DMSO‐__d__~

NMR chemical shift mapping of the bindin
NMR chemical shift mapping of the binding site of a protein proteinase inhibitor: changes in the 1H, 13C and 15N NMR chemical shifts of turkey ovomucoid third domain upon binding to bovine chymotrypsin Aα
✍ Jikui Song; John L. Markley 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 201 KB

## Abstract The substrate‐like inhibition of serine proteinases by avian ovomucoid domains has provided an excellent model for protein inhibitor‐proteinase interactions of the standard type. ^1^H,^15^N and ^13^C NMR studies have been undertaken on complexes formed between turkey ovomucoid third dom

Rapid acquisition of 1H–13C and 1H–15N h
Rapid acquisition of 1H–13C and 1H–15N heteronuclear chemical shift correlation data at the submilligram level using SMIDG (submicro inverse-detection gradient) NMR probe technology
✍ Gary E. Martin; Chad E. Hadden; Albert N. Tackie; Maged M. H. Sharaf; Paul L. Sc 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 132 KB 👁 1 views

The application of submicro inverse-detection gradient (SMIDG) NMR probe technology at 600 MHz is demonstrated for the rapid acquisition of both 1 H-13 C and 1 H-15 N heteronuclear chemical shift correlation data. Using a 750 µg (ca 1.5 µmol, MW 505) sample of the complex spirononacyclic alkaloid cr