𝔖 Bobbio Scriptorium
✦   LIBER   ✦

In SituMeasurements of Ribulose-1,5-bisphosphate Carboxylase Activity by Nuclear Magnetic Resonance

✍ Scribed by Zheng-Yu Wang; Shen Luo; Kazuhiro Sato; Masayuki Kobayashi; Tsunenori Nozawa


Publisher
Elsevier Science
Year
1998
Tongue
English
Weight
298 KB
Volume
257
Category
Article
ISSN
0003-2697

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Structural investigation of 3,5-disubsti
✍ Mario Sechi; Luciano Sannia; Maria Orecchioni; Fabrizio Carta; Giuseppe Pagliett πŸ“‚ Article πŸ“… 2003 πŸ› Journal of Heterocyclic Chemistry 🌐 English βš– 55 KB

## Abstract HIV‐1 integrase (IN) is a very promising and validated target for the development of therapeutic agents against AIDS. In an effort to design and synthesize biological isosteric analogs of β‐diketoacid‐containing inhibitors of IN, we prepared a series of substituted isoxazole carboxylic

Enzyme-catalyzed polymerization of 8-hyd
✍ K. Shridhara Alva; Lynne Samuelson; Jayant Kumar; Sukant Tripathy; Ashok L. Chol πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 187 KB πŸ‘ 2 views

In this report, we describe the use of in situ NMR spectroscopy to elucidate the mechanism of horseradish peroxidase-catalyzed oxidative free-radical coupling of phenols. We demonstrate the potential of the technique for the polymerization of 8-hydroxyquinoline-5-sulfonate (HQS). Based on the struct

Effect of condensed tannins prepared fro
✍ McNabb, Warren C; Peters, Jason S; Foo, L Yeap; Waghorn, Garry C; Jackson, Felic πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 443 KB πŸ‘ 3 views

A series of in vitro experiments was undertaken to determine the extent to which Sephadex LH-20 treated extracts from a range of temperate forages precipitated ribulose-1,5-bisphosphate carboxylase (Rubisco) and a †ected the enzymatic hydrolysis of Rubisco protein by trypsin and chymotrypsin at a ra

Configurational assignment of Ξ²-phenylas
✍ M. Barrelle; C. Gey; C. G. BΓ©guin πŸ“‚ Article πŸ“… 1988 πŸ› John Wiley and Sons 🌐 English βš– 345 KB

Vicinal 3J(HH) and 3J( 13CH) coupling constants are reported for the two diastereoisomers of p-pbenylaspartic acid at various pH values. A comparison between these coupling constants and those expected from the possible conformations of these molecules allows configurational assignments to be made.