نتایج جستجو برای: amine substrate

تعداد نتایج: 159961  

2015
Maika Genz Clare Vickers Tom van den Bergh Henk-Jan Joosten Mark Dörr Matthias Höhne Uwe T. Bornscheuer Vladimír Křen

To alter the amine donor/acceptor spectrum of an (S)-selective amine transaminase (ATA), a library based on the Vibrio fluvialis ATA targeting four residues close to the active site (L56, W57, R415 and L417) was created. A 3DM-derived alignment comprising fold class I pyridoxal-5'-phosphate (PLP)-dependent enzymes allowed identification of positions, which were assumed to determine substrate sp...

Journal: :Journal of biochemistry and molecular biology 2003
S Zahra Moosavi-Nejad Ali-Akbar Moosavi-Movahedi Mostafa Rezaei-Tavirani Giovanni Floris Rosaria Medda

The kinetics of thermal inactivation of copper-containing amine oxidase from lentil seedlings were studied in a 100 mM potassium phosphate buffer, pH 7, using putrescine as the substrate. The temperature range was between 47-60 degrees C. The thermal inactivation curves were not linear at 52 and 57 degrees C; three linear phases were shown. The first phase gave some information about the number...

Journal: :The Journal of biological chemistry 1986
T J Williams M C Falk

The ortho-, meta-, and para-trifluoromethylphenylhydrazine inhibitors of porcine plasma amine oxidase were synthesized. Titrations of plasma amine oxidase with these inhibitors demonstrated that 1 mol of trifluoromethylphenylhydrazine completely and irreversibly modifies 1 mol of enzyme by covalently binding to the active carbonyl cofactor. NMR relaxation measurements on the fluorine nuclei wer...

Journal: :The Journal of biological chemistry 1993
M A Shah C H Scaman M M Palcic H M Kagan

The structural specificity of amine oxidation by lysyl oxidase was investigated using kinetic and NMR spectroscopic analyses. Substrate efficiency increased with increasing molecular distance from the alpha-carbon of the aromatic moiety substituted on the aliphatic chains of a series of primary amines. The p-hydroxyl substituent of p-hydroxybenzylamine significantly increased kcat over that of ...

Journal: :The Journal of biological chemistry 1967
J E Folk P W Cole J P Mullooly

The transglutaminase-catalyzed hydrolysis and transfer reactions have been studied kinetically in the forward direction at pH 8 in the presence of a 0.1 M level of the activating metal ion, Ca++. Isotope exchange and product inhibition studies were also conducted. The initial velocity, product inhibition, and isotope exchange patterns are consistent with a ping pong mechanism in which (a) gluta...

Journal: :Biomaterials 2010
Shih T Khew Pradeep P Panengad Michael Raghunath Yen W Tong

Transglutaminase (TGase)-modified proteins are commonly observed in a wide range of biological systems. Therefore, the identification of TGase substrates and respective consensus sites may contribute to a better understanding of the physiological role of TGase. In this study, we identified enzyme-specific properties of two peptide sequences, EDGFFKI, derived from human fibrillin-1, and the prev...

Journal: :Chemical communications 2013
Lina Xu Shugui Hua Shuhua Li

Density functional theory investigations reveal that a cavitand with an introverted aldehyde group not only provides the host-guest interaction for preorganizing the substrate and stabilizing the hemiaminal intermediate, but also acts as an acid/base catalyst in the subsequent dehydration step in its reaction with a primary amine.

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