نتایج جستجو برای: active site cavity

تعداد نتایج: 828256  

Journal: :Organic & biomolecular chemistry 2012
Santosh Rudrawar Philip S Kerry Marie-Anne Rameix-Welti Andrea Maggioni Jeffrey C Dyason Faith J Rose Sylvie van der Werf Robin J Thomson Nadia Naffakh Rupert J M Russell Mark von Itzstein

Novel 3-C-alkylated-Neu5Ac2en derivatives have been designed to target the expanded active site cavity of influenza virus sialidases with an open 150-loop, currently seen in X-ray crystal structures of influenza A virus group-1 (N1, N4, N5, N8), but not group-2 (N2, N9), sialidases. The compounds show selectivity for inhibition of H5N1 and pdm09 H1N1 sialidases over an N2 sialidase, providing e...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1988
D S Peterson D Walliker T E Wellems

Analysis of a genetic cross of Plasmodium falciparum and of independent parasite isolates from Southeast Asia, Africa, and South America indicates that resistance to pyrimethamine, an antifolate used in the treatment of malaria, results from point mutations in the gene encoding dihydrofolate reductase-thymidylate synthase (EC 1.5.1.3 and EC 2.1.1.45, respectively). Parasites having a mutation f...

The buoyancy-driven fluid flow and heat transfer in a square cavity with partially active side walls filled with Cu-water nanofluid is investigated numerically. The active parts of the left and the right side-walls of the cavity are maintained at temperatures Th and Tc, respectively, with Th>Tc. The enclosure’s top and bottom walls, as well as, the inactive parts of its side walls are kept insu...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2000
R H van Den Heuvel M W Fraaije M Ferrer A Mattevi W J van Berkel

Vanillyl-alcohol oxidase (VAO) is the prototype of a newly recognized family of structurally related oxidoreductases sharing a conserved FAD-binding domain. The active site of VAO is formed by a cavity where the enzyme is able to catalyze many reactions with phenolic substrates. Among these reactions is the stereospecific hydroxylation of 4-ethylphenol-forming (R)-1-(4'-hydroxyphenyl)ethanol. D...

Journal: :The Journal of biological chemistry 2011
Natalia Mast Andrew J Annalora David T Lodowski Krzysztof Palczewski C David Stout Irina A Pikuleva

Mitochondrial cytochrome P450 11A1 (CYP11A1 or P450 11A1) is the only known enzyme that cleaves the side chain of cholesterol, yielding pregnenolone, the precursor of all steroid hormones. Pregnenolone is formed via three sequential monooxygenation reactions that involve the progressive production of 22R-hydroxycholesterol (22HC) and 20α,22R-dihydroxycholesterol, followed by the cleavage of the...

Journal: :Biochemistry 2008
Jiayin Zheng Balendu Sankara Avvaru Chingkuang Tu Robert McKenna David N Silverman

Catalysis by the zinc metalloenzyme human carbonic anhydrase II (HCA II) is limited in maximal velocity by proton transfer between His64 and the zinc-bound solvent molecule. Asn62 extends into the active site cavity of HCA II adjacent to His64 and has been shown to be one of several hydrophilic residues participating in a hydrogen-bonded solvent network within the active site. We compared sever...

Journal: :Journal of chemical information and modeling 2011
Tanya Singh D. Biswas Bhyravabhotla Jayaram

We report here a robust automated active site detection, docking, and scoring (AADS) protocol for proteins with known structures. The active site finder identifies all cavities in a protein and scores them based on the physicochemical properties of functional groups lining the cavities in the protein. The accuracy realized on 620 proteins with sizes ranging from 100 to 600 amino acids with know...

Journal: :Molecular pharmacology 2018
Mei-Hui Hsu Uzen Savas Eric F Johnson

The contributions of cytochrome P450 3A5 to the metabolic clearance of marketed drugs is unclear, but its probable role is to augment the metabolism of several drugs that are largely cleared by P450 3A4. Selective metabolism by 3A4 is often a concern in drug development owing to potential drug-drug interactions and the variability of 3A4 and 3A5 expression. The contribution of P450 3A5 to these...

The present study reports a microwave-assisted method for the synthesis of twelve novel tricyclic 1,4-dihydropyridine derivatives in which dimethyl-substituted cyclohexane and / or tetrahydrothiophene rings are fused to the DHP ring. The structures of the compounds were confirmed by spectral methods and elemental analysis. The potassium channel opening effects of the compounds were determined o...

The present study reports a microwave-assisted method for the synthesis of twelve novel tricyclic 1,4-dihydropyridine derivatives in which dimethyl-substituted cyclohexane and / or tetrahydrothiophene rings are fused to the DHP ring. The structures of the compounds were confirmed by spectral methods and elemental analysis. The potassium channel opening effects of the compounds were determined o...

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