Virtual screening, selection and development of a benzindolone structural scaffold for inhibition of lumazine synthase - Wikidata - wikimedia - TriplyDB

Virtual screening, selection and development of a benzindolone structural scaffold for inhibition of lumazine synthase

Virtual screening, selection and development of a benzindolone structural scaffold for inhibition of lumazine synthase

http://www.wikidata.org/entity/Q30494491

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Discovery of novel MDR-Mycobacterium tuberculosis inhibitor by new FRIGATE computational screen Analysis and hit filtering of a very large library of compounds screened against Mycobacterium tuberculosis.O-Nucleoside, S-nucleoside, and N-nucleoside probes of lumazine synthase and riboflavin synthase.The lumazine synthase/riboflavin synthase complex: shapes and functions of a highly variable enzyme system.In-silico docking based design and synthesis of [1H,3H] imidazo[4,5-b] pyridines as lumazine synthase inhibitors for their effective antimicrobial activity.Design, Synthesis, and Evaluation of Dihydrobenzo[cd]indole-6-sulfonamide as TNF-α Inhibitors.Synthesis, antiviral, cytotoxic and cytostatic evaluation of N 1-(phosphonoalkyl)uracil derivatives

P2860

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P2860

Virtual screening, selection and development of a benzindolone structural scaffold for inhibition of lumazine synthase

http://www.wikidata.org/entity/Q30494491

description

2010 nî lūn-bûn

@nan

2010 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Virtual screening, selection a ...... nhibition of lumazine synthase

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Virtual screening, selection a ...... nhibition of lumazine synthase

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type

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Virtual screening, selection a ...... nhibition of lumazine synthase

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Virtual screening, selection a ...... nhibition of lumazine synthase

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prefLabel

Virtual screening, selection a ...... nhibition of lumazine synthase

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Virtual screening, selection a ...... nhibition of lumazine synthase

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J.BMC.2010.03.072

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Bioorganic & Medicinal Chemistry

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Virtual screening, selection a ...... nhibition of lumazine synthase

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Arindam Talukdar

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Boris Illarionov

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Jianxin Duan

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Mark Cushman

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Markus Fischer

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Rudolf Ladenstein

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Winfried Meining

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P2860

The atomic structure of pentameric lumazine synthase from Saccharomyces cerevisiae at 1.85 A resolution reveals the binding mode of a phosphonate intermediate analogue

X-ray structure analysis and crystallographic refinement of lumazine synthase from the hyperthermophile Aquifex aeolicus at 1.6 A resolution: determinants of thermostability revealed from structural comparisons

The structural basis of riboflavin binding to Schizosaccharomyces pombe 6,7-dimethyl-8-ribityllumazine synthase

Studies on the reaction mechanism of riboflavin synthase: X-ray crystal structure of a complex with 6-carboxyethyl-7-oxo-8-ribityllumazine

A structure-based model of the reaction catalyzed by lumazine synthase from Aquifex aeolicus

Structure of 3,4-dihydroxy-2-butanone 4-phosphate synthase from Methanococcus jannaschii in complex with divalent metal ions and the substrate ribulose 5-phosphate: implications for the catalytic mechanism

Lumazine synthase from Candida albicans as an anti-fungal target enzyme: structural and biochemical basis for drug design

A new series of N-[2,4-dioxo-6-d-ribitylamino-1,2,3,4-tetrahydropyrimidin-5-yl]oxalamic acid derivatives as inhibitors of lumazine synthase and riboflavin synthase: design, synthesis, biochemical evaluation, crystallography, and mechanistic implicat

ZINC--a free database of commercially available compounds for virtual screening

Studies on the lumazine synthase/riboflavin synthase complex of Bacillus subtilis: crystal structure analysis of reconstituted, icosahedral beta-subunit capsids with bound substrate analogue inhibitor at 2.4 A resolution

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3518-3534

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scholarly article

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10.1016/J.BMC.2010.03.072

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Adelbert Bacher

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Nicolas Foloppe

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