Virtual Screening for UDP-Galactopyranose Mutase Ligands Identifies a New Class of Antimycobacterial Agents - Test2 - elhamkhani - TriplyDB

Virtual Screening for UDP-Galactopyranose Mutase Ligands Identifies a New Class of Antimycobacterial Agents

Virtual Screening for UDP-Galactopyranose Mutase Ligands Identifies a New Class of Antimycobacterial Agents

http://www.wikidata.org/entity/Q27657362

about

OpenZika: An IBM World Community Grid Project to Accelerate Zika Virus Drug Discovery In Silico Exploration for Novel Type-I Inhibitors of Tie-2/TEK: The Performance of Different Selection Strategy in Selecting Virtual Screening Candidates Bioinformatics and Drug Discovery.Computational Methods Applied to Rational Drug Design.Comparing Galactan Biosynthesis in Mycobacterium tuberculosis and Corynebacterium diphtheriae.Carboxylate Surrogates Enhance the Antimycobacterial Activity of UDP-Galactopyranose Mutase Probes.Natural and Synthetic Flavonoids as Potent Mycobacterium tuberculosis UGM Inhibitors.Conformational Control of UDP-Galactopyranose Mutase Inhibition.A Second, Druggable Binding Site in UDP-Galactopyranose Mutase from Mycobacterium tuberculosis?Deleterious Consequences of UDP-Galactopyranose Mutase Inhibition for Nematodes.Identification of inhibitors targeting Mycobacterium tuberculosis cell wall biosynthesis via dynamic combinatorial chemistry.

P2860

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P2860

Virtual Screening for UDP-Galactopyranose Mutase Ligands Identifies a New Class of Antimycobacterial Agents

http://www.wikidata.org/entity/Q27657362

description

2015 nî lūn-bûn

@nan

2015 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2015 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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Virtual Screening for UDP-Gala ...... ss of Antimycobacterial Agents

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Virtual Screening for UDP-Gala ...... ss of Antimycobacterial Agents

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ACSCHEMBIO.5B00370

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ACS Chemical Biology

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Virtual Screening for UDP-Gala ...... ss of Antimycobacterial Agents

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Adel M Talaat

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Annie Héroux

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Brian K Shoichet

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Katrina T Forest

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Lyudmila Nedyalkova

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Virginia A Kincaid

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P2860

A Common Mechanism Underlying Promiscuous Inhibitors from Virtual and High-Throughput Screening

Hierarchical docking of databases of multiple ligand conformations

UDP-galactopyranose mutase has a novel structure and mechanism

Comprehensive Mechanistic Analysis of Hits from High-Throughput and Docking Screens against β-Lactamase

Ligand Binding and Substrate Discrimination by UDP-Galactopyranose Mutase

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

X-ray crystallography reveals a reduced substrate complex of UDP-galactopyranose mutase poised for covalent catalysis by flavin

Structural basis of substrate binding to UDP-galactopyranose mutase: crystal structures in the reduced and oxidized state complexed with UDP-galactopyranose and UDP

Complementarity Between a Docking and a High-Throughput Screen in Discovering New Cruzain Inhibitors

Chemoenzymatic synthesis, inhibition studies, and X-ray crystallographic analysis of the phosphono analog of UDP-Galp as an inhibitor and mechanistic probe for UDP-galactopyranose mutase

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2209-2218

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scholarly article

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2889492

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10.1021/ACSCHEMBIO.5B00370

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10

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10

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Laura Lee Kiessling

Kittikhun Wangkanont

Darryl A Wesener

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2015-10-16T00:00:00Z

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26214585

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4669066

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