Structural genomics for drug design against the pathogen Coxiella burnetii - Wikidata - awgldk - TriplyDB

Structural genomics for drug design against the pathogen Coxiella burnetii

Structural genomics for drug design against the pathogen Coxiella burnetii

http://www.wikidata.org/entity/Q27700949

about

Loss of the RNA-binding protein TACO1 causes late-onset mitochondrial dysfunction in mice The SCP2-thiolase-like protein (SLP) of Trypanosoma brucei is an enzyme involved in lipid metabolism Resistance gene identification from Larimichthys crocea with machine learning techniques.GMP Synthase Is Required for Virulence Factor Production and Infection by Cryptococcus neoformans.Inhibition of homologous phosphorolytic ribonucleases by citrate may represent an evolutionarily conserved communicative link between RNA degradation and central metabolism.Ligand co-crystallization of aminoacyl-tRNA synthetases from infectious disease organisms Multiple Substrate Usage of Coxiella burnetii to Feed a Bipartite Metabolic Network.Evolution of plant δ(1)-pyrroline-5-carboxylate reductases from phylogenetic and structural perspectives.Crystal Structure of the Chloroplastic Oxoene Reductase ceQORH from Arabidopsis thaliana Resolving the cofactor-binding site in the proline biosynthetic enzyme human pyrroline-5-carboxylate reductase 1.Analysis of Coxiela burnetti dihydrofolate reductase via in silico docking with inhibitors and molecular dynamics simulation.Structure determination of uracil-DNA N-glycosylase from Deinococcus radiodurans in complex with DNA.Crystallographic analysis of RsmA, a ribosomal RNA small subunit methyltransferase A from Staphylococcus aureus.Active site geometry of a novel aminopropyltransferase for biosynthesis of hyperthermophile-specific branched-chain polyamine.Conformational variability of the stationary phase survival protein E from Xylella fastidiosa revealed by X-ray crystallography, small-angle X-ray scattering studies, and normal mode analysis.8-Mercaptoguanine Derivatives as Inhibitors of Dihydropteroate Synthase.Insights into stabilizing interactions in the distorted domain-swapped dimer of Salmonella typhimurium survival protein.Structural and functional insights into the stationary-phase survival protein SurE, an important virulence factor of Brucella abortus.

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Structural genomics for drug design against the pathogen Coxiella burnetii

http://www.wikidata.org/entity/Q27700949

description

2015 nî lūn-bûn

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2015 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

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2015 թվականի դեկտեմբերին 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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name

Structural genomics for drug design against the pathogen Coxiella burnetii

@ast

Structural genomics for drug design against the pathogen Coxiella burnetii

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Structural genomics for drug design against the pathogen Coxiella burnetii

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type

label

Structural genomics for drug design against the pathogen Coxiella burnetii

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Structural genomics for drug design against the pathogen Coxiella burnetii

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Structural genomics for drug design against the pathogen Coxiella burnetii

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prefLabel

Structural genomics for drug design against the pathogen Coxiella burnetii

@ast

Structural genomics for drug design against the pathogen Coxiella burnetii

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Structural genomics for drug design against the pathogen Coxiella burnetii

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Structural genomics for drug design against the pathogen Coxiella burnetii

@en

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Brandan Hillerich

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Ebony Gary

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Fiana Burshteyn

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James D Love

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Jonah Cheung

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Matthew C Franklin

http://www.w3.org/2001/XMLSchema#string

Maxim Totrov

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Michael Cassidy

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Michael J Rudolph

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P2860

Complete genome sequence of the Q-fever pathogen Coxiella burnetii

Protein production and purification

Host cell-free growth of the Q fever bacterium Coxiella burnetii

The subsystems approach to genome annotation and its use in the project to annotate 1000 genomes

The infectious dose of coxiella burnetii (Q Fever)

Basic local alignment search tool

The ChEMBL bioactivity database: an update

Three-dimensional structure of M. tuberculosis dihydrofolate reductase reveals opportunities for the design of novel tuberculosis drugs

Crystal structure of the anthrax drug target, Bacillus anthracis dihydrofolate reductase

Differential inhibition of class I and class II 5-enolpyruvylshikimate-3-phosphate synthases by tetrahedral reaction intermediate analogues

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2124-2136

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scholarly article

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652920

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10.1002/PROT.24841

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12

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83

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Paul R. Carlier

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2015-12-01T00:00:00Z

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26033498

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