The AEROPATH project targetingPseudomonas aeruginosa: crystallographic studies for assessment of potential targets in early-stage drug discovery

The AEROPATH project targetingPseudomonas aeruginosa: crystallographic studies for assessment of potential targets in early-stage drug discovery

Item
http://www.wikidata.org/entity/Q27675787
Structure ofPseudomonas aeruginosainosine 5′-monophosphate dehydrogenaseStructural Insights into the UbiD Protein Family from the Crystal Structure of PA0254 from Pseudomonas aeruginosaStructure of diaminohydroxyphosphoribosylaminopyrimidine deaminase/5-amino-6-(5-phosphoribosylamino)uracil reductase fromAcinetobacter baumanniiSubstrate Channel Flexibility in Pseudomonas aeruginosa MurB Accommodates Two Distinct SubstratesDiscovery of an Allosteric Inhibitor Binding Site in 3-Oxo-acyl-ACP Reductase from Pseudomonas aeruginosaHigh-resolution structure of the M14-type cytosolic carboxypeptidase fromBurkholderia cenocepaciarefined exploitingPDB_REDOstrategiesHigh-resolution structure of a papaya plant-defense barwin-like protein solved by in-house sulfur-SAD phasingCrystallographic studies of two variants of Pseudomonas aeruginosa IMPDH with impaired allosteric regulationTo Hit or Not to Hit, That Is the Question - Genome-wide Structure-Based Druggability Predictions for Pseudomonas aeruginosa ProteinsCrystal structure of the flavoenzyme PA4991 from Pseudomonas aeruginosaAgainst the odds? De novo structure determination of a pilin with two cysteine residues by sulfur SAD.The bacterial septal ring protein RlpA is a lytic transglycosylase that contributes to rod shape and daughter cell separation in Pseudomonas aeruginosaGuanine nucleotide binding to the Bateman domain mediates the allosteric inhibition of eukaryotic IMP dehydrogenases.Lytic transglycosylases: concinnity in concision of the bacterial cell wall.Open and compressed conformations of Francisella tularensis ClpP.Novel drug targets in cell wall biosynthesis exploited by gene disruption in Pseudomonas aeruginosa.Structures of Pseudomonas aeruginosa β-ketoacyl-(acyl-carrier-protein) synthase II (FabF) and a C164Q mutant provide templates for antibacterial drug discovery and identify a buried potassium ion and a ligand-binding site that is an artefact of the
P2860

The AEROPATH project targetingPseudomonas aeruginosa: crystallographic studies for assessment of potential targets in early-stage drug discovery

Item
http://www.wikidata.org/entity/Q27675787
description
2013 nî lūn-bûn
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2013 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2013年の論文
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2013年論文
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2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
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2013年論文
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2013年论文
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name
The AEROPATH project targeting ...... in early-stage drug discovery
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The AEROPATH project targeting ...... in early-stage drug discovery
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The AEROPATH project targeting ...... in early-stage drug discovery
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The AEROPATH project targeting ...... in early-stage drug discovery
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The AEROPATH project targeting ...... in early-stage drug discovery
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The AEROPATH project targeting ...... in early-stage drug discovery
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The AEROPATH project targeting ...... in early-stage drug discovery
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The AEROPATH project targeting ...... in early-stage drug discovery
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The AEROPATH project targeting ...... in early-stage drug discovery
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P1433
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P2093
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The AEROPATH project targeting ...... in early-stage drug discovery
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P2093
P2860
P304
P31
P356
P433
P478
P50
P577
P5875
P698
P921
P932