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Controlled Construction of Cyclic d / l Peptide Nanorods.
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- Angewandte Chemie, 2019, v. 131, n. 2, p. 606, doi. 10.1002/ange.201811910
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- Article
Application of Fragment-Based Screening to the Design of Inhibitors of Escherichia coli DsbA.
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- Angewandte Chemie, 2015, v. 127, n. 7, p. 2207, doi. 10.1002/ange.201410341
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- Article
Conserved features in TamA enable interaction with TamB to drive the activity of the translocation and assembly module.
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- Scientific Reports, 2015, p. 12905, doi. 10.1038/srep12905
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- Article
Redox-stable cyclic peptide inhibitors of the SPSB2-iNOS interaction.
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- FEBS Letters, 2016, v. 590, n. 6, p. 696, doi. 10.1002/1873-3468.12115
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- Article
<sup>19</sup>F NMR as a Probe of Ligand Interactions with the iNOS Binding site of SPRY Domain-Containing SOCS Box Protein 2.
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- Chemical Biology & Drug Design, 2014, v. 84, n. 5, p. 616, doi. 10.1111/cbdd.12355
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- Article
The Fragment-Based Development of a Benzofuran Hit as a New Class of Escherichia coli DsbA Inhibitors.
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- Molecules, 2019, v. 24, n. 20, p. 3756, doi. 10.3390/molecules24203756
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- Article
Targeting Bacterial Dsb Proteins for the Development of Anti-Virulence Agents.
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- Molecules, 2016, v. 21, n. 7, p. 811, doi. 10.3390/molecules21070811
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- Article
Fragment-Based Discovery of Inhibitors of the Bacterial DnaG-SSB Interaction.
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- Antibiotics (2079-6382), 2018, v. 7, n. 1, p. 14, doi. 10.3390/antibiotics7010014
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- Article
Neurokinin 1 receptor signaling in endosomes mediates sustained nociception and is a viable therapeutic target for prolonged pain relief.
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- Science Translational Medicine, 2017, v. 9, n. 392, p. 1, doi. 10.1126/scitranslmed.aal3447
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- Article
Fluoromethylketone‐Fragment Conjugates Designed as Covalent Modifiers of EcDsbA are Atypical Substrates.
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- ChemMedChem, 2024, v. 19, n. 16, p. 1, doi. 10.1002/cmdc.202300684
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- Article
Selective Binding of Small Molecules to Vibrio cholerae DsbA Offers a Starting Point for the Design of Novel Antibacterials.
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- ChemMedChem, 2022, v. 17, n. 6, p. 1, doi. 10.1002/cmdc.202100673
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- Article
Identification of the Binding Site of Apical Membrane Antigen 1 (AMA1) Inhibitors Using a Paramagnetic Probe.
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- ChemMedChem, 2019, v. 14, n. 5, p. 603, doi. 10.1002/cmdc.201800802
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- Article
Cyclic Hexapeptide Mimics of the LEDGF Integrase Recognition Loop in Complex with HIV‐1 Integrase.
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- ChemMedChem, 2018, v. 13, n. 15, p. 1555, doi. 10.1002/cmdc.201800129
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- Publication type:
- Article
Application of Fragment-Based Screening to the Design of Inhibitors of Escherichia coli DsbA.
- Published in:
- Angewandte Chemie International Edition, 2015, v. 54, n. 7, p. 2179, doi. 10.1002/anie.201410341
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- Publication type:
- Article
Controlled Construction of Cyclic d / l Peptide Nanorods.
- Published in:
- Angewandte Chemie International Edition, 2019, v. 58, n. 2, p. 596, doi. 10.1002/anie.201811910
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- Publication type:
- Article
Fatty Acid-Binding Protein 5 at the Blood–Brain Barrier Regulates Endogenous Brain Docosahexaenoic Acid Levels and Cognitive Function.
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- Journal of Neuroscience, 2016, v. 36, n. 46, p. 11755, doi. 10.1523/JNEUROSCI.1583-16.2016
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- Article
NMR fragment screening reveals a novel small molecule binding site near the catalytic surface of the disulfide–dithiol oxidoreductase enzyme DsbA from Burkholderia pseudomallei.
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- Journal of Biomolecular NMR, 2020, v. 74, n. 10/11, p. 595, doi. 10.1007/s10858-020-00339-5
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- Article
Colloidal characteristics and formulation of pure protein particulate vaccines.
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- Journal of Pharmacy & Pharmacology, 2012, v. 64, n. 10, p. 1386, doi. 10.1111/j.2042-7158.2012.01513.x
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- Article
Molecular Insights into the Interaction Between the SPRY Domain-Containing SOCS Box Protein SPSB2 and Peptides Based on the Binding Motif from iNOS.
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- Australian Journal of Chemistry, 2017, v. 70, n. 2, p. 191, doi. 10.1071/CH16510
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- Article
Propargyloxyproline Regio- and Stereoisomers for Click-Conjugation of Peptides: Synthesis and Application in Linear and Cyclic Peptides.
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- Australian Journal of Chemistry, 2015, v. 68, n. 9, p. 1365, doi. 10.1071/CH15146
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- Article
Blind Man's Bluff - Elaboration of Fragment Hits in the Absence of Structure for the Development of Antitrypsin Deficiency Inhibitors.
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- Australian Journal of Chemistry, 2013, v. 66, n. 12, p. 1525, doi. 10.1071/CH13290
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- Article
Detection and Prevention of Aggregation-based False Positives in STD-NMR-based Fragment Screening.
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- Australian Journal of Chemistry, 2013, v. 66, n. 12, p. 1518, doi. 10.1071/CH13286
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- Article
Design and Evaluation of the Performance of an NMR Screening Fragment Library.
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- Australian Journal of Chemistry, 2013, v. 66, n. 12, p. 1465, doi. 10.1071/CH13280
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- Article
Interrogating Fragments Using a Protein Thermal Shift Assay.
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- Australian Journal of Chemistry, 2013, v. 66, n. 12, p. 1502, doi. 10.1071/CH13279
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- Article
Development of Inhibitors of Plasmodium falciparum Apical Membrane Antigen 1 Based on Fragment Screening.
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- Australian Journal of Chemistry, 2013, v. 66, n. 12, p. 1530, doi. 10.1071/CH13266
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- Article
Molecular Insights into the Interaction between Plasmodium falciparum Apical Membrane Antigen 1 and an Invasion-Inhibitory Peptide.
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- PLoS ONE, 2014, v. 9, n. 10, p. 1, doi. 10.1371/journal.pone.0109674
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- Article
The Role of Oxidoreductases in Determining the Function of the Neisserial Lipid A Phosphoethanolamine Transferase Required for Resistance to Polymyxin.
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- PLoS ONE, 2014, v. 9, n. 9, p. 1, doi. 10.1371/journal.pone.0106513
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- Article
Comparative Sequence, Structure and Redox Analyses of <i>Klebsiella pneumoniae</i> DsbA Show That Anti-Virulence Target DsbA Enzymes Fall into Distinct Classes.
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- PLoS ONE, 2013, v. 8, n. 11, p. 1, doi. 10.1371/journal.pone.0080210
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- Article
Production, biophysical characterization and initial crystallization studies of the N‐ and C‐terminal domains of DsbD, an essential enzyme in <italic>Neisseria meningitidis</italic>.
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- Acta Crystallographica: Section F, Structural Biology Communications, 2018, v. 74, n. 1, p. 31, doi. 10.1107/S2053230X17017800
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- Article
Corrigendum: Fragment-Based Design of Ligands Targeting a Novel Site on the Integrase Enzyme of Human Immunodeficiency Virus 1.
- Published in:
- ChemMedChem, 2011, v. 6, n. 4, p. 583, doi. 10.1002/cmdc.201190013
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- Article
Fragment-Based Design of Ligands Targeting a Novel Site on the Integrase Enzyme of Human Immunodeficiency Virus 1.
- Published in:
- ChemMedChem, 2011, v. 6, n. 2, p. 258, doi. 10.1002/cmdc.201000483
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- Article
Targeting virulence not viability in the search for future antibacterials.
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- British Journal of Clinical Pharmacology, 2015, v. 79, n. 2, p. 208, doi. 10.1111/bcp.12356
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- Article
Solution NMR characterization of apical membrane antigen 1 and small molecule interactions as a basis for designing new antimalarials.
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- Journal of Molecular Recognition, 2016, v. 29, n. 6, p. 281, doi. 10.1002/jmr.2529
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- Article
Solution structure and DNA binding of the catalytic domain of the large serine resolvase TnpX.
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- Journal of Molecular Recognition, 2015, v. 28, n. 5, p. 316, doi. 10.1002/jmr.2446
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- Article
Fragment library screening identifies hits that bind to the non-catalytic surface of Pseudomonas aeruginosa DsbA1.
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- PLoS ONE, 2017, v. 12, n. 3, p. 1, doi. 10.1371/journal.pone.0173436
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- Article
Dietary docosahexaenoic acid supplementation enhances expression of fatty acid‐binding protein 5 at the blood–brain barrier and brain docosahexaenoic acid levels.
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- Journal of Neurochemistry, 2018, v. 146, n. 2, p. 186, doi. 10.1111/jnc.14342
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- Publication type:
- Article
Reduced blood-brain barrier expression of fatty acid-binding protein 5 is associated with increased vulnerability of APP/PS1 mice to cognitive deficits from low omega-3 fatty acid diets.
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- Journal of Neurochemistry, 2018, v. 144, n. 1, p. 81, doi. 10.1111/jnc.14249
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- Article
Identification and characterization of two drug‐like fragments that bind to the same cryptic binding pocket of Burkholderia pseudomallei DsbA.
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- Acta Crystallographica: Section D, Structural Biology, 2022, v. 78, n. 1, p. 75, doi. 10.1107/S2059798321011475
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- Article
Methyl probes in proteins for determining ligand binding mode in weak protein–ligand complexes.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-13561-y
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- Article
A novel two-chain proteinase inhibitor generated by circularization of a multidomain precursor protein.
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- Nature Structural Biology, 1999, v. 6, n. 6, p. 526
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- Article
DSB proteins and bacterial pathogenicity.
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- Nature Reviews Microbiology, 2009, v. 7, n. 3, p. 215, doi. 10.1038/nrmicro2087
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- Article
Novel small molecules that increase the susceptibility of Neisseria gonorrhoeae to cationic antimicrobial peptides by inhibiting lipid A phosphoethanolamine transferase.
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- Journal of Antimicrobial Chemotherapy (JAC), 2022, v. 77, n. 9, p. 2441, doi. 10.1093/jac/dkac204
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- Article
Crystal structure of the HIV-1 integrase core domain in complex with sucrose reveals details of an allosteric inhibitory binding site
- Published in:
- FEBS Letters, 2010, v. 584, n. 8, p. 1455, doi. 10.1016/j.febslet.2010.03.016
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- Article