Found: 14
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NADPH oxidase (NOX) isoforms are inhibited by celastrol with a dual mode of action.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Structure‐based drug design and in vitro testing reveal new inhibitors of enoyl‐acyl carrier protein reductases.
- Published in:
- Chemical Biology & Drug Design, 2019, v. 94, n. 2, p. 1545, doi. 10.1111/cbdd.13536
- By:
- Publication type:
- Article
Temperature-Dependent NMR and CD Spectra of β-Peptides: On the Thermal Stability of β-Peptide Helices - Is the Folding Process of β-Peptides Non-cooperative?
- Published in:
- Helvetica Chimica Acta, 1999, v. 82, n. 1, p. 1, doi. 10.1002/(SICI)1522-2675(19990113)82:1<1::AID-HLCA1>3.0.CO;2-N
- By:
- Publication type:
- Article
Crystal Structures of T. b. rhodesiense Adenosine Kinase Complexed with Inhibitor and Activator: Implications for Catalysis and Hyperactivation.
- Published in:
- PLoS Neglected Tropical Diseases, 2011, v. 5, n. 5, p. 1, doi. 10.1371/journal.pntd.0001164
- By:
- Publication type:
- Article
Crystal Structures of T. b. rhodesiense Adenosine Kinase Complexed with Inhibitor and Activator: Implications for Catalysis and Hyperactivation.
- Published in:
- PLoS Neglected Tropical Diseases, 2011, v. 5, n. 5, p. 1, doi. 10.1371/journal.pntd.0001164
- By:
- Publication type:
- Article
Adenosine Kinase of T. b. rhodesiense Identified as the Putative Target of 4-[5-(4-phenoxyphenyl)-2H-pyrazol-3-yl]morpholine Using Chemical Proteomics.
- Published in:
- PLoS Neglected Tropical Diseases, 2009, v. 3, n. 8, p. 1, doi. 10.1371/journal.pntd.0000506
- By:
- Publication type:
- Article
Adenosine Kinase of T. b. rhodesiense Identified as the Putative Target of 4-[5-(4-phenoxyphenyl)-2H-pyrazol-3- yl]morpholine Using Chemical Proteomics.
- Published in:
- PLoS Neglected Tropical Diseases, 2009, v. 3, n. 8, p. 1, doi. 10.1371/journal.pntd.0000506
- By:
- Publication type:
- Article
The crystal structure of PfFabZ, the unique β-hydroxyacyl-ACP dehydratase involved in fatty acid biosynthesis of Plasmodium falciparum.
- Published in:
- Protein Science: A Publication of the Protein Society, 2005, v. 14, n. 6, p. 1570, doi. 10.1110/ps.051373005
- By:
- Publication type:
- Article
Targeting RNA structure in SMN2 reverses spinal muscular atrophy molecular phenotypes.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-04110-1
- By:
- Publication type:
- Article
Naphthoquinone Derivatives Exert Their Antitrypanosomal Activity via a Multi-Target Mechanism.
- Published in:
- PLoS Neglected Tropical Diseases, 2013, v. 7, n. 1, p. 1, doi. 10.1371/journal.pntd.0002012
- By:
- Publication type:
- Article
Calpain-mediated cleavage of Atg5 switches autophagy to apoptosis.
- Published in:
- Nature Cell Biology, 2006, v. 8, n. 10, p. 1124, doi. 10.1038/ncb1482
- By:
- Publication type:
- Article
Nucleoside binding site of Herpes simplex type 1 thymidine kinase analyzed by X-ray crystallography.
- Published in:
- Proteins, 2000, v. 41, n. 4, p. 545, doi. 10.1002/1097-0134(20001201)41:4<545::AID-PROT110>3.0.CO;2-8
- By:
- Publication type:
- Article
From compound to target: chemical proteomics and in silico screening identify Hsp90 and CDPK2 as putative targets in Plasmodium falciparum.
- Published in:
- 2012
- By:
- Publication type:
- Abstract
The periplasmic domain of the histidine autokinase CitA functions as a highly specific citrate receptor.
- Published in:
- Molecular Microbiology, 1999, v. 33, n. 4, p. 858, doi. 10.1046/j.1365-2958.1999.01536.x
- By:
- Publication type:
- Article