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Sorcin in Cancer Development and Chemotherapeutic Drug Resistance.
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- Cancers, 2024, v. 16, n. 16, p. 2810, doi. 10.3390/cancers16162810
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- Article
Structural basis of Sorcin-mediated calcium-dependent signal transduction.
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- Scientific Reports, 2015, p. 16828, doi. 10.1038/srep16828
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- Article
Structure-based discovery of the first non-covalent inhibitors of Leishmania major tryparedoxin peroxidase by high throughput docking.
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- Scientific Reports, 2015, p. 9705, doi. 10.1038/srep09705
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The phosphoglycerate kinase 1 variants found in carcinoma cells display different catalytic activity and conformational stability compared to the native enzyme.
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- PLoS ONE, 2018, v. 13, n. 7, p. 1, doi. 10.1371/journal.pone.0199191
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- Article
Identification of the pyridoxal 5′‐phosphate allosteric site in human pyridox(am)ine 5′‐phosphate oxidase.
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- Protein Science: A Publication of the Protein Society, 2024, v. 33, n. 2, p. 1, doi. 10.1002/pro.4900
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- Article
Targeting Trypanothione Reductase, a Key Enzyme in the Redox Trypanosomatid Metabolism, to Develop New Drugs against Leishmaniasis and Trypanosomiases.
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- Molecules, 2020, v. 25, n. 8, p. 1924, doi. 10.3390/molecules25081924
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Sorcin, a Calcium Binding Protein Involved in the Multidrug Resistance Mechanisms in Cancer Cells.
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- Molecules, 2014, v. 19, n. 9, p. 13976, doi. 10.3390/molecules190913976
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Investigation of the Entry Pathway and Molecular Nature of σ1 Receptor Ligands.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 7, p. 6367, doi. 10.3390/ijms24076367
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Known Drugs Identified by Structure-Based Virtual Screening Are Able to Bind Sigma-1 Receptor and Increase Growth of Huntington Disease Patient-Derived Cells.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 3, p. 1293, doi. 10.3390/ijms22031293
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Spiro-containing derivatives show antiparasitic activity against Trypanosoma brucei through inhibition of the trypanothione reductase enzyme.
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- PLoS Neglected Tropical Diseases, 2020, p. 1, doi. 10.1371/journal.pntd.0008339
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The Crystal Structures of the Tryparedoxin-Tryparedoxin Peroxidase Couple Unveil the Structural Determinants of Leishmania Detoxification Pathway.
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- PLoS Neglected Tropical Diseases, 2012, v. 6, n. 8, p. 1, doi. 10.1371/journal.pntd.0001781
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- Article
The Crystal Structures of the Tryparedoxin-Tryparedoxin Peroxidase Couple Unveil the Structural Determinants of Leishmania Detoxification Pathway.
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- PLoS Neglected Tropical Diseases, 2012, v. 6, n. 8, p. 1, doi. 10.1371/journal.pntd.0001781
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- Article
Folding propensity of anoplin: A molecular dynamics study of the native peptide and four mutated isoforms.
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- Biopolymers, 2015, v. 103, n. 12, p. 692, doi. 10.1002/bip.22714
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The Crystal Structure of <i>Giardia duodenalis</i> 14-3-3 in the Apo Form: When Protein Post-Translational Modifications Make the Difference.
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- PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0092902
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Metal-Based Compounds as Prospective Antileishmanial Agents: Inhibition of Trypanothione Reductase by Selected Gold Complexes.
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- ChemMedChem, 2013, v. 8, n. 10, p. 1634, doi. 10.1002/cmdc.201300276
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- Article
Inhibition of Leishmania infantum Trypanothione Reductase by Azole-Based Compounds: a Comparative Analysis with Its Physiological Substrate by X-ray Crystallography.
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- ChemMedChem, 2013, v. 8, n. 7, p. 1175, doi. 10.1002/cmdc.201300176
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The X-ray structure of N-methyltryptophan oxidase reveals the structural determinants of substrate specificity.
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- Proteins, 2008, v. 71, n. 4, p. 2065, doi. 10.1002/prot.21898
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Crystal structure of a family 16 endoglucanase from the hyperthermophile Pyrococcus furiosus– structural basis of substrate recognition.
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- FEBS Journal, 2009, v. 276, n. 4, p. 1048, doi. 10.1111/j.1742-4658.2008.06848.x
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Re-Discovery of Giardiavirus : Genomic and Functional Analysis of Viruses from Giardia duodenalis Isolates.
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- Biomedicines, 2021, v. 9, n. 6, p. 654, doi. 10.3390/biomedicines9060654
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Roles of Sorcin in Drug Resistance in Cancer: One Protein, Many Mechanisms, for a Novel Potential Anticancer Drug Target.
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- Cancers, 2020, v. 12, n. 4, p. 887, doi. 10.3390/cancers12040887
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Identification and binding mode of a novel Leishmania Trypanothione reductase inhibitor from high throughput screening.
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- PLoS Neglected Tropical Diseases, 2018, v. 12, n. 11, p. 1, doi. 10.1371/journal.pntd.0006969
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Huntingtin Ubiquitination Mechanisms and Novel Possible Therapies to Decrease the Toxic Effects of Mutated Huntingtin.
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- Journal of Personalized Medicine, 2021, v. 11, n. 12, p. 1309, doi. 10.3390/jpm11121309
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Short peptides from leucyl-tRNA synthetase rescue disease-causing mitochondrial tRNA point mutations.
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- Human Molecular Genetics, 2016, v. 25, n. 5, p. 903, doi. 10.1093/hmg/ddv619
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Structure-guided approach to identify a novel class of anti-leishmaniasis diaryl sulfide compounds targeting the trypanothione metabolism.
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- Amino Acids, 2020, v. 52, n. 2, p. 247, doi. 10.1007/s00726-019-02731-4
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Glucose transportation in the brain and its impairment in Huntington disease: one more shade of the energetic metabolism failure?
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- Amino Acids, 2017, v. 49, n. 7, p. 1147, doi. 10.1007/s00726-017-2417-2
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A gold-containing drug against parasitic polyamine metabolism: the X-ray structure of trypanothione reductase from Leishmania infantum in complex with auranofin reveals a dual mechanism of enzyme inhibition.
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- Amino Acids, 2012, v. 42, n. 2/3, p. 803, doi. 10.1007/s00726-011-0997-9
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Structure and metal‐binding properties of PA4063, a novel player in periplasmic zinc trafficking by Pseudomonas aeruginosa.
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- Acta Crystallographica: Section D, Structural Biology, 2021, v. 77, n. 11, p. 1401, doi. 10.1107/S2059798321009608
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The structure of maize polyamine oxidase K300M mutant in complex with the natural substrates provides a snapshot of the catalytic mechanism of polyamine oxidation.
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- FEBS Journal, 2011, v. 278, n. 5, p. 809, doi. 10.1111/j.1742-4658.2010.08000.x
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- Article