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Results for
""Spider Venoms""[mesh_terms]

9 Results

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Fluorescent- and tagged-protoxin II peptides: potent markers of the Na 1.7 channel pain target.

Michel Partiseti, Rachid Boukaiba, Massimo Mantegazza, Rémy Béroud, Jérôme Montnach, Stephan De Waard, Sébastien Nicolas, Sophie Burel, Nancy Osorio, Claude Zoukimian, Céline Marionneau, Michel De Waard, Patrick Delmas

British journal of pharmacology 2021;178(13):2632-2650

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Spider venoms: a rich source of acylpolyamines and peptides as new leads for CNS drugs.

Elba Villegas, Gerardo Corzo, Georgina Estrada

Natural product reports 2007;24(1):145-61

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Structure and activity analysis of two spider toxins that alter sodium channel inactivation kinetics.

Alessandra Matavel, Cécile Fleury, Leida C Oliveira, Franck Molina, Maria Elena de Lima, Jader S Cruz, Marta N Cordeiro, Michael Richardson, Carlos H I Ramos, Paulo S L Beirão

Biochemistry 2009;48(14):3078-88

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Neonatal Na 1.5 channels: pharmacological distinctiveness of a cancer-related voltage-gated sodium channel splice variant.

Scott P Fraser, Rustem Onkal, Margaux Theys, Frank Bosmans, Mustafa B A Djamgoz

British journal of pharmacology 2022;179(3):473-486

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Combination of Ambiguous and Unambiguous Data in the Restraint-driven Docking of Flexible Peptides with HADDOCK: The Binding of the Spider Toxin PcTx1 to the Acid Sensing Ion Channel (ASIC) 1a.

Evelyne Deplazes, Josephine Davies, Alexandre M J J Bonvin, Glenn F King, Alan E Mark

Journal of chemical information and modeling 2016;56(1):127-38

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Computational reverse-engineering of a spider-venom derived peptide active against Plasmodium falciparum SUB1.

Giacomo Bastianelli, Anthony Bouillon, Christophe Nguyen, Elodie Crublet, Stéphane Pêtres, Olivier Gorgette, Dung Le-Nguyen, Jean-Christophe Barale, Michael Nilges

PloS one 2011;6(7):e21812

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Docking and MD simulations of the interaction of the tarantula peptide psalmotoxin-1 with ASIC1a channels using a homology model.

Francesco Pietra

Journal of chemical information and modeling 2009;49(4):972-7

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Potency-Enhancing Mutations of Gating Modifier Toxins for the Voltage-Gated Sodium Channel Na1.7 Can Be Predicted Using Accurate Free-Energy Calculations.

Dan Sindhikara, Dana Katz, Michael DiMattia, Abba E Leffler

Toxins 2021;13(3):193

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Ion-channel modulators: more diversity than previously thought.

Sébastien Dilly, Cédric Lamy, Neil V Marrion, Jean-François Liégeois, Vincent Seutin

Chembiochem : a European journal of chemical biology 2011;12(12):1808-12

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Results: 1 – 9 / 9

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Results for ""Spider Venoms""[mesh_terms]

Fluorescent- and tagged-protoxin II peptides: potent markers of the Na 1.7 channel pain target.

Spider venoms: a rich source of acylpolyamines and peptides as new leads for CNS drugs.

Structure and activity analysis of two spider toxins that alter sodium channel inactivation kinetics.

Neonatal Na 1.5 channels: pharmacological distinctiveness of a cancer-related voltage-gated sodium channel splice variant.

Combination of Ambiguous and Unambiguous Data in the Restraint-driven Docking of Flexible Peptides with HADDOCK: The Binding of the Spider Toxin PcTx1 to the Acid Sensing Ion Channel (ASIC) 1a.

Computational reverse-engineering of a spider-venom derived peptide active against Plasmodium falciparum SUB1.

Docking and MD simulations of the interaction of the tarantula peptide psalmotoxin-1 with ASIC1a channels using a homology model.

Potency-Enhancing Mutations of Gating Modifier Toxins for the Voltage-Gated Sodium Channel Na1.7 Can Be Predicted Using Accurate Free-Energy Calculations.

Ion-channel modulators: more diversity than previously thought.

Results for
""Spider Venoms""[mesh_terms]