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Plos Computational Biology
|
December 18, 2019
Revisiting the "satisfaction of spatial restraints" approach of MODELLER for protein homology modeling
Giacomo Janson, Alessandro Grottesi, Marco Pietrosanto, et al.
Biophysical Journal
|
March 8, 2005
Conformational dynamics of the ligand-binding domain of inward rectifier K channels as revealed by molecular dynamics simulations: toward an understanding of Kir channel gating
Shozeb Haider, Alessandro Grottesi, Benjamin A Hall, et al.
Channels (Austin, Tex.)
|
February 10, 2009
Contribution of the central hydrophobic residue in the PXP motif of voltage-dependent K+ channels to S6 flexibility and gating properties
Paola Imbrici, Alessandro Grottesi, Maria Cristina D'Adamo, et al.
Biochemistry
|
September 28, 2006
Vstx1, a modifier of Kv channel gating, localizes to the interfacial region of lipid bilayers
Daniele Bemporad, Zara A Sands, Chze Ling Wee, et al.
Biochemistry
|
October 23, 2018
Cysteine 180 Is a Redox Sensor Modulating the Activity of Human Pyridoxal 5'-Phosphate Histidine Decarboxylase
Giada Rossignoli, Alessandro Grottesi, Giovanni Bisello, et al.
Proteins
|
November 5, 2004
Early events in protein aggregation: molecular flexibility and hydrophobicity/charge interaction in amyloid peptides as studied by molecular dynamics simulations
Mariacristina Valerio, Alfredo Colosimo, Filippo Conti, et al.
American Journal of Physiology. Cell Physiology
|
April 4, 2008
A Kv channel with an altered activation gate sequence displays both "fast" and "slow" activation kinetics
Alain J Labro, Alessandro Grottesi, Mark S P Sansom, et al.
Proteins
|
July 6, 2023
Conformational response to ligand binding of TMPRSS2, a protease involved in SARS-CoV-2 infection: Insights through computational modeling
Giorgia Frumenzio, Balasubramanian Chandramouli, Neva Besker, et al.
Neuropharmacology
|
March 10, 2016
Voltage-sensor conformation shapes the intra-membrane drug binding site that determines gambierol affinity in Kv channels
Ivan Kopljar, Alessandro Grottesi, Tessa de Block, et al.
The Journal of General Physiology
|
November 26, 2008
Kv channel gating requires a compatible S4-S5 linker and bottom part of S6, constrained by non-interacting residues
Alain J Labro, Adam L Raes, Alessandro Grottesi, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 46) with videos related to
Sort By:
Page
of 5
Plos Computational Biology
|
December 18, 2019
Revisiting the "satisfaction of spatial restraints" approach of MODELLER for protein homology modeling
Giacomo Janson, Alessandro Grottesi, Marco Pietrosanto, et al.
Biophysical Journal
|
March 8, 2005
Conformational dynamics of the ligand-binding domain of inward rectifier K channels as revealed by molecular dynamics simulations: toward an understanding of Kir channel gating
Shozeb Haider, Alessandro Grottesi, Benjamin A Hall, et al.
Channels (Austin, Tex.)
|
February 10, 2009
Contribution of the central hydrophobic residue in the PXP motif of voltage-dependent K+ channels to S6 flexibility and gating properties
Paola Imbrici, Alessandro Grottesi, Maria Cristina D'Adamo, et al.
Biochemistry
|
September 28, 2006
Vstx1, a modifier of Kv channel gating, localizes to the interfacial region of lipid bilayers
Daniele Bemporad, Zara A Sands, Chze Ling Wee, et al.
Biochemistry
|
October 23, 2018
Cysteine 180 Is a Redox Sensor Modulating the Activity of Human Pyridoxal 5'-Phosphate Histidine Decarboxylase
Giada Rossignoli, Alessandro Grottesi, Giovanni Bisello, et al.
Proteins
|
November 5, 2004
Early events in protein aggregation: molecular flexibility and hydrophobicity/charge interaction in amyloid peptides as studied by molecular dynamics simulations
Mariacristina Valerio, Alfredo Colosimo, Filippo Conti, et al.
American Journal of Physiology. Cell Physiology
|
April 4, 2008
A Kv channel with an altered activation gate sequence displays both "fast" and "slow" activation kinetics
Alain J Labro, Alessandro Grottesi, Mark S P Sansom, et al.
Proteins
|
July 6, 2023
Conformational response to ligand binding of TMPRSS2, a protease involved in SARS-CoV-2 infection: Insights through computational modeling
Giorgia Frumenzio, Balasubramanian Chandramouli, Neva Besker, et al.
Neuropharmacology
|
March 10, 2016
Voltage-sensor conformation shapes the intra-membrane drug binding site that determines gambierol affinity in Kv channels
Ivan Kopljar, Alessandro Grottesi, Tessa de Block, et al.
The Journal of General Physiology
|
November 26, 2008
Kv channel gating requires a compatible S4-S5 linker and bottom part of S6, constrained by non-interacting residues
Alain J Labro, Adam L Raes, Alessandro Grottesi, et al.
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of 5