[NMR paper] Targeting the cryptic sites: NMR-based strategy to improve protein druggability by controlling the conformational equilibrium.
Targeting the cryptic sites: NMR-based strategy to improve protein druggability by controlling the conformational equilibrium.
http://www.bionmr.com//www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--highwire.stanford.edu-icons-externalservices-pubmed-advances.gif Targeting the cryptic sites: NMR-based strategy to improve protein druggability by controlling the conformational equilibrium.
Sci Adv. 2020 Sep;6(40):
Authors: Mizukoshi Y, Takeuchi K, Tokunaga Y, Matsuo H, Imai M, Fujisaki M, Kamoshida H, Takizawa T, Hanzawa H, Shimada I
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A persulfidation-based mechanism controls aquaporin-8 conductance - Science Advances
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A persulfidation-based mechanism controls aquaporin-8 conductance
Science Advances
1Protein Transport and Secretion Unit, Division of Genetics and Cell Biology, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Ospedale San Raffaele, UniversitÃ* Vita-Salute San Raffaele, 20132 Milan, Italy. 2Biomolecular Nuclear Magnetic ...
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A persulfidation-based mechanism controls aquaporin-8 conductance - Science Advances
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[NMR paper] Characterization of conformational dynamics of bistable RNA by equilibrium and non-equilibrium NMR.
Characterization of conformational dynamics of bistable RNA by equilibrium and non-equilibrium NMR.
Characterization of conformational dynamics of bistable RNA by equilibrium and non-equilibrium NMR.
Curr Protoc Nucleic Acid Chem. 2014;55:11.13.1-11.13.16
Authors: Fürtig B, Reining A, Sochor F, Oberhauser EM, Heckel A, Schwalbe H
Abstract
Unlike proteins, a given RNA sequence can adopt more than a single conformation. The two (or more) conformations are long-lived and have similar stabilities, but interconvert only slowly. Such...
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01-30-2015 12:15 PM
[NMR paper] Druggability indices for protein targets derived from NMR-based screening data.
Druggability indices for protein targets derived from NMR-based screening data.
Related Articles Druggability indices for protein targets derived from NMR-based screening data.
J Med Chem. 2005 Apr 7;48(7):2518-25
Authors: Hajduk PJ, Huth JR, Fesik SW
An analysis of heteronuclear-NMR-based screening data is used to derive relationships between the ability of small molecules to bind to a protein and various parameters that describe the protein binding site. It is found that a simple model including terms for polar and apolar surface area,...