Rajeevan Selvaratnam
Affiliations: | University of Minnesota, Twin Cities, Minneapolis, MN |
Area:
Clinical ChemistryGoogle:
"Rajeevan Selvaratnam"Mean distance: 9.32 | S | N | B | C | P |
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Publications
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Mohamed H, Baryar U, Bashiri A, et al. (2022) Identification of Core Allosteric Sites through Temperature- and Nucleus-Invariant Chemical Shift Covariance. Biophysical Journal |
Boulton S, Selvaratnam R, Ahmed R, et al. (2019) Mechanisms of Specific versus Nonspecific Interactions of Aggregation-Prone Inhibitors and Attenuators. Journal of Medicinal Chemistry |
Boulton S, Selvaratnam R, Blondeau JP, et al. (2018) Mechanism of Selective Enzyme Inhibition through Uncompetitive Regulation of an Allosteric Agonist. Journal of the American Chemical Society |
Boulton S, Selvaratnam R, Ahmed R, et al. (2018) Implementation of the NMR CHEmical Shift Covariance Analysis (CHESCA): A Chemical Biologist's Approach to Allostery. Methods in Molecular Biology (Clifton, N.J.). 1688: 391-405 |
VanSchouwen B, Selvaratnam R, Giri R, et al. (2015) Mechanism of cAMP Partial Agonism in Protein Kinase G (PKG). The Journal of Biological Chemistry |
Boulton S, Akimoto M, Selvaratnam R, et al. (2015) A Tool Set to Map Dynamic Allosteric Networks through the NMR Chemical Shift Covariance Analysis (CHESCA) Biophysical Journal. 108: 60a |
Boulton S, Akimoto M, Selvaratnam R, et al. (2014) A tool set to map allosteric networks through the NMR chemical shift covariance analysis. Scientific Reports. 4: 7306 |
Akimoto M, Zhang Z, Boulton S, et al. (2014) A mechanism for the auto-inhibition of hyperpolarization-activated cyclic nucleotide-gated (HCN) channel opening and its relief by cAMP Journal of Biological Chemistry. 289: 22205-22220 |
Boulton S, Akimoto M, VanSchouwen B, et al. (2014) Tapping the translation potential of cAMP signalling: molecular basis for selectivity in cAMP agonism and antagonism as revealed by NMR. Biochemical Society Transactions. 42: 302-7 |
Akimoto M, Moleschi K, Boulton S, et al. (2014) Allosteric linkers in cAMP signalling. Biochemical Society Transactions. 42: 139-44 |