Sunhwan Jo to Humans
This is a "connection" page, showing publications Sunhwan Jo has written about Humans.
Connection Strength
0.089
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CHARMM-GUI 10 years for biomolecular modeling and simulation. J Comput Chem. 2017 06 05; 38(15):1114-1124.
Score: 0.019
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CHARMM-GUI PDB manipulator for advanced modeling and simulations of proteins containing nonstandard residues. Adv Protein Chem Struct Biol. 2014; 96:235-65.
Score: 0.017
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H(1) antihistamine drug promethazine directly blocks hERG K(+) channel. Pharmacol Res. 2009 Nov; 60(5):429-37.
Score: 0.012
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Identification and characterization of fragment binding sites for allosteric ligand design using the site identification by ligand competitive saturation hotspots approach (SILCS-Hotspots). Biochim Biophys Acta Gen Subj. 2020 04; 1864(4):129519.
Score: 0.006
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Exploring protein-protein interactions using the site-identification by ligand competitive saturation methodology. Proteins. 2019 04; 87(4):289-301.
Score: 0.006
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CHARMM-GUI Membrane Builder for Complex Biological Membrane Simulations with Glycolipids and Lipoglycans. J Chem Theory Comput. 2019 Jan 08; 15(1):775-786.
Score: 0.006
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Roles of glycans in interactions between gp120 and HIV broadly neutralizing antibodies. Glycobiology. 2016 Mar; 26(3):251-60.
Score: 0.005
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GS-align for glycan structure alignment and similarity measurement. Bioinformatics. 2015 Aug 15; 31(16):2653-9.
Score: 0.004
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Application of binding free energy calculations to prediction of binding modes and affinities of MDM2 and MDMX inhibitors. J Chem Inf Model. 2012 Jul 23; 52(7):1821-32.
Score: 0.004
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An ensemble dynamics approach to decipher solid-state NMR observables of membrane proteins. Biochim Biophys Acta. 2012 Feb; 1818(2):252-62.
Score: 0.003
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Novel pyrrolopyrimidine-based a-helix mimetics: cell-permeable inhibitors of protein-protein interactions. J Am Chem Soc. 2011 Feb 02; 133(4):676-9.
Score: 0.003
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Papaverine, a vasodilator, blocks the pore of the HERG channel at submicromolar concentration. J Cardiovasc Pharmacol. 2008 Dec; 52(6):485-93.
Score: 0.003
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A novel hypothesis for the binding mode of HERG channel blockers. Biochem Biophys Res Commun. 2006 May 26; 344(1):72-8.
Score: 0.002