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Analytical Biochemistry|November 5, 2002
Physical methods to determine the binding mode of putative ligands for hepatitis C virus NS3 helicaseRonald W Sarver, Joseph M Rogers, Brian J Stockman, et al.
Acta Crystallographica. Section D, Biological Crystallography|January 15, 2014
Ligand placement based on prior structures: the guided ligand-replacement methodHerbert E Klei, Nigel W Moriarty, Nathaniel Echols, et al.
Journal of Chemical Information and Modeling|July 9, 2011
Conserved core substructures in the overlay of protein-ligand complexesBarry C Finzel, Ramprasad Akavaram, Aravind Ragipindi, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 30, 2022
Human endogenous retrovirus-K (HERV-K) reverse transcriptase (RT) structure and biochemistry reveals remarkable similarities to HIV-1 RT and opportunities for HERV-K-specific inhibitionEric T Baldwin, Matthias Götte, Egor P Tchesnokov, et al.
Acta Crystallographica. Section D, Biological Crystallography|November 28, 2002
Co-crystallization of Staphylococcus aureus peptide deformylase (PDF) with potent inhibitorsMelissa S Harris, Jeffrey H Bock, Gil Choi, et al.
The Journal of Biological Chemistry|June 6, 2002
Crystal structure of type II peptide deformylase from Staphylococcus aureusEric T Baldwin, Melissa S Harris, Anthony W Yem, et al.
Protein Expression and Purification|June 14, 2011
Affinity purification of a chimeric nicotinic acetylcholine receptor in the agonist and antagonist bound statesShenping Liu, Merrill S Babcock, Jacob Bode, et al.
The Journal of Biological Chemistry|April 28, 2006
Crystal structure of the herpes simplex virus 1 DNA polymeraseShenping Liu, John D Knafels, Jeanne S Chang, et al.
Bioorganic & Medicinal Chemistry Letters|April 8, 2015
Discovery of new acylaminopyridines as GSK-3 inhibitors by a structure guided in-depth exploration of chemical space around a pyrrolopyridinone corePrasanna Sivaprakasam, Xiaojun Han, Rita L Civiello, et al.
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