Identification of and Structural Insights into Hit Compounds Targeting N-Myristoyltransferase for Cryptosporidium Drug Development
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Structure-guided discovery of potent human NMT inhibitors a, Structures
Frontiers Mode of action studies confirm on-target engagement of lysyl-tRNA synthetase inhibitor and lead to new selection marker for Cryptosporidium
Rudimentary Structure-Activity-Relationship study of the MMV Pathogen Box compound MMV675968 (2,4-diaminoquinazoline) unveils novel inhibitors of Trypanosoma brucei brucei DHFR enzyme
How To Design Selective Ligands for Highly Conserved Binding Sites: A Case Study Using N-Myristoyltransferases as a Model System
Cellular levels of NMT in T. cruzi life-cycle stages Immunoblots of
Identification of and Structural Insights into Hit Compounds Targeting N- Myristoyltransferase for Cryptosporidium Drug Development
Prioritization of Molecular Targets for Antimalarial Drug Discovery
Identification of and Structural Insights into Hit Compounds Targeting N- Myristoyltransferase for Cryptosporidium Drug Development
PDF) Structure-Based Design of Potent and Selective Leishmania N- Myristoyltransferase Inhibitors
Michael FENWICK, Research Associate, Seattle Structural Genomics Center for Infectious Disease, Seattle, SSGCID
Discovery of Plasmodium vivaxN-Myristoyltransferase Inhibitors: Screening, Synthesis, and Structural Characterization of their Binding Mode
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