PubMed:28287727
Annnotations
GoldHamster
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Acceptor-Based Peptidomimetic Inhibitor of Main Protease from Porcine Epidemic Diarrhea Virus.\nPorcine epidemic diarrhea virus (PEDV) causes high mortality in pigs. PEDV main protease (M(pro)) plays an essential role in viral replication. We solved the structure of PEDV M(pro) complexed with peptidomimetic inhibitor N3 carrying a Michael acceptor warhead, revealing atomic level interactions. We further designed a series of 17 inhibitors with altered side groups. Inhibitors M2 and M17 demonstrated enhanced specificity against PEDV M(pro). These compounds have potential as future therapeutics to combat PEDV infection."}
PubMed_ArguminSci
{"project":"PubMed_ArguminSci","denotations":[{"id":"T1","span":{"begin":103,"end":172},"obj":"DRI_Background"},{"id":"T2","span":{"begin":247,"end":402},"obj":"DRI_Approach"},{"id":"T3","span":{"begin":403,"end":474},"obj":"DRI_Approach"},{"id":"T4","span":{"begin":475,"end":551},"obj":"DRI_Approach"},{"id":"T5","span":{"begin":552,"end":631},"obj":"DRI_FutureWork"}],"text":"Michael Acceptor-Based Peptidomimetic Inhibitor of Main Protease from Porcine Epidemic Diarrhea Virus.\nPorcine epidemic diarrhea virus (PEDV) causes high mortality in pigs. PEDV main protease (M(pro)) plays an essential role in viral replication. We solved the structure of PEDV M(pro) complexed with peptidomimetic inhibitor N3 carrying a Michael acceptor warhead, revealing atomic level interactions. We further designed a series of 17 inhibitors with altered side groups. Inhibitors M2 and M17 demonstrated enhanced specificity against PEDV M(pro). These compounds have potential as future therapeutics to combat PEDV infection."}
Goldhamster2_Cellosaurus
{"project":"Goldhamster2_Cellosaurus","denotations":[{"id":"T1","span":{"begin":193,"end":199},"obj":"CVCL_5430|Spontaneously_immortalized_cell_line|Mus musculus"},{"id":"T2","span":{"begin":195,"end":198},"obj":"CVCL_N817|Cancer_cell_line|Homo sapiens"},{"id":"T3","span":{"begin":207,"end":209},"obj":"CVCL_8754|Cancer_cell_line|Homo sapiens"},{"id":"T4","span":{"begin":207,"end":209},"obj":"CVCL_H241|Cancer_cell_line|Homo sapiens"},{"id":"T5","span":{"begin":234,"end":245},"obj":"CVCL_XY58|Transformed_cell_line|Mus musculus"},{"id":"T6","span":{"begin":247,"end":249},"obj":"CVCL_5M23|Cancer_cell_line|Mesocricetus auratus"},{"id":"T7","span":{"begin":279,"end":285},"obj":"CVCL_5430|Spontaneously_immortalized_cell_line|Mus musculus"},{"id":"T8","span":{"begin":281,"end":284},"obj":"CVCL_N817|Cancer_cell_line|Homo sapiens"},{"id":"T9","span":{"begin":326,"end":328},"obj":"CVCL_D435|Transformed_cell_line|Mus musculus"},{"id":"T10","span":{"begin":326,"end":328},"obj":"CVCL_ZU49|Transformed_cell_line|Homo sapiens"},{"id":"T11","span":{"begin":338,"end":339},"obj":"CVCL_6479|Finite_cell_line|Mus musculus"},{"id":"T12","span":{"begin":403,"end":405},"obj":"CVCL_5M23|Cancer_cell_line|Mesocricetus auratus"},{"id":"T13","span":{"begin":423,"end":424},"obj":"CVCL_6479|Finite_cell_line|Mus musculus"},{"id":"T14","span":{"begin":486,"end":488},"obj":"CVCL_M543|Cancer_cell_line|Homo sapiens"},{"id":"T15","span":{"begin":486,"end":488},"obj":"CVCL_W291|Cancer_cell_line|Homo sapiens"},{"id":"T16","span":{"begin":486,"end":488},"obj":"CVCL_XD77|Embryonic_stem_cell|Homo sapiens"},{"id":"T17","span":{"begin":493,"end":496},"obj":"CVCL_D028|Cancer_cell_line|Homo sapiens"},{"id":"T18","span":{"begin":544,"end":550},"obj":"CVCL_5430|Spontaneously_immortalized_cell_line|Mus musculus"},{"id":"T19","span":{"begin":546,"end":549},"obj":"CVCL_N817|Cancer_cell_line|Homo sapiens"}],"text":"Michael Acceptor-Based Peptidomimetic Inhibitor of Main Protease from Porcine Epidemic Diarrhea Virus.\nPorcine epidemic diarrhea virus (PEDV) causes high mortality in pigs. PEDV main protease (M(pro)) plays an essential role in viral replication. We solved the structure of PEDV M(pro) complexed with peptidomimetic inhibitor N3 carrying a Michael acceptor warhead, revealing atomic level interactions. We further designed a series of 17 inhibitors with altered side groups. Inhibitors M2 and M17 demonstrated enhanced specificity against PEDV M(pro). These compounds have potential as future therapeutics to combat PEDV infection."}