Pages that link to "Q27653428"

The following pages link to Structural Basis of Inhibition Specificities of 3C and 3C-like Proteases by Zinc-coordinating and Peptidomimetic Compounds (Q27653428):

Displaying 48 items.

• From SARS to MERS: crystallographic studies on coronaviral proteases enable antiviral drug design (Q26992345) (← links)
• Insights into cleavage specificity from the crystal structure of foot-and-mouth disease virus 3C protease complexed with a peptide substrate (Q27658042) (← links)
• Structure and mechanism ofEscherichia coliglutathionylspermidine amidase belonging to the family of cysteine; histidine-dependent amidohydrolases/peptidases (Q27666555) (← links)
• Crystal structure of human enterovirus 71 3C protease (Q27666945) (← links)
• Enterovirus 71 and Coxsackievirus A16 3C Proteases: Binding to Rupintrivir and Their Substrates and Anti-Hand, Foot, and Mouth Disease Virus Drug Design (Q27671020) (← links)
• Crystal Structures of Enterovirus 71 3C Protease Complexed with Rupintrivir Reveal the Roles of Catalytically Important Residues (Q27671472) (← links)
• Broad-spectrum antivirals against 3C or 3C-like proteases of picornaviruses, noroviruses, and coronaviruses. (Q27671667) (← links)
• Structural Basis for Antiviral Inhibition of the Main Protease, 3C, from Human Enterovirus 93 (Q27671687) (← links)
• Terpyridine platinum(II) complexes inhibit cysteine proteases by binding to active-site cysteine (Q27672388) (← links)
• 3C Protease of Enterovirus 68: Structure-Based Design of Michael Acceptor Inhibitors and Their Broad-Spectrum Antiviral Effects against Picornaviruses (Q27676219) (← links)
• Inhibition of Enterovirus 71 replication by 7-hydroxyflavone and diisopropyl-flavon7-yl Phosphate (Q28541413) (← links)
• Atlas of coronavirus replicase structure. (Q30357066) (← links)
• The coxsackievirus B 3C protease cleaves MAVS and TRIF to attenuate host type I interferon and apoptotic signaling (Q33855429) (← links)
• Virtual screening identification of novel severe acute respiratory syndrome 3C-like protease inhibitors and in vitro confirmation (Q33864377) (← links)
• Recent development of 3C and 3CL protease inhibitors for anti-coronavirus and anti-picornavirus drug discovery (Q34218166) (← links)
• Crystallization and preliminary crystallographic study of Porcine epidemic diarrhea virus main protease in complex with an inhibitor (Q34652825) (← links)
• Metal impurities cause false positives in high-throughput screening campaigns (Q35181932) (← links)
• Human coronavirus OC43 3CL protease and the potential of ML188 as a broad-spectrum lead compound: homology modelling and molecular dynamic studies. (Q35544702) (← links)
• Benserazide, the first allosteric inhibitor of Coxsackievirus B3 3C protease (Q35645639) (← links)
• Reversal of the Progression of Fatal Coronavirus Infection in Cats by a Broad-Spectrum Coronavirus Protease Inhibitor. (Q35973652) (← links)
• Potential Broad Spectrum Inhibitors of the Coronavirus 3CLpro: A Virtual Screening and Structure-Based Drug Design Study (Q36403490) (← links)
• X-Ray Structure and Inhibition of 3C-like Protease from Porcine Epidemic Diarrhea Virus (Q36897887) (← links)
• The newly emerged SARS-like coronavirus HCoV-EMC also has an "Achilles' heel": current effective inhibitor targeting a 3C-like protease (Q36923117) (← links)
• Macrocyclic inhibitors of 3C and 3C-like proteases of picornavirus, norovirus, and coronavirus. (Q37114506) (← links)
• A Novel Enterovirus 71 (EV71) Virulence Determinant: The 69th Residue of 3C Protease Modulates Pathogenicity (Q37622718) (← links)
• Picornaviral 3C protease inhibitors and the dual 3C protease/coronaviral 3C-like protease inhibitors (Q37658853) (← links)
• Focal adhesion kinase is a component of antiviral RIG-I-like receptor signaling (Q38567618) (← links)
• Application of a cell-based protease assay for testing inhibitors of picornavirus 3C proteases (Q39037067) (← links)
• Structure-based antivirals for emerging and neglected RNA viruses: an emerging field for medicinal chemistry in academia (Q39067597) (← links)
• Identification and evaluation of potent Middle East respiratory syndrome coronavirus (MERS-CoV) 3CLPro inhibitors. (Q40068309) (← links)
• Coxsackievirus B3 protease 3C: expression, purification, crystallization and preliminary structural insights (Q40441657) (← links)
• Irreversible inhibitors of the 3C protease of Coxsackie virus through templated assembly of protein-binding fragments (Q40525758) (← links)
• Chalcones isolated from Angelica keiskei inhibit cysteine proteases of SARS-CoV. (Q42164714) (← links)
• Synthesis and evaluation of pyrazolone compounds as SARS-coronavirus 3C-like protease inhibitors (Q42858751) (← links)
• Dieckol, a SARS-CoV 3CL(pro) inhibitor, isolated from the edible brown algae Ecklonia cava (Q44440454) (← links)
• Inhibitory zinc sites in enzymes (Q44954333) (← links)
• Picornain 3C (human rhinovirus) (Q57014295) (← links)
• Coxsackievirus B3 Responds to Polyamine Depletion via Enhancement of 2A and 3C Protease Activity. (Q64997513) (← links)
• Flavonoid-mediated inhibition of SARS coronavirus 3C-like protease expressed in Pichia pastoris (Q83476348) (← links)
• Structure of Mpro from COVID-19 virus and discovery of its inhibitors (Q87967188) (← links)
• α-Ketoamides as Broad-Spectrum Inhibitors of Coronavirus and Enterovirus Replication: Structure-Based Design, Synthesis, and Activity Assessment (Q89654680) (← links)
• Structural Basis for Inhibiting Porcine Epidemic Diarrhea Virus Replication with the 3C-Like Protease Inhibitor GC376 (Q89878619) (← links)
• Structure of the HRV-C 3C-Rupintrivir Complex Provides New Insights for Inhibitor Design (Q89903079) (← links)
• Structure of Mpro from COVID-19 virus and discovery of its inhibitors (Q89975279) (← links)
• Structural Biology of the Enterovirus Replication-Linked 5'-Cloverleaf RNA and Associated Virus Proteins (Q90436716) (← links)
• Conserved interactions required for inhibition of the main protease of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (Q103804911) (← links)
• X-ray screening identifies active site and allosteric inhibitors of SARS-CoV-2 main protease (Q108146970) (← links)
• Zinc2+ ion inhibits SARS-CoV-2 main protease and viral replication in vitro (Q108581897) (← links)