In vitro and ex vivo inhibition of hepatitis A virus 3C proteinase by a peptidyl monofluoromethyl ketone. (Q41111799)

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4 November 2019

title

In vitro and ex vivo inhibition of hepatitis A virus 3C proteinase by a peptidyl monofluoromethyl ketone (English)

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4 November 2019

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John Christopher Vederas

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4 November 2019

Christopher Lowe

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S U Emerson

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R H Purcell

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4 November 2019

author name string

T S Morris

1

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4 November 2019

S Frormann

2

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4 November 2019

S Shechosky

3

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4 November 2019

M S Lall

5

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4 November 2019

V Gauss-Müller

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B A Malcolm

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4 November 2019

language of work or name

English

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publication date

1 May 1997

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Bioorganic & Medicinal Chemistry

4 November 2019

published in

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4 November 2019

volume

5

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issue

5

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page(s)

797-807

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Cleavage specificity of purified recombinant hepatitis A virus 3C proteinase on natural substrates.

4 November 2019

cites work

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The picornaviral 3C proteinases: cysteine nucleophiles in serine proteinase folds

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Peptide aldehyde inhibitors of hepatitis A virus 3C proteinase

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The crystal structure of cruzain: a therapeutic target for Chagas' disease

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Cysteine proteinase inhibitors decrease articular cartilage and bone destruction in chronic inflammatory arthritis

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Dirofilaria immitis: effect of fluoromethyl ketone cysteine protease inhibitors on the third- to fourth-stage molt

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Synthesis of peptide fluoromethyl ketones and the inhibition of human cathepsin B.

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Inhibition of serine proteases by peptidyl fluoromethyl ketones

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The synthesis of peptidylfluoromethanes and their properties as inhibitors of serine proteinases and cysteine proteinases

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Picornaviral 3C cysteine proteinases have a fold similar to chymotrypsin-like serine proteinases

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Structure of human rhinovirus 3C protease reveals a trypsin-like polypeptide fold, RNA-binding site, and means for cleaving precursor polyprotein

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On the size of the active site in proteases. I. Papain

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Hepatitis A virus 3C proteinase substrate specificity

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Chloroketone hydrolysis by chymotrypsin and N-methylhistidyl-57-chymotrypsin: implications for the mechanism of chymotrypsin inactivation by chloroketones

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Three-dimensional structure of chymotrypsin inactivated with (2S)-N-acetyl-L-alanyl-L-phenylalanyl alpha-chloroethane: implications for the mechanism of inactivation of serine proteases by chloroketones

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Evidence for hemiketals as intermediates in the inactivation of serine proteinases with halomethyl ketones

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An x-ray crystallographic study of the binding of peptide chloromethyl ketone inhibitors to subtilisin BPN'

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The isomorphous structures of prethrombin2, hirugen-, and PPACK-thrombin: changes accompanying activation and exosite binding to thrombin

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Binding of chloromethyl ketone substrate analogues to crystalline papain

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Proteinase 3C of hepatitis A virus (HAV) cleaves the HAV polyprotein P2-P3 at all sites including VP1/2A and 2A/2B.

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Simple in vitro translation assay to analyze inhibitors of rhinovirus proteases

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Expression and characterization of recombinant hepatitis A virus 3C proteinase

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Synthesis and Testing of Heterocyclic Analogs of Diaminopimelic Acid (DAP) as Inhibitors of DAP Dehydrogenase and DAP Epimerase

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7 January 2021

Determination of the rate constant of enzyme modification by measuring the substrate reaction in the presence of the modifier.

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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

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An infectious cDNA clone of a cytopathic hepatitis A virus: genomic regions associated with rapid replication and cytopathic effect

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Identifiers

DOI

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4 November 2019

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