(Q27640115)

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Crystal structures of reversible ketone-Based inhibitors of the cysteine protease cruzain

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Crystal structures of reversible ketone-Based inhibitors of the cysteine protease cruzain (English)

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Lily Huang

1

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Linda S Brinen

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2

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Jonathan A Ellman

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3

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language of work or name

English

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publication date

2 January 2003

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published in

Bioorganic & Medicinal Chemistry

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volume

11

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issue

1

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page(s)

21-9

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cites work

Inhibition of cruzipain visualized in a fluorescence quenched solid-phase inhibitor library assay. D-amino acid inhibitors for cruzipain, cathepsin B and cathepsin L.

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Cysteine protease inhibitors as chemotherapy for parasitic infections

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Cysteine protease inhibitors cure an experimental Trypanosoma cruzi infection

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

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Structural determinants of specificity in the cysteine protease cruzain

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A target within the target: probing cruzain's P1' site to define structural determinants for the Chagas' disease protease

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Identification of potent and selective mechanism-based inhibitors of the cysteine protease cruzain using solid-phase parallel synthesis

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Peptidyl (acyloxy)methyl ketones and the quiescent affinity label concept: the departing group as a variable structural element in the design of inactivators of cysteine proteinases

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Potent dipeptidylketone inhibitors of the cysteine protease cathepsin K

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7 January 2021

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17 The kinetics of reversible tight-binding inhibition

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Crystallographic R factor refinement by molecular dynamics

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MAB, a generally applicable molecular force field for structure modelling in medicinal chemistry.

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DOI

10.1016/S0968-0896(02)00427-3

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PubMed publication ID

12467703

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(Q27640115)

Crystal structures of reversible ketone-Based inhibitors of the cysteine protease cruzain

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