(Q27639638)

2

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Joseph D Ho

3

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John R. Somoza

1

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James T. Palmer

2

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Joseph D. Ho

Journal of Molecular Biology

3

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language of work or name

English

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publication date

20 September 2002

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September 2002

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published in

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volume

322

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issue

3

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page(s)

559-68

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559-568

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cites work

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Human cathepsin V functional expression, tissue distribution, electrostatic surface potential, enzymatic characterization, and chromosomal localization

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Role for cathepsin F in invariant chain processing and major histocompatibility complex class II peptide loading by macrophages

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Crystal structure of human cathepsin K complexed with a potent inhibitor

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Potentiometric determination of ionizations at the active site of papain

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Proton Equilibria in the Binding of Zn2+ and of Methylmercuric Iodide to Papain

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Crystal structure of cathepsin B inhibited with CA030 at 2.0-A resolution: A basis for the design of specific epoxysuccinyl inhibitors

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Structure-based design of non-peptide, carbohydrazide-based cathepsin K inhibitors

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Structure-based design, synthesis and evaluation of conformationally constrained cysteine protease inhibitors

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Identification of dipeptidyl nitriles as potent and selective inhibitors of cathepsin B through structure-based drug design

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Crystal structure of porcine cathepsin H determined at 2.1 A resolution: location of the mini-chain C-terminal carboxyl group defines cathepsin H aminopeptidase function

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Structure of human dipeptidyl peptidase I (cathepsin C): exclusion domain added to an endopeptidase framework creates the machine for activation of granular serine proteases

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Crystal structure of cathepsin X: a flip-flop of the ring of His23 allows carboxy-monopeptidase and carboxy-dipeptidase activity of the protease

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