High-molecular-weight kininogen binds two molecules of cysteine proteinases with different rate constants (Q28284858)

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V Turk

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G Johansson

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J J Cazzulo

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I Björk

Structure and functions of human kininogens

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language of work or name

English

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publication date

5 August 1996

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published in

FEBS Letters

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volume

391

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issue

1-2

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page(s)

109-12

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cites work

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Isolation of a human cDNA for alpha 2-thiol proteinase inhibitor and its identity with low molecular weight kininogen

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Human plasma kininogens are identical with alpha-cysteine proteinase inhibitors. Evidence from immunological, enzymological and sequence data

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Human low-Mr kininogen contains three copies of a cystatin sequence that are divergent in structure and in inhibitory activity for cysteine proteinases

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Nomenclature and classification of the proteins homologous with the cysteine-proteinase inhibitor chicken cystatin.

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High-affinity binding of two molecules of cysteine proteinases to low-molecular-weight kininogen.

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The Purification of Papain by Affinity Chromatography

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Reactivity of small thiolate anions and cysteine-25 in papain toward methyl methanethiosulfonate

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How to measure and predict the molar absorption coefficient of a protein

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The proteolytic activities of chymopapain, papain, and papaya proteinase III.

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High molecular weight kininogen potentiates the heparin-accelerated inhibition of plasma kallikrein by antithrombin: role for antithrombin in the regulation of kallikrein

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Binding of heparin to human high molecular weight kininogen

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Comparison of cysteine-proteinases inhibitory properties of human high-molecular-weight-kininogen (HMrK) purified from plasma and serum

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Protein Inhibitors of Cysteine Proteinases. III. Amino-Acid Sequence of Cystatin from Chicken Egg White

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Isolation and structure of T-kinin

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Inhibition of cruzipain, the major cysteine proteinase of the protozoan parasite, Trypanosoma cruzi, by proteinase inhibitors of the cystatin superfamily

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EQUILIBRIUM ULTRACENTRIFUGATION OF DILUTE SOLUTIONS

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Cloning, expression and characterization of human kininogen domain 3

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