protease binding

Interacting selectively and non-covalently with any protease or peptidase. [GOC:hjd]
National Institutes of Health

Topic mentions per year

Topic mentions per year

1977-2017
02419772017

Papers overview

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2012
2012
RNase R, an important exoribonuclease involved in degradation of structured RNA, is subject to a novel mechanism of regulation… (More)
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2011
2011
Using a shape analysis technique, a Dataset of 79 (19 wild-type and 60 mutated) HIV-1 protease crystal structures was analyzed… (More)
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2011
2011
The human severe acute respiratory syndrome coronavirus (SARS-CoV) and the NL63 coronaviruses are human respiratory pathogens for… (More)
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2010
2010
The efficiency of canonical serine protease inhibitors is conventionally attributed to the rigidity of their protease binding… (More)
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2002
2002
Hepatocyte growth factor activator inhibitor type 1 (HAI-1) is a Kunitz-type serine protease inhibitor identified as a strong… (More)
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2000
2000
The three-dimensional structure of the 56 residue polypeptide Apis mellifera chymotrypsin/cathepsin G inhibitor 1 (AMCI-1… (More)
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1991
1991
We have examined in detail the kinetics of binding of the serpin alpha 2-antiplasmin to the serine proteases alpha-chymotrypsin… (More)
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1988
1988
Sequence homology comparisons between serum serine protease inhibitors led to the prediction that the C-terminal sequences are… (More)
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1983
1983
Human alpha 2-macroglobulin (alpha 2M) undergoes a conformational change after reaction with proteases. In this report, it is… (More)
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1983
1983
Human alpha 2-macroglobulin (alpha 2M) half-molecules were prepared by limited reduction and alkylation of the native protein… (More)
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