Identifying common metalloprotease inhibitors by protein fold types using Fourier Transform Mass Spectrometry
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Mitchell, Jennifer K
Pitcher, Desley
McArdle, Bernadette M
Alnefelt, Terese
Duffy, Sandra
Avery, Vicky
Quinn, Ronald J
Pitcher, Desley
McArdle, Bernadette M
Alnefelt, Terese
Duffy, Sandra
Avery, Vicky
Quinn, Ronald J
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2007
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Abstract
Fourteen natural products, known to inhibit other proteins of the Zincin-like fold class, were screened for inhibition of the Zincin-like fold metalloprotease thermolysin using mass spectrometry. Fourier Transform Mass Spectrometry was successful in identifying actinonin, a known inhibitor of astacin and stromelysin, to be an inhibitor of thermolysin. Molecular modelling studies have shown that specificity within the Zincin-like fold is determined by Protein Fold Topology.
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Bioorganic & Medicinal Chemistry Letters
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17
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Medicinal and biomolecular chemistry
Organic chemistry
Pharmacology and pharmaceutical sciences