Title of article
Identifying common metalloprotease inhibitors by protein fold types using Fourier Transform Mass Spectrometry
Author/Authors
Jennifer K. Mitchell، نويسنده , , Desley Pitcher، نويسنده , , Bernadette M. McArdle، نويسنده , , Terese Alnefelt، نويسنده , , Sandra Duffy، نويسنده , , Vicky Avery، نويسنده , , Ronald J. Quinn، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2007
Pages
4
From page
6521
To page
6524
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.
Keywords
FTMS , Protein–ligand complex , Protein Fold
Journal title
Bioorganic & Medicinal Chemistry Letters
Serial Year
2007
Journal title
Bioorganic & Medicinal Chemistry Letters
Record number
798836
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