|کد مقاله||کد نشریه||سال انتشار||مقاله انگلیسی||ترجمه فارسی||نسخه تمام متن|
|15266||1398||2011||7 صفحه PDF||سفارش دهید||دانلود رایگان|
The selectivity of a known arylsulfonamides inhibitor for two isozymes II and VII of human carbonic anhydrases (hCAs) was studied by homology modeling, molecular docking and molecular dynamics methods. The results show that the selectivity of the inhibitor for two isozymes is due to the different side chain lengths between N67 of hCA II and Q64 of hCA VII. One more methene group in the side chain of Q64 of hCA VII makes it possible to form the hydrogen bond with the bromide atom of the known inhibitor. From the point of view, the modification to the known inhibitor was performed to obtain an inhibitor with higher selectivity. The complex conformations of the new designed inhibitor and two isozymes designate the formation of the hydrogen bond between the newly added group (hydroxypropyl group) and Q64 of hCA VII but N67 of hCA II. The results of the binding free energy from the MM/PBSA approach also prove the selectivity improvement of the new inhibitor in comparison with the known inhibitor. The work will help the design of the isozyme-specific inhibitors of hCA VII.
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► The selective mechanism of a known inhibitor for two isozymes (II and VII) of human carbonic anhydrase (hCA) was investigated by homology modeling, molecular docking and molecular dynamics methods.
► On the basis of the obtained results, the modification to the known inhibitor was performed to design a new hCA VII-specific inhibitor.
► The new inhibitor strengthens the interaction with hCA VII by a newly added group and increases the selectivity for hCA VII.
Journal: Computational Biology and Chemistry - Volume 35, Issue 1, February 2011, Pages 50–56