Successful development of inhibitors of proteases (for example HIV-1 protease) further supports the choice of target.
研制成功的抑制剂蛋白酶(例如HIV - 1蛋白酶)，进一步支持的选择目标。
The algorithm is applied to the docking of several simple model molecules and the docking between the benzamidine and HIV 1 protease.
首先将该算法应用于假想分子模型间的刚性对接，然后将算法应用于HIV - 1蛋白酶与苯甲醚配体的刚性对接。
The algorithm is applied to the docking of several simple model molecules and the docking between the benzamidine and HIV 1 protease.
首先将该算法应用于假想分子模型间的刚性对接，然后将算法应用于HIV - 1蛋白酶与苯甲醚配体的刚性对接。
应用推荐