Functionality map analysis of the active site cleft of human thrombin

被引:25
作者
Grootenhuis, PDJ
Karplus, M
机构
[1] HARVARD UNIV, DEPT CHEM, CAMBRIDGE, MA 02138 USA
[2] NV ORGANON, DEPT COMPUTAT MED CHEM, 5340 BH OSS, NETHERLANDS
关键词
thrombin inhibitors; molecular modelling; rational drug design; MCSS method;
D O I
10.1007/BF00124460
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Multiple Copy Simultaneous Search methodology has been used to construct functionality maps for an extended region of human thrombin, including the active site. This method allows the determination of energetically favorable positions and orientations for functional groups defined by the user on the three-dimensional surface of a protein. The positions of 10 functional group sites are compared with those of corresponding groups of four thrombin-inhibitor complexes. Many, but not all features, of known thrombin inhibitors are reproduced by the method. The results indicate that certain aspects of the binding modes of these inhibitors are not optimal. In addition, suggestions are made for improving binding by interaction with functional group sites on the thrombin surface that are not used by the thrombin inhibitors.
引用
收藏
页码:1 / 10
页数:10
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