Structure-based inhibitor design

被引:7
作者
Craig, SP [1 ]
Eakin, AE [1 ]
机构
[1] Univ N Carolina, Sch Pharm, Lab Mol Parasitol & Drug Design, Chapel Hill, NC 27599 USA
来源
VITAMINS AND HORMONES - ADVANCES IN RESEARCH AND APPLICATIONS, VOL 58 | 2000年 / 58卷
关键词
D O I
10.1016/S0083-6729(00)58024-8
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
引用
收藏
页码:149 / +
页数:22
相关论文
共 63 条
[1]   An experimental approach to mapping the binding surfaces of crystalline proteins [J].
Allen, KN ;
Bellamacina, CR ;
Ding, XC ;
Jeffery, CJ ;
Mattos, C ;
Petsko, GA ;
Ringe, D .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (07) :2605-2611
[2]   Structure-based drug design [J].
Amzel, LM .
CURRENT OPINION IN BIOTECHNOLOGY, 1998, 9 (04) :366-369
[3]   Retention of marked sensitivity to (S)-4-isopropoxycarbonyl-6-methoxy-3-(methylthiomethyl)-3,4-dihydroquinoxaline-2(1H)-thione (HBY 097) by an azidothymidine (AZT)-resistant human immunodeficiency virus type 1 (HIV-1) strain subcultured in the combined presence of quinoxaline HBY 097 and 2′,3′-dideoxy-3′-thiacytidine (lamivudine) [J].
Balzarini, J ;
Pelemans, H ;
Riess, G ;
Roesner, M ;
Winkler, I ;
De Clercq, E ;
Kleim, JP .
BIOCHEMICAL PHARMACOLOGY, 1998, 55 (05) :617-625
[4]  
Bohacek RS, 1996, MED RES REV, V16, P3, DOI 10.1002/(SICI)1098-1128(199601)16:1<3::AID-MED1>3.3.CO
[5]  
2-D
[6]   DRUGS BY DESIGN [J].
BUGG, CE ;
CARSON, WM ;
MONTGOMERY, JA .
SCIENTIFIC AMERICAN, 1993, 269 (06) :92-98
[7]   Bacterial complementation as a means to test enzyme-ligand interactions [J].
Canyuk, B ;
Craig, SP ;
Eakin, AE .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 1998, 50 (02) :181-186
[8]   Structure-based design of potent inhibitors of scytalone dehydratase: Displacement of a water molecule from the active site [J].
Chen, JM ;
Xu, SL ;
Wawrzak, Z ;
Basarab, GS ;
Jordan, DB .
BIOCHEMISTRY, 1998, 37 (51) :17735-17744
[9]   ANALYTICAL MOLECULAR-SURFACE CALCULATION [J].
CONNOLLY, ML .
JOURNAL OF APPLIED CRYSTALLOGRAPHY, 1983, 16 (OCT) :548-558
[10]  
De Clercq E, 1998, Verh K Acad Geneeskd Belg, V60, P13