X-ray studies on Ligands

被引:9
|
作者
Deschamps, JR [1 ]
Flippen-Anderson, JL [1 ]
George, C [1 ]
机构
[1] USN, Res Lab, Struct Matter Lab, Washington, DC 20375 USA
关键词
x-ray crystallographic studies; ligands; atomic resolution; opioids; pharmacophores;
D O I
10.1002/bip.10308
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
Advances in x-ray crystallographic data collection, structure solution, and refinement/ validation have reduced the time required and expanded the range of samples amenable to x-ray crystallographic studies. Consequently, we can now collect complete atomic resolution data sets on physically smaller crystals and solve larger problems by direct methods beyond what could have been accomplished even five years ago. Applying these improved methods to the study of opioid ligands has enhanced our knowledge of the opioid pharmacophore. Despite considerable progress, it is still difficult to define the pharmacophoric parameters required for highly selective and potent opioid peptides. In part this is due to the conformational flexibility remaining even in conformationally constrained peptides. (C) 2003 Wiley Periodicals, Inc.
引用
收藏
页码:287 / 293
页数:7
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