Drug-protein interactions: Two-site binding of heterocyclic ligands to a monomeric hemoglobin

被引:143
作者
Stephanos, JJ [1 ]
机构
[1] DREXEL UNIV, DEPT CHEM, PHILADELPHIA, PA 19104 USA
关键词
D O I
10.1016/0162-0134(95)00144-1
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 reactivity response of the heme proteins to the heterotropic effecters, purine, caffeine, theophylline, and (C2H5N+, have been examined. The heterotropic effecters influence the heme ligation affinities. The heme axial ligation of pyridine and pyrazole;have not influenced the hemoglobin's affinity for caffeine and theophylline. The imidazole ligation indicates a mutual interaction between the heme active site and the noncoordinate binding site.
引用
收藏
页码:155 / 169
页数:15
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