Accurate measurement of HN-Hα residual dipolar couplings in proteins

被引:33
作者
Cai, ML [1 ]
Wang, H [1 ]
Olejniczak, ET [1 ]
Meadows, RP [1 ]
Gunasekera, AH [1 ]
Xu, N [1 ]
Fesik, SW [1 ]
机构
[1] Abbott Labs, Div Pharmaceut Discovery, Abbott Pk, IL 60064 USA
关键词
residual dipolar coupling; protein alignment; bicelle; lipid; phage;
D O I
10.1006/jmre.1999.1819
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A method for accurately measuring H-N-H-alpha residual dipolar couplings is described. Using this technique, both the sign and magnitude of the coupling can be determined easily. Residual dipolar coupling between H-N(i)-H-alpha(i) and H-N(i)-H-alpha(i-1) were measured for the FK506 binding protein complexed to FK506, The experimental values were in excellent agreement with predictions based on an X-ray crystal structure of the protein/ligand complex, suggesting that these residual dipolar couplings will provide accurate structural constraints for the refinement of protein structures determined by NMR. (C) 1999 Academic Press.
引用
收藏
页码:451 / 453
页数:3
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