Refinement of the NMR solution structure of a protein to remove distortions arising from neglect of internal motion.
Refinement of the NMR solution structure of a protein to remove distortions arising from neglect of internal motion.
复制标题
细化蛋白质的 NMR 溶液结构,以消除因忽略内部运动而产生的扭曲。
DOI:
10.1021/bi00230a001
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发表时间:
1991
期刊:
影响因子:
2.9
通讯作者:
Markley,JL
中科院分区:
文献类型:
--
作者:
Fejzo,J;Krezel,AM;Westler,WM;Macura,S;Markley,JL
Jasna Fejzo, t, § Andrzej M. Krezel, § William M. Westler, 5 Slobodan Macura, 1, 11 and John L. Markley*’5 Biochemistry Department, College of Agricultural and Life Sciences, University of Wisconsin, 420 Henry Mall, Madison, Wisconsin 53706, and Faculty of Physical Chemistry, University of Belgrade, 11000 Beograd, POB 550, Yugoslavia Received January 29, 1991 abstract: The effect of internal motion on the quality of a protein structure derived from nuclear magnetic resonance (NMR) cross relaxation has been investigated experimentally. Internal rotation of the tyrosine-31 ring of turkey ovomucoid third domain was found to mediate magnetization transfer; the effect led to underestimation of proton-proton distances in its immediate neighborhood. Experimental methods that distinguish pure cross relaxation from chemical exchange mediated cross relaxation were used to separate true distances from distorted ones. Uncorrected and corrected sets of distances, where the corrections took internal motion into account, each were used as input to a distance geometry program for structural modeling. Each set of distances yielded a family of similar (converged) structures. The two families of structures differed considerably (2 A) in the region of tyrosine-31. In addition, differences as large as 1