Zuiderweg E R, Henkin J, Mollison K W, Carter G W, Greer J
NMR Research Group, Abbott Laboratories, Abbott Park, Illinois 60064.
Proteins. 1988;3(3):139-45. doi: 10.1002/prot.340030302.
The model structure previously proposed for human C5a, based upon the crystal structure of the homologous protein human C3a, is compared to the solution structure of human C5a recently determined by nuclear magnetic resonance (NMR) methods in our laboratory. The general folding and helix topography of the C5a protein were modeled very well. The N-terminus, which is disordered in the C3a crystal, was correctly predicted in the C5a model both as to its being a helix and as to its docking site on the rest of the molecule. On the other hand, the NMR data show that the biologically important C-terminal residues are disordered in solution, unlike the model and the C3a crystal structure where this region was helical.
基于同源蛋白人C3a的晶体结构先前提出的人C5a模型结构,与我们实验室最近通过核磁共振(NMR)方法确定的人C5a溶液结构进行了比较。C5a蛋白的总体折叠和螺旋拓扑结构模拟得非常好。在C3a晶体中无序的N末端,在C5a模型中关于其作为螺旋以及其在分子其余部分上的对接位点都被正确预测。另一方面,NMR数据表明,具有生物学重要性的C末端残基在溶液中是无序的,这与该区域为螺旋结构的模型和C3a晶体结构不同。