Greer J
Science. 1985 May 31;228(4703):1055-60. doi: 10.1126/science.3992245.
The complement cleavage product C5a is a potent stimulant of inflammatory processes; thus, inhibition of C5a activity is of therapeutic interest. The three-dimensional structure of the major portion of C5a was modeled from the homologous C3a crystal structure by comparative modeling techniques. The model shows that core residues of C5a are completely conserved, while external residues differ from C3a. Even though the amino-terminal 12 residues of C3a are disordered in the crystal, this sequence in C5a may form an amphipathic helix. The distribution of species sequence differences in the complete C5a structure suggests a possible receptor binding site.
补体裂解产物C5a是炎症过程的强效刺激物;因此,抑制C5a活性具有治疗意义。通过比较建模技术,根据同源的C3a晶体结构对C5a主要部分的三维结构进行了建模。该模型表明,C5a的核心残基完全保守,而外部残基与C3a不同。尽管C3a的氨基末端12个残基在晶体中无序,但C5a中的该序列可能形成两亲性螺旋。完整C5a结构中物种序列差异的分布提示了一个可能的受体结合位点。