摘要
依据高峰淀粉酶的晶体结构数据对它的分子可及性进行了计算和分析,得到了极性与非极性氨基酸的分布、极性原子与非极性原子对可及性的贡献、催化活性中心裂隙的构象、C末端结构域空间拓扑等信息。活性部位氨基酸残基的可及性研究结果与酶-底物复合物模型相符。
In this paper, the molecular accessibility of Taka-Amylase A (TAA) was calculated and analyzed on the basis of its crystal structure data. Some useful information, such as the distribution of polar and non-polar amino acids in surface and core of the molecules, the comformation and function of the catalytic cleft, the folding topology of the C-terminal domain, were obtained. The result of the accesibility analysis of the residues in the active center tallied with the enzyme-substrated complex model.
出处
《生物物理学报》
CAS
CSCD
北大核心
1995年第2期134-138,共5页
Acta Biophysica Sinica