| 1. | A primary study on anticonvulsant parts of bombyx mori l
僵蚕抗惊厥活性部位的初步研究 |
| 2. | Allosteric enzymes possess an allosteric site in addition to their active site
别构酶控制着别构部位和它的活性部位。 |
| 3. | Experimental study of huixincao against active site of acute myocardial ischemia in rats
回心草抗大鼠急性心肌缺血活性部位的实验研究 |
| 4. | Conclusion the ethanol extract method should be used to extract the potent active components of " yueju pills "
结论乙醇冷浸为越鞠丸方药抗抑郁活性部位的较佳提取方法。 |
| 5. | Binding of an inhibiting compound elsewhere on the enzyme molecule may change this configuration and hence the efficiency of the enzyme activity
活性部位如果结合了抑制性的化合物则其构象就要发生改变影响酶的活性。 |
| 6. | The active site consists of amino acids arranged in a configuration specific to a particular substrate or type of substrate
构成酶活性部位的这些基团由于肽链的盘绕折叠使它们在空间结构上彼此靠近，形成具有一定空间结构的区域。 |
| 7. | Because the catalytic site of a - aldc has not been certified and the catalytic mechanism has to be also further proved , it is difficult to enhance the enzyme activity in low temperature by the rational design
由于- aldc的活性部位尚未完全确定，催化机理也需进一步证实，在这种条件下通过酶的合理化设计来提高酶在低温下的活力有一定困难。 |
| 8. | Though zn 2 + and co 2 + are divalent ions , they probably can not substitute ca2 + from the active center of tcs , or can substitute ca2 + but does not change the structure of tcs . there is no significant change observed for the fluorescence intensity of tcs
‘ “是二价金属离子，但这两种离子与天花粉蛋白作用时可能并没有取代天花粉蛋白活性部位的ca ‘ ” ，或部分取代但并没有改变天花粉蛋白分子的空间结构，以致天花粉蛋白的荧光强度无明显变化。 |
| 9. | This is a problem vitally important to both molecular biologists and bioinformatists today . we herein become interests in comparing ( - sheet topologies of protein main - chain , identifying combination of the side - chain , introducing structural mobility into secondary structure and conformation , and simulating enzyme active site fluctuation by intelligent polymer catalysts
本文致力于比较蛋白质主链的( -折叠片拓扑，识别侧链的组合，并将结构的运动性引入二级结构和构象，且用智能高分子催化剂来模拟酶活性部位的涨落。 |
| 10. | Part iv computer - aided molecule modelling of tnfa mimotopes and tnfa - binding peptides : to investigate the interaction between tnfa mimotopes and tnfa - binding peptides , the computational docking program autodock ( with confirming calculations using discover ) was used to predict the binding modes of llt - 18 with tnfa firstly , then lcs - 7 was docked to llt - 18 by manual . the interaction between llt - 18 and tnfa or lcs - 7 showed electrostatic interaction and h - bond dominant
进行对接，对两者间结合位点进行分析；在此基础之上，以insight11软件构建lcs刁分于三维结构， autodock程序对接llt和lcs 7两个短肽分子，找寻两者结合的关键性残基，结果表明llt与tnfa及lcs 7分子间相互作用以静电相互作用为主， lcs刀和tnfa活性部位的arg在分于间相互作用中起重要作用。 |
