 Side-specific post-transpiration after modification of proteins have disappeared the same amount of adhesion, because it can add in functionality to proteins. We have been working in little and diluted side-specific protein modifications. So, the focus of our use is on proteins, so to say, that provides a better adhesion. The enzyme is becoming an important tool for protein material, such as to serve as flavoring protein peptide circulation and protein chemophysiation. The enzyme directly becomes an anti-alcoholic acid, and creates a peptide bond between the swelling and guise to form and seal the enzyme in the media at the active site. The intermediate is resolved by necrophilic attack of the combined group and olivaricin, to generate a peptide bond between swelling and olivaricin. The activity of the enzyme is strongly dependent on the calcium concentration, and the activity grounds for it is at low calcium concentration. So, the application of this enzyme is very restricted. The calcium binding site is dissolved in the active site. The role of calcium ion is known to survive the 36xm group. This group contacts with the other activity, so calcium ion can not involve in the product cycle. Actually, so there is an enzyme from other protein bacteria, shown closely in the enzyme appendix. This part here, the enzyme can be extended to specific to some of the glucose ions, so it is an enzyme. Now, the enzyme can be obtained because of the tendency by mutagenesis. We found two glutamate molecules in the classified bucket are not conserved, in so-called enzyme enzymes, from glycococcus and genesis, and process aggressive. In the objective, the glycococcus is always sorted there by making the process independent, so it is the enzyme. The writing of the application of glutamate 1.5 is not affected by glycococcus. The application of glutamate 1.8 will add more productivity, more calcium dependency. However, the activities are very low, so we have to get more independent subjects there by the limitations. Interestingly, as a combination of limitations, we can enhance the activity in the absence of calcium ion. In general, the activities are almost the same with those in the presence of calcium ion. So there is a difference also within high-summit specificity. In the Gaussian, it depends on the amount of high-summit specificity to increase the effectiveness of this sort of enzyme, as a tool for working in theory, including for integral for demonstration and writing. For more detail, please read our article in 5G and 5G. If you have any interest in our research, please contact us. Thank you.