We apologize for Proteopedia being slow to respond. For the past two years, a new implementation of Proteopedia has been being built. Soon, it will replace this 18-year old system. All existing content will be moved to the new system at a date that will be announced here.

Sandbox GGC7

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 21: Line 21:
Another significant feature of this protein is <scene name='75/752270/Ggc7/7'>Tyr150</scene> , which has an aromatic ring that interferes with the mobility of Arg193 and helps stabilize it (2). This protein is similar to human trypsin I, but has a few notable differences, such as a <scene name='75/752270/Ggc7/8'>Threonine in position 21</scene> instead of Asparagine.
Another significant feature of this protein is <scene name='75/752270/Ggc7/7'>Tyr150</scene> , which has an aromatic ring that interferes with the mobility of Arg193 and helps stabilize it (2). This protein is similar to human trypsin I, but has a few notable differences, such as a <scene name='75/752270/Ggc7/8'>Threonine in position 21</scene> instead of Asparagine.
== References ==
== References ==
 +
 +
1.Wang, Y., Luo, W., & Reiser, G. (2008). Trypsin and trypsin-like proteases in the brain: proteolysis and cellular functions. Cellular And Molecular Life Sciences: CMLS, 65(2), 237-252.
 +
 +
2. Katona, G., Berglund, G., Hajdu, J., Gráf, L., & Szilágyi, L. (2002). Crystal structure reveals basis for the inhibitor resistance of human brain trypsin 1 1 Edited by R. Huber. Journal of Molecular Biology, 315(5), 1209-1218.
 +
<references/>
<references/>

Revision as of 00:15, 23 April 2018

Structure of Brain Trypsin (human trypsin IV)

Triose phosphate isomerase

Drag the structure with the mouse to rotate

This portion of the protein contains which provides resistance to the inhibitor due to its large size and positive charge (2). Another significant feature of this protein is , which has an aromatic ring that interferes with the mobility of Arg193 and helps stabilize it (2). This protein is similar to human trypsin I, but has a few notable differences, such as a instead of Asparagine.

References

1.Wang, Y., Luo, W., & Reiser, G. (2008). Trypsin and trypsin-like proteases in the brain: proteolysis and cellular functions. Cellular And Molecular Life Sciences: CMLS, 65(2), 237-252.

2. Katona, G., Berglund, G., Hajdu, J., Gráf, L., & Szilágyi, L. (2002). Crystal structure reveals basis for the inhibitor resistance of human brain trypsin 1 1 Edited by R. Huber. Journal of Molecular Biology, 315(5), 1209-1218.


Personal tools