Sandbox 1666
From Proteopedia
(Difference between revisions)
Line 8: | Line 8: | ||
== Biological Relevance and Broader Implications == | == Biological Relevance and Broader Implications == | ||
- | This protein causes drug resistance, which is a problem. It is a problem because if we can understand it better, we can change the way we treat | + | Since Beta-Lactam antibiotics are used very often in antimicrobial therapy to treat bacterial infections, bacterial resistance often ocurrs. This protein, CTX-M Beta-Lactamase, causes this drug resistance, which is a problem. It is a problem because if we can understand it better, we can change the way we treat to fight off the bacteria better. |
+ | |||
+ | The research of this protein is very significant because it has a direct clinical application. | ||
== Important Amino Acids == | == Important Amino Acids == | ||
An important ligand of this protein is GOL (glycerol), which is the only ligand in this protein. GOL helps with stability of this protein. The catalytic amino acids of this protein include Ser^70, Ser^130, and Lys^73. Ser^70 interacts with the oxygen on the ampicillin, and it is also cross-linked with clavulanic acid. Ser^130 is also cross-linked with clavulanic acid and interacts with the ligand through hydrogen bonds. Lys^73 also interacts with the ligand through hydrogen bonds. This amino acid is used to lower the pka value of the hydroxyl group as well. | An important ligand of this protein is GOL (glycerol), which is the only ligand in this protein. GOL helps with stability of this protein. The catalytic amino acids of this protein include Ser^70, Ser^130, and Lys^73. Ser^70 interacts with the oxygen on the ampicillin, and it is also cross-linked with clavulanic acid. Ser^130 is also cross-linked with clavulanic acid and interacts with the ligand through hydrogen bonds. Lys^73 also interacts with the ligand through hydrogen bonds. This amino acid is used to lower the pka value of the hydroxyl group as well. | ||
+ | Another important amino acid includes Lys^234. This amino acid plays an important role in proton transfer during the catalysis of the antibiotics. | ||
+ | An active site residue of this protein that causes deacylation to occur is Glu^166. This residue activates a catalytic water molecule. e | ||
== Structural highlights == | == Structural highlights == |
Revision as of 20:22, 16 April 2021
CTX-M Beta-Lactamase
|
References
- ↑ Hanson, R. M., Prilusky, J., Renjian, Z., Nakane, T. and Sussman, J. L. (2013), JSmol and the Next-Generation Web-Based Representation of 3D Molecular Structure as Applied to Proteopedia. Isr. J. Chem., 53:207-216. doi:http://dx.doi.org/10.1002/ijch.201300024
- ↑ Herraez A. Biomolecules in the computer: Jmol to the rescue. Biochem Mol Biol Educ. 2006 Jul;34(4):255-61. doi: 10.1002/bmb.2006.494034042644. PMID:21638687 doi:10.1002/bmb.2006.494034042644