Sandbox Reserved 1102
From Proteopedia
(Difference between revisions)
| Line 22: | Line 22: | ||
Helicase from Zika virus with a specific domain : a [https://en.wikipedia.org/wiki/Serine_protease serine protease]. It is a specific class of protein that hydrolysis peptide bonds from proteins. | Helicase from Zika virus with a specific domain : a [https://en.wikipedia.org/wiki/Serine_protease serine protease]. It is a specific class of protein that hydrolysis peptide bonds from proteins. | ||
| - | The helicase active site has a serine residue that serves as a nucleophilic amino acid. This residue is essential for the catalytic activity of the enzyme.The serine protases present a catalytic triad composed of 3 amino acids His57 Asp102 and Ser195.These 3 amino acids have a specific interaction which is due to the folding of the protein. The tridimentional conformation of the protein brings closer these 3 residues. Their side chains have a specific function : | + | The helicase active site has a serine residue that serves as a nucleophilic amino acid. This residue is essential for the catalytic activity of the enzyme.The serine protases present a catalytic triad composed of 3 amino acids His57 Asp102 and Ser195<ref>Enrico Di Cera, Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine, Box 8231, St. Louis, MO, USA; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2675663/</ref>.These 3 amino acids have a specific interaction which is due to the folding of the protein. The tridimentional conformation of the protein brings closer these 3 residues. Their side chains have a specific function : |
[[Image:Serine protease catalysis.png | thumb | upright=3 | Serine protease catalysis]] | [[Image:Serine protease catalysis.png | thumb | upright=3 | Serine protease catalysis]] | ||
'''Ser195''': the hydroxyl group plays the role of a nucleophile that attack the substrate. | '''Ser195''': the hydroxyl group plays the role of a nucleophile that attack the substrate. | ||
| Line 54: | Line 54: | ||
== Relevance == | == Relevance == | ||
| - | There are still no vaccines against Zika virus but the study of zika helicase is one of the most promising area for scientific research. It is an enzyme essential for the virulence of Zika virus and blocking its activity may be a means to struggle against this virus. The development of inhibitors targeting the viral helicase is becoming more and more studied by researchers. | + | There are still no vaccines against Zika virus but the study of zika helicase is one of the most promising area for scientific research. It is an enzyme essential for the virulence of Zika virus and blocking its activity may be a means to struggle against this virus.<ref>Xu S, Ci Y, Wang, Yang, Zhang L, Xu C, Qin C, Shi L. Zika virus NS3 is a canonical RNA helicase stimulated by NS5 RNA polymerase.Nucleic Acids Res. 2019 Sep 19;47(16):8693-8707. doi: 10.1093/nar/gkz650.https://www.ncbi.nlm.nih.gov/pubmed/31361901</ref> The development of inhibitors targeting the viral helicase is becoming more and more studied by researchers. |
== References == | == References == | ||
<references/> | <references/> | ||
Revision as of 01:42, 16 January 2020
| This Sandbox is Reserved from 25/11/2019, through 30/9/2020 for use in the course "Structural Biology" taught by Bruno Kieffer at the University of Strasbourg, ESBS. This reservation includes Sandbox Reserved 1091 through Sandbox Reserved 1115. |
To get started:
More help: Help:Editing |
5y6n- Zika virus helicase in complex with ADP
5y6n is a 1 chain protein structure. It’s the only helicase that belongs to zika virus. Zika helicase plays an important role in the pathogenocity of this virus.
| |||||||||||

