H-TSAVLQSGFRK-NH2

Ref. 3D-PP46750

Produktinformation

• Name: H-TSAVLQSGFRK-NH2
• Synonyme: NH2-Thr-Ser-Ala-Val-Leu-Gln-Ser-Gly-Phe-Arg-Lys-amide

Beschreibung

Peptide H-TSAVLQSGFRK-NH2 is a Research Peptide with significant interest within the field academic and medical research. This peptide is available for purchase at Cymit Quimica in multiple sizes and with a specification of your choice. Recent citations using H-TSAVLQSGFRK-NH2 include the following: Virtual screening of novel noncovalent inhibitors for SARS-CoV 3C-like proteinase Z Liu, C Huang, K Fan, P Wei , H Chen - Journal of chemical , 2005 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/ci049809b Molecular mechanisms of SARS-CoV-2 resistance to nirmatrelvir Y Duan, H Zhou, X Liu, S Iketani , M Lin, X Zhang - Nature, 2023 - nature.comhttps://www.nature.com/articles/s41586-023-06609-0 Structures of two coronavirus main proteases: implications for substrate binding and antiviral drug design X Xue , H Yu, H Yang, F Xue, Z Wu, W Shen , J Li - Journal of , 2008 - Am Soc Microbiolhttps://journals.asm.org/doi/abs/10.1128/JVI.02114-07 Production of authentic SARS-CoV Mpro with enhanced activity: application as a novel tag-cleavage endopeptidase for protein overproduction X Xue , H Yang, W Shen , Q Zhao , J Li , K Yang - Journal of molecular , 2007 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0022283606016329 Severe acute respiratory syndrome coronavirus 3C-like proteinase N terminus is indispensable for proteolytic activity but not for enzyme dimerization: biochemical and S Chen, L Chen, J Tan, J Chen, L Du , T Sun - Journal of Biological , 2005 - ASBMBhttps://www.jbc.org/article/S0021-9258(20)76576-2/abstract Interaction of 8-anilinonaphthalene-1-sulfonate with SARS-CoV-2 main protease and its application as a fluorescent probe for inhibitor identification P Deetanya, K Hengphasatporn , P Wilasluck - Computational and , 2021 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S2001037021002415 Structures of Two Coronavirus Main ML Zhang, M Bartlam , Z Rao, W Shen, J Li, Z Zhou - J. Virol, 2008 - Citeseerhttps://citeseerx.ist.psu.edu/document?repid=rep1&type=pdf&doi=6cc23c00a217bc6d21a3f0009ae9eebe6d00fa4e Promising SARS-CoV-2 main protease inhibitor ligand-binding modes evaluated using LB-PaCS-MD/FMO K Hengphasatporn , R Harada , P Wilasluck - Scientific Reports, 2022 - nature.comhttps://www.nature.com/articles/s41598-022-22703-1 Viral proteases: Structure, mechanism and inhibition J Zephyr , NK Yilmaz, CA Schiffer - The Enzymes, 2021 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S1874604721000214 A proteomics-MM/PBSA dual approach for the analysis of SARS-CoV-2 main protease substrate peptide specificity G Gallo, U Barcick , C Coelho, M Salardani - Peptides, 2022 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0196978122000808 Characterization of SARS main protease and inhibitor assay using a fluorogenic substrate CJ Kuo, YH Chi , JTA Hsu, PH Liang - Biochemical and biophysical , 2004 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0006291X04008526 Crystal-structures-guided design of fragment-based drugs for inhibiting the main protease of SARS-CoV-2 B Luan , T Huynh - Proteins: Structure, Function, and , 2022 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/prot.26260 A genetically encoded BRET-based SARS-CoV-2 Mpro protease activity sensor AM Geethakumari , WS Ahmed , S Rasool - Communications , 2022 - nature.comhttps://www.nature.com/articles/s42004-022-00731-2

• Marke: Biosynth