Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Yiyin Xia"'
Autor:
Yiyin Xia, Fupeng Li, Xiaohong Zhang, Seetharamsing Balamkundu, Fan Tang, Side Hu, Julien Lescar, James P. Tam, Chuan-Fa Liu
Enzymatic peptide ligation holds great promise in the study of protein functions and development of protein therapeutics. Owing to their high catalytic efficiency and a minimal tripeptide recognition motif, peptidyl asparaginyl ligases (PALs) are par
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2815ca7450ad5dfe57d54e2fdda4e7ad
https://hdl.handle.net/10356/169065
https://hdl.handle.net/10356/169065
Autor:
Side Hu, Seetharamsing Balamkundu, James P. Tam, Heng Tai Liew, Janet To, Xiaohong Zhang, Julien Lescar, Chuan-Fa Liu, Surajit Bhattacharjya, Ning-Yu Chan, Yiyin Xia
Publikováno v:
Angewandte Chemie. 133:22381-22385
Peptidyl asparaginyl ligases (PALs) are powerful tools for peptide macrocyclization. Herein, we report that a derivative of Asn, namely Nγ -hydroxyasparagine or Asn(OH), is an unnatural P1 substrate of PALs. By Asn(OH)-mediated cyclization, we prepa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af6b33c50224dba4f6e15de1b10b312a
https://doi.org/10.1002/ange.202108125
https://doi.org/10.1002/ange.202108125
Autor:
Yiyin, Xia, Janet, To, Ning-Yu, Chan, Side, Hu, Heng Tai, Liew, Seetharamsing, Balamkundu, Xiaohong, Zhang, Julien, Lescar, Surajit, Bhattacharjya, James P, Tam, Chuan-Fa, Liu
Publikováno v:
Angewandte Chemie (International ed. in English). 60(41)
Peptidyl asparaginyl ligases (PALs) are powerful tools for peptide macrocyclization. Herein, we report that a derivative of Asn, namely N
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c995c35b64af49d225a65cc4adc3d66c
https://pubmed.ncbi.nlm.nih.gov/34396662
https://pubmed.ncbi.nlm.nih.gov/34396662
Autor:
Valentin Paul Nicu, Wybren Jan Buma, Juana M. Pérez, Yiyin Xia, Syuzanna R. Harutyunyan, Mark A. J. Koenis, Juan F. Collados, Pablo Ortiz
Publikováno v:
European Journal of Organic Chemistry. 2018:3900-3903
The Brook rearrangement of simple, chiral tertiary benzylic -hydroxysilanes is presented. The rearrangement followed by proton trapping is enantiospecific and proceeds with inversion of the configuration at the carbon center. Importantly, the [1,2]-B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2399e2f472b75d3ce66906cceda3903
https://doi.org/10.1002/ejoc.201701469
https://doi.org/10.1002/ejoc.201701469
Autor:
Mark A. J. Koenis, Valentin P. Nicu, Wybren Jan Buma, Lucas Visscher, Sérgio R. Domingos, Yiyin Xia
Publikováno v:
Chemical Science, 10, 7680-7689
Chemical Science, 10(33), 7680-7689. Royal Society of Chemistry
Chemical Science, 10, 33, pp. 7680-7689
Koenis, M A J, Xia, Y, Domingos, S R, Visscher, L, Buma, W J & Nicu, V P 2019, ' Taming conformational heterogeneity in and with vibrational circular dichroism spectroscopy ', Chemical Science, vol. 10, no. 33, pp. 7680-7689 . https://doi.org/10.1039/c9sc02866h
Chemical Science
Chemical science 10, 7680-7689 (2019). doi:10.1039/C9SC02866H
Chemical Science, 10(33), 7680-7689. Royal Society of Chemistry
Chemical Science, 10, 33, pp. 7680-7689
Koenis, M A J, Xia, Y, Domingos, S R, Visscher, L, Buma, W J & Nicu, V P 2019, ' Taming conformational heterogeneity in and with vibrational circular dichroism spectroscopy ', Chemical Science, vol. 10, no. 33, pp. 7680-7689 . https://doi.org/10.1039/c9sc02866h
Chemical Science
Chemical science 10, 7680-7689 (2019). doi:10.1039/C9SC02866H
Chemical science 10, 7680 -7689 (2019). doi:10.1039/C9SC02866H
The flexibility of a molecule has important consequences on its function and application. Vibrational Circular Dichroism (VCD) is intrinsically an excellent experimental technique to
The flexibility of a molecule has important consequences on its function and application. Vibrational Circular Dichroism (VCD) is intrinsically an excellent experimental technique to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72c67d81530ab107146eba0c37d396d3
https://doi.org/10.1039/c9sc02866h
https://doi.org/10.1039/c9sc02866h