Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Xinjian Ji"'
Autor:
Leixia Chu, Jinduo Cheng, Chengzeng Zhou, Tianlu Mo, Xinjian Ji, Taoting Zhu, Jie Chen, Suze Ma, Jiangtao Gao, Qi Zhang
Publikováno v:
ACS Chemical Biology. 17:3198-3206
Linaridins and lanthipeptides are two classes of natural products belonging to the ribosomally synthesized and posttranslationally modified peptide (RiPP) superfamily. Although these two RiPP classes share similar structural motifs such as dehydroami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::363ce2983b7499f12a202c70617f1cd0
https://doi.org/10.1021/acschembio.2c00657
https://doi.org/10.1021/acschembio.2c00657
Herein, we report a novel strategy for the modification of peptides based on the introduction of highly reactive hypervalent iodine reagents - ethynylbenziodoxolones (EBXs)- onto peptides. These peptide-EBXs can be easily accessed, both via solution
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2f5d3f2c65572f594aafc4e8d983ce2
https://doi.org/10.26434/chemrxiv-2023-jskfd
https://doi.org/10.26434/chemrxiv-2023-jskfd
Publikováno v:
Proceedings of the 4th International Conference on Economic Management and Model Engineering, ICEMME 2022, November 18-20, 2022, Nanjing, China.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8066490b08525828dd661752ba17b4c1
https://doi.org/10.4108/eai.18-11-2022.2326913
https://doi.org/10.4108/eai.18-11-2022.2326913
Autor:
Thomas A. Scott, Marjan Verest, Jakob Farnung, Clarissa C. Forneris, Serina L. Robinson, Xinjian Ji, Florian Hubrich, Clara Chepkirui, Daniel U. Richter, Stefanie Huber, Philipp Rust, Alena B. Streiff, Qi Zhang, Jeffrey W. Bode, Jörn Piel
Publikováno v:
Chem, 8 (10)
β-Amino residues are regarded as extremely rare features among ribosomal products. They can be installed by a remarkable non-canonical enzymatic splicing process occurring in some Nif11-type ribosomally synthesized and posttranslationally modified p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fddd4bd2c294c8e54a752eb14b923d0d
https://hdl.handle.net/20.500.11850/578198
https://hdl.handle.net/20.500.11850/578198
Publikováno v:
Chinese Journal of Chemistry. Jan2020, Vol. 38 Issue 1, p39-42. 4p.
Publikováno v:
Angewandte Chemie. 133:20110-20117
Aminomalonate (Ama) is a widespread structural motif in Nature, whereas its biosynthetic route is only partially understood. In this study, we show that a radical S-adenosylmethionine (rSAM) enzyme involved in cyclophane biosynthesis exhibits remarka
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcc887d56fdd68dafebfca2cff2d2f02
https://doi.org/10.1002/ange.202107192
https://doi.org/10.1002/ange.202107192
Publikováno v:
Chinese Journal of Chemistry. 39:2417-2421
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3938508befee442c0e6a61e083d6893f
https://doi.org/10.1002/cjoc.202100304
https://doi.org/10.1002/cjoc.202100304
Publikováno v:
Angewandte Chemie International Edition. 60:7570-7575
Arsenosugars are a group of arsenic-containing ribosides that are found predominantly in marine algae but also in terrestrial organisms. It has been proposed that arsenosugar biosynthesis involves a key intermediate 5'-deoxy-5'-dimethylarsinoyl-adeno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::488baaad998ba06ea3a71f167e2fcacc
https://doi.org/10.1002/anie.202015177
https://doi.org/10.1002/anie.202015177
Publikováno v:
Chinese Journal of Chemistry. 38:959-962
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2bf99ad98923a30211c701df90ad2485
https://doi.org/10.1002/cjoc.202000119
https://doi.org/10.1002/cjoc.202000119
Publikováno v:
Current Opinion in Chemical Biology. 55:86-95
The radical S-adenosylmethionine (SAM) superfamily enzymes reductively cleave SAM to produce a highly reactive 5'-deoxyadenosyl (dAdo) radical, which in most cases abstracts a hydrogen from the substrate and initiates highly diverse reactions. In rar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d57a91c2481590163c3689597bfc37dd
https://doi.org/10.1016/j.cbpa.2020.01.007
https://doi.org/10.1016/j.cbpa.2020.01.007