Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Anissa Ouald Chaib"'
Autor:
Anissa Ouald Chaib, Alessandro Fracassi, Ankita Ray, Dominik Schauenburg, Nako Nakatsuka, Antonella Rossi, Jeffrey W. Bode, Matthias Tanriver, Simon Scherrer, Yoko Yamakoshi, Cristiana Passiu, Joydeb Mandal, Nicholas D. Spencer, Shivaprakash N. Ramakrishna
Publikováno v:
ACS Applied Materials & Interfaces. 13:29113-29121
The efficient and bioorthogonal chemical ligation reaction between potassium acyltrifluoroborates (KATs) and hydroxylamines (HAs) was used for the surface functionalization of a self-assembled monolayer (SAM) with biomolecules. An alkane thioether mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1529e2f401aa3f277c752ac118dfa1e
https://doi.org/10.1021/acsami.1c05652
https://doi.org/10.1021/acsami.1c05652
Autor:
Yakov Kipnis, Anissa Ouald Chaib, Anastassia A. Vorobieva, Guangyang Cai, Gabriella Reggiano, Benjamin Basanta, Eshan Kumar, Peer R.E. Mittl, Donald Hilvert, David Baker
Publikováno v:
Protein science : a publication of the Protein Society. 31(11)
While native scaffolds offer a large diversity of shapes and topologies for enzyme engineering, their often unpredictable behavior in response to sequence modification makes de novo generated scaffolds an exciting alternative. Here we explore the cus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::204fd9138c0e3c632eda3e39e3d8db2e
https://pubmed.ncbi.nlm.nih.gov/36305767
https://pubmed.ncbi.nlm.nih.gov/36305767
Publikováno v:
ACS Catal
Here we report a cytochrome P450 variant that catalyzes C(2)-amidation of 1-methylindoles with tosyl azide via nitrene transfer. Before evolutionary optimization the enzyme exhibited two undesired side reactivities resulting in reduction of the putat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ac3618c2d0cd61c6f0e3d98ac256b5a
https://pubmed.ncbi.nlm.nih.gov/31938573
https://pubmed.ncbi.nlm.nih.gov/31938573
Publikováno v:
Biochimica et Biophysica Acta (BBA) - General Subjects. 1860:1043-1055
Background Small molecules targeting the dimerization interface of the C-terminal domain of Hsp90, a validated target for cancer treatment, have yet to be identified. Methods Three peptides were designed with the aim to inhibit the dimerization of Hs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35bc3720888997600bfb8c3e84b29395
https://doi.org/10.1016/j.bbagen.2016.01.005
https://doi.org/10.1016/j.bbagen.2016.01.005