Deciphering the Fluorine Code The Many Hats Fluorine Wears in a Protein Environment
AA Berger, JS Völler, N Budisa… - Accounts of chemical …, 2017 - ACS Publications
Conspectus Deciphering the fluorine code is how we describe not only the focus of this
Account, but also the systematic approach to studying the impact of fluorine's incorporation …
Account, but also the systematic approach to studying the impact of fluorine's incorporation …
Perfluorocarbons in chemical biology
MA Miller, EM Sletten - ChemBioChem, 2020 - Wiley Online Library
Perfluorocarbons, saturated carbon chains in which all the hydrogen atoms are replaced
with fluorine, form a separate phase from both organic and aqueous solutions. Though …
with fluorine, form a separate phase from both organic and aqueous solutions. Though …
Asymmetric synthesis of tailor-made amino acids using chiral Ni (II) complexes of Schiff bases. An update of the recent literature
Y Zou, J Han, AS Saghyan, AF Mkrtchyan, H Konno… - Molecules, 2020 - mdpi.com
Tailor-made amino acids are indispensable structural components of modern medicinal
chemistry and drug design. Consequently, stereo-controlled preparation of amino acids is …
chemistry and drug design. Consequently, stereo-controlled preparation of amino acids is …
The alanine world model for the development of the amino acid repertoire in protein biosynthesis
V Kubyshkin, N Budisa - International journal of molecular sciences, 2019 - mdpi.com
A central question in the evolution of the modern translation machinery is the origin and
chemical ethology of the amino acids prescribed by the genetic code. The RNA World …
chemical ethology of the amino acids prescribed by the genetic code. The RNA World …
Cu-catalysed three-component C–H trifluoroalkylation of glycine derivatives: access to diverse CF 3-containing amino acids
Y Li, D Lu, Y Gong - Organic Chemistry Frontiers, 2023 - pubs.rsc.org
A Cu-catalysed method that selectively incorporates a trifluoromethyl group and an alkene
moiety onto the α carbon of glycine derivatives has been developed using commercialized …
moiety onto the α carbon of glycine derivatives has been developed using commercialized …
Expanding the DOPA universe with genetically encoded, mussel‐inspired bioadhesives for material Sciences and medicine
N Budisa, T Schneider - ChemBioChem, 2019 - Wiley Online Library
Catechols are a biologically relevant group of aromatic diols that have attracted much
attention as mediators of adhesion of “bio‐glue” proteins in mussels of the genus Mytilus …
attention as mediators of adhesion of “bio‐glue” proteins in mussels of the genus Mytilus …
Non‐canonical Amino Acid Substrates of E. coli Aminoacyl‐tRNA Synthetases
MCT Hartman - ChemBioChem, 2022 - Wiley Online Library
In this comprehensive review, I focus on the twenty E. coli aminoacyl‐tRNA synthetases and
their ability to charge non‐canonical amino acids (ncAAs) onto tRNAs. The promiscuity of …
their ability to charge non‐canonical amino acids (ncAAs) onto tRNAs. The promiscuity of …
Engineering aminoacyl-tRNA synthetases for use in synthetic biology
Within the broad field of synthetic biology, genetic code expansion (GCE) techniques enable
creation of proteins with an expanded set of amino acids. This may be invaluable for …
creation of proteins with an expanded set of amino acids. This may be invaluable for …
Unexpected trends in the hydrophobicity of fluorinated amino acids reflect competing changes in polarity and conformation
Fluorination can dramatically improve the thermal and proteolytic stability of proteins and
their enzymatic activity. Key to the impact of fluorination on protein properties is the …
their enzymatic activity. Key to the impact of fluorination on protein properties is the …
Practical Method for Preparation of (S)-2-Amino-5,5,5-trifluoropentanoic Acid via Dynamic Kinetic Resolution
Practical Method for Preparation of (S)-2-Amino-5,5,5-trifluoropentanoic Acid via Dynamic
Kinetic Resolution | ACS Omega ACS ACS Publications C&EN CAS Find my institution Log In …
Kinetic Resolution | ACS Omega ACS ACS Publications C&EN CAS Find my institution Log In …