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Interestingly, the two internal IdoA residues of a heparin hexasaccharide bound to the basic fibroblast growth factor exist in different conformations (Faham et al. 1996).
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Yeast two hybrid and in vitro experiments indicate that Nkd directly binds to the basic-PDZ region of Dsh.
PDB code 1H8F was chosen as an initial starting structure since the small ligand HEPES (4- 2-hydroxyethyl -1-piperazineethanesulfonic acid), from the crystallization buffer, has a sulfonate ion bound to the Ser(p) basic binding pocket of Arg, Arg, and Lys with extensive hydrogen bonds.
During pregnancy, circulating PAPP-A is largely bound to the proform of Major Basic Protein (ProMBP) [ 30], which also forms a covalent complex with angiotensinogen [ 31].
The 2-OG binding is less well conserved, and the cofactor coordinates the iron in a bidentate manner via its 2-oxo group and one of its 1-carboxylate oxygens, whereas the 5-carboxylate is usually bound to the side-chain of a basic residue (Arg/Lys) and to a hydroxyl group from a Ser/Thr or Tyr residue.
Signatories of the Convention of the Right of the Child are duty bound to protect the basic human dignity of all children including the fundamental rights specific to the CRC.
Extracellular PPi directly binds to the surface of basic calcium phosphate hydroxyapatites and interferes with propagation of crystal formation, contributing to the formation of poorly ordered bone crystal structure [ 95, 96].
This article describes several strategies used to design peptides that bind to the basic region leucine zipper (bZIP) domain of the viral transcription factor BZLF1, which is encoded by the Epstein Barr virus.
The C-terminal domain (Dot1) harbors the catalytic activity and the acidic patch that binds to the basic patch on the tail of histone H4 [ 26, 27, 52].
As a constituent of myosin, radixin binds to the basic canalicular structure, whereas DPPIV/CD26 and Mrp2 represent functional bile canalicular proteins where loss of expression can occur, for example under conditions of inflammation.
This phase is selective for nucleosides thanks to the vicinal hydroxyl groups in their structure (during extraction the vicinal groups of nucleosides bind to the phenylboronic acid phase under basic conditions).
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