Exact(3)
The different complexation mode in the 2Ca2+ 3TIG versus 1Ca2+ 3MIN complex is attributed to the N-t-butylglycylamido group, which is unique to TIG, participating in Ca2+ coordination along with the β-ketoenol moiety common to all three antibiotics.
The lack of such polar interactions in Bad peptide complex is attributed to specific basic residues present before and after the highly conserved Leu residue.
Traditionally, the creation of the Alchi complex is attributed to the famous scholar-translator Rinchen Zangpo (958 1055) in the 10th century, along with the Lamayuru Monastery, the Wanla, the Mang-gyu and the Sumda.
Similar(57)
The low residual signal observed in the presence of fully formed complex was attributed to the free ligand produced by the complex dissociation, having a kinetic constant estimated 0.2 s−1.
Previous publications have demonstrated ubiquitination activity of Ring1A [32], [32] however this activity was very weak and the main ubiquitination activity of the PRC1 complex was attributed to Ring1B.
The predominant species generated in solution (below the m/z values of the intact complex) are attributed to losses of Sm-B/B', U1-C and U1-A.
The preference of MIN and TIG for higher order complexes is attributed to their stronger affinity for Ca2+ and more lipophilic nature.
The driving force for the adsorption of formation of the metal complexes is attributed to the entropic gain associated with the disruption of a highly ordered hydrogen-bonding network of hydrating water molecules; the interplay of electrostatic forces (hard base/hard acid interactions) and complex specific ion/surface interactions [38].
The greater robustness at high P of the HSPC (C16(15%),C18 85%)) complexes relative to the DMPC ((C14 2) or POPC (C16, C18 1) complexes is attributed to the stronger van der Waals attraction between the HSPC acyl tails, relative to the shorter or un-saturated tails of the other two lipids.
The ability of FHL2 to assemble multiple partners into protein complexes is attributed to its LIM-domain structure that serves as protein binding interface through double zinc finger motifs [17].
The choice of ternary complexes was attributed to two considerations.
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