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To determine whether secondary TF-DNA binding modes are conserved, we compared secondary modes of binding between TFs in several structural families.
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In all cases where sufficiently high quality data existed for detection of weaker binding sites in both species, the secondary modes were conserved, indicating that TF specificity does not commonly evolve by loss or gain of secondary binding modes.
A comparison between eIF3a⋅eIF3c and Thp1⋅Sac3 shows that, although the overall interaction mode is conserved between these two PCI complexes, the relative positions of the WHDs differ by up to 6 Å between these two heterodimers.
Since the phosphate-binding mode is conserved in the HAD catalytic core domain we begin by covalently attaching a pentavalent, trigonal-bipyrimidal phosphate to the catalytic aspartate (Oδ P bond length = 1.9 ± 0.3Å; Cγ Oδ P angle = 120 ± 10°; Figure 1).
The measured binding affinities (Kd of 115 382 nM) and Δ H (−6.1 to −10.0 kcal/mol) compared well with those reported for unmodified JQ1 (literature values for BRD4 bromodomains shown in Figure 1c, entries 7, 8), suggesting that JQ1 binding mode is conserved within the context of our PROTACs.
We present the C. floridanus immunome using sequence-based protein orthology with the previously published data of D. melanogaster, A. mellifera and N. vitripennis assuming their functions and modes of action are conserved (Fig. 3).
(i) TargetScan database (30) is operated in two modes: (a) Sites that are conserved across most vertebrates and (b) site that are only conserved across mammals.
We observed a repeat cycle of cell deformation and cell protrusion formation at 105 160 min and 185 200 min (arrows), each followed by a spontaneous division generating progeny cells after 170 min and 205 min. It thus appears that the general features of the L-form mode of cell proliferation are conserved between Gram-positive and Gram-negative bacteria.
The guanylyltransferases and cap methyltransferases are conserved in structure and mode of action from yeast to metazoa, whereas the RNA triphosphatases are quite different in structure and mode of action in yeast and metazoa [ 1].
So by identifying God's conserving activity with his activity as creator ex nihilo, Malebranche appears to arguing that even in cases where the creatures are conserved, God is the unique cause of both their esse and modes.
The main residues are conserved.
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