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Intriguingly, as shown in Figure 7A, the peak position of inactive Av1 shifted to an earlier elution time, relative to the position observed for native Av1 or for Av1 incubated at pH 9.5 in the absence of turnover components.
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The journalists and others on the plane started to drop into sleep, leaving Shakira in the unaccustomed position of being inactive.
The first ensemble of the conformations is characterized by the broken Y2195.58 Y3267.53 hydrogen bond, the second ensemble has, in addition, F2826.44 at the position of the inactive state, and the third ensemble has the fully inward position of helix 6.
c Rotation of TM6 shown by the position of Lys618 in the inactive and active states.
The biphasic behavior strongly suggests a mechanism in which the low occupancy binding of N-terminal domains of cMyBP-C activates the thin filaments by a mechanism similar to the activation of the thin filament by rigor S1 heads and NEM-S1, which shifts the position of tropomyosin from the inactive to active position at low ratios of S1 to actin.
The shift in elution position indicates that the hydrodynamic radius of inactive Av1 has increased relative to that of native Av1.
Notably, charged substitutions at the buried positions resulted in a higher fraction of inactive variants (type "×"; 41%) than the other three types and polar substitutions predominantly reduced activity (type "−"; 32 41% for all three organic solvents) of BSLA.
Compound 11, which differs from the highly active compound 3 only in the position of the heterocyclic nitrogen, was inactive as revealed by in vitro kinase assays.
Comprehensive and elegant experimentation revealed substantial differences in the relative positions of the PH and kinase domains of inactive and membrane-associated AKT [12], [13], [14], [15], [16], resulting in the inactive form being termed the closed or 'PH-in' conformation; whereas the membrane-associated form is referred to as the open or 'PH-out' conformation.
On the contrary, modifications at 2′-OH position of araC and araG, have provided inactive derivatives against TK2 and dGK, respectively.
Both α1 and α2 are catalytic subunits, but the α1 alone is sufficient to catalyze the removal of the acetyl moiety at the sn-2 position of PAF to generate the biologically inactive lyso-PAF [17].
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CEO of Professional Science Editing for Scientists @ prosciediting.com