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DOI: http://dx.doi.org/10.7554/eLife.04387.008 The selectivity for Na+ ions in vertebrate Nav channels is attributed to an asymmetric ring of 4 amino acids (Asp, Glu, Lys, and Ala: DEKA) contributed by each of the pore-lining loops of the 4 domains (Catterall, 2012).
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The spectral feature at 1170 cm−1 can be attributed to an ester C-O asymmetric stretch [ 13].
The 1H NMR spectra of the PHAs extracted from Bacillus sp. NA10 shows a doublet at 1.26 ppm which is attributed to the methyl group coupled to one proton, a doublet of quadruplet at 2.580 ppm which is attributed to a methylene group adjacent to an asymmetric carbon atom bearing a single proton, and a multiplet at 5.25 ppm characteristic of the methyne group.
The asymmetric behavior is attributed to a thin, passivating film of Na2O at the interface between beta″-alumina and liquid sodium.
We further assessed asymmetric evolution in the annotated protein domains and found that a large fraction of the asymmetry detected at the whole protein level can be attributed to a specific domain.
The absorption at 1550 cm−1 is attributed to the asymmetric stretch of a nitro group attached to a tertiary carbon.
This suggests that the asymmetry in the rate of evolution of gene duplicates can be largely attributed to the asymmetric evolution of a specific protein domain.
The low energetic asymmetric d d band in curve (a) can be attributed to the asymmetric, quasi-octahedral T 1g→T 1g(P) transition of the Co(H2O) 6 2+ aquo-ion.
The wind-induced motion of modern tall buildings is generally found to involve with significant coupled lateral and torsional effects, which are attributed to the asymmetric three-dimensional (3D) mode shapes of these buildings.
This absorption band can be attributed to the asymmetric vibrations of –CH2 bonds.
The maximum absorption recorded at 1,095.37, 1,064.51 and 985.447 cm−1 was attributed to the asymmetric stretching of Si O (Fig. 2).
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