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Our analysis of 3413 protein structures having from 51 to 350 residues revealed that packing efficiency, indeed, is the same for proteins from different structural classes evidenced by the molecular volume per atom (for all-α proteins – 18.520±0.010 Å3, for all-β proteins −18.577±0.009 Å3, for α/β proteins −18.618±0.007 Å3, and for α+β proteins −18.598±0.009 Å3).
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Per molecular volume type, this effectively produced three different maps, one per quadrupole component (Qx, Qy, and Qz), of allowed values for the similarity metric, shape Tanimoto (ST) ≥ 0.8.
where μ∞ is the chemical potential of a flat surface, γ is the surface energy of SiC per unit area, and Ω is the molecular volume of SiC, and kT has the usual meaning of thermal energy.
Assuming a molecular volume of about 1 nm and a sputter yield of ∼50 to 100 molecules per primary impact, the 1.7 × 10 ions cm 2 dose is well beyond the static limit and almost all the molecules in a 1 μm × 10 nm surface volume will be removed.
Again, we discover molecular volume in the chapter on thermometry, and polarimetry in the chapter entitled "The Spectroscope "!
However, when a constant ST thresh value is used across a range of volumes, each increase in the molecular volume may result in a very rapid growth of the shape space, and hence, the number of reference shapes per volume.
Since changes in molecular volume were negligible, p∆V ≈ 0.
Molecular mobility and molecular volume increase from crystalline to amorphous to liquid forms.
Since the applied pressure changes the molecular volume, the inter-molecular interaction is changed.
The solvent accessible volume is larger than the molecular volume.
The CNS drugs tend to have less molecular flexibility, lighter molecular weights and less molecular volume.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com