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All models of N excretion appeared to underestimate N excretion.
Because most ecosystems are N limited and plants can potentially access multiple forms of N in the environment, more information is needed on the generality of direct acquisition of amino acids by plants to fully assess current models of N cycling for a wider range of environments.
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We created a whole model of the human Sirt-1 by comparing modelling using as templates the previously obtained models of N-terminal, allosteric site, catalytic site and C-terminal site.
Two recently developed detailed kinetics models of n-butanol oxidation were used to simulate the experiments.
Ligand-based pharmacophore models of N-Aryl and N-Heteroaryl piperazine α1A-antagonists were developed using two separate training sets.
Discrepancies are noted and discussed, which are of direct relevance for further improvement of kinetic models of n-decane at conditions of elevated pressures and low-to-intermediate temperatures.
The technique that we use for the simulations is a combination of the configurational-bias Monte Carlo method (used for efficient generation of molecular models of n-alkane chains) and the dual control-volume grand-canonical MD method.
We define and investigate the main properties of the metric and nonlinear and connection structures and compute their torsions and curvatures and related almost Hermitian models of N-anholonomic manifolds.
Moreover, animal models of n-hexane exposure identified 2,5-hexanedione (2,5-HD) as a neurotoxic n-hexane metabolite [29], inducing deterioration in visual function [30].
The TIMP molecule was tilted towards the prime side of the active site, such that Phe of the TIMP was no longer in contact with the enzyme, as in the models of N-TIMP-3 docked into ADAMTS-4 and ADAMTS-5.
This set contains 185 N-terminal 25-mers, each of which has a glycine at position 2. The reason the set was limited to sequences with a glycine at position two is that all current models of N-myristoylation in plants, animals, and fungi stipulate that this residue is required for activity as a myristoylation substrate.
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