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Computational modelling was used to build into a solvent exposed pocket near the opening of the ATP binding site, which led to potent inhibitors of HSP90 (25 30).
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These metalloregulatory proteins, in principle, sense the intracellular levels of specific metal ions by binding them to a metal binding site, which leads to conformational changes affecting the regulator's ability to bind operator sites in regulatory DNA regions [ 7].
Biochemical studies have recently demonstrated that Bacillus subtilis PerR senses H2O2 by Fe2+-catalyzed oxidation of two histidines in its regulatory binding site, which leads to Fe2+ release and subsequent de-repression of PerR target genes [ 23].
Jiang et al. also demonstrated that, in macrophages, neither COX-2 protein or mRNA expression was affected by tocopherol treatment, leading to the speculation that RRR-γ-tocopherol may compete for the arachidonic acid binding site which leads to protein inhibition and reduced activity [ 13].
For example, several independent studies found that the actionable mutations in the EGFR gene could activate EGFR by altering the ATP binding site, which ultimately leads to an enhancement of drug response to gefitinib [ 24, 25].
The T-to-C substitution was initially hypothesized to create an Sp-1 binding site, which could lead to up-regulation of transcriptional activation of the variant allele and higher activity of the enzyme [ 8, 9], but this was not observed in experimental studies [ 10- 12].
Any binding site which had a p < 0.01 was annotated as a potential miRNA binding site.
Often, the base pairing occurs at the ribosome binding site (RBS), which leads to blockage of ribosome entry and thus to translation inhibition.
The amount of regulatory substrate, or ncDNA, is then a function of population size; and so, if binding site accumulation, which leads to regulatory complexity and organismal complexity, is a function of ncDNA, then it is also a function of population size.
Primer binding sites which contain polymorphic sites will lead to impaired or even absent PCR amplification of the mismatched alleles.
Subsequently, low-temperature carbonization (500 800 °C) and KOH activation leads to abundant ultrasmall pores and strong oxygen molecule binding sites, which are essential in enhancing the capacitance as well as ORR activity.
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