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Specific inhibitors that bind to the interface of DNA-Top complexes can stabilize Top-mediated transient DNA breaks.
While most modulators can only bind to one position with a one modulator per dimer ratio, some thiazide-based modulators can bind to the interface in two symmetrical positions with a two modulator per dimer ratio.
Several reports (Kuhn et al. 2013; Wang, Thijssen, et al. 2013) have proposed that pharmacological treatment is necessary to restore the function of the perturbed network as drugs often bind to the interface of the disease-associated proteins.
Importantly, on the basis of related SF2 helicases, ATP was shown to bind to the interface of the RecA-fold subdomains and stabilize a 'closed' state (Sengoku et al., 2006).
Overall, our results from the present study show that the dimer interface should be considered a potential target for cancer treatment, where the identification of small molecules that bind to the interface of procaspase-3, resulting in its activation, may be a viable alternative to current therapies.
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Therefore, if the Gibbs energy of the peptide bound to the interface decreases when binding improves, we would expect the transfer to the bilayer interior from the interface to become more unfavorable, which would slow down translocation and efflux.
The proposed inhibition mechanism is represented that EBR28 binds to the interface of IN1 to form the IN1_EBR28 complex and preventes the formation of IN dimmer, finally leads to the partial loss of binding potency for IN with viral DNA.
One c-di-GMP binds to the interface of STING dimer with a unique mode.
where depending on the model, is either a bulk penetration depth of states bound to the interface at z = z 0 or a thickness of the interface, see [24].
Traditional plasmonic materials usable in visible/near infrared range, noble metals, are unsuitable for uses in the THz regime due to low confinement to the metal; the wave is weakly bound to the interface, a phenomenon sometimes called the Zenneck plasmon [7].
STA-21 is a small molecule inhibitor of Stat3 identified through virtual ligand screening of compounds that bound to the interface of Stat3 Shomodimersers [17].
More suggestions(18)
bind to the surface
bind to the biotin
bind to the peptide
bind to the promoter
bind to the end
bind to the androgen
bind to the tyrosinase
bind to the active-site
bind to the target
bind to the bone
bind to the invading
bind to the repeat
bind to the serotonin
bind to the AhR
bind to the protein
bind to the enzyme
bind to the interspace
bind to the glucocorticoid
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