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Binding of hEBV321 to VEGF-G88A resembled its binding to the wild type VEGF, but binding of Bevacizumab to VEGF-G88A was substantially reduced as compared to hEBV321 (Figure 3D).
In comparing to proteins binding to the wild type eIF5B, several proteins were found to preferentially bind to eIF5B-S214E mutant, but not eIF5B-S214A mutast as displayed in Fig. 2C.
Here we used structural and biophysical approaches to characterize genistein binding to the wild type (TTRwt) and to its most frequent amyloidogenic variant, the V30M mutant.
Furthermore, we could also identify potential allosteric movements caused by genistein binding to the wild type TTR that explains, at least in part, the frequently observed negatively cooperative process between the two sites of TTRwt when binding ligands.
In vitro affinity measurements of Hfq for RydC show similar binding to the wild type.
We found that K2 > K1/4, which implies that putrescine binding to the wild type AdoMetDC protein has positive cooperativity.
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GCs exert their effects by binding to the wild-type GR, GRα.
Combined with mutation analysis and molecular dynamics simulations with apelin-13 binding to the wild-type APJR, this structure provides a mechanistic understanding of apelin recognition and binding specificity.
Additionally, a non-extendable primer with more mismatches to the mutant allele than to the wild-type allele (blocker primer, BP) competes with the MSP for binding to the wild-type allele, thereby reducing background amplification from the wild-type allele.
Rapamycin and analogs promoted FKBP12 binding to the wild-type Tor1 kinase but not to a rapamycin-resistant Tor1 mutant kinase (S1972R).
Among the six mutations tested, five of them reduced the binding of -crebanine (1) by more than 40% relative to binding to the wild-type receptor, displaying the importance of hydrophobic interactions.
More suggestions(16)
binding to the N-domain
binding to the anti-BL
binding to the upper
binding to the bacterial
binding to the AMP-lid
binding to the imprinted
binding to the degenerate
binding to the Smad
binding to the wild-type
binding to the cellular
binding to the extracellular
binding to the 16-base
binding to the hydroxyapatite
binding to the human
binding to the nucleobase
binding to the urinary
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