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Protein-protein complexes show good complementarity in surface shape and polarity and are stabilized largely by weak interactions, such as burial of hydrophobic surface, hydrogen bonds, and van der Waals forces.
This favorable result may be due to several factors such as: the high content of secondary structures; the good complementarity of the partners and the significant decrease of exposed aminoacids in the complex state; and/or to the MD-SA step used to refine PECr which brings the system into a deep local minimum of the energy function.
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Several compounds showed stronger HSA binding than can be expected from their lipophilicity alone, and comparison between predicted and experimental binding affinity allows the identification of compounds that have good complementarities with any of the known binding sites.
This illustrates that the predictions based on different complex detection algorithms have good complementarities.
Large positive FTDOCK scores denote complex formation with good surface complementarity, a score of zero indicates that the molecules do not interact at all and the score is negative if the smaller molecule significantly overlaps with the larger one.
This simplified energy function yields docked structures that have good shape complementarity, but have no favorable electrostatic or chemical interactions.
ClusPro [ 19] develops a fast algorithm for filtering docked conformations with good surface complementarity, and ranks them based on their properties.
16 In general there was good shape complementarity between the ligand and the active site; however, visual inspection of the adjoining areas indicated that it might be possible to modify the ligand to improve both specificity and efficacy.
This simplified energy function yields docked structures that have good shape complementarity, but have no favorable electrostatic or chemical interactions (fourth paragraph of the Results section entitled "PRE experiments and theoretical PRE profiles based on structure").
The SH3 rotation results in a polar interface between SH3 and PH-TH, with good electrostatic complementarity, which preserves the interactions between the SH3 domain, the linker and the N lobe of the kinase.
In the crystal structure presented here, the good precomplex complementarity between the shape of the channel entryway and the shape of the toxin (i.e., the absence of channel structural change upon toxin binding) suggests a possible explanation for two prominent features of pore-blocking toxins.
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