Exact(9)
Z33, a 33 amino acid peptide sequence derived from Protein A, is a minimized binding domain with comparable interaction potential.
The pi pi stacking interaction with Tyr1230 appears important for MET inhibition, but no comparable interaction is seen in the ALK structure.
The reversible competitive and covalent active site-directed (Conduritol B epoxide, CBE) inhibitors of GCase showed comparable interaction with both enzymes [34], [35], [36] (Table 2).
Therefore, in a full trial, comparable interaction of the subjects with the instructor is desirable.
A comparable interaction is observed in our structure of PepTSt between Asn328 (H8) and Glu400 (H10).
A minimal 16-mer without the proline cluster produces a comparable interaction, showing that this cluster is dispensable in this binding assay.
Similar(50)
The results suggest that both molecules have comparable interactions and better docking scores.
The results suggest that both the molecules have comparable interactions and better docking scores.
The results obtained reveals that both the molecules have comparable interactions and better docking scores.
A comparison of the circular-dichroism and fluorescence spectra of the purified chimera and the SH3 circular permutant showed that the proline-rich sequence occupies the putative SH3 binding site in a similar conformation and with comparable interactions to those found in complexes between SH3 and proline-rich peptides.
Comparable interactions between genes and cis-regulatory elements have been demonstrated for several other gene loci (e.g.[9], [10]).
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