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Two sterol binding proteins were studied as well (PDB IDs: 1ZHY and 2A1B).
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Herein, the Zn2+-induced folding kinetics of a small zinc-binding protein are studied; the CH11 peptide is derived from the first cysteine/histidine-rich region (CH1 domain) of the protein interaction domains of the transcriptional coregulator CREB-binding protein.
The gene expression of insulin-like growth factor 1, insulin-like growth factor type 1 receptor and insulin-like growth factor binding proteins were also studied.
Our approach also showed some false negatives because some known methylated DNA binding proteins were not identified in this study (Mann et al., 2013; Spruijt et al., 2013).
Interestingly, calcium ion binding proteins were previously identified in another proteomic study that compared HCV-induced HCC with cirrhosis [43].
In our study, GTP binding proteins were found to be the major class of nucleotide binding proteins in susceptible as well as resistant genotypes.
Calb3 (Calbindin 3), a vitamin D-dependent Ca2+ binding protein, was previously studied in the intestine, uterus, placenta, and lung epithelium [ 23].
In addition, the plasmatic protein binding properties were studied both by experimental and theoretical techniques.
The expression of these genes, together with that of JH esterase and JH binding proteins, is consistent with previous studies implicating tight control of JH during embryogenesis [ 63].
The quantity of protein loading and the binding time were studied over 3.5 h (data not shown).
The resulting mutant proteins were purified, and their binding affinities were studied by surface plasmon resonance.
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