Sentence examples for binding proteins were deduced from inspiring English sources

General shared features with other nucleotide binding proteins were deduced from overall statistics on the available structure complexes at the Protein Data Bank and compared with the particularities of selected representative endoribonuclease families.

The number of theoretical E-box-binding sites likely to bind USF proteins was deduced based on the TYMS G>C genotype: one E-box for genotypes 2RC/3RC or 2RC/2RG, two E-boxes for genotypes 2RG/2RG or 2RG/3RC or 3RC/3RC or 2RC/3RG, three E-boxes for 2RG/3RG or 3RC/3RG, four E-boxes for 3RG/3RG or 2RG/4R or 3RC/4R and five E-boxes for 3RG/4R.

The full length sequence of Ae_10AL7886 was determined and domain organization of the predicted protein was deduced (Figure 3).

More precisely, the function of a protein is deduced, where such function was previously unknown.

The RBCS1-Ce (CaCe) protein was deduced from the unigene SGN-U607188 from C. arabica and was identical to that deduced from the CaRBCS1 cDNA and gene sequences.

The Sox2-TALE-TF binding sequences were deduced from the Sox2 effector binding domain, and used for construction of its dual reporter.

The resulting putative mRNA sequences were extended by in silico EST assembly and the encoded protein sequences were deduced.

Putative protein sequences were deduced from nucleotide sequences, analysed and compared.

The overall peptide binding preferences for the DR1201 allele were deduced by incubating these peptides in competition with the reference H1MP40 54 to determine the relative binding affinities of each to recombinant DR1201 protein.

Given that there are still relatively few proteins for which binding sites can be deduced from their corresponding structures, it is particularly interesting to be able to predict substrate binding sites and regions of interaction with other protein effectors.

Its putative lipopolysaccharide (LPS) binding domain was deduced to be important for its activities.