Sentence examples for potentially bind to from inspiring English sources

Exact(52)

Our examination revealed that a novel scaffold (5) in Figure 1C might potentially bind to CDK2 with high affinity (Estimated binding free energy ΔG∼8.6 kcal/mol).

Our modeling results show that these urea-sulfonamides potentially bind to the intramolecular ammonia tunnel, which transports ammonia from the glutaminase domain to the active site of the enzyme.

AQPs possess six α-helical TM (TM1 TM6) domains that are tilted along the plane of PM and linked one to the other by five connecting loops (LA LE 21,29, LB, LD, and both N-terminal and C-terminal regions locate inside the cell and potentially bind to cytosolic substrates51,69.

To test the hypothesis, we searched human proteins database and found a number of candidates (including UHRF1, histone H3, histone H2A) contain such consensus motif and potentially bind to TUDUSP7 (Fig. 2B).

To determine if PZ-34 and PZ-38 potentially bind to ABCG2, we performed staining analyses of ABCG2 using 5D3 in the presence or absence of PZ-34 and PZ-38.

Only probes 102 and 110(14) potentially bind to J11/12, however, and both may bind elsewhere (Table 2).

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Similar(8)

Furthermore when vitamin D3 is produced in the skin 100% of it is potentially bound to the vitamin D binding protein (Fig. 17).

GLM potentially binds to ATP-sensitive potassium channel receptors on the pancreatic beta cell surface, dropping potassium conductance across the membrane and causing depolarization of the membrane which stimulates calcium ion influx through voltage-sensitive calcium channels.

In the homozygote, enhanced expression of both PEG11 and PEG11as would occur through the cis-mediated action of the mutation; however their ratio may not significantly alter thereby resulting in little change in the level of PEG11 that is not potentially bound to miRNA derived from PEG11as.

This suggested that the selected candidates potentially bound to common antigens expressed in multiple strains of E. coli [ 42].

Through structure-function analysis, we propose that kinesin-1 potentially binds to MTs with its C-terminal tail domain and slides anti-parallel MTs against each other.

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