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However, if the T-20 peptides were too closely spaced, steric hindrance could conceivably inhibit their activity by preventing T-20 from binding to the deep hydrophobic pockets.
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Additionally, the substantial α2→3 sialylated glycan binding of Alb58 observed in the glycan array assay was also reflected in its binding to the human deep lung alveolar tissue (Figure 1B) that predominantly expresses these glycans [10], [21].
The in silico design of ligands binding to the protein surface instead of deep binding pockets is still a great challenge.
"It is binding to the upper respiratory tract rather than deep in the lungs," she said.
When the L protomer transitions to the T state, drugs translocate to a binding pocket deeper in the protein; low molecular-mass drugs, however, can apparently bind directly to the deep binding pocket in the T protomer without binding to the access pocket first (Nakashima et al., 2011).
QA ions are known to inhibit both Kv channels and Kir channels from the intracellular side by binding to a site deep within the pore just below the selectivity filter.
Thus, although containing no physically rotating parts, the periplasmic porter domain cycles through three sequential phases, (1) capturing a lipophilic substrate from the peripheral periplasm membrane interface, (2) transferring the substrate to the deep binding pocket, and (3) squeezing the substrate through the exit cleft into the central chamber.
This finding indicates that the covalent linking of the cRGDfK moiety does not affect the affinity of the HtBv compound to PSMA, as long as the urea-based scaffold is efficiently delivered to the deep PSMA binding site using a linker of suitable length.
The non-reducing end Man4 of oligomannose-3 (Figure 1) is attracted to the deep, monomannose-binding polar pocket (Figure 3A, red) through a hydrophobic tyrosine gate (Figure 3A, blue) to make previously well-defined interactions [47], [53].
In the L to T transition, substrate binding in the deep binding pocket of the porter domain causes a structural change within the PN2/PC1 unit.
The cloning and prokaryotic/bacterial protein expression of AAL-2 provided clues to the deep investigation of the glycan-binding mechanism of AAL-2 and further application of AAL-2 in probing GlcNAc-related glycans or glycoconjugates.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com