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In summary, we describe the intrahelical binding site of a highly potent, specific CXCR3 antagonist.
Ligand binding site of a fraction of integrin αIIbβ3 becomes activated on agonist induced platelet aggregates at stenosis.
To identify locations on the Rv3 oligosaccharide at which to incorporate D3-like branches, the Rv3 crystal structure19 was modeled into the binding site of a PGT128 crystal structure21 using the UCSF Chimera software package46.
The ability of a peptide to react specifically with the functional binding site of a complementary antibody is known as its antigenic reactivity or antigenicity.
Computational design of protein ligand interfaces finds optimal amino acid sequences within a small-molecule binding site of a protein for tight binding of a specific small molecule.
This review discusses the major methods and programs specifically developed for the purpose of designing combinatorial libraries under the constraint of the binding site of a biological target, with emphasis on their advantages and disadvantages.
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With the growing understanding of the molecular biology of protein tyrosine kinases and the use of structural information, the design of potential drugs directed towards the bind adenosine triphosphate (ATP -binding site of ATP -bindingget hasitecofe possible.
The metal-binding site of a Helicobacter pylori ATPase 439 (heliWT-tag) was successfully used as a new fusion peptide for immobilized metal ion affinity chromatography (IMAC).
The crystal lattice revealed an interaction between eight sequential residues in one iASPP molecule and the p53-binding site of a neighboring molecule.
Based on the crystal structure of human glutathione transferase M1-1, cysteine residues were introduced in the substrate-binding site of a Cys-free mutant of the enzyme, which were subsequently alkylated with 1-iodoalkanes.
This system, Light-Inducible Transcription using Engineered Zinc finger proteins (LITEZ), is based on the blue light-induced interaction of GIGANTEA and the LOV domain of FKF1 that drives the localization of a transcriptional activator to the DNA-binding site of a highly customizable engineered zinc finger protein.
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