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2002
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2005
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Molecular basis for the recognition and cleavages of IGF-II, TGF-alpha, and amylin by human insulin-degrading enzyme.
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The C-terminal domain of human insulin degrading enzyme is required for dimerization and substrate recognition.
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Molecular analysis of the interaction of anthrax adenylyl cyclase toxin, edema factor, with 2'(3')-O-(N-(methyl)anthraniloyl)-substituted purine and pyrimidine nucleotides.
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Mol Pharmacol
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Molecular analysis of the interaction of Bordetella pertussis adenylyl cyclase with fluorescent nucleotides.
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Structural and kinetic analyses of the interaction of anthrax adenylyl cyclase toxin with reaction products cAMP and pyrophosphate.
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Real-time analysis of ternary complex on particles: direct evidence for partial agonism at the agonist-receptor-G protein complex assembly step of signal transduction.
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A 1.3-A structure of zinc-bound N-terminal domain of calmodulin elucidates potential early ion-binding step.
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The amino terminus of varicella-zoster virus (VZV) glycoprotein E is required for binding to insulin-degrading enzyme, a VZV receptor.
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Insights from atomic-resolution X-ray structures of chemically synthesized HIV-1 protease in complex with inhibitors.
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Protein-protein docking and analysis reveal that two homologous bacterial adenylyl cyclase toxins interact with calmodulin differently.
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Structure of anthrax edema factor-calmodulin-adenosine 5'-(alpha,beta-methylene)-triphosphate complex reveals an alternative mode of ATP binding to the catalytic site.
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