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Solution structure of the chimera of the C-terminal tail peptide of APP and the C-terminal PID domain of Fe65L[PROTEIN BINDING]
View in iCn3D Similar StructuresPubMedProteinsConserved Domains
Solution structure of the chimera of the C-terminal PID domain of Fe65L and the C-terminal tail peptide of APP[PROTEIN BINDING]
Crystal structure of the human Fe65-PTB1 domain with bound phosphate (trigonal crystal form)[PROTEIN BINDING]
View in iCn3D Similar StructuresPubMedProteinsConserved DomainsPubChem Compound
Crystal structure of the human Fe65-PTB1 domain (trigonal crystal form)[PROTEIN BINDING]
Crystal structure of the human Fe65-PTB1 domain[PROTEIN BINDING]
Crystal structure of the intracellular domain of human APP (T668A mutant) in complex with Fe65-PTB2[PROTEIN BINDING]
Crystal structure of the intracellular domain of human APP (T668E mutant) in complex with Fe65-PTB2[PROTEIN BINDING]
Crystal structure of the intracellular domain of human APP in complex with Fe65-PTB2[PROTEIN BINDING]
Crystal Structure of the C-terminal Phophotyrosine Interaction Domain of Human APBB3[PROTEIN BINDING]
View in iCn3D Similar StructuresProteinsConserved Domains
Solution structure of Fe65 WW domain[PROTEIN BINDING]
Solution structure of the WW domain from the human amyloid beta A4 precursor protein-binding family B member 3, APBB3[PROTEIN BINDING]
Human NUMB-like protein, phosphotyrosine interaction domain[SIGNALING PROTEIN]
View in iCn3D Similar StructuresProteinsConserved DomainsPubChem Compound
DISCOVERY OF CELL-ACTIVE PHENYL-IMIDAZOLE PIN1 INHIBITORS BY STRUCTURE-GUIDED FRAGMENT EVOLUTION[ISOMERASE]
Structure-guided design of alpha-amino acid-derived Pin1 inhibitors[ISOMERASE]
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